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Dietary diversity moderates household economic inequalities in the double burden of malnutrition in Tanzania

Published online by Cambridge University Press:  16 May 2024

Sanmei Chen*
Affiliation:
Global Health Nursing, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8553, Japan
Yoko Shimpuku
Affiliation:
Global Health Nursing, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8553, Japan
Takanori Honda
Affiliation:
Center for Cohort Studies, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
Dorkasi L Mwakawanga
Affiliation:
Global Health Nursing, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8553, Japan
Beatrice Mwilike
Affiliation:
Department of Community Health Nursing, School of Nursing, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania
*
*Corresponding author: Email chens@hiroshima-u.ac.jp
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Abstract

Objective:

Improved food availability and a growing economy in Tanzania may insufficiently decrease pre-existing nutritional deficiencies and simultaneously increase overweight within the same individual, household or population, causing a double burden of malnutrition (DBM). We investigated economic inequalities in DBM at the household level, expressed as a stunted child with a mother with overweight/obesity, and the moderating role of dietary diversity in these inequalities.

Design:

We used cross-sectional data from the 2015–2016 Tanzania Demographic and Health Survey.

Setting:

A nationally representative survey.

Participants:

Totally, 2867 children (aged 6–23 months) and their mothers (aged 15–49 years). The mother–child pairs were categorised into two groups based on dietary diversity score: achieving and not achieving minimum dietary diversity.

Results:

The prevalence of DBM was 5·6 % (sd = 0·6) and significantly varied by region (ranging from 0·6 % to 12·2 %). Significant interaction was observed between dietary diversity and household wealth index (Pfor interaction < 0·001). The prevalence of DBM monotonically increased with greater household wealth among mother–child pairs who did not achieve minimum dietary diversity (Pfor trend < 0·001; however, this association was attenuated in those who achieved minimum dietary diversity (Pfor trend = 0·16), particularly for the richest households (P = 0·44). Analysing household wealth index score as a continuous variable yielded similar results (OR (95 % CI): 2·10 (1·36, 3·25) for non-achievers of minimum dietary diversity, 1·38 (0·76, 2·54) for achievers).

Conclusions:

Greater household wealth was associated with higher odds of DBM in Tanzania; however, the negative impact of household economic status on DBM was mitigated by minimum dietary diversity.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

Countries worldwide are now experiencing a fast-evolving and more complex nutrition paradigm(1). Instead of focusing on a single side of malnutrition, combating all forms of malnutrition is among the top priorities of the United Nations Decade of Action on Nutrition and the Sustainable Development Goals (SDG, Target 2·2)(2,Reference Nilsson, Griggs and Visbeck3) . Undernutrition and overweight or obesity have been historically addressed as separate challenges affecting distinct populations with contrast risk factors(Reference Wells, Sawaya and Wibaek4). However, the changing global nutrition reality is that these two distinct forms of malnutrition frequently coexist within individuals, households and populations, with common mechanisms (e.g. economic inequalities(Reference Alao, Nur and Fivian5)) and consequences on health(Reference Wells, Sawaya and Wibaek4). This growing recognition in the global health community forms the basis of the emerging concept of double burden of malnutrition (DBM)(Reference Khan, Ning and Wilkins6,Reference Demaio and Branca7) . This global double burden of undernutrition and obesity and its great developmental and socio-economic impact have been recognised as serious and lasting in low- and middle-income countries (LMIC) undergoing rapid nutrition transition(8Reference Nugent, Levin and Hale10); however, they have not yet been examined extensively.

Tanzania is experiencing improved food availability as its economy is growing rapidly. Economic transition with an increased average household income enables more households to purchase more food(11), which potentially improves undernutrition. However, the rates of decline in undernutrition in children under age five in Tanzania (e.g. stunting from 34·4 % in 2014 to 31·8 % in 2018) are still too slow to meet the SDG targets by 2030(12). Even worse, the prevalence of child underweight increased from 13·7 % in 2014 to 14·6 % in 2018(12). Simultaneously overweight and obesity is rapidly growing, affecting over 30 % of Tanzanian women aged 15–49 years(12), perhaps mainly due to major reductions in physical activities at work, transportation and home and increased consumption of cheap ultra-processed fast food and beverages(Reference Pallangyo, Mkojera and Hemed13,Reference Popkin, Corvalan and Grummer-Strawn14) . The coexistence of persisting undernutrition and rising obesity may increase DBM in Tanzania(Reference Faustini, Mniachi and Msengwa15).

