PROCOMIDA, a Food-Assisted Maternal and Child Health and Nutrition Program, Reduces Child Stunting in Guatemala: A Cluster-Randomized Controlled Intervention Trial

Deanna K Olney, Jef Leroy, Lilia Bliznashka, Marie T Ruel, Deanna K Olney, Jef Leroy, Lilia Bliznashka, Marie T Ruel

Abstract

Background: Food-assisted maternal and child health and nutrition (FA-MCHN) programs may foster child growth during the first 1000 d (pregnancy and the first 2 y of a child's life), but evidence is scant.

Objective: We evaluated the impact of an FA-MCHN program, PROCOMIDA, on linear growth (stunting [length-for-age z score (LAZ) < -2] and length-for-age difference [LAD]) among children aged 1-24 mo. PROCOMIDA was implemented in Guatemala by Mercy Corps and was available to beneficiaries throughout the first 1000 d.

Methods: We used a longitudinal, cluster-randomized controlled trial with groups varying in family ration sizes [full (FFR), reduced (RFR), and none (NFR)] and individual ration types provided to mothers (pregnancy to 6 mo postpartum) and children (6-24 mo of age) [corn-soy blend (CSB), lipid-based nutrient supplement (LNS), micronutrient powder (MNP)]: 1) FFR + CSB (n = 576); 2) RFR + CSB (n = 575); 3) NFR + CSB (n = 542); 4) FFR + LNS (n = 550); 5) FFR + MNP (n = 587); 6) control (n = 574). Program impacts compared with control, and differential impacts between groups varying family ration size or individual ration type, were assessed through the use of linear mixed-effects models and post hoc simple effect tests (significant if P < 0.05).

Results: PROCOMIDA significantly reduced stunting at age 1 mo in FFR + CSB, RFR + CSB, and FFR + MNP groups compared with control [5.05, 4.06, and 3.82 percentage points (pp), respectively]. Stunting impact increased by age 24 mo in FFR + CSB and FFR + MNP relative to control (impact = 11.1 and 6.5 pp at age 24 mo, respectively). For CSB recipients, the FFR compared with RFR or NFR significantly reduced stunting (6.47-9.68 pp). CSB reduced stunting significantly more than LNS at age 24 mo (8.12 pp).

Conclusions: FA-MCHN programs can reduce stunting during the first 1000 d, even in relatively energy/food-secure populations. Large family rations with individual rations of CSB or MNP were most effective. The widening of impact as children age highlights the importance of intervening throughout the full first 1000 d. This trial was registered at clinicaltrials.gov as NCT01072279.

Figures

FIGURE 1
FIGURE 1
Study flow diagram. CC, convergence center; CSB, corn-soy blend; FFR, full family ration; LNS, lipid-based nutrient supplement; MNP, micronutrient powder; NFR, no family ration; RFR, reduced family ration.
FIGURE 2
FIGURE 2
Proportion of eligible beneficiaries participating in PROCOMIDA at each time point by study group. Participation was assessed by self-report of participation in the PROCOMIDA program. Enrollment into the survey was done during pregnancy and when the child was 1, 4, 6, 9, 12, 18, and 24 mo of age. Among those currently enrolled in PROCOMIDA, participation in the monthly behavior change communication and food distributions was >95% at all time points for all study groups. CSB, corn-soy blend; FFR, full family ration; LNS, lipid-based nutrient supplement; MNP, micronutrient powder; NFR, no family ration; RFR, reduced family ration.
FIGURE 3
FIGURE 3
Estimated marginal mean prevalence of stunting (length-for-age z score <−2) among children in treatment compared with control groups at 1, 4, 9, 12, 18, and 24 mo of age. Estimated marginal means (unadjusted means are presented in Tables 5 and 6), *P < 0.05, **< 0.01 for impact on stunting of treatment group [FFR + CSB (n = 576); RFR + CSB (n = 575); NFR + CSB (n = 542); FFR + LNS (n = 550); FFR + MNP (n = 587)] compared with the control group (n = 574) (Table 4). CSB, corn-soy blend; FFR, full family ration; LNS, lipid-based nutrient supplement; MNP, micronutrient powder; NFR, no family ration; RFR, reduced family ration.

