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Neuroinflammation and cognition across psychiatric conditions

Published online by Cambridge University Press:  04 February 2019

Célia Fourrier Open the ORCID record for Célia Fourrier [Opens in a new window] ,
Gaurav Singhal  and
Bernhard T. Baune
Célia Fourrier
Affiliation:
Discipline of Psychiatry, University of Adelaide, Adelaide, Australia
Gaurav Singhal
Affiliation:
Discipline of Psychiatry, University of Adelaide, Adelaide, Australia
Bernhard T. Baune*
Affiliation:
Department of Psychiatry, Melbourne Medical School, The University of Melbourne, Melbourne, Australia
*
*Address for correspondence: Prof. Bernhard T. Baune, MD, PhD, FRANZCP, Department of Psychiatry and Psychotherapy, University Hospital Münster, University of Münster, Münster, Germany (Email: bernhard.baune@me.com)
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Abstract

Cognitive impairments reported across psychiatric conditions (ie, major depressive disorder, bipolar disorder, schizophrenia, and posttraumatic stress disorder) strongly impair the quality of life of patients and the recovery of those conditions. There is therefore a great need for consideration for cognitive dysfunction in the management of psychiatric disorders. The redundant pattern of cognitive impairments across such conditions suggests possible shared mechanisms potentially leading to their development. Here, we review for the first time the possible role of inflammation in cognitive dysfunctions across psychiatric disorders. Raised inflammatory processes (microglia activation and elevated cytokine levels) across diagnoses could therefore disrupt neurobiological mechanisms regulating cognition, including Hebbian and homeostatic plasticity, neurogenesis, neurotrophic factor, the HPA axis, and the kynurenine pathway. This redundant association between elevated inflammation and cognitive alterations across psychiatric disorders hence suggests that a cross-disorder approach using pharmacological and nonpharmacological (ie, physical activity and nutrition) anti-inflammatory/immunomodulatory strategies should be considered in the management of cognition in psychiatry.

Keywords

Cognitioncognitive dysfunctioncross-diagnoses approachinflammationpsychiatric disorders

Information

Type
Review
Information
CNS Spectrums , Volume 24 , Issue 1 , February 2019 , pp. 4 - 15
Copyright
© Cambridge University Press 2019 

Introduction

Cognition has been described as “a suite of interrelated conscious (and unconscious) mental activities, including: pre-attentional sensory gating; attention; learning and memory; problem solving, planning, reasoning and judgment; understanding, knowing and representing; creativity, intuition and insight; ‘spontaneous’ thought; introspection; as well as mental time travel, self-awareness and meta-cognition (thinking and knowledge about cognition).”Reference Millan, Agid and Brune 1 The range of cognitive impairments reported in psychiatric disorders is wide and redundant across conditions.Reference Millan, Agid and Brune 1 These alterations do not only aggravate the course of the disorders but also strongly compromise patients’ quality of life and recovery. For example, cognitive symptoms (eg, working memory impairments) in bipolar disorder (BD) or schizophrenia (SCZ) predict the development and the severity of psychotic symptoms, suggesting that they may participate in the development of the diseases.Reference Jenkins, Bodapati, Sharma and Rosen 2 In addition, symptom severity (ie, intrusive thoughts, nightmares, and flashbacks) in patients with posttraumatic stress disorder (PTSD) is significantly correlated with impairments in attention, learning, memory, executive function, and visuospatial attention.Reference Qureshi, Long and Bradshaw 3 Cognitive deficits in attention, verbal learning, and verbal memory predict poorer general and psychosocial functioning in BD patients and impair recovery in later stages of the disease.Reference Baune, Li and Beblo 4 , Reference Andreou and Bozikas 5 They also negatively affect employment status and occupational functioning in adults with mood disorders or SCZ.Reference Baune, Li and Beblo 4 , Reference Tse, Chan, Ng and Yatham 6 – Reference Baune and Renger 8 There is therefore a great need for consideration for cognitive function in remission and recovery processes in psychiatry, which is emphasized by elevated rates of cognitive impairments after remissionReference Kar and Jain 7 , Reference Rock, Roiser, Riedel and Blackwell 9 , Reference Soni, Singh, Shah and Bagotia 10 representing a risk factor for relapse.Reference Majer, Ising and Kunzel 11

A better knowledge of the biological mechanisms underlying cognitive dysfunctions in patients suffering from psychiatric disorders is needed, as they would represent potential therapeutic targets in the management of cognition across psychiatric conditions. Numerous studies have implicated inflammation in the development of psychiatric disorders. In particular, it has been suggested that inflammation might underlie core symptoms of the disorders, such as somatic symptoms (eg, fatigue, sleep disturbances, appetite disturbances).Reference Dooley, Kuhlman, Robles, Eisenberger, Craske and Bower 12 However, there is less evidence linking elevated inflammation to cognitive deficits across psychiatric disorders.Reference Dooley, Kuhlman, Robles, Eisenberger, Craske and Bower 12 Thus, the purpose of this review is to summarize evidence that supports a role for inflammatory processes in the establishment of cognitive impairments across major depressive disorder (MDD), BD, SCZ, and PTSD.

Biological underpinnings of cognitive function

Various brain areas and mechanisms participate in the regulation of cognitive function in physiological conditions. In particular, these mechanisms have been extensively described in the hippocampus for learning and memory, whereas the mechanisms underlying other cognitive processes remain understudied. Mechanisms underlying learning and memory processes in the hippocampus encompass changes in neurotransmission at the synapse, namely Hebbian synaptic plasticity (including long term potentiation [LTP] and long term depression [LTD]).Reference Citri and Malenka 13 Hippocampal LTP inhibition through blockade or knockout of N-methyl-D-aspartate (NMDA) receptors impairs spatial learning and memory,Reference Martin and Morris 14 whereas enhancing LTP improves learning and memory performances.Reference Perusini, Cajigas and Cohensedgh 15 In addition, mice exhibiting impaired LTD display behavioral flexibility deficits.Reference Dong, Bai and Wu 16 To compensate with prolonged activity changes driven by Hebbian synaptic plasticity, homeostatic mechanisms relying on post-synaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors adjust average synaptic strength to bring the level of post-synaptic response into an appropriate range.Reference Fernandes and Carvalho 17 It has been suggested that homeostatic plasticity could be a fundamental mechanism for the dynamic process of memory, providing a link between early and late memory formation processes.Reference Tetzlaff, Kolodziejski, Timme, Tsodyks and Worgotter 18 Hippocampal Hebbian plasticity is also tightly interrelated with the formation of new neurons, namely neurogenesis,Reference Bruel-Jungerman, Davis, Rampon and Laroche 19 , Reference Nissant, Bardy, Katagiri, Murray and Lledo 20 which also contributes to learning and memory. Indeed, the rate of neurogenesis in rodents was found to be positively correlated to spatial learning and memory performances.Reference Hollands, Tobin and Hsu 21 , Reference Aarse, Herlitze and Manahan-Vaughan 22 In the hippocampus, these key regulatory mechanisms are dependent on the synthesis of neurotrophic factors such as brain-derived neurotrophic factor (BDNF)Reference Kino 23 – Reference Aarse, Herlitze and Manahan-Vaughan 26 and the activation of various pathways such as the HPA axisReference Kino 27 – Reference Pocivavsek, Wu, Potter, Elmer, Pellicciari and Schwarcz 31 and the kynurenine pathway, which are therefore able to modulate learning and memory.Reference de Quervain, Schwabe and Roozendaal 32 – Reference Pocivavsek, Wu, Elmer, Bruno and Schwarcz 36

Inflammation and cognitive function in physiological conditions: mechanisms

The relationship between raised levels of inflammation and cognitive changes across inflammation-associated conditions (eg, obesity, rheumatoid arthritis, HIV infection)Reference Castanon, Lasselin and Capuron 37 – Reference Saylor, Dickens and Sacktor 39 has suggested a role for inflammation in the regulation of cognition in physiological conditions. The role of peripheral and brain inflammatory mediators (ie, cytokines) in influencing learning and memory was previously reviewed under the name of “cytokine model of cognitive function.”Reference McAfoose and Baune 40 Microglia, the immune cells of the brain, do not only play a role in brain immune function but are also strong regulators of neurological functionReference Singhal and Baune 41 (see Figure 1) and cognition in physiological conditions. Indeed, microglia depletion or inhibition in mice negatively impairs learning and memory.Reference Torres, Danver and Ji 42 Although microglia can directly modulate cognition, it is noteworthy that they can also perform this role by secreting inflammatory mediators such as cytokines. As previously reviewed, inflammatory cytokines (ie, interleukin-1β [IL-1β], IL-6, and tumor necrosis factor-α [TNF-α]) are required for the physiological regulation of memory processes since disrupting their signaling pathway leads to decreased learning and memory.Reference Baune, Wiede, Braun, Golledge, Arolt and Koerner 43 – Reference Hryniewicz, Bialuk, Kamiński and Winnicka 46 However, the regulatory role of these cytokines on cognition is dose-dependent since overexpression of IL-1β or TNF-α disrupts normal learning and memory in rodents.Reference Barrientos, Higgins, Sprunger, Watkins, Rudy and Maier 47 , Reference Fiore, Angelucci, Alleva, Branchi, Probert and Aloe 48

Figure 1 Role of neuroinflammation in the dysregulation of neurobiological processes underlying cognition. The activation of microglia within the brain induces neuroinflammation through the secretion of local pro-inflammatory cytokines and the enhanced expression of chemokine receptors on microglia. Neuroinflammation can then induce dysregulations of neurobiological mechanisms regulating cognitive processes by: (1) changing the expression and activity of AMPAR, therefore impairing homeostatic plasticity; (2) inhibiting LTP and LTD processes and hence impairing Hebbian plasticity; (3) dysregulating the tryptophan-kynurenine pathway, subsequently causing neurodegeneration; (4) impairing neurotrophin metabolism; and (5) dysregulating HPA axis, leading to hypercortisolemia and subsequent neurotoxicity. In addition, the processes (3), (4), and (5) also participate to impairment of neurogenesis and Hebbian plasticity processes.