DBM at the household level is defined as multiple family members affected by different forms of malnutrition(8). Household-level DBM varies between countries and often arises in lower-middle-income countries including Tanzania(Reference Popkin, Corvalan and Grummer-Strawn14). Evidence showed that the prevalence of the total household-level DBM ranged between 3 % and 35 % across 126 LMIC, with child stunting and maternal overweight/obesity being the most prevalent DBM type (ranging between 1 % and 24 %)(Reference Popkin, Corvalan and Grummer-Strawn14,Reference Garrett and Ruel16) . Household-level DBM has been shown to be primarily driven by socio-economic inequalities; however, the effect of household economic status on DBM is heterogeneous(Reference Doak, Adair and Monteiro17Reference Fooken and Vo21). In poorer LMIC higher household economic levels were linked to increased odds of DBM, while in richer LMIC lower household economic levels were associated with higher odds of DBM(Reference Seferidi, Hone and Duran22). In Tanzania, it remains uncertain how household economic inequalities are associated with DBM. A univariate analysis in Tanzania reported a 1·4 times higher crude likelihood of DBM among richer households; however, this study did not account for important household characteristics such as place of residence when quantifying this association(Reference Faustini, Mniachi and Msengwa15).

Dietary diversity, a practical and valid indicator of nutrient/micronutrient adequacy in assessing maternal and child nutrition in LMIC, is hypothesised to be an underrated action target for addressing DBM(Reference Miller, Webb and Micha23,Reference Hawkes, Ruel and Salm24) . However, the role of dietary diversity in this association remains uncertain(Reference Doak, Adair and Monteiro17Reference Seferidi, Hone and Duran22). Poor dietary diversity remains prevalent in Africa(Reference Kumssa, Joy and Ander25,26) , especially among populations with diets based on starchy staples like Tanzanians(Reference Forsythe, Njau and Martin27,Reference Swindale and Bilinsky28) . Generally, dietary diversity increases as household income increases(Reference Swindale and Bilinsky28), thus it may mediate the beneficial effects of household income on improving nutrient adequacy and diet-related health outcomes(Reference Verger, Le Port and Borderon29). Paradoxically, in emerging economies and African countries, economic growth or family income has not yet efficiently improved dietary diversity(26,Reference Iziga30,Reference Ren, Li and Wang31) , but worsened nutrition-related health outcomes(Reference Alao, Nur and Fivian5,Reference Seferidi, Hone and Duran22,Reference Ren, Li and Wang31) . This is partly because other factors, such as cultural preferences(Reference Forsythe, Njau and Martin27), lack of nutrition knowledge(Reference Forsythe, Njau and Martin27), and unimproved food systems(32), contribute significantly(Reference Iziga30). We assumed that the unimproved dietary diversity may play a moderating role in attenuating the potential adverse impact of household wealth on DBM in Tanzania.

In this study, we aimed to investigate household economic inequalities in DBM, expressed as child stunting and maternal overweight/obesity, and the moderating role of dietary diversity in these inequalities. We hypothesised that the association between household wealth and DBM may be weaker among mother–child pairs with a higher dietary diversity.

Methods

Data

We obtained cross-sectional data from the 2015–2016 Tanzania Demographic and Health Survey, provided by the United States Agency for International Development(33). The data were from nationally representative household surveys of girls and women of productive age (15–49 years) and their children born in the five years preceding the survey, using a stratified two-stage cluster sampling method. This sampling technique allowed each household to have an equal probability of participating in the survey. In the present study, we used the dataset for children under the age of five and their mothers. This dataset provides anthropometric information for each child, as well as the characteristics of the mother and household (n 10 233)(34). For the analysis, we included children aged 6–23 months old (n 3320), who were recommended by the WHO/UNICEF as key targets for assessing infant and young child feeding practices using diet quality indicators such as dietary diversity(35). We excluded children who were not alive (n 137), children who were not living with their mothers (n 47) and children with height missing values (n 55). Moreover, we excluded mothers who were pregnant (n 207) and those with missing values of weight or height (n 7). Our final sample consisted of 2867 mother–child pairs (weighted sample size: n 2850) (see online supplementary material, Supplemental Fig. S1).

Double burden of malnutrition

Anthropometric data (weight and height) were collected based on the standard procedures from the WHO(34,36,37) . Weight was measured with an electronic SECA 874 flat scale in 0·1 kg increments(34). For very young children, the mother or caretaker was weighed first and then weighed again while holding the child(34). The weight scale allowed the mother’s stored weight to be deducted and showed the child’s weight on the display. Height was measured with a short measuring board in a standing position, while children younger than 24 months or shorter than 85 cm were measured lying down on the board (recumbent length)(34).

DBM can occur in different scenarios, including when a child is both stunted and overweight, when a child is wasted with a mother who is overweight/obese, when a child is stunted with a mother who is overweight/obese or when a child is overweight with a mother who is underweight(Reference Popkin, Corvalan and Grummer-Strawn14). We defined DBM as child stunting and maternal overweight/obesity in the same household, as it is the most prevalent and well-studied measure for assessing household-level DBM in LMIC(Reference Popkin, Corvalan and Grummer-Strawn14,Reference Seferidi, Hone and Duran22) . A child was considered stunted if their height-for-age Z-score was below minus two standard deviations (–2 sd) from the 2006 WHO Child Growth Standards median Z-score(36). A mother was considered overweight if her BMI was 25 kg/m2 or higher(37). The DBM variable was coded 1 if a child was stunted and the mother was overweight and 0 otherwise.