References

    1. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, Ezzati M, Grantham-McGregor S, Katz J, Martorell R et al. . Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 2013;382:427–51.
    1. International Food Policy Research Institute (IFPRI) Global nutrition report 2016: from promise to impact: ending malnutrition by 2030. Washington (DC): International Food Policy Research Institute; 2016.
    1. Delgado HL. Technical report. Status and trends in chronic malnutrition in Guatemala. Chevy Chase, MD: University Research Co., LLC; 2010.
    1. Schroeder DG, Martorell R, Rivera JA, Ruel MT, Habicht JP. Age differences in the impact of nutritional supplementation on growth. J Nutr 1995;125:1051S–9S.
    1. Martorell R, Schroeder DG, Rivera JA, Kaplowitz HJ. Patterns of linear growth in rural Guatemalan adolescents and children. J Nutr 1995;125:1060S–7S.
    1. Martorell R, Melgar P, Maluccio JA, Stein AD, Rivera JA. The nutrition intervention improved adult human capital and economic productivity. J Nutr 2010;140:411–14.
    1. Panjwani A, Heidkamp R. Complementary feeding interventions have a small but significant impact on linear and ponderal growth of children in low- and middle-income countries: a systematic review and meta-analysis. J Nutr 2017;147:2169S–78S.
    1. Bhandari N, Bahl R, Taneja S. Effect of micronutrient supplementation on linear growth of children. Br J Nutr 2001;85(Suppl 2):S131–7.
    1. Christian P, Shaikh S, Shamim AA, Mehra S, Wu L, Mitra M, Ali H, Merrill RD, Choudhury N, Parveen M et al. . Effect of fortified complementary food supplementation on child growth in rural Bangladesh: a cluster-randomized trial. Int J Epidemiol 2015;44:1862–76.
    1. Allen LH, Peerson JM, Olney DK. Provision of multiple rather than two or fewer micronutrients more effectively improves growth and other outcomes in micronutrient-deficient children and adults. J Nutr 2009;139:1022–30.
    1. Shafique S, Sellen DW, Lou W, Jalal CS, Jolly SP, Zlotkin SH. Mineral- and vitamin-enhanced micronutrient powder reduces stunting in full-term low-birth-weight infants receiving nutrition, health, and hygiene education: a 2 × 2 factorial, cluster-randomized trial in Bangladesh. Am J Clin Nutr 2016;103:1357–69.
    1. Adu-Afarwuah S, Lartey A, Okronipa H, Ashorn P, Peerson JM, Arimond M, Ashorn U, Zeilani M, Vosti S, Dewey KG. Small-quantity, lipid-based nutrient supplements provided to women during pregnancy and 6 mo postpartum and to their infants from 6 mo of age increase the mean attained length of 18-mo-old children in semi-urban Ghana: a randomized controlled trial. Am J Clin Nutr 2016;104:797–808.
    1. Ashorn P, Alho L, Ashorn U, Cheung YB, Dewey KG, Harjunmaa U, Lartey A, Nkhoma M, Phiri N, Phuka J et al. . The impact of lipid-based nutrient supplement provision to pregnant women on newborn size in rural Malawi: a randomized controlled trial. Am J Clin Nutr 2015;101:387–97.
    1. Imdad A, Bhutta ZA. Maternal nutrition and birth outcomes: effect of balanced protein-energy supplementation. Paediatr Perinat Epidemiol 2012;26:178–90.
    1. Haider BA, Bhutta ZA. Multiple-micronutrient supplementation for women during pregnancy. In: Bhutta ZA, editor Cochrane database of systematic reviews. Chichester, UK: John Wiley & Sons, Ltd; 2015.
    1. Lu W-P, Lu M-S, Li Z-H, Zhang C-X, Lind T. Effects of multimicronutrient supplementation during pregnancy on postnatal growth of children under 5 years of age: a meta-analysis of randomized controlled trials. PLoS One 2014;9:e88496.
    1. Christian P, Kim J, Mehra S, Shaikh S, Ali H, Shamim AA, Wu L, Klemm R, Labrique AB, West KP. Effects of prenatal multiple micronutrient supplementation on growth and cognition through 2 y of age in rural Bangladesh: the JiVitA-3 trial. Am J Clin Nutr 2016;104:1175–82.
    1. Ruel MT, Menon P, Habicht J-P, Loechl C, Bergeron G, Pelto G, Arimond M, Maluccio J, Michaud L, Hankebo B. Age-based preventive targeting of food assistance and behaviour change and communication for reduction of childhood undernutrition in Haiti: a cluster randomised trial. Lancet 2008;371:588–95.
    1. Leroy JL, Olney D, Ruel M. Tubaramure, a food-assisted integrated health and nutrition program, reduces child stunting in Burundi: a cluster-randomized controlled intervention trial. J Nutr 2018;148:445–52.
    1. MSPAS; INE; ICF Encuesta Nacional de Salud Materno Infantil 2014-2015. Informe final. Guatemala City: MSPAS; INE; ICF; 2017.
    1. Richter S, Harris J, Leroy J, Olney D, Ruel M. Strengthening and evaluating the “Preventing Malnutrition in children under two years of age Approach” (PM2A) in Guatemala. Washington (DC): Poverty, Health, and Nutrition Division, FHI 360/FANTA; 2011.