Recent evidence suggests that disruption of microglia activation alters hippocampus-dependent neuronal plasticity and learning and memory performance in adulthood.Reference Maggi, Scianni, Branchi, D’Andrea, Lauro and Limatola 49 , Reference Rogers, Morganti and Bachstetter 50 Microglial processes continuously interact with synapses in a glutamate-dependent way,Reference Eyo, Peng, Swiatkowski, Mukherjee, Bispo and Wu 51 suggesting a role in learning and memory through their impact on synaptic plasticity. In addition, microglia indirectly modulate synaptic plasticity through the production of inflammatory cytokines.Reference Pickering and O’Connor 52 IL-1β and TNF-α are critical in the establishment of synaptic plasticity since their knockout induces impaired LTPReference Avital, Goshen and Kamsler 53 and LTD,Reference Albensi and Mattson 54 respectively. Glial-derived TNF-α also strongly regulates homeostatic plasticity by inducing exocytosis of AMPA receptors and inhibiting astrocyte glutamatergic transporters at the synapse.Reference Stellwagen, Beattie, Seo and Malenka 55 – Reference Beattie, Stellwagen and Morishita 57 However, the effect of inflammatory cytokines on synaptic plasticity often follows an inverted U-shape since supra-physiological doses of IL-1β, IL-6, and TNF-α disrupts normal LTP,Reference Murray and Lynch 58 – Reference Cumiskey, Butler, Moynagh and O’Connor 60 possibly linking raised inflammation to cognitive impairments. Similarly to what has been reported for pro-inflammatory cytokines, anti-inflammatory cytokines, such as IL-10, also participate in the regulation of hippocampal synaptic plasticity in a dose-dependent manner.Reference Kelly, Lynch and Vereker 61 – Reference Almolda, de Labra and Barrera 63 Microglia and pro- and anti-inflammatory cytokines do not only regulate Hebbian and homeostatic plasticity but can also influence brain function through their effects on neurogenesis. During development, microglia coordinate synaptic pruning, ie, the elimination of weak synapses in order to maintain and strengthen functional synapses.Reference Hua and Smith 64 During adulthood, neurogenesis is then highly dependent on the crosstalk between microglia and neurons through the CX3C chemokine receptor 1/CX3C chemokine ligand 1 (CX3CR1/CX3CL1) pathway.Reference Delpech, Madore, Nadjar, Joffre, Wohleb and Laye 65 , Reference de Miranda, Zhang, Katsumoto and Teixeira 66 Cytokines such as IL-1β and IL-6 have a dual role on adult neurogenesis in the hippocampus. On one hand, they exert a critical role in the establishment of neurogenesis.Reference Meng, Zhang, Shi, Zhang and Yuan 67 , Reference Spulber, Oprica, Bartfai, Winblad and Schultzberg 68 On the other hand, their overexpression in the brain negatively affects adult neurogenesis.Reference Vallieres, Campbell, Gage and Sawchenko 69 , Reference Wu, Hein, Moravan, Shaftel, Olschowka and O’Banion 70 Similarly, TNF-α may exert a dual role on adult neurogenesis, through a differential effect of its receptors TNF-R1 and TNF-R2,Reference Chen and Palmer 71 although the underlying mechanisms remain understudied. Recently, IL-10 was also described as an enhancer of postnatal neurogenesis.Reference Pereira, Font-Nieves, Van den Haute, Baekelandt, Planas and Pozas 72

Microglia and inflammatory mediators may also have an indirect effect on cognition-associated biological mechanisms through modulation of neurotrophic factors levels and signaling pathway activation. Although the link between inflammation, cognition, and neurotrophic factors needs further consideration, there is evidence that cytokines can modulate BDNF levels and activity.Reference Calabrese, Rossetti, Racagni, Gass, Riva and Molteni 73 In particular, immune stimulation decreases brain BDNF expression and activity,Reference Gonzalez, Machado and Vilcaes 74 , Reference Tong, Prieto and Kramar 75 therefore altering synaptic plasticity in the hippocampus.Reference Tong, Prieto and Kramar 75 In mice, BDNF removal from microglia revealed that these cells regulate memory by promoting synapse formation through BDNF signaling.Reference Parkhurst, Yang and Ninan 76 Along with altering neurotrophic factor activity, cytokine signaling pathways can interact with GC receptor signaling and therefore change GC action.Reference Pace, Hu and Miller 77 Inflammatory cytokines can indeed influence the production of all the hormones produced along the hypothalamic–pituitary–adrenal (HPA) axisReference Silverman and Sternberg 78 and modulate GR function at multiple levels, from expression to translocation and associated signaling pathways.Reference Pace and Miller 79 In addition to their effects on neurotrophic factors and the HPA axis, inflammatory processes can influence kynurenine pathway activation. Pro-inflammatory cytokines induce hippocampal activation of the kynurenine-producing enzyme indoleamine 2,3-dioxygenase (IDO),Reference Andre, O’Connor, Kelley, Lestage, Dantzer and Castanon 80 , Reference O’Connor, Andre and Wang 81 which participates in the regulation of learning and memory.Reference Heisler and O’Connor 35 , Reference Too, Li and Suarna 82

Inflammation and Cognition Across Psychiatric Conditions

The key role that inflammatory processes play in the regulation of the neurobiological processes underlying cognition in physiological conditions suggests that dysregulations of the immune system could participate in cognitive alterations reported across psychiatric diseases. In agreement with this hypothesis, alterations of neurobiological mechanisms regulating cognition are redundant across disorders (see Table 1). Here, we review the evidence suggesting that inflammatory processes, in particular activated microglia and inflammatory cytokines, play a role in impaired cognitive performance associated with psychiatric disorders through the regulation of the neurobiological processes underlying cognitive function (see Figure 1).

Table 1 Main biological mechanisms impairments across psychiatric conditions

0: essentially absent; 0/+: anecdotal, poorly documented, ambiguous; +: preclinical; ++: clinical; +++: clinical, consistent; ?: not clearly evaluated.

Reference numbers are in parentheses.

Inflammation and cognition in major depressive disorder

Levels of inflammatory markers have been found to be associated with cognitive performance in MDD. In patients with MDD, elevated serum levels of TNF-α, TNF-R1, and TNF-R2 negatively correlate with performance in executive functioning, attention, learning, working, and declarative memories.Reference Bobinska, Galecka, Szemraj, Galecki and Talarowska 83 Similarly, elevated plasma levels of C-reactive protein (CRP) and IL-6 are associated with impaired cognitive performance in the domains of attention and executive function and of verbal memory and psychomotor speed, respectively.Reference Chang, Lee and Gean 84 – Reference Goldsmith, Haroon and Woolwine 86 It is noteworthy that CRP and IL-6 levels are not only associated with cognitive symptoms of depression at baseline but also predict those symptoms at 12 years follow-up, suggesting that inflammation contributes to the progression of MDD rather than to the later stages of the disease.Reference Gimeno, Kivimaki and Brunner 87 This relationship appears to be unilateral since cognitive symptoms of depression at baseline are not predictive of inflammatory status at follow-up. Although double-blind, randomized, placebo-controlled trials with anti-inflammatory agents are necessary to establish a causal link between inflammation and cognition in MDD, acute treatment with the cyclooxygenase (COX)-2 inhibitor Celecoxib has been reported to improve cognitive function in an elderly depressed woman with recurrent MDD.Reference Chen, Tzeng and Chen 88

It is noteworthy that individuals with MDD display dysregulations of the kynurenine (KYNA) pathway, which could mediate the relationship between elevated levels of inflammatory markers and cognitive function through its effects on brain plasticity. Elevated levels of inflammatory markers were found to be associated with decreased urinary KYNA in MDD patients.Reference Peacock, Scheiderer and Kellermann 89 Interestingly, KYNA/3-hydroxykynurenine (3-HK) was also reported to negatively correlate with hippocampal activity during memory recall, and KYNA/quinolinic acid (QA) correlated with negative specific memory recall and with hippocampal and amygdala volume in MDD patients.Reference Young, Drevets, Dantzer, Teague, Bodurka and Savitz 90 , Reference Savitz, Drevets and Smith 91 It might be hypothesized that the kynurenine pathway could participate in the impairment of cognitive functions observed in MDD by influencing glutamatergic transmission in brain structures associated with cognitive processes. Numerous alterations in glutamatergic synaptic plasticity have indeed been reported in animal models of depression.Reference Mahati, Bhagya, Christofer, Sneha and Shankaranarayana Rao 92 Inhibition of microglia activation prevents impairments of both spatial memory and hippocampal LTP in a rodent model of depression. This effect is likely to involve a role of GluR1 phosphorylation.Reference Liu, Li and Dai 93 BDNF is also likely to be a mediator of inflammation-associated cognitive impairments in MDD. In cancer patients with depression, plasma IL-6 levels predict serum BDNF levels, which are significantly associated with short-term memory performance.Reference Jehn, Becker and Flath 94 In addition, inhibiting TNF-α in a rat model of depression prevents stress-induced cognitive impairments as well as the associated reduction of hippocampal BDNF expression.Reference Sahin, Karson, Balci, Yazir, Bayramgurler and Utkan 95

