Impact of vitamin A with zinc supplementation on malaria morbidity in Ghana

Seth Owusu-Agyei, Sam Newton, Emmanuel Mahama, Lawrence Gyabaa Febir, Martha Ali, Kwame Adjei, Kofi Tchum, Latifa Alhassan, Thabisile Moleah, Sherry A Tanumihardjo, Seth Owusu-Agyei, Sam Newton, Emmanuel Mahama, Lawrence Gyabaa Febir, Martha Ali, Kwame Adjei, Kofi Tchum, Latifa Alhassan, Thabisile Moleah, Sherry A Tanumihardjo

Abstract

Background: Malaria is a leading cause of morbidity and mortality among young children and is estimated to cause at least 1 million deaths each year especially among pregnant women and young children under the age of five years. Vitamin A supplementation is known to reduce morbidity and mortality in young children. Zinc is required for growth and immunity and we sought to replicate the study by Zeba et al. which showed 30% lower cases of clinical malaria in children on a combination of zinc and a large dose of vitamin A compared with children on vitamin A alone based on the hypothesis that combined vitamin A and zinc reduced symptomatic malaria compared to vitamin A alone.

Objectives: The primary objective was to determine the effect of vitamin A alone vs. vitamin A and zinc supplements on the incidence of clinical malaria and other anthropometric indices. It also sought to assess the effects on the incidence of anaemia, diarrhoea and pneumonia.

Methods: The study was community-based and 200 children between the ages of 6-24 months were randomised to receive either vitamin A (100,000 IU for infants less than 12 months & 200,000 IU for children greater than 12 months and 10 mg daily zinc in the intervention group or vitamin A and zinc placebo for 6 months in the control group.

Results: The number of children who were diagnosed with uncomplicated malaria in the intervention group was 27% significantly lower compared with the children in the control group (p = 0.03). There were, however, no effects on severe malaria, pneumonia, anaemia and diarrhea.

Conclusions: Our study confirms a significant role of vitamin A and zinc in reducing malaria morbidity.

Figures

Figure 1
Figure 1
Trial profile of infants recruited into the trial and lost to follow up.