Household economic status

Household economic affluence was measured using the DHS wealth index(33,34) . The DHS wealth index is a composite measure of a household’s cumulative living standard, constructed using household-level information on ownership of selected assets, such as television and bicycles, materials for housing construction and type of water access and sanitation facilities(Reference Rutstein38). It is one of the most useful indicators of household financial well-being in LMIC where it is difficult to obtain reliable data on household income from surveys(33,34) . This is because a significant portion of the population in LMIC do not receive market-level transactions and engage in significant home production(Reference Fooken and Vo21). A continuous measure of relative wealth (i.e. wealth index factor score) was assessed for each household using principal component analysis(33,34) . Based on the distribution of the wealth index factor score in the whole survey sample of the 2015–2016 Tanzania DHS, all households were categorised into quintiles(33,34) .

Dietary diversity

In the 2015–2016 Tanzania DHS, training of field staff on the nutritional survey was provided by the trainers from the Ifakara Health Institute and Tanzania Food and Nutrition Centre, with support from the Inner City Fund International(34). Mothers were asked if the child was receiving breastmilk and provided a 24-h recall of foods and food groups given to their children(39). Data were collected on the following foods and beverages that the child had consumed the previous day: juice; tinned, powdered or fresh milk; formula milk; fortified baby food (cerelac, etc.); other porridge/gruel; soup/clear broth; other liquids; chicken, duck, or other birds; bread, noodles, other grains; potatoes, cassava, tubers; eggs; meat (beef, pork, lamb, chicken, etc.); pumpkin, carrots, squash; dark green leafy vegetables; mangoes, papayas, other vitamin A fruits; any other fruits; liver, heart, other organ meat; fish or shellfish; beans, peas, lentils, nuts; cheese, yogurt, other milk products; oil, fats, butter, products made of them and other solid/semi-solid food. Eight food groups were defined following the WHO/UNICEF Infant and Young Child Feeding practices guidelines(39,40) : (1) breastmilk; (2) grains, roots and tubers; (3) legumes and nuts; (4) dairy products (infant formula, milk, yogurt and cheese); (5) flesh foods (meat, fish, poultry and liver/organ meats); (6) eggs; (7) fruits and vegetables rich in vitamin A and (8) other fruits and vegetables(41).

Dietary diversity is a commonly used indicator of diet quality estimated using the number of different food groups consumed within over a given reference period(35). For each child, a dietary diversity score was computed by counting the number of consumed food groups (ranging from zero to eight). Minimum dietary diversity was defined as having a dietary diversity score > 5, according to the 2021 WHO/UNICEF Infant and Young Child Feeding practices guideline(40) and the DHS statistics guide(39). We used minimum dietary diversity for children as a proxy indicator at the household level since data on the mothers’ diet were not available. Mother–child pairs were categorised into two groups: achieving and not achieving minimum dietary diversity.

Covariates

We considered the following demographic and socio-economic covariates that may affect both household economic status and the presence of DBM: the mother’s age (in years), education (no completed education, completed primary education or completed secondary education and above), marital status (never married, currently married and formerly married), place of residence (urban or rural), number of children in the household, child’s age (in months) and sex (male or female) and the number of household members.

Statistical analysis

All statistical analyses were performed using the SAS software (version 9.4; SAS Institute) and R version 4.3.0 (R Foundation for Statistical Computing). All analyses were weighted using sampling weights, which considered the stratified cluster sampling design and non-response rate. The prevalence of DBM by region was illustrated as a choropleth map, and regional differences were tested using χ2 tests. We summarised the sample characteristics according to the wealth index quintiles among non-achievers and achievers of minimum dietary diversity. Descriptive statistics were presented as weighted means and SE for continuous variables and weighted frequencies (%) and their SE for categorical variables. We tested the trends in the sample characteristics across quintiles of wealth index using logistic regression model for categorical variables and linear regression model for continuous variables.