Inflammation and cognition in bipolar disorder

Currently, few studies have reported associations between inflammatory processes and cognitive performances in BD.Reference Bauer, Pascoe, Wollenhaupt-Aguiar, Kapczinski and Soares 96 In individuals with BD, plasma CRP levels are negatively correlated with immediate memory, language, and attention.Reference Dickerson, Stallings, Origoni, Vaughan, Khushalani and Yolken 97 Similarly, elevated levels of IL-1ra and TNF-α are associated with worse memory performances, even during euthymic states.Reference Hope, Hoseth and Dieset 98 , Reference Doganavsargil-Baysal, Cinemre and Aksoy 99 Elevated plasma levels of soluble TNF (sTNF)-RI were also found to be associated with impaired declarative memory in patients with BD.Reference Hoseth, Westlye and Hope 100 The only study assessing the relationship between cerebrospinal fluid (CSF) inflammatory markers and cognition in BD reported a negative association between CSF concentration of the inflammatory biomarker YLK-40 and executive function in those patients.Reference Rolstad, Jakobsson and Sellgren 101 It is noteworthy that in addition to elevated peripheral inflammation reported in BD patients with cognitive impairments, increased microglial activation was reported in the right hippocampus of BD patients in comparison to healthy controls.Reference Haarman, Riemersma-Van der Lek and de Groot 102 Hence, these studies provide evidence that elevated inflammatory profile is negatively associated with cognitive function in BD.

Various neurobiological systems have been reported to potentially participate in inflammation-associated cognitive impairments in BD. A recent study reported that pro-inflammatory cytokines such as TNF-α decrease white matter integrity in BD individuals,Reference Benedetti, Poletti and Hoogenboezem 103 which could be mediated by alterations in neurogenesis.Reference Czeh and Lucassen 104 Cytokines may also alter cognition by influencing the activity of the HPA axis, subsequently leading to impaired neuroplasticity. Indeed, HPA axis alterations are associated with impaired cognition in individuals with BD. GR insensitivity was reported in BD,Reference Fries, Vasconcelos-Moreno and Gubert 105 and mifepristone (GR antagonist) treatment for 1 week improves spatial working memory performance in BD.Reference Watson, Gallagher and Porter 106 In addition, a very recent study showed that adult males with BD display elevated plasma 3-HK/KYNA ratio, which is significantly associated with poorer declarative memory performances.Reference Platzer, Dalkner and Fellendorf 107 Given the role that inflammatory cytokines play in the regulation of the IDO pathway, inflammation may dysregulate this pathway, leading to an imbalance between neuroprotective and neurotoxic metabolites and to a subsequent cognitive impairment in BD patients. Finally, it is worth mentioning that peripheral BDNF levels, which can also be regulated by inflammation, predict cognitive function in BD. Moreover, the BDNF val66met polymorphism could be a risk factor for cognitive impairment in this disease,Reference Bauer, Pascoe, Wollenhaupt-Aguiar, Kapczinski and Soares 96 further reinforcing the possible role of BDNF in mediating the effects of inflammation on cognition in BD.

Inflammation and cognition in schizophrenia

Inflammation has also been extensively reported to be a potential player in the etiology and pathophysiology of SCZ. Epidemiological studies have reported elevated risk of schizophrenia following prenatal or childhood exposure to infection. Infection then mediates peripheral and central inflammatory responses which in turn alter brain development (for a review, see MeyerReference Meyer 108 ). Similarly to what has been reported in other psychiatric conditions, cognitive impairments associated with schizophrenia are correlated with raised peripheral inflammation. A recent systemic review conducted on SCZ patients reported an association between plasma CRP levels and worse cognitive performance including in the domains of attention, memory, and learning abilities.Reference Misiak, Stanczykiewicz, Kotowicz, Rybakowski, Samochowiec and Frydecka 109 Similarly, significant negative associations have been reported between general cognitive function and serum IL-6, sTNF-R1, and IL-1ra levels,Reference Hope, Hoseth and Dieset 98 , Reference Frydecka, Misiak and Pawlak-Adamska 110 and elevated peripheral IL-1β mRNA levels are associated with both impairments in verbal fluency and brain volume reduction in a subgroup of patients with SCZ.Reference Fillman, Weickert and Lenroot 111 It is noteworthy that an association has also been reported between cognitive impairments and anti-inflammatory cytokines in SCZ, since serum IL-10 levels negatively correlate with cognitive factor (made up of 3 items of the Positive and Negative Syndrome Scale).Reference Xiu, Tian and Chen 112 , Reference Xiu, Yang and Tan 113 Particularly, patients who carry the AA allele of the IL10-592 A/C polymorphism perform worse in attention, suggesting that this IL-10 allele could contribute to cognitive impairments in SCZ.Reference Xiu, Tian and Chen 112 Moreover, inflammatory pathways are enriched in mutations associated with cognitive impairments in SCZ patients.Reference Fischer and Drago 114 In addition to these studies showing association between inflammation and cognition in SCZ, Müller et al Reference Müller, Riedel, Schwarz and Engel 115 reported that decreasing inflammation through anti-inflammatory add-on to risperidone treatment for 5 weeks trends to improve cognition factor in SCZ patients (F1,47=3.64; p=0.06).

A longitudinal, double-blind, randomized, placebo-controlled study showed that minocycline add-on to atypical antipsychotic treatment has a beneficial effect on executive functioning (such as working memory, cognitive shifting, and cognitive planning), suggesting that inhibiting microglia activation in patients with SCZ could be a strategy to decrease SCZ-associated cognitive impairments.Reference Levkovitz, Mendlovich and Riwkes 116 This is in agreement with the microglia hypothesis of SCZ, which states that the neuropathology of SCZ is closely associated with elevated microglia activation.Reference Monji, Kato and Kanba 117 , Reference Laskaris, Di Biase and Everall 118 Indeed, inflammatory cytokines and free radicals produced by activated microglia in animal models of SCZ lead to decreased neurogenesis, white matter abnormalities, and neuronal degeneration, which may participate in the pathophysiology of the disease.

Similarly to what has been suggested for MDD and BD, inflammation-mediated kynurenine pathway dysfunctions could also participate in cognitive alterations in SCZ, since patients display raised levels of KYNA in the CSF.Reference Linderholm, Skogh and Olsson 119 This effect could be mediated by changes in glutamatergic neurotransmission. MüllerReference Müller 120 suggested that elevated inflammation in SCZ may promote the production of the NMDA antagonist KYNA, therefore resulting in a glutamatergic imbalance. The glutamate hypothesis of SCZ suggests that a deficit in glutamatergic transmission in the brain of SCZ patients may lead to dopaminergic system dysfunction, which may in turn exacerbate glutamatergic transmission impairments, eventually leading to psychotic and cognitive symptoms.Reference Müller 120 Decreased glutamatergic neurotransmission may be associated with alterations in synaptic vesicles transportation, which is linked to IL-10 levels in the brain of SCZ patients.Reference Xiu, Tian and Chen 112

Inflammation and cognition in PTSD

Currently, the link between inflammatory processes and cognitive impairments remains understudied in the context of PTSD. However, a few recent studies reported elevated levels of inflammatory markers (such as CRP, TNF-α, IL-6, and IL-1β) in the plasma of individuals with a diagnosis of PTSD.Reference Passos, Vasconcelos-Moreno and Costa 121 – Reference Miller, Driscoll, Smith and Ramaswamy 123 In a rat model of PTSD, chronic consumption of curcumin, a component with anti-inflammatory properties, impairs the consolidation and reconsolidation of fear memories, suggesting a possible role for inflammation in memory processes.Reference Monsey, Gerhard, Boyle, Briones, Seligsohn and Schafe 124 Interestingly, plasma levels of sTNF-RII are associated with reduced hippocampal volume in Gulf War veterans with current and past PTSD.Reference O’Donovan, Chao and Paulson 125 Hence, one can hypothesize that inflammation could impair cognition by reducing hippocampal volume via its deleterious effect on neurogenesis or HPA axis activation.Reference Boku, Nakagawa, Toda and Hishimoto 126 In agreement with this last assumption, the GC receptor antagonist mifepristone improves cognition in Gulf War veterans with PTSD.Reference Golier, Caramanica and Michaelides 127

Future Directions

Anti-inflammatory strategies to improve cognition across psychiatric conditions

The redundant association between inflammatory alterations and cognitive processes across psychiatric disorders suggests that deconstructing psychiatric disorders to account for the heterogeneity across individuals and consider patients’ endophenotypes may be promising in the development of novel strategies in the management of cognitive alterations in psychiatry. A cross-disorder approach is in agreement with the Research Domain Criteria (RDoC) initiative led by the National Institute of Mental Health (NIH), which is aimed at developing new ways of classifying mental disorders based on dimensions of both observable behavior and neurobiological measures, in order to develop new and individualized treatments. The evidence reviewed here suggests that the use of anti-inflammatory strategies as adjunctive therapies across diagnoses could improve the management of cognitive impairments in psychiatry.