    1. Olney D, Arriola M, Carranza R, Leroy J, Richter S, Harris J, Ruel M, Becker E. Report of formative research conducted in Alta Verapaz, Guatemala, to help inform the health-strengthening activities and the social and behavior change communication strategy that will be implemented through the Mercy Corps PM2A program – PROCOMIDA. Washington (DC): FHI 360/FANTA; 2012.
    1. Donegan S, Maluccio JA, Myers CK, Menon P, Ruel MT, Habicht J-P. Two food-assisted maternal and child health nutrition programs helped mitigate the impact of economic hardship on child stunting in Haiti. J Nutr 2010;140:1139–45.
    1. Cogill B. Anthropometric indicators measurement guide. Washington (DC): Food and Nutrition Technical Assistance Project, Academy for Educational Development; 2003.
    1. Ballard T, Coates J, Swindale A, Deitchler M. Household Hunger Scale (HHS): indicator definition and measurement guide FHI 360; 2011.
    1. World Health Organization Indicators for assessing infant and young child feeding practices: part II measurement. Geneva: World Health Organization; 2010.
    1. WHO Multicentre Growth Reference Study Group 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; 2006.
    1. Leroy JL, Ruel M, Habicht J-P, Frongillo EA. Linear growth deficit continues to accumulate beyond the first 1000 days in low- and middle-income countries: global evidence from 51 national surveys. J Nutr 2014;144:1460–6.
    1. Filmer D, Pritchett LH. Estimating wealth effects without expenditure data—or tears: an application to educational enrollments in states of India. Demography 2001;38:115–32.
    1. de Onis M, Dewey KG, Borghi E, Onyango AW, Blössner M, Daelmans B, Piwoz E, Branca F. The World Health Organization's global target for reducing childhood stunting by 2025: rationale and proposed actions. Matern Child Nutr 2013;9:6–26.
    1. Dewey KG, Mridha MK, Matias SL, Arnold CD, Cummins JR, Khan MSA, Maalouf-Manasseh Z, Siddiqui Z, Ullah MB, Vosti SA. Lipid-based nutrient supplementation in the first 1000 d improves child growth in Bangladesh: a cluster-randomized effectiveness trial. Am J Clin Nutr 2017;105:944–57.
    1. Arimond M, Zeilani M, Jungjohann S, Brown KH, Ashorn P, Allen LH, Dewey KG. Considerations in developing lipid-based nutrient supplements for prevention of undernutrition: experience from the International Lipid-Based Nutrient Supplements (iLiNS) project. Matern Child Nutr 2015;11:31–61.
    1. De-Regil LM, Suchdev PS, Vist GE, Walleser S, Peña-Rosas JP. Home fortification of foods with multiple micronutrient powders for health and nutrition in children under two years of age (review). Evid Based Child Health 2013;8:112–201.
    1. Thakwalakwa CM, Ashorn P, Jawati M, Phuka JC, Cheung YB, Maleta KM. An effectiveness trial showed lipid-based nutrient supplementation but not corn–soya blend offered a modest benefit in weight gain among 6- to 18-month-old underweight children in rural Malawi. Public Health Nutr 2012;15:1755–62.
    1. Lanou H, Huybregts L, Roberfroid D, Nikièma L, Kouanda S, Van Camp J, Kolsteren P. Prenatal nutrient supplementation and postnatal growth in a developing nation: an RCT. Pediatrics 2014;133:e1001–8.
    1. Adu-Afarwuah S, Lartey A, Okronipa H, Ashorn P, Zeilani M, Peerson JM, Arimond M, Vosti S, Dewey KG. Lipid-based nutrient supplement increases the birth size of infants of primiparous women in Ghana. Am J Clin Nutr 2015;101:835–46.
    1. Olney DK, Richter S, Becker E, Roopnaraine T, Margolies A, Kennedy A, Leroy JL, Ruel MT. A process evaluation of the PROCOMIDA “Preventing Malnutrition in children under 2 Approach” in Guatemala. Washington (DC): FHI 360; 2013.
    1. Shuaib FMB, Jolly PE, Ehiri JE, Yatich N, Jiang Y, Funkhouser E, Person SD, Wilson C, Ellis WO, Wang J-S et al. . Association between birth outcomes and aflatoxin B1 biomarker blood levels in pregnant women in Kumasi, Ghana. Trop Med Int Heal 2010;15:160–7.
    1. Turner PC, Collinson AC, Cheung YB, Gong Y, Hall AJ, Prentice AM, Wild CP. Aflatoxin exposure in utero causes growth faltering in Gambian infants. Int J Epidemiol 2007;36:1119–25.
    1. Gong YY, Cardwell K, Hounsa A, Egal S, Turner PC, Hall AJ, Wild CP. Dietary aflatoxin exposure and impaired growth in young children from Benin and Togo: cross sectional study. BMJ 2002;325:20–1.
    1. Gong Y, Hounsa A, Egal S, Turner PC, Sutcliffe AE, Hall AJ, Cardwell K, Wild CP. Postweaning exposure to aflatoxin results in impaired child growth: a longitudinal study in Benin, West Africa. Environ Health Perspect 2004;112:1334–8.
    1. Wild CP, Miller JD, Groopman JD. Mycotoxin control in low- and middle-income countries. Geneva: World Health Organization; 2016.

Source: PubMed

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