We built logistic regression models for stratified cluster sampling to assess the OR and 95 % CI of DBM according to the wealth index levels. Given that there were too few cases of DBM among mother–child pairs who achieved minimum dietary diversity in the poorest group to build logistic regression models, we merged the poorest group with the poorer group. We used both a continuous estimate of the wealth index score and groups of the wealth index as independent variables in separate models. First, we performed unadjusted analyses. We then adjusted the models for all covariates as mentioned above. We tested the trend in the association between the wealth index and DBM by assigning ordinal numbers (0, 1, 2 and 3) to the wealth index categories, treating it as a continuous variable. Based on the hypothesis that the household wealth index might exhibit varying associations with DBM depending on the presence of minimum dietary diversity, we initially tested the heterogeneity in the associations between the two groups of minimum dietary diversity. This was achieved by adding a multiplicative interaction term (minimum dietary diversity × household wealth index). We tested this interaction effect using the likelihood ratio test by comparing the log-likelihood of the model containing the interaction term and that of the model not containing the interaction term. We conducted primary analyses separately for non-achievers and achievers of minimum dietary diversity. We performed a restricted cubic spline analysis without assuming a linear association between the wealth index score and the DBM to visualise the shape of this association. We placed four knots at the 20th (the reference), 40th, 60th and 80th percentiles of the wealth index score. Collinearity between independent variables was checked using the variance inflation factor test.

We performed the following sensitivity analyses: (1) additionally adjusting for region to account for the potential confounding effect in which the association between household wealth and DBM is attributed to regional differences only and (2) removing the variable of place of residence from the covariates to address the potential collinearity between place of residence and the household wealth index (with a variance inflation factor value = 2·3). Statistical tests were two-sided, and a P value for the interaction term < 0·05 was considered statistically significant.

Results

The estimated prevalence (s e) of DBM was 5·6 % (0·6). The prevalence (se) of child stunting was 31·1 % (1·2), and maternal overweight was 21·4 % (1·0). Figure 1 shows the regional distribution of the DBM prevalence in Tanzania, which ranged from the lowest rate of 0·6 % in Manyara to the highest rate of 12·2 % in Kusini Unguja, with significant regional differences (P = 0·03). In total, 21·8 % (1·0) of mother–child pairs achieved minimum dietary diversity. The estimated prevalence (se) of DBM was 5·4 % (0·6) among non-achievers of minimum dietary diversity and 6·7 % (1·2) among achievers of minimum dietary diversity.

Fig. 1 The estimated prevalence of double burden of malnutrition in Tanzania by region

Table 1 shows the characteristics of mother–child pairs according to the quintiles of the household wealth index among non-achievers and achievers of minimum dietary diversity. In both groups, households with a higher wealth index were more likely to have mothers with higher education, had few living children and household members and lived in urban areas. They were also more likely to have children with lower height-for-age and mothers with higher BMI. In non-achievers, households with a higher wealth index were more likely to have mothers who were younger and never or formerly married.

Table 1 Characteristics of mother–child pairs according to the household wealth index among non-achievers and achievers of minimum dietary diversity

Values are frequency (%) or mean. Frequencies, means and SEs are weighted using the sampling weights.

Figure 2 shows the prevalence of DBM according to the household wealth level among non-achievers and achievers of minimum dietary diversity. The prevalence of DBM showed a statistically significant increase with increasing household wealth index among non-achievers of minimum dietary diversity. However, this was not observed among achievers. The DBM prevalence reached a plateau in the richer group and then decreased in the richest group.

Fig. 2 The estimated prevalence and 95 % CI of DBM according to the household wealth index levels among non-achievers and achievers of minimum dietary diversity. The error bar denotes 95 % CI of the prevalence. The poorest group was merged with the poorer group as there was only one case of DBM in the poorest group among those who achieved minimum dietary diversity. *The trend of the association was assessed by assigning ordinal numbers to each group of the household wealth index and modelling this variable as a continuous variable. DBM, double burden of malnutrition

Table 2 shows the associations of household wealth index with DBM significantly differed by minimum dietary diversity, with P for interaction = 0·006. The multivariable-adjusted odds of DBM in non-achievers of minimum dietary diversity were approximately two times higher for both middle and richer groups and more than five times higher in the richest group, as compared with the poorest/poorer groups (P for trend < 0·001). However, the multivariable-adjusted odds of DBM among achievers were not statistically different in the middle and the richest groups, but they were approximately five times higher in the richer group. Similar results were observed when modelling the continuous variable of the wealth index score (mean (sd): 0·16 (0·94)), with an OR (95 % CI) per unit increase in the wealth index score of 2·10 (1·36, 3·25) among non-achievers of minimum dietary diversity and an OR (95 % CI) of 1·38 (0·76, 2·54) among achievers. Restricted cubic spline analyses showed a similar shape association between the wealth index score and DBM among non-achievers and achievers of minimum dietary diversity (see online supplementary material, Supplemental Fig. S2). The prevalence of child stunting decreased as household wealth increased, especially among achievers of minimum dietary diversity. However, the prevalence of maternal overweight increased with the household wealth levels in both non-achievers and achievers of minimum dietary diversity (see online supplementary material, Supplemental Fig. S3).

Table 2 Associations between household wealth index and the double burden of malnutrition among non-achievers and achievers of minimum dietary diversity (MDD)

DBM, double burden of malnutrition. Adjusted models were adjusted for mother’s age (in years), education (no completed education, completed primary education or completed secondary education and above), marital status (never married, currently married and formerly married), place of residence (urban or rural), number of children in the household, child’s age (in months) and sex (male or female) and number of household members.