Pharmacological approaches

Nonsteroidal anti-inflammatory drugs (NSAIDs) such as celecoxib (COX-2 inhibitor) are widely used in the treatment of inflammatory conditions (eg, arthritis, multiple sclerosis). In the last decades, they have also been used as effective additional therapies to antidepressant and antipsychotic treatments across psychiatric conditions.Reference Müller, Riedel and Schwarz 128 – Reference Kohler, Benros and Nordentoft 130 However, only a few preliminary data suggest a possible enhancing effect of the anti-inflammatory medication celecoxib on cognition in psychiatric disorders.Reference Chen, Tzeng and Chen 88 , Reference Müller, Riedel, Schwarz and Engel 115 Interestingly, NSAIDs were shown to improve memory in mouse models of neurotoxicityReference Syed, Ikram, Yaqinuddin and Ahmed 131 and Parkinson’s disease,Reference Naeem, Ikram, Khan and Rao 132 suggesting that their impact on cognition across psychiatric conditions requires further examination.

Nutritional interventions

Numerous research efforts have reported a beneficial effect of nutrients such as n-3 polyunsaturated fatty acids (n-3 PUFAs) and flavonoids on inflammatory processes underlying cognitive dysfunctions.Reference Vauzour, Martinsen and Laye 133 Indeed, these nutrients and their metabolites have been extensively described to potently reduce microglia activation and cytokine production in inflammatory conditions and improve associated alterations in HPA axis activation, synaptic plasticity, and BDNF production.Reference Vauzour, Martinsen and Laye 133 – Reference Rey, Nadjar and Buaud 136 It is noteworthy that polyphenols (such as flavonoids) and n-3 PUFAs can alleviate cognitive impairments in inflammation-associated conditions such as aging and disorders such as Parkinson’s disease and Alzheimer’s disease.Reference Vauzour, Martinsen and Laye 133 , Reference Bensalem, Servant and Alfos 137 There is also evidence that they have a beneficial effect on psychiatric disorders,Reference Müller, Riedel and Schwarz 128 although it is unclear whether those cognitive improvements are mediated by inflammatory changes.

Physical activity

Physical activity has been reported to decrease inflammation in both preclinical and clinical models of psychiatric conditions such as MDD.Reference Eyre and Baune 138 , Reference Gleeson, Bishop, Stensel, Lindley, Mastana and Nimmo 139 In rodents, exercise does not only enhance anti-inflammatory processes at the cellular level, by changing microglial phenotype, but also at the molecular level by increasing the production of anti-inflammatory cytokines in the brain.Reference Eyre and Baune 138 This anti-inflammatory effect of exercise positively influences the activity of the HPA axis as well as neuronal proliferation, neurotrophic factor levels, and the activation of the kynurenine pathway,Reference Eyre and Baune 138 which suggests that it could positively impact cognition across psychiatric conditions. In agreement with this hypothesis, moderate physical activity has a beneficial effect on cognition in patients with psychiatric conditions.Reference Jahshan, Rassovsky and Green 140 – Reference Greer, Furman and Trivedi 142

Conclusion

The numerous cognitive impairments across major psychiatric disorders highlight a strong need for consideration since they not only affect the quality of life but also the treatment and recovery of patients. However, the mechanisms underlying these deficits are still understudied and must be addressed to allow a better management of the disorders. The common pattern of cognitive impairments across psychiatric conditions suggests shared mechanisms potentially leading to their causation. As described in this review, inflammation could be a shared mechanism underlying the development of cognitive impairments in MDD, BD, SCZ, and PTSD. Indeed, raised inflammatory processes (ie, activated microglia and elevated levels of inflammatory cytokines) can disrupt neurobiological mechanisms regulating cognitive processes (see Figure 2). However, although most studies report associations or correlations between inflammatory biomarkers, cognitive-related biological mechanisms, and cognitive performance, causal evidence is still strongly lacking. Few studies have evaluated the role of inflammation in cognitive alterations in other psychiatric conditions such as autism or attention deficit hyperactivity disorder, but one may hypothesize that the underlying mechanisms could be similar given the shared pattern of cognitive alteration across psychiatric conditions.Reference Millan, Agid and Brune 1

Figure 2 Role of neuroinflammation in the cognitive alterations and disease outcomes across psychiatric conditions. The detection of damage-associated molecular patterns (DAMPs) or pathogen-associated molecular patterns (PAMPs) by the immune system following psychological stress, infections or injury induces a switch of the microglia phenotype from a quiescent M2 phenotype to an activated or reactive M1 phenotype. As described in Figure 1, this induces neuroinflammation, therefore dysregulating neurobiological processes underlying cognition. The cognitive alterations resulting from this inflammatory state are redundant across psychiatric conditions and encompass impaired episodic memory, processing speed, social cognition, fear-extinction learning, attention, executive function, and declarative learning and memory. Importantly, this common pattern of cognitive alterations in psychiatric disorders increases the severity of symptoms, decreases the quality of life and workplace and psychosocial functioning of patients, has a negative effect on remission and recovery processes, and increases the risk of relapse.

Disclosures

Célia Fourrier and Gaurav Singha have nothing to disclose. Bernhard Baune has the following disclosure: Grants from Fay Fuller Foundation, during the conduct of the study.

Footnotes

This study is financially supported by a generous research donation of the Fay Fuller Foundation, Adelaide. The funders had no role in preparation of the manuscript or decision to publish.

