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17 - Investigational strategies: treatment of rapid cycling, mixed episodes, and atypical bipolar mood disorder

Published online by Cambridge University Press:  10 August 2009

Gary Sachs
Affiliation:
Massachusetts General Hospital Partners Bipolar Treatment Center Boston, MA USA
Mandy Graves
Affiliation:
Massachusetts General Hospital Partners Bipolar Treatment Center Boston, MA USA
Andreas Marneros
Affiliation:
Martin Luther-Universität Halle-Wittenburg, Germany
Frederick Goodwin
Affiliation:
George Washington University, Washington DC
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Summary

The psychiatric literature includes relatively few adequately powered controlled double-blind clinical trials reporting results for bipolar disorders. The majority of these randomized clinical trials report results for treatment of acute mania in hospitalized bipolar I (BP-I) patients. The majority of bipolar patients are, however, not BP-I and manic states are relatively infrequent. Why are there so few published controlled treatment studies dealing with common clinical problems like rapid cycling, mixed episodes, and atypical bipolar disorder?

Rapid cycling, mixed episodes, and atypical bipolar mood disorder each challenge clinical researchers in distinctly different ways. This chapter explores the issues as they relate to study design in general and offers suggestions for study methodology.

The first consideration is the conceptual dissimilarity of the terms rapid cycling, mixed episodes, and atypical bipolar disorder. These terms correspond to three distinct organizational levels used in the Diagnostic and Statistical Manual of Mental Disorders, 4th edn (DSM-IV) mood-disorder nosology and represent the concepts of course specifier, acute episode, and subtype of bipolar (American Psychiatric Association, 1994). Study designs for each require attention to sample selection, outcome measures, and an analysis plan matched to the appropriate level in the organizational hierarchy of the DSM-IV mood-disorder classification.

Difficulties in conducting clinical trials for atypical bipolar disorder

The DSM-IV bipolar mood disorder category is subtyped into BP-I, BP-II, cyclothymia, and bipolar disorder not otherwise specified. The latter encompasses all forms of “atypical bipolar disorder” which do not meet criteria for one of the three defined subtypes.

Type
Chapter
Information
Bipolar Disorders
Mixed States, Rapid Cycling and Atypical Forms
, pp. 369 - 385
Publisher: Cambridge University Press
Print publication year: 2005

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References

Akiskal, H. and Pinto, O. C. (1999). The evolving bipolar spectrum: prototypes I, II, III, and IV. Psychiatr. Clin. North Am., 22, 517–34.Google Scholar
Alda, M., Grof, P., and Grof, E. (1998). MN blood groups and bipolar disorder: evidence of genotypic association and Hardy–Weinberg disequilibrium. Biol. Psychiatry, 44, 361–3.Google Scholar
American Psychiatric Association (1994). Diagnostic and Statistical Manual of Mental Disorders, 4th edn. Washington, DC: American Psychiatric Association.
Baldessarini, R., Tondo, L., Floris, G.et al. (2000). Effects of rapid cycling on response to lithium maintenance treatment in 360 bipolar I and II disorder patients. J. Affect. Disorder, 61, 13–22.Google Scholar
Bauer, M. S. and Whybrow, P. C. (1990). Rapid cycling bipolar affective disorder. II. Treatment of refractory rapid cycling with high-dose levothyroxine: a preliminary study. Arch. Gen. Psychiatry, 47, 435–40.Google Scholar
Bauer, M. S., Calabrese, J., Dunner, D. L.et al. (1994). Multisite data reanalysis of the validity of rapid cycling as a course modifier for bipolar disorder in DSM-IV. Am. J. Psychiatry, 151, 506–15.Google Scholar
Bowden, C. L. and McElroy, S. L. (1995). History of the development of valproate for treatment of bipolar disorder. J. Clin. Psychiatry, 56 (suppl. 3:), 3–5.Google Scholar
Calabrese, J. R., Suppes, T., Bowden, C. L.et al. (2000). A double blind, placebo-controlled, prophylaxis study of lamotrigine in rapid-cycling bipolar disorder. J. Clin. Psychopharmacol, 61, 841–50.Google Scholar
Coryell, W., Endicott, J., and Keller, M. (1992). Rapid cycling affective disorder: demographics, family history and course. Arch. Gen. Psychiatry, 49, 126–31.Google Scholar
Dunner, D. L., Patrick, V. and Fieve, R. R. (1977). Rapid cycling manic depressive patients. Compr. Psychiatry, 18, 561–6.Google Scholar
Goodwin, F. and Jamison, K. (1990). Manic Depressive Illness. New York: Oxford University Press.
Grof, E., Haag, M., Grof, P., et al. (1987). Lithium response and the sequence of episode polarities: preliminary report on a Hamilton sample. Progr. Neuropsychopharmacol. Biol. Psychiatry, 11, 199–203.Google Scholar
Haag, H., Heidorn, A., Haag, M.et al. (1987). Sequence of affective polarity and lithium response: preliminary report on Munich sample. Progr. Neuropsychopharmacol. Biol. Psychiatry, 11, 205–8.Google Scholar
Himmelhoch, J. M., Mulla, D., Neil, J. F.et al. (1976). Incidence and significance of mixed affective states in a bipolar population. Arch. Gen. Psychiatry, 33, 1062–6.Google Scholar
Judd, L. L., Akiskal, H. S., Schettler, P. J.et al. (2002). The long-term natural history of the weekly symptomatic status of bipolar I disorder. Arch. Gen. Psychiatry, 59, 530–7.Google Scholar
Keller, M. B., Lavori, P. W., Friedman, B.et al. (1987). The longitudinal interval follow-up evaluation. A comprehensive method for assessing outcome in prospective longitudinal studies. Arch. Gen. Psychiatry, 44, 540–8.Google Scholar
Koukopoulos, A., Reginaldi, D., and Laddomada, P. (1980). Course of the manic–depressive cycle and changes caused by treatments. Pharmacopsychiatry, 13, 156–67.Google Scholar
Kraepelin, E. (1921). Manic-Depressive Insanity and Paranoia. Edinburgh: E. and S. Livingstone.
Kramlinger, K. and Post, R. M. (1996). Ultra-rapid and ultradian cycling in bipolar affective illness. Br. J. Psychiatry, 168, 314–23.Google Scholar
Kupfer, D. J., Chengappa, K. N., Gelenberg, A. J.et al. (2001). Citalopram as adjunctive therapy in bipolar depression. J. Clin. Psychiatry, 62, 985–90.Google Scholar
Maj, M., Pirozzi, R. and Starace, F. (1989). Previous pattern of course of the illness as a predictor of response to lithium prophylaxis in bipolar patients. J. Affect. Disord., 17, 237–41.Google Scholar
Robb, J. C., Cooke, R. G., Devins, G. M.et al. (1997). Quality of life and lifestyle disruption in euthymic bipolar disorder. J. Psychiatr. Res., 31, 509–17.Google Scholar
Sachs, G. S, Guille, C., and McMurrich, S. A (2002a). Clinical monitoring form for mood disorders. Bipolar. Disord, 4, 323–7.Google Scholar
Sachs, G., et al. (2002b). The systematic treatment enhancement program for bipolar disorder: a model for collaborative research. Biol. Psychiatry. (in press).Google Scholar
Tohen, M., Sanger, T. M., McElroy, S. L.et al. (1999). Olanzapine versus placebo in the treatment of acute mania. Olanzapine HGEH study group. J. Psychiatry., 156, 702–9.Google Scholar

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