* The poorest group was merged with the poorer group as there was only 1 case of DBM in the poorest group among those who achieved minimum dietary diversity to build the logistic regression model.

Trend association was assessed by assigning ordinal numbers to each group of household wealth index and modelling this variable as a continuous variable.

In the sensitivity analyses, the results minimally changed after further adjustment for regions (see online supplementary material, Supplemental Table S1), or without adjustment for the place of residence (see online supplementary material, Supplemental Table S2).

Discussion

This analysis demonstrated that the prevalence of household-level DBM varied regionally and was unequally distributed across levels of household wealth. Inequalities in DBM across household wealth levels were moderated by minimum dietary diversity. Richer households had higher odds of DBM, but this association was less pronounced in mother–child pairs achieving minimum dietary diversity. Our findings suggest that household wealth increased DBM in Tanzania; however, dietary diversity could potentially mitigate this negative impact. This study is one of the few attempts to examine the economic inequalities in DBM at the household level in Tanzania by considering the moderating role of dietary diversity in these inequalities.

Our observation of the prevalence of DBM at the household level in Tanzania is comparable with the results from analyses of LMIC (5·6 % v. 6·0 %)(Reference Seferidi, Hone and Duran22). However, our observations indicate relatively higher rates of DBM compared with LMIC in Asia, where the prevalence was mostly < 1 %(Reference Fooken and Vo21). This disparity may be primarily driven by the high prevalence of maternal overweight or obesity in Tanzania (31·7 % in 2018)(12). We also observed regional differences in the prevalence of DBM. DBM tended to be disproportionately concentrated in regions with relatively higher economic development levels, such as Kusini Unguja, Mwanza, Tanga and Dar es Salaam. This observation could be partly explained by the fact that economic growth of an entire area might exacerbate the DBM prevalence(Reference Fooken and Vo21,Reference Seferidi, Hone and Duran22) . Taken together, our findings suggest the importance of accounting for regional differences including varying economic development levels, when addressing DBM in Tanzania.

Our findings on the negative impact of household economic affluence on household-level DBM in Tanzania agree with findings from previous limited analysis in fifty-five LMIC(Reference Seferidi, Hone and Duran22) and eleven LMIC in Asia(Reference Fooken and Vo21), as well as other analyses using nationally representative data(Reference Hong19,Reference Oddo, Rah and Semba20) . In contrast, some analyses showed no or opposite direction of the association(Reference Doak, Adair and Monteiro17,Reference Nakphong and Beltrán-Sánchez18) . Of note, no previous analysis has examined the interaction between household economic affluence and dietary diversity on DBM. This study expands on existing evidence regarding the adverse impact of household wealth on DBM and demonstrated that dietary diversity could potentially alleviate these negative impacts. This moderating effect of dietary diversity could be driven by the observed dramatic decrease in the child stunting rate among the richest households that embraced a minimum level of dietary diversity. A more diverse diet is highly correlated with higher micronutrient intake among children, thus helping prevent child stunting(Reference Swindale and Bilinsky28). The dramatic decrease in child stunting in the richest households could be attributed to the fact that their mothers were more likely to have a higher level of nutritional literacy, in addition to more food expenditure to sustain a high overall diet quality for their children(Reference Mohsen, Sacre and Hanna-Wakim42). We also observed a persistent increase in maternal overweight as household wealth increased, even among the group that achieved minimum dietary diversity. This result indicates that affluent Tanzanian women have a high level of total energy intake, regardless of dietary diversity. This finding could be partly explained by the cultural beliefs held by Tanzanian women that associate overweight/obesity with beauty and consider it a symbol of success in life(Reference Keding, Msuya and Maass43). Our findings support that dietary diversity might be an underrated action target for addressing DBM(Reference Miller, Webb and Micha23,Reference Hawkes, Ruel and Salm24) .

A recent Lancet Commission advocated double-duty actions to simultaneously address different forms of malnutrition, aligning with the United Nations’ SDG and global nutrition targets(Reference Miller, Webb and Micha23,Reference Hawkes, Ruel and Salm24) . Our findings indicate that double-duty actions promoting dietary diversity for children while simultaneously reducing total energy intake among mothers could be an effective strategy to address DBM in Tanzania. Additionally, the design of such double-duty actions should consider the uneven impact of economic affluence, as well as cultural and regional differences.