References

1. Millan, MJ, Agid, Y, Brune, M, et al. Cognitive dysfunction in psychiatric disorders: characteristics, causes and the quest for improved therapy. Nat Rev Drug Discov. 2012; 11(2): 141–168.Google Scholar
2. Jenkins, LM, Bodapati, AS, Sharma, RP, Rosen, C. Working memory predicts presence of auditory verbal hallucinations in schizophrenia and bipolar disorder with psychosis. J Clin Exp Neuropsychol. 2018; 40(1): 84–94.Google Scholar
3. Qureshi, SU, Long, ME, Bradshaw, MR, et al. Does PTSD impair cognition beyond the effect of trauma? J Neuropsychiatry Clin Neurosci. 2011; 23(1): 16–28.Google Scholar
4. Baune, BT, Li, X, Beblo, T. Short- and long-term relationships between neurocognitive performance and general function in bipolar disorder. J Clin Exp Neuropsychol. 2013; 35(7): 759–774.Google Scholar
5. Andreou, C, Bozikas, VP. The predictive significance of neurocognitive factors for functional outcome in bipolar disorder. Curr Opin Psychiatry. 2013; 26(1): 54–59.Google Scholar
6. Tse, S, Chan, S, Ng, KL, Yatham, LN. Meta-analysis of predictors of favorable employment outcomes among individuals with bipolar disorder. Bipolar Disord. 2014; 16(3): 217–229.Google Scholar
7. Kar, SK, Jain, M. Current understandings about cognition and the neurobiological correlates in schizophrenia. J Neurosci Rural Pract. 2016; 7(3): 412–418.Google Scholar
8. Baune, BT, Renger, L. Pharmacological and non-pharmacological interventions to improve cognitive dysfunction and functional ability in clinical depression—a systematic review. Psychiatry Res. 2014; 219(1): 25–50.Google Scholar
9. Rock, PL, Roiser, JP, Riedel, WJ, Blackwell, AD. Cognitive impairment in depression: a systematic review and meta-analysis. Psychol Med. 2014; 44(10): 2029–2040.Google Scholar
10. Soni, A, Singh, P, Shah, R, Bagotia, S. Impact of cognition and clinical factors on functional outcome in patients with bipolar disorder. East Asian Arch Psychiatry. 2017; 27(1): 26–34.Google Scholar
11. Majer, M, Ising, M, Kunzel, H, et al. Impaired divided attention predicts delayed response and risk to relapse in subjects with depressive disorders. Psychol Med. 2004; 34(8): 1453–1463.Google Scholar
12. Dooley, LN, Kuhlman, KR, Robles, TF, Eisenberger, NI, Craske, MG, Bower, JE. The role of inflammation in core features of depression: insights from paradigms using exogenously-induced inflammation. Neurosci Biobehav Rev. 2018; 94: 219–237.Google Scholar
13. Citri, A, Malenka, RC. Synaptic plasticity: multiple forms, functions, and mechanisms. Neuropsychopharmacology. 2008; 33(1): 18–41.Google Scholar
14. Martin, SJ, Morris, RG. New life in an old idea: the synaptic plasticity and memory hypothesis revisited. Hippocampus. 2002; 12(5): 609–636.Google Scholar
15. Perusini, JN, Cajigas, SA, Cohensedgh, O, et al. Optogenetic stimulation of dentate gyrus engrams restores memory in Alzheimer’s disease mice. Hippocampus. 2017; 27(10): 1110–1122.Google Scholar
16. Dong, Z, Bai, Y, Wu, X, et al. Hippocampal long-term depression mediates spatial reversal learning in the Morris water maze. Neuropharmacology. 2013; 64: 65–73.Google Scholar
17. Fernandes, D, Carvalho, AL. Mechanisms of homeostatic plasticity in the excitatory synapse. J Neurochem. 2016; 139(6): 973–996.Google Scholar
18. Tetzlaff, C, Kolodziejski, C, Timme, M, Tsodyks, M, Worgotter, F. Synaptic scaling enables dynamically distinct short- and long-term memory formation. PLoS Comput Biol. 2013; 9(10): e1003307.Google Scholar
19. Bruel-Jungerman, E, Davis, S, Rampon, C, Laroche, S. Long-term potentiation enhances neurogenesis in the adult dentate gyrus. J Neurosci. 2006; 26(22): 5888–5893.Google Scholar
20. Nissant, A, Bardy, C, Katagiri, H, Murray, K, Lledo, PM. Adult neurogenesis promotes synaptic plasticity in the olfactory bulb. Nat Neurosci. 2009; 12(6): 728–730.Google Scholar
21. Hollands, C, Tobin, MK, Hsu, M, et al. Depletion of adult neurogenesis exacerbates cognitive deficits in Alzheimer’s disease by compromising hippocampal inhibition. Mol Neurodegener. 2017; 12(1): 64.Google Scholar
22. Richetin, K, Leclerc, C, Toni, N, et al. Genetic manipulation of adult-born hippocampal neurons rescues memory in a mouse model of Alzheimer’s disease. Brain. 2015; 138(Pt 2): 440–455.Google Scholar
23. Leal, G, Bramham, CR, Duarte, CB. BDNF and hippocampal synaptic plasticity. Vitam Horm. 2017; 104: 153–195.Google Scholar
24. Carvalho, AL, Caldeira, MV, Santos, SD, Duarte, CB. Role of the brain-derived neurotrophic factor at glutamatergic synapses. Br J Pharmacol. 2008; 153(Suppl 1): S310–324.Google Scholar
25. Scharfman, H, Goodman, J, Macleod, A, Phani, S, Antonelli, C, Croll, S. Increased neurogenesis and the ectopic granule cells after intrahippocampal BDNF infusion in adult rats. Exp Neurol. 2005; 192(2): 348–356.Google Scholar
26. Aarse, J, Herlitze, S, Manahan-Vaughan, D. The requirement of BDNF for hippocampal synaptic plasticity is experience-dependent. Hippocampus. 2016; 26(6): 739–751.Google Scholar
27. Kino, T. Stress, glucocorticoid hormones, and hippocampal neural progenitor cells: implications to mood disorders. Front Physiol. 2015; 6: 230.Google Scholar
28. Groc, L, Choquet, D, Chaouloff, F. The stress hormone corticosterone conditions AMPAR surface trafficking and synaptic potentiation. Nat Neurosci. 2008; 11(8): 868–870.Google Scholar
29. Joëls, M, Karst, H. Corticosteroid effects on calcium signaling in limbic neurons. Cell Calcium. 2012; 51(3–4): 277–283.Google Scholar
30. Howland, JG, Cazakoff, BN. Effects of acute stress and GluN2B-containing NMDA receptor antagonism on object and object-place recognition memory. Neurobiol Learn Mem. 2010; 93(2): 261–267.Google Scholar
31. Pocivavsek, A, Wu, HQ, Potter, MC, Elmer, GI, Pellicciari, R, Schwarcz, R. Fluctuations in endogenous kynurenic acid control hippocampal glutamate and memory. Neuropsychopharmacology. 2011; 36(11): 2357–2367.Google Scholar
32. de Quervain, D, Schwabe, L, Roozendaal, B. Stress, glucocorticoids and memory: implications for treating fear-related disorders. Nat Rev Neurosci. 2017; 18(1): 7–19.Google Scholar
33. Allison, DJ, Ditor, DS. The common inflammatory etiology of depression and cognitive impairment: a therapeutic target. J Neuroinflammation. 2014; 11: 151.Google Scholar
34. Alexander, KS, Wu, HQ, Schwarcz, R, Bruno, JP. Acute elevations of brain kynurenic acid impair cognitive flexibility: normalization by the alpha7 positive modulator galantamine. Psychopharmacology (Berl). 2012; 220(3): 627–637.Google Scholar
35. Heisler, JM, O’Connor, JC. Indoleamine 2,3-dioxygenase-dependent neurotoxic kynurenine metabolism mediates inflammation-induced deficit in recognition memory. Brain Behav Immun. 2015; 50: 115–124.Google Scholar
36. Pocivavsek, A, Wu, HQ, Elmer, GI, Bruno, JP, Schwarcz, R. Pre- and postnatal exposure to kynurenine causes cognitive deficits in adulthood. Eur J Neurosci. 2012; 35(10): 1605–1612.Google Scholar
37. Castanon, N, Lasselin, J, Capuron, L. Neuropsychiatric comorbidity in obesity: role of inflammatory processes. Front Endocrinol (Lausanne). 2014; 5: 74.Google Scholar
38. Joaquim, AF, Appenzeller, S. Neuropsychiatric manifestations in rheumatoid arthritis. Autoimmun Rev. 2015; 14(12): 1116–1122.Google Scholar
39. Saylor, D, Dickens, AM, Sacktor, N, et al. HIV-associated neurocognitive disorder—pathogenesis and prospects for treatment. Nat Rev Neurol. 2016; 12(5): 309.Google Scholar
40. McAfoose, J, Baune, BT. Evidence for a cytokine model of cognitive function. Neurosci Biobehav Rev. 2009; 33(3): 355–366.Google Scholar
41. Singhal, G, Baune, BT. Microglia: an interface between the loss of neuroplasticity and depression. Front Cell Neurosci. 2017; 11: 270.Google Scholar
42. Torres, L, Danver, J, Ji, K, et al. Dynamic microglial modulation of spatial learning and social behavior. Brain Behav Immun. 2016; 55: 6–16.Google Scholar
43. Baune, BT, Wiede, F, Braun, A, Golledge, J, Arolt, V, Koerner, H. Cognitive dysfunction in mice deficient for TNF- and its receptors. Am J Med Genet B. 2008; 147b(7): 1056–1064.Google Scholar
44. Camara, ML, Corrigan, F, Jaehne, EJ, et al. TNF-alpha and its receptors modulate complex behaviours and neurotrophins in transgenic mice. Psychoneuroendocrinology. 2013; 38(12): 3102–3114.Google Scholar
45. Goshen, I, Kreisel, T, Ounallah-Saad, H, et al. A dual role for interleukin-1 in hippocampal-dependent memory processes. Psychoneuroendocrinology. 2007; 32(8–10): 1106–1115.Google Scholar
46. Hryniewicz, A, Bialuk, I, Kamiński, KA, Winnicka, MM. Impairment of recognition memory in interleukin (IL)-6 knock-out mice. Eur J Pharmacol. 2007; 577(1–3): 219–220.Google Scholar
47. Barrientos, RM, Higgins, EA, Sprunger, DB, Watkins, LR, Rudy, JW, Maier, SF. Memory for context is impaired by a post context exposure injection of interleukin-1 beta into dorsal hippocampus. Behav Brain Res. 2002; 134(1–2): 291–298.Google Scholar
48. Fiore, M, Angelucci, F, Alleva, E, Branchi, I, Probert, L, Aloe, L. Learning performances, brain NGF distribution and NPY levels in transgenic mice expressing TNF-alpha. Behavioural Brain Research. 2000; 112(1-2): 165–175.Google Scholar
49. Maggi, L, Scianni, M, Branchi, I, D’Andrea, I, Lauro, C, Limatola, C. CX(3)CR1 deficiency alters hippocampal-dependent plasticity phenomena blunting the effects of enriched environment. Front Cell Neurosci. 2011; 5: 22.Google Scholar
50. Rogers, JT, Morganti, JM, Bachstetter, AD, et al. CX3CR1 deficiency leads to impairment of hippocampal cognitive function and synaptic plasticity. J Neurosci. 2011; 31(45): 16241–16250.Google Scholar
51. Eyo, UB, Peng, J, Swiatkowski, P, Mukherjee, A, Bispo, A, Wu, LJ. Neuronal hyperactivity recruits microglial processes via neuronal NMDA receptors and microglial P2Y12 receptors after status epilepticus. J Neurosci. 2014; 34(32): 10528–10540.Google Scholar
52. Pickering, M, O’Connor, JJ. Pro-inflammatory cytokines and their effects in the dentate gyrus. Prog Brain Res. 2007; 163: 339–354.Google Scholar
53. Avital, A, Goshen, I, Kamsler, A, et al. Impaired interleukin-1 signaling is associated with deficits in hippocampal memory processes and neural plasticity. Hippocampus. 2003; 13(7): 826–834.Google Scholar
54. Albensi, BC, Mattson, MP. Evidence for the involvement of TNF and NF-kappaB in hippocampal synaptic plasticity. Synapse. 2000; 35(2): 151–159.Google Scholar
55. Stellwagen, D, Beattie, EC, Seo, JY, Malenka, RC. Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-alpha. J Neurosci. 2005; 25(12): 3219–3228.Google Scholar
56. Stellwagen, D, Malenka, RC. Synaptic scaling mediated by glial TNF-alpha. Nature. 2006; 440(7087): 1054–1059.Google Scholar
57. Beattie, EC, Stellwagen, D, Morishita, W, et al. Control of synaptic strength by glial TNFalpha. Science. 2002; 295(5563): 2282–2285.Google Scholar
58. Murray, CA, Lynch, MA. Evidence that increased hippocampal expression of the cytokine interleukin-1 beta is a common trigger for age- and stress-induced impairments in long-term potentiation. J Neurosci. 1998; 18(8): 2974–2981.Google Scholar
59. Tancredi, V, D’Antuono, M, Cafe, C, et al. The inhibitory effects of interleukin-6 on synaptic plasticity in the rat hippocampus are associated with an inhibition of mitogen-activated protein kinase ERK. J Neurochem. 2000; 75(2): 634–643.Google Scholar