References

    1. Chuma JM, Thiede M, Molyneux CS. Rethinking the economic costs of malaria at the household level: Evidence from applying a new analytical framework in rural Kenya. Malar J. 2006;30:5–76.
    1. Holding PA, Kitsao-Wekulo PK. Describing the burden of malaria on child development: what should We Be measuring and How should We Be measuring It? Am J Trop Med Hyg. 2004;71(Suppl 2):71–79.
    1. Dewey KG, Peerson MJ, Heinig MJ, Noomsen LA, Lonnerdal B, Lopez De Roman G, De Kanashiro HC, Black RE, Brown KH. Growth patterns of breast fed infants in affluent (United States) and poor (Peru) communities: implications for timing of complementary feeding. Am J Clin Nutr. 1992;56:1012–1018.
    1. Adu-Afarwuah S, Lartey A, Brown KH, Zlotkin KH, Briend A, Dewey KG. Home fortification of complementary foods with micronutrient supplements is well accepted and has positive effects in infant iron status in Ghana. Am J Clin Nutr. 2008;87(4):929–938.
    1. Nestel P, Briend A, de Benoist B, Decker E, Ferguson E, Fontaine O, Micardi A, Nalubola R. Complementary food supplements to achieve micronutrient adequacy for infants and young children. J Pediatr Gastroenterol Nutr. 2003;36(3):316–328. doi: 10.1097/00005176-200303000-00005.
    1. Ghana Vast Study Team Vitamin A supplementation in Northern Ghana. Effects on clinic attendances, hospital admissions and child mortality. Lancet. 1994;344:228–231. doi: 10.1016/S0140-6736(94)92998-X.
    1. Barreto ML, Santos LMP, Assis AMO, Araujo MPN, Farenzena GG, Santos PAB, Fiaccone RL. Effect of vitamin A supplementation on diarrhoea and acute lower respiratory infections in young children in Brazil. Lancet. 1994;344:228–231. doi: 10.1016/S0140-6736(94)92998-X.
    1. Beaton GH, Martorell R, Aronson KJ, Effectiveness of vitamin A supplementation in the control of young child morbidity and mortality in developing countries. Geneva: ACC/SCN; 1993.
    1. Sommer A, Davidson FR. Assessment and control of vitamin a deficiency: the Annecy accords. J Nutr. 2002;132(Suppl):S2845–S2850.
    1. Semba RD. The role of vitamin A and related retinoids in immune function. Nutr Rev. 1998;56:S38–S48.
    1. Veenemans J, Milligan P, Prentice AM, Schouten LR, Inja N, der Heijden V, De Boer LC, Jansen EJ, Koopmans AE, Enthoven WT, Kraaijenhagen RJ, Demir AY, Uges DRA, Mbugi EV, Savelkou HF, Verhoef H. Effect of supplementation with zinc and other micronutrients on malaria in Tanzanian children: a randomised trial. PloS Med. 2011;8(11):e1001125. doi: 10.1371/journal.pmed.1001125.
    1. Brown K, Wehler S, Person J. The importance of zinc in humans nutrition and estimation of the global prevalence of zinc deficiency. Food Nutr Bull. 2001;22:113–125.
    1. Keen CL. Gershwin ME Zinc deficiency and immune function. Annu Rev Nutr. 1990;10:415–431. doi: 10.1146/annurev.nu.10.070190.002215.
    1. Zeba AN, Sorgho H, Rouamba N, Zongo I, Rouamba J, Guiguemde RT, Hamer DH, Mokhtar N, Ouedraogo JB. Major reduction of malaria morbidity with combined vitamin A and zinc supplementation in young children in Burkina Faso: a randomized double blind tria. Nut J. 2008;7:7. doi: 10.1186/1475-2891-7-7.
    1. WHO/CHD immunization linked Vitamin A Supplementation Study Group. Randomised trial to assess benefits and safety of vitamin A supplementation linked to immunization in early infancy. Lancet. 1998;352:1257–1263.
    1. Newton S, Cousens S, Owusu Agyei S, Filteau S, Stanley C, Linsell L, Kirkwood B. Vitamin a supplementation does not affect Infants’ immune responses to polio and tetanus vaccines. J Nutr. 2005;135:2669–2673.
    1. Owusu-Agyei S, Nettey OE, Zandoh C, Sulemana A, Adda R, Amenga-Etego S, Mbacke C. Demographic patterns and trends in Central Ghana: baseline indicators from the kintampo health and demographic surveillance system. Glob Health Action. 2012;5(0):1–11. doi: 10.3402/gha.v5i0.19033.
    1. Domellof M, Dewey KG, Lonnerdal B, Cohen RJ, Hernell O. The diagnostic criteria for iron deficiency in infants should be reevaluated. J Nutr. 2002;132:3680–3686.