This study used a large nationally representative sample and employed robust methodological approaches, including interactions between household wealth and dietary diversity and restricted cubic splines to avoid assuming linear associations. Our results remained robust under different sensitivity analyses. However, this study has several limitations. The cross-sectional nature precludes causal inferences. We did not include children aged 2 years and older because the DHS employed the WHO-designed indicator of minimum dietary diversity specifically for children 6–23 months(35). Future studies should validate our findings among children aged 24–59 months and their mothers in LMIC(Reference Diop, Becquey and Turowska44). This study was also limited by the lack of data on mother’s diet. In Tanzania, there is a food culture in which women and children eat from the same pot(Reference Forsythe, Njau and Martin27), indicating that what mothers eat is strongly related to what their children eat(Reference Hasan, Islam and Mubarak45). Nevertheless, we could not rule out the possibility of misclassification of mother–child pairs’ minimum dietary diversity, which may have led to an underestimation of the moderating effect of dietary diversity on DBM. There is a chance that the statistical power could be inadequate for the analysis among achievers of minimum dietary diversity. However, we observed significantly higher odds of DBM among non-achievers compared with their counterparts. Thus, this is unlikely to alter our conclusion. Although we used the most prevalent measure of DBM, other forms of DBM exist and may exhibit different associations with household wealth. The wealth index is a country-specific and relative measure of household wealth affluence. We urge caution when generalising our findings to other countries.

In conclusion, the prevalence of household-level DBM was unequally distributed across regions of Tanzania and increased with higher household wealth. However, the association between household wealth and DBM was mitigated by dietary diversity levels. Our findings highlight the importance of increasing dietary diversity to address the negative impact of household wealth on DBM in Tanzania.

Financial support

This work was supported by Grants-in-Aid for Early-Career Scientists KAKENHI from the Ministry of Education, Culture, Sports, Science and Technology of Japan (23K16471) to SC. The funder had no role in the analysis and interpretation of data, the writing of the report or in the decision to submit the paper for publication.

Conflict of interest

We have no competing interests to declare.

Authorship

S.C. conceptualised and designed this study. S.C. performed the statistical analysis. S.C., Y.S. and T.H. contributed to verification of the statistical results. S.C., Y.S., T.H., D.L.B. and B.M. contributed to the interpretation of the results. All authors had access to the data in the study. S.C. had primary responsibility for the final content. S.C. wrote the first draft of the manuscript, and all authors contributed to the manuscript revision.

Ethics of human subject participation

This research involved analysis of publicly available, de-idenified data. This data collection was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the Medical Research Council of Tanzania and the Zanzibar Health Research Institute and reviewed by the Internal Review Board of the Inner City Fund.

The maps included in this research paper are for illustrative purposes only. The boundaries, names, and designations used in the maps do not imply official endorsement or acceptance by the authors or affiliated institutions. The depiction of any specific geographic area, including political boundaries, does not imply any position regarding legal or political status. Users are advised to exercise caution and consult additional reliable sources for precise and up-to-date information. The authors and affiliated institutions bear no responsibility for any errors or omissions in the maps or for any consequences arising from the use or interpretation of the information presented.

Supplementary material

For supplementary material accompanying this paper visit https://doi.org/10.1017/S136898002400106X