60. Cumiskey, D, Butler, MP, Moynagh, PN, O’Connor, J J. Evidence for a role for the group I metabotropic glutamate receptor in the inhibitory effect of tumor necrosis factor-alpha on long-term potentiation. Brain Res. 2007; 1136(1): 13–19.Google Scholar
61. Kelly, A, Lynch, A, Vereker, E, et al. The anti-inflammatory cytokine, interleukin (IL)-10, blocks the inhibitory effect of IL-1 beta on long term potentiation. A role for JNK. J Biol Chem. 2001; 276(49): 45564–45572.Google Scholar
62. Lynch, AM, Walsh, C, Delaney, A, Nolan, Y, Campbell, VA, Lynch, MA. Lipopolysaccharide-induced increase in signalling in hippocampus is abrogated by IL-10--a role for IL-1 beta? J Neurochem. 2004; 88(3): 635–646.Google Scholar
63. Almolda, B, de Labra, C, Barrera, I, et al. Alterations in microglial phenotype and hippocampal neuronal function in transgenic mice with astrocyte-targeted production of interleukin-10. Brain Behav Immun. 2015; 45: 80–97.Google Scholar
64. Hua, JY, Smith, SJ. Neural activity and the dynamics of central nervous system development. Nat Neurosci. 2004; 7(4): 327–332.Google Scholar
65. Delpech, JC, Madore, C, Nadjar, A, Joffre, C, Wohleb, ES, Laye, S. Microglia in neuronal plasticity: influence of stress. Neuropharmacology. 2015; 96(Pt A): 19–28.Google Scholar
66. de Miranda, AS, Zhang, CJ, Katsumoto, A, Teixeira, AL. Hippocampal adult neurogenesis: does the immune system matter? J Neurol Sci. 2017; 372: 482–495.Google Scholar
67. Meng, C, Zhang, JC, Shi, RL, Zhang, SH, Yuan, SY. Inhibition of interleukin-6 abolishes the promoting effects of pair housing on post-stroke neurogenesis. Neuroscience. 2015; 307: 160–170.Google Scholar
68. Spulber, S, Oprica, M, Bartfai, T, Winblad, B, Schultzberg, M. Blunted neurogenesis and gliosis due to transgenic overexpression of human soluble IL-1ra in the mouse. Eur J Neurosci. 2008; 27(3): 549–558.Google Scholar
69. Vallieres, L, Campbell, IL, Gage, FH, Sawchenko, PE. Reduced hippocampal neurogenesis in adult transgenic mice with chronic astrocytic production of interleukin-6. J Neurosci. 2002; 22(2): 486–492.Google Scholar
70. Wu, MD, Hein, AM, Moravan, MJ, Shaftel, SS, Olschowka, JA, O’Banion, MK. Adult murine hippocampal neurogenesis is inhibited by sustained IL-1beta and not rescued by voluntary running. Brain Behav Immun. 2012; 26(2): 292–300.Google Scholar
71. Chen, Z, Palmer, TD. Differential roles of TNFR1 and TNFR2 signaling in adult hippocampal neurogenesis. Brain Behav Immun. 2013; 30: 45–53.Google Scholar
72. Pereira, L, Font-Nieves, M, Van den Haute, C, Baekelandt, V, Planas, AM, Pozas, E. IL-10 regulates adult neurogenesis by modulating ERK and STAT3 activity. Front Cell Neurosci. 2015; 9: 57.Google Scholar
73. Calabrese, F, Rossetti, AC, Racagni, G, Gass, P, Riva, MA, Molteni, R. Brain-derived neurotrophic factor: a bridge between inflammation and neuroplasticity. Front Cell Neurosci. 2014; 8: 430.Google Scholar
74. Gonzalez, P, Machado, I, Vilcaes, A, et al. Molecular mechanisms involved in interleukin 1-beta (IL-1beta)-induced memory impairment. Modulation by alpha-melanocyte-stimulating hormone (alpha-MSH). Brain Behav Immun. 2013; 34: 141–150.Google Scholar
75. Tong, L, Prieto, GA, Kramar, EA, et al. Brain-derived neurotrophic factor-dependent synaptic plasticity is suppressed by interleukin-1beta via p38 mitogen-activated protein kinase. J Neurosci. 2012; 32(49): 17714–17724.Google Scholar
76. Parkhurst, CN, Yang, G, Ninan, I, et al. Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor. Cell. 2013; 155(7): 1596–1609.Google Scholar
77. Pace, TW, Hu, F, Miller, AH. Cytokine-effects on glucocorticoid receptor function: relevance to glucocorticoid resistance and the pathophysiology and treatment of major depression. Brain Behav Immun. 2007; 21(1): 9–19.Google Scholar
78. Silverman, MN, Sternberg, EM. Glucocorticoid regulation of inflammation and its functional correlates: from HPA axis to glucocorticoid receptor dysfunction. Ann N Y Acad Sci. 2012; 1261(1): 55–63.Google Scholar
79. Pace, TW, Miller, AH. Cytokines and glucocorticoid receptor signaling. Relevance to major depression. Ann N Y Acad Sci. 2009; 1179(1): 86–105.Google Scholar
80. Andre, C, O’Connor, JC, Kelley, KW, Lestage, J, Dantzer, R, Castanon, N. Spatio-temporal differences in the profile of murine brain expression of proinflammatory cytokines and indoleamine 2,3-dioxygenase in response to peripheral lipopolysaccharide administration. J Neuroimmunol. 2008; 200(1–2): 90–99.Google Scholar
81. O’Connor, JC, Andre, C, Wang, Y, et al. Interferon-gamma and tumor necrosis factor-alpha mediate the upregulation of indoleamine 2,3-dioxygenase and the induction of depressive-like behavior in mice in response to bacillus Calmette-Guerin. J Neurosci. 2009; 29(13): 4200–4209.Google Scholar
82. Too, LK, Li, KM, Suarna, C, et al. Deletion of TDO2, IDO-1 and IDO-2 differentially affects mouse behavior and cognitive function. Behav Brain Res. 2016; 312: 102–117.Google Scholar
83. Bobinska, K, Galecka, E, Szemraj, J, Galecki, P, Talarowska, M. Is there a link between TNF gene expression and cognitive deficits in depression? Acta Biochim Pol. 2017; 64(1): 65–73.Google Scholar
84. Chang, HH, Lee, IH, Gean, PW, et al. Treatment response and cognitive impairment in major depression: association with C-reactive protein. Brain Behav Immun. 2012; 26(1): 90–95.Google Scholar
85. Grassi-Oliveira, R, Bauer, ME, Pezzi, JC, Teixeira, AL, Brietzke, E. Interleukin-6 and verbal memory in recurrent major depressive disorder. Neuro Endocrinol Lett. 2011; 32(4): 540–544.Google Scholar
86. Goldsmith, DR, Haroon, E, Woolwine, BJ, et al. Inflammatory markers are associated with decreased psychomotor speed in patients with major depressive disorder. Brain Behav Immun. 2016; 56: 281–288.Google Scholar
87. Gimeno, D, Kivimaki, M, Brunner, EJ, et al. Associations of C-reactive protein and interleukin-6 with cognitive symptoms of depression: 12-year follow-up of the Whitehall II study. Psychol Med. 2009; 39(3): 413–423.Google Scholar
88. Chen, CY, Tzeng, NS, Chen, YC. Maintenance therapy of celecoxib for major depression with mimicking neuropsychological dysfunction. Gen Hosp Psychiatry. 2010; 32(6): e647–649.Google Scholar
89. Peacock, BN, Scheiderer, DJ, Kellermann, GH. Biomolecular aspects of depression: a retrospective analysis. Compr Psychiatry. 2017; 73: 168–180.Google Scholar
90. Young, KD, Drevets, WC, Dantzer, R, Teague, TK, Bodurka, J, Savitz, J. Kynurenine pathway metabolites are associated with hippocampal activity during autobiographical memory recall in patients with depression. Brain Behav Immun. 2016; 56: 335–342.Google Scholar
91. Savitz, J, Drevets, WC, Smith, CM, et al. Putative neuroprotective and neurotoxic kynurenine pathway metabolites are associated with hippocampal and amygdalar volumes in subjects with major depressive disorder. Neuropsychopharmacology. 2015; 40(2): 463–471.Google Scholar
92. Mahati, K, Bhagya, V, Christofer, T, Sneha, A, Shankaranarayana Rao, BS. Enriched environment ameliorates depression-induced cognitive deficits and restores abnormal hippocampal synaptic plasticity. Neurobiol Learn Mem. 2016; 134 Pt B: 379–391.Google Scholar
93. Liu, M, Li, J, Dai, P, et al. Microglia activation regulates GluR1 phosphorylation in chronic unpredictable stress-induced cognitive dysfunction. Stress. 2015; 18(1): 96–106.Google Scholar
94. Jehn, CF, Becker, B, Flath, B, et al. Neurocognitive function, brain-derived neurotrophic factor (BDNF) and IL-6 levels in cancer patients with depression. J Neuroimmunol. 2015; 287: 88–92.Google Scholar
95. Sahin, TD, Karson, A, Balci, F, Yazir, Y, Bayramgurler, D, Utkan, T. TNF-alpha inhibition prevents cognitive decline and maintains hippocampal BDNF levels in the unpredictable chronic mild stress rat model of depression. Behav Brain Res. 2015; 292: 233–240.Google Scholar
96. Bauer, IE, Pascoe, MC, Wollenhaupt-Aguiar, B, Kapczinski, F, Soares, JC. Inflammatory mediators of cognitive impairment in bipolar disorder. J Psychiatr Res. 2014; 56: 18–27.Google Scholar
97. Dickerson, F, Stallings, C, Origoni, A, Vaughan, C, Khushalani, S, Yolken, R. Elevated C-reactive protein and cognitive deficits in individuals with bipolar disorder. J Affect Disord. 2013; 150(2): 456–459.Google Scholar
98. Hope, S, Hoseth, E, Dieset, I, et al. Inflammatory markers are associated with general cognitive abilities in schizophrenia and bipolar disorder patients and healthy controls. Schizophr Res. 2015; 165(2–3): 188–194.Google Scholar
99. Doganavsargil-Baysal, O, Cinemre, B, Aksoy, UM, et al. Levels of TNF-alpha, soluble TNF receptors (sTNFR1, sTNFR2), and cognition in bipolar disorder. Hum Psychopharmacol. 2013; 28(2): 160–167.Google Scholar
100. Hoseth, EZ, Westlye, LT, Hope, S, et al. Association between cytokine levels, verbal memory and hippocampus volume in psychotic disorders and healthy controls. Acta Psychiatr Scand. 2016; 133(1): 53–62.Google Scholar
101. Rolstad, S, Jakobsson, J, Sellgren, C, et al. CSF neuroinflammatory biomarkers in bipolar disorder are associated with cognitive impairment. Eur Neuropsychopharmacol. 2015; 25(8): 1091–1098.Google Scholar
102. Haarman, BC, Riemersma-Van der Lek, RF, de Groot, JC, et al. Neuroinflammation in bipolar disorder—a [(11)C]-(R)-PK11195 positron emission tomography study. Brain Behav Immun. 2014; 40: 219–225.Google Scholar
103. Benedetti, F, Poletti, S, Hoogenboezem, TA, et al. Inflammatory cytokines influence measures of white matter integrity in bipolar disorder. J Affect Disord. 2016; 202: 1–9.Google Scholar
104. Czeh, B, Lucassen, PJ. What causes the hippocampal volume decrease in depression? Are neurogenesis, glial changes and apoptosis implicated? Eur Arch Psychiatry Clin Neurosci. 2007; 257(5): 250–260.Google Scholar
105. Fries, GR, Vasconcelos-Moreno, MP, Gubert, C, et al. Hypothalamic-pituitary-adrenal axis dysfunction and illness progression in bipolar disorder. Int J Neuropsychopharmacol. 2014; 18(1): pyu043.Google Scholar
106. Watson, S, Gallagher, P, Porter, RJ, et al. A randomized trial to examine the effect of mifepristone on neuropsychological performance and mood in patients with bipolar depression. Biol Psychiatry. 2012; 72(11): 943–949.Google Scholar
107. Platzer, M, Dalkner, N, Fellendorf, FT, et al. Tryptophan breakdown and cognition in bipolar disorder. Psychoneuroendocrinology. 2017; 81: 144–150.Google Scholar
108. Meyer, U. Developmental neuroinflammation and schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 2013; 42: 20–34.Google Scholar
109. Misiak, B, Stanczykiewicz, B, Kotowicz, K, Rybakowski, JK, Samochowiec, J, Frydecka, D. Cytokines and C-reactive protein alterations with respect to cognitive impairment in schizophrenia and bipolar disorder: a systematic review. Schizophr Res. 2018; 192: 16–29.Google Scholar
110. Frydecka, D, Misiak, B, Pawlak-Adamska, E, et al. Interleukin-6: the missing element of the neurocognitive deterioration in schizophrenia? The focus on genetic underpinnings, cognitive impairment and clinical manifestation. Eur Arch Psychiatry Clin Neurosci. 2015; 265(6): 449–459.Google Scholar