References

High Level Panel of Experts on Food Security and Nutrition (2020) Food Security and Nutrition: Building a Global Narrative Towards 2030. A Report by the High Level Panel of Experts on Food Security and Nutrition of the Committee on World Food Security. Rome: HLPE.Google Scholar
UN (2019) The United Nations Decade of Action on Nutrition: Addressing the Challenge. https://www.un.org/nutrition/commitments (accessed January 2023).Google Scholar
Nilsson, M, Griggs, D & Visbeck, M (2016) Policy: map the interactions between Sustainable Development Goals. Nature 534, 320322.CrossRefGoogle ScholarPubMed
Wells, JC, Sawaya, AL, Wibaek, R et al. (2020) The double burden of malnutrition: aetiological pathways and consequences for health. Lancet 395, 7588.CrossRefGoogle ScholarPubMed
Alao, R, Nur, H, Fivian, E et al. (2021) Economic inequality in malnutrition: a global systematic review and meta-analysis. BMJ Glob Heal 6, e006906.CrossRefGoogle ScholarPubMed
Khan, SS, Ning, H, Wilkins, JT et al. (2018) Association of body mass index with lifetime risk of cardiovascular disease and compression of morbidity. JAMA Cardiol 3, 280287.CrossRefGoogle ScholarPubMed
Demaio, AR & Branca, F (2017) Decade of action on nutrition: our window to act on the double burden of malnutrition. BMJ Glob Heal 3, e000492.CrossRefGoogle ScholarPubMed
World Health Organization (2017) The Double Burden of Malnutrition. Policy Brief. Geneva: WHO.Google Scholar
Popkin, BM, Horton, S, Kim, S et al. (2001) Trends in diet, nutritional status, and diet-related noncommunicable diseases in China and India: the economic costs of the nutrition transition. Nutr Rev 59, 379390.CrossRefGoogle Scholar
Nugent, R, Levin, C, Hale, J et al. (2020) Economic effects of the double burden of malnutrition. Lancet 395, 156164.CrossRefGoogle ScholarPubMed
The World Bank (2022) The World Bank in Tanzania. https://www.worldbank.org/en/country/tanzania/overview (accessed January 2023).Google Scholar
Ministry of Health Community Development Gender Elderly and Children, Ministry of Health, Tanzania Food and Nutrition Center et al. (2019) Tanzania National Nutrition Survey 2018. Dar es Salaamm, Tanzania: MoHCDGEC, MoH, TFNC, NBS, OCGS, and UNICEF.Google Scholar
Pallangyo, P, Mkojera, ZS, Hemed, NR et al. (2020) Obesity epidemic in urban Tanzania: a public health calamity in an already overwhelmed and fragmented health system. BMC Endocr Disord 20, 147.CrossRefGoogle Scholar
Popkin, BM, Corvalan, C & Grummer-Strawn, LM (2020) Dynamics of the double burden of malnutrition and the changing nutrition reality. Lancet 395, 6574.CrossRefGoogle ScholarPubMed
Faustini, FT, Mniachi, AR & Msengwa, AS (2022) Coexistence and correlates of forms of malnutrition among mothers and under-five child pairs in Tanzania. J Nutr Sci 11, e103.CrossRefGoogle ScholarPubMed
Garrett, JL & Ruel, MT (2005) Stunted child-overweight mother pairs: prevalence and association with economic development and urbanization. Food Nutr Bull 26, 209221.CrossRefGoogle ScholarPubMed
Doak, CM, Adair, LS, Monteiro, C et al. (2000) Overweight and underweight coexist within households in Brazil, China and Russia. J Nutr 130, 29652971.CrossRefGoogle ScholarPubMed
Nakphong, MK & Beltrán-Sánchez, H (2021) Socio-economic status and the double burden of malnutrition in Cambodia between 2000 and 2014: overweight mothers and stunted children. Public Health Nutr 24, 18061817.CrossRefGoogle ScholarPubMed
Hong, SA (2021) Prevalence and regional variations of coexistence of child stunting and maternal overweight or obesity in Myanmar. Public Health Nutr 24, 22482258.CrossRefGoogle ScholarPubMed
Oddo, VM, Rah, JH, Semba, RD et al. (2012) Predictors of maternal and child double burden of malnutrition in rural Indonesia and Bangladesh. Am J Clin Nutr 95, 951958.CrossRefGoogle ScholarPubMed
Fooken, J & Vo, LK (2021) Exploring the macroeconomic and socioeconomic determinants of simultaneous over and undernutrition in Asia: an analysis of stunted child – overweight mother households. Soc Sci Med 269, 113570.CrossRefGoogle ScholarPubMed
Seferidi, P, Hone, T, Duran, AC et al. (2022) Global inequalities in the double burden of malnutrition and associations with globalisation: a multilevel analysis of Demographic and Health Surveys from 55 low-income and middle-income countries, 1992–2018. Lancet Glob Heal 10, e482e490.CrossRefGoogle ScholarPubMed
Miller, V, Webb, P, Micha, R et al. (2020) Defining diet quality: a synthesis of dietary quality metrics and their validity for the double burden of malnutrition. Lancet Planet Heal 4, e352e370.CrossRefGoogle ScholarPubMed
Hawkes, C, Ruel, MT, Salm, L et al. (2020) Double-duty actions: seizing programme and policy opportunities to address malnutrition in all its forms. Lancet 395, 142155.CrossRefGoogle ScholarPubMed
Kumssa, DB, Joy, EJM, Ander, EL et al. (2015) Dietary calcium and zinc deficiency risks are decreasing but remain prevalent. Sci Rep 5, 10974.CrossRefGoogle ScholarPubMed
FAO, IFAD (International Fund for Agricultural Development), UNICEF (United Nations Children’s Fund), et al. (2020) The State of Food Security and Nutrition in the World 2020. Transforming Food Systems for Affordable Healthy Diets. Rome: FAO.Google Scholar
Forsythe, L, Njau, M, Martin, A et al. (2017) Staple food cultures: a case study of cassava ugali preferences in Dar es Salaam, Tanzania. Natural Resources Institute and CGIAR Research Program on Roots, Tubers and Bananas (RTB). RTB Working Paper. https://gala.gre.ac.uk/22350/7/22350%20FORSYTHE_Staple_Food_Cultures_2017.pdf (accessed April 2023).Google Scholar
Swindale, A & Bilinsky, P (2006) Household Dietary Diversity Score (HDDS) for Measurement of Household Food Access: Indicator Guide (v.2). Washington, DC: FHI 360/FANTA.Google Scholar
Verger, EO, Le Port, A, Borderon, A et al. (2021) Dietary diversity indicators and their associations with dietary adequacy and health outcomes: a systematic scoping review. Adv Nutr 12, 16591672.CrossRefGoogle ScholarPubMed
Iziga, JI (2023) Prioritizing Economic Development for Increasing Dietary Diversity. Sapporo, Japan: Hokkaido University.Google Scholar
Ren, Y, Li, H & Wang, X (2019) Family income and nutrition-related health: evidence from food consumption in China. Soc Sci Med 232, 5876.CrossRefGoogle ScholarPubMed
World Food Programme (2021) Food Systems in Tanzania: Investing in Distribution to Trigger Systemic Change. Dar es Salaam: WFP Tanzania Country Office.Google Scholar
USAID DHS Overview (2018). https://dhsprogram.com/Methodology/Survey-Types/DHS.cfm (accessed January 2023).Google Scholar
Ministry of Health, Community Development, Gender, Elderly and Children (MoHCDGEC) (Tanzania Mainland), Ministry of Health (MoH) (Zanzibar), National Bureau of Statistics (NBS), et al. (2016) Tanzania Demographic and Health Survey and Malaria Indicator Survey (TDHS-MIS) 2015–2016. Dar es Salaam, Tanzania; Rockville, MD: MoHCDGEC, MoH, NBS, OCGS, and ICF.Google Scholar
WHO & UNICEF (2017) Global Nutrition Monitoring Framework. Operational Guidance for Tracking Progress in Meeting Targets for 2025. Geneva: WHO.Google Scholar
World Health Organization (2006) WHO Child Growth Standards: Length/Height-for-Age, Weight-for-Age, Weight for-Length, Weight-for-Height and Body Mass Index for-Age: Methods and Development. Geneva: World Health Organization.Google Scholar
World Health Organization (1995) Physical Status: The Use and Interpretation of Anthropometry: Report of a World Health Organization (WHO) Expert Committee. Geneva: World Health Organization.Google Scholar
Rutstein, S (2008) The DHS: Approaches for Rural and Urban Areas. DHS Working Paper Series. https://www.dhsprogram.com/pubs/pdf/WP60/WP60.pdf (accessed February 2023).Google Scholar
USAID (2019) Guide to DHS Statistics DHS-7: Minimum Dietary Diversity, Minimum Meal Frequency and Minimum Acceptable Diet. https://dhsprogram.com/data/Guide-to-DHS-Statistics/Minimum_Dietary_Diversity_Minimum_Meal_Frequency_and_Minimum_Acceptable_Diet.htm (accessed January 2023).Google Scholar
World Health Organization and the United Nations Children’s Fund (UNICEF) (2021) Indicators for Assessing Infant and Young Child Feeding Practices: Definitions and Measurement Methods. Geneva: World Health Organization and the United Nations Children’s Fund (UNICEF).Google Scholar
World Health Organisation (2010) Indicators for Assessing Infant and Young Child Feeding Practices (Part 1, Definitions). Geneva, Switzerland: World Health Organization.Google Scholar
Mohsen, H, Sacre, Y, Hanna-Wakim, L et al. (2022) Nutrition and food literacy in the MENA region: a review to inform nutrition research and policy makers. Int J Environ Res Public Health 19, 10190.CrossRefGoogle ScholarPubMed
Keding, GB, Msuya, JM, Maass, BL et al. (2013) Obesity as a public health problem among adult women in rural Tanzania. Glob Heal Sci Pract 1, 359371.CrossRefGoogle ScholarPubMed
Diop, L, Becquey, E, Turowska, Z et al. (2021) Standard minimum dietary diversity indicators for women or infants and young children are good predictors of adequate micronutrient intakes in 24–59-month-old children and their nonpregnant nonbreastfeeding mothers in rural Burkina Faso. J Nutr 151, 412422.CrossRefGoogle ScholarPubMed
Hasan, M, Islam, MM, Mubarak, E et al. (2019) Mother’s dietary diversity and association with stunting among children < 2 years old in a low socio-economic environment: a case–control study in an urban care setting in Dhaka, Bangladesh. Matern Child Nutr 15, e12665.CrossRefGoogle Scholar
Figure 0

Fig. 1 The estimated prevalence of double burden of malnutrition in Tanzania by region

Figure 1

Table 1 Characteristics of mother–child pairs according to the household wealth index among non-achievers and achievers of minimum dietary diversity

Figure 2

Fig. 2 The estimated prevalence and 95 % CI of DBM according to the household wealth index levels among non-achievers and achievers of minimum dietary diversity. The error bar denotes 95 % CI of the prevalence. The poorest group was merged with the poorer group as there was only one case of DBM in the poorest group among those who achieved minimum dietary diversity. *The trend of the association was assessed by assigning ordinal numbers to each group of the household wealth index and modelling this variable as a continuous variable. DBM, double burden of malnutrition

Figure 3

Table 2 Associations between household wealth index and the double burden of malnutrition among non-achievers and achievers of minimum dietary diversity (MDD)

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