111. Fillman, SG, Weickert, TW, Lenroot, RK, et al. Elevated peripheral cytokines characterize a subgroup of people with schizophrenia displaying poor verbal fluency and reduced Broca’s area volume. Mol Psychiatry. 2016; 21(8): 1090–1098.Google Scholar
112. Xiu, MH, Tian, L, Chen, S, et al. Contribution of IL-10 and its -592 A/C polymorphism to cognitive functions in first-episode drug-naive schizophrenia. Brain Behav Immun. 2016; 57: 116–124.Google Scholar
113. Xiu, MH, Yang, GG, Tan, YL, et al. Decreased interleukin-10 serum levels in first-episode drug-naive schizophrenia: relationship to psychopathology. Schizophr Res. 2014; 156(1): 9–14.Google Scholar
114. Fischer, EK, Drago, A. A molecular pathway analysis stresses the role of inflammation and oxidative stress towards cognition in schizophrenia. J Neural Transm (Vienna). 2017; 124(7): 765–774.Google Scholar
115. Müller, N, Riedel, M, Schwarz, MJ, Engel, RR. Clinical effects of COX-2 inhibitors on cognition in schizophrenia. Eur Arch Psychiatry Clin Neurosci. 2005; 255(2): 149–151.Google Scholar
116. Levkovitz, Y, Mendlovich, S, Riwkes, S, et al. A double-blind, randomized study of minocycline for the treatment of negative and cognitive symptoms in early-phase schizophrenia. J Clin Psychiatry. 2010; 71(2): 138–149.Google Scholar
117. Monji, A, Kato, T, Kanba, S. Cytokines and schizophrenia: microglia hypothesis of schizophrenia. Psychiatry Clin Neurosci. 2009; 63(3): 257–265.Google Scholar
118. Laskaris, LE, Di Biase, MA, Everall, I, et al. Microglial activation and progressive brain changes in schizophrenia. Br J Pharmacol. 2016; 173(4): 666–680.Google Scholar
119. Linderholm, KR, Skogh, E, Olsson, SK, et al. Increased levels of kynurenine and kynurenic acid in the CSF of patients with schizophrenia. Schizophr Bull. 2012; 38(3): 426–432.Google Scholar
120. Müller, N. Inflammation and the glutamate system in schizophrenia: implications for therapeutic targets and drug development. Expert Opin Ther Targets. 2008; 12(12): 1497–1507.Google Scholar
121. Passos, IC, Vasconcelos-Moreno, MP, Costa, LG, et al. Inflammatory markers in post-traumatic stress disorder: a systematic review, meta-analysis, and meta-regression. Lancet Psychiatry. 2015; 2(11): 1002–1012.Google Scholar
122. Eraly, SA, Nievergelt, CM, Maihofer, AX, et al. Assessment of plasma C-reactive protein as a biomarker of posttraumatic stress disorder risk. JAMA Psychiatry. 2014; 71(4): 423–431.Google Scholar
123. Miller, K, Driscoll, D, Smith, LM, Ramaswamy, S. The role of inflammation in late-life post-traumatic stress disorder. Mil Med. 2017; 182(11): e1815–e1818.Google Scholar
124. Monsey, MS, Gerhard, DM, Boyle, LM, Briones, MA, Seligsohn, M, Schafe, GE. A diet enriched with curcumin impairs newly acquired and reactivated fear memories. Neuropsychopharmacology. 2015; 40(5): 1278–1288.Google Scholar
125. O’Donovan, A, Chao, LL, Paulson, J, et al. Altered inflammatory activity associated with reduced hippocampal volume and more severe posttraumatic stress symptoms in Gulf War veterans. Psychoneuroendocrinology. 2015; 51: 557–566.Google Scholar
126. Boku, S, Nakagawa, S, Toda, H, Hishimoto, A. Neural basis of major depression: beyond monoamine hypothesis. Psychiatry Clin Neurosci. 2018; 72(1): 3–12.Google Scholar
127. Golier, JA, Caramanica, K, Michaelides, AC, et al. A randomized, double-blind, placebo-controlled, crossover trial of mifepristone in Gulf War veterans with chronic multisymptom illness. Psychoneuroendocrinology. 2016; 64: 22–30.Google Scholar
128. Müller, N, Riedel, M, Schwarz, MJ. Psychotropic effects of COX-2 inhibitors--a possible new approach for the treatment of psychiatric disorders. Pharmacopsychiatry. 2004; 37(6): 266–269.Google Scholar
129. Ayorech, Z, Tracy, DK, Baumeister, D, Giaroli, G. Taking the fuel out of the fire: evidence for the use of anti-inflammatory agents in the treatment of bipolar disorders. J Affect Disord. 2015; 174: 467–478.Google Scholar
130. Kohler, O, Benros, ME, Nordentoft, M, et al. Effect of anti-inflammatory treatment on depression, depressive symptoms, and adverse effects: a systematic review and meta-analysis of randomized clinical trials. JAMA Psychiatry. 2014; 71(12): 1381–1391.Google Scholar
131. Syed, H, Ikram, MF, Yaqinuddin, A, Ahmed, T. Cyclooxygenase I and II inhibitors distinctly enhance hippocampal- and cortex-dependent cognitive functions in mice. Mol Med Rep. 2015; 12(5): 7649–7656.Google Scholar
132. Naeem, S, Ikram, R, Khan, SS, Rao, SS. NSAIDs ameliorate cognitive and motor impairment in a model of parkinsonism induced by chlorpromazine. Pak J Pharm Sci. 2017; 30(3): 801–808.Google Scholar
133. Vauzour, D, Martinsen, A, Laye, S. Neuroinflammatory processes in cognitive disorders: is there a role for flavonoids and n-3 polyunsaturated fatty acids in counteracting their detrimental effects? Neurochem Int. 2015; 89: 63–74.Google Scholar
134. Bazinet, RP, Laye, S. Polyunsaturated fatty acids and their metabolites in brain function and disease. Nat Rev Neurosci. 2014; 15(12): 771–785.Google Scholar
135. Fourrier, C, Remus-Borel, J, Greenhalgh, AD, et al. Docosahexaenoic acid-containing choline phospholipid modulates LPS-induced neuroinflammation in vivo and in microglia in vitro. J Neuroinflammation. 2017; 14(1): 170.Google Scholar
136. Rey, C, Nadjar, A, Buaud, B, et al. Resolvin D1 and E1 promote resolution of inflammation in microglial cells in vitro. Brain Behav Immun. 2016; 55: 249–259.Google Scholar
137. Bensalem, J, Servant, L, Alfos, S, et al. Dietary polyphenol supplementation prevents alterations of spatial navigation in middle-aged mice. Front Behav Neurosci. 2016; 10: 9.Google Scholar
138. Eyre, H, Baune, BT. Neuroimmunological effects of physical exercise in depression. Brain Behav Immun. 2012; 26(2): 251–266.Google Scholar
139. Gleeson, M, Bishop, NC, Stensel, DJ, Lindley, MR, Mastana, SS, Nimmo, MA. The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease. Nat Rev Immunol. 2011; 11(9): 607–615.Google Scholar
140. Jahshan, C, Rassovsky, Y, Green, MF. Enhancing neuroplasticity to augment cognitive remediation in schizophrenia. Front Psychiatry. 2017; 8: 191.Google Scholar
141. Mittal, VA, Vargas, T, Osborne, KJ, et al. Exercise treatments for psychosis: a review. Curr Treat Options Psychiatry. 2017; 4(2): 152–166.Google Scholar
142. Greer, TL, Furman, JL, Trivedi, MH. Evaluation of the benefits of exercise on cognition in major depressive disorder. Gen Hosp Psychiatry. 2017; 49: 19–25.Google Scholar
143. Workman, ER, Niere, F, Raab-Graham, KF. Engaging homeostatic plasticity to treat depression. Mol Psychiatry. 2018; 23: 26–35.Google Scholar
144. Ren, Z, Pribiag, H, Jefferson, SJ, et al. Bidirectional homeostatic regulation of a depression-related brain state by gamma-aminobutyric acidergic deficits and ketamine treatment. Biol Psychiatry. 2016; 80(6): 457–468.Google Scholar
145. Eisch, AJ, Petrik, D. Depression and hippocampal neurogenesis: a road to remission? Science. 2012; 338(6103): 72–75.Google Scholar
146. Fischer, S, Strawbridge, R, Vives, AH, Cleare, AJ. Cortisol as a predictor of psychological therapy response in depressive disorders: systematic review and meta-analysis. Br J Psychiatry. 2017; 210(2): 105–109.Google Scholar
147. Zorn, JV, Schur, RR, Boks, MP, Kahn, RS, Joels, M, Vinkers, CH. Cortisol stress reactivity across psychiatric disorders: a systematic review and meta-analysis. Psychoneuroendocrinology. 2017; 77: 25–36.Google Scholar
148. Ribolsi, M, Lisi, G, Ponzo, V, et al. Left hemispheric breakdown of LTP-like cortico-cortical plasticity in schizophrenic patients. Clin Neurophysiol. 2017; 128(10): 2037–2042.Google Scholar
149. Strube, W, Bunse, T, Nitsche, MA, Palm, U, Falkai, P, Hasan, A. Differential response to anodal tDCS and PAS is indicative of impaired focal LTP-like plasticity in schizophrenia. Behav Brain Res. 2016; 311: 46–53.Google Scholar
150. Wang, HX, Gao, WJ. Prolonged exposure to NMDAR antagonist induces cell-type specific changes of glutamatergic receptors in rat prefrontal cortex. Neuropharmacology. 2012; 62(4): 1808–1822.Google Scholar
151. Inta, D, Meyer-Lindenberg, A, Gass, P. Alterations in postnatal neurogenesis and dopamine dysregulation in schizophrenia: a hypothesis. Schizophr Bull. 2011; 37(4): 674–680.Google Scholar
152. Kheirollahi, M, Kazemi, E, Ashouri, S. Brain-derived neurotrophic factor gene Val66Met polymorphism and risk of schizophrenia: a meta-analysis of case-control studies. Cell Mol Neurobiol. 2016; 36(1): 1–10.Google Scholar
153. Fernandes, BS, Steiner, J, Berk, M, et al. Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications. Mol Psychiatry. 2015; 20(9): 1108–1119.Google Scholar
154. Sanz-Garcia, A, Knafo, S, Pereda-Perez, I, Esteban, JA, Venero, C, Armario, A. Administration of the TrkB receptor agonist 7,8-dihydroxyflavone prevents traumatic stress-induced spatial memory deficits and changes in synaptic plasticity. Hippocampus. 2016; 26(9): 1179–1188.Google Scholar
155. Li, X, Han, F, Liu, D, Shi, Y. Changes of Bax, Bcl-2 and apoptosis in hippocampus in the rat model of post-traumatic stress disorder. Neurol Res. 2010; 32(6): 579–586.Google Scholar
156. Burgdorf, J, Kroes, RA, Zhang, XL, et al. Rapastinel (GLYX-13) has therapeutic potential for the treatment of post-traumatic stress disorder: characterization of a NMDA receptor-mediated metaplasticity process in the medial prefrontal cortex of rats. Behav Brain Res. 2015; 294: 177–185.Google Scholar
157. Andrews, JA, Neises, KD. Cells, biomarkers, and post-traumatic stress disorder: evidence for peripheral involvement in a central disease. J Neurochem. 2012; 120(1): 26–36.Google Scholar
158. Kheirbek, MA, Klemenhagen, KC, Sahay, A, Hen, R. Neurogenesis and generalization: a new approach to stratify and treat anxiety disorders. Nat Neurosci. 2012; 15(12): 1613–1620.Google Scholar
159. Gao, J, Chen, C, Liu, Y, et al. Lycium barbarum polysaccharide improves traumatic cognition via reversing imbalance of apoptosis/regeneration in hippocampal neurons after stress. Life Sci. 2015; 121: 124–134.Google Scholar
160. Martinotti, G, Sepede, G, Brunetti, M, et al. BDNF concentration and impulsiveness level in post-traumatic stress disorder. Psychiatry Res. 2015; 229(3): 814–818.Google Scholar
161. Stratta, P, Sanita, P, Bonanni, RL, et al. Clinical correlates of plasma brain-derived neurotrophic factor in post-traumatic stress disorder spectrum after a natural disaster. Psychiatry Res. 2016; 244: 165–170.Google Scholar
162. Angelucci, F, Ricci, V, Gelfo, F, et al. BDNF serum levels in subjects developing or not post-traumatic stress disorder after trauma exposure. Brain Cogn. 2014; 84(1): 118–122.Google Scholar
163. Morris, MC, Compas, BE, Garber, J. Relations among posttraumatic stress disorder, comorbid major depression, and HPA function: a systematic review and meta-analysis. Clin Psychol Rev. 2012; 32(4): 301–315.Google Scholar
164. Klaassens, ER, Giltay, EJ, Cuijpers, P, van Veen, T, Zitman, FG. Adulthood trauma and HPA-axis functioning in healthy subjects and PTSD patients: a meta-analysis. Psychoneuroendocrinology. 2012; 37(3): 317–331.Google Scholar
Figure 0

Figure 1 Role of neuroinflammation in the dysregulation of neurobiological processes underlying cognition. The activation of microglia within the brain induces neuroinflammation through the secretion of local pro-inflammatory cytokines and the enhanced expression of chemokine receptors on microglia. Neuroinflammation can then induce dysregulations of neurobiological mechanisms regulating cognitive processes by: (1) changing the expression and activity of AMPAR, therefore impairing homeostatic plasticity; (2) inhibiting LTP and LTD processes and hence impairing Hebbian plasticity; (3) dysregulating the tryptophan-kynurenine pathway, subsequently causing neurodegeneration; (4) impairing neurotrophin metabolism; and (5) dysregulating HPA axis, leading to hypercortisolemia and subsequent neurotoxicity. In addition, the processes (3), (4), and (5) also participate to impairment of neurogenesis and Hebbian plasticity processes.

Figure 1

Table 1 Main biological mechanisms impairments across psychiatric conditions

Figure 2

Figure 2 Role of neuroinflammation in the cognitive alterations and disease outcomes across psychiatric conditions. The detection of damage-associated molecular patterns (DAMPs) or pathogen-associated molecular patterns (PAMPs) by the immune system following psychological stress, infections or injury induces a switch of the microglia phenotype from a quiescent M2 phenotype to an activated or reactive M1 phenotype. As described in Figure 1, this induces neuroinflammation, therefore dysregulating neurobiological processes underlying cognition. The cognitive alterations resulting from this inflammatory state are redundant across psychiatric conditions and encompass impaired episodic memory, processing speed, social cognition, fear-extinction learning, attention, executive function, and declarative learning and memory. Importantly, this common pattern of cognitive alterations in psychiatric disorders increases the severity of symptoms, decreases the quality of life and workplace and psychosocial functioning of patients, has a negative effect on remission and recovery processes, and increases the risk of relapse.