    1. Valentine AR, Tanumihardjo SA. Adjustments to the modified relative dose response MRDR) test for assessment of vitamin A status minimize the blood volume used in piglets. J Nutr. 2004;134:1186–1192.
    1. Olson JA. In: Handbook of Vitamins. 3. Rucker RB, Suttie JW, McCormick DB, Machlin LJ, editor. New York, NY: Marcel Dekker; 2001. Vitamin A; pp. 1–50.
    1. Tanumihardjo SA, Cheng JC, Permaesih D, Muherdiyantiningsih E, Rustan M, Muhilal Karyadi D, Olson JA. Refinement of the modified-relative-dose–response test as a method for assessing vitamin A status in a field setting: experience with Indonesian children. Am J Clin Nutr. 1996;64:966–971.
    1. Smith JC, Butrimovitz GP, Purdy WC. Direct measurement of zinc in plasma by atomic absorption spectroscopy. Clin Chem. 1979;25:1487–1491.
    1. Shankar A, Genton B, Semba R, Baisor M, Paino J. et al.Effect of vitamin A supplementation on morbidity due to Plamodium falciparum in young children in Papua New Guinea: A randomized trial. Lancet. 1999;354:203–209. doi: 10.1016/S0140-6736(98)08293-2.
    1. Gibson RS, Heywood A, Yaman C, Sohlstrom A, Thompson LU, Heywood P. Growth in children from the Wosera sub district, Papua New Guinea in relation to energy and protein intakes and zinc status. Am J Clin Nutr. 1991;53:782–789.
    1. Gibson RS, Huddle JM. Sub optimal zinc status in pregnant Malawian women: its association with low intakes of poorly available zinc, frequent reproductive cycling and malaria. Am J Clin Nutr. 1998;67:702–709.
    1. Shankar AH, Genton B, Baisor M, Paino J, Tamja S. et al.The influence of zinc supplementation on morbidity due to Plasmodium falciparum: a randomised trial in preschool children in Papua New Guinea. Am J Trop Med Hyg. 2000;62:663–669.
    1. Bates C, Evans PH, Dardene M, Prentice A, Lunn PG. et al.A trial of zinc supplementation in young rural Gambian children. Br J Nutr. 1993;69:243–255. doi: 10.1079/BJN19930026.
    1. Muller O, Becher H, van Zweeden AB, Ye Y, Diallo DA. Effect of zinc supplementation on malaria and other causes of morbidity in West African children: randomised double blind placebo controlled trial. BMJ. 2001;322:1567. doi: 10.1136/bmj.322.7302.1567.
    1. Binka F, Ross D, Morris S. Vitamin A supplementation and childhood malaria in northern Ghana. Am J Clin Nutr. 1995;61:853–859.
    1. Rahman MM, Tofail F, Wahed MA, Fuchs GJ, Baqui AH, Alvarez JO. Short term supplementation with zinc and vitamin A gas no significant effect on the growth of undernourished Bangladeshi children. AM J Clin Nutr. 2002;75:87–91.
    1. Michaelson KF, Samuelson G, Graham TW, Lonnerdal B. Zinc intake, zinc status and growth in a longitudinal study of health Danish Infants. Acta Pediatr. 1994;83:1115–1121. doi: 10.1111/j.1651-2227.1994.tb18262.x.
    1. Krebs NF, Reidinger C, Robertson AD, Hambridge KM. Growth and intakes of energy and zinc in infants fed human milk. J Pediatr. 1994;124:32–39. doi: 10.1016/S0022-3476(94)70251-9.
    1. Samenpera L, Perheentupa J, Nanto V, Siimes MA. Low zinc intake during exclusive-breastfeeding does not impair growth. J Pediatr Gastroenterol Nutr. 1994;18:361–370. doi: 10.1097/00005176-199404000-00019.
    1. World Health Organization. Trace Elements in Human Nutrition and Health. Geneva: WHO; 1996. Zinc; pp. 72–104.
    1. Brown KH, Peerson JM, Rivera J, Allen LH. Effect of supplemented zinc on the growth and serum zinc concentrations of prepubertal children: a meta analyses of randomized controlled trials. Am J Clin Nutr. 2002;75:1062–1071.
    1. Bhutta ZA, Black R, Brown KH. et al.Prevention of diarrhoea and pneumonia by zinc supplementation in children in developing countries: pooled analyses of randomized controlled trials. Zinc investigators collaborative group. J Pediatr. 1999;135:689–697. doi: 10.1016/S0022-3476(99)70086-7.
    1. Jones G, Steketee RW, Black RE, Bhutta ZA, Morris SS. Bellabio: child survival study. How many deaths can we prevent this year? Lancet. 2003;362:65–71. doi: 10.1016/S0140-6736(03)13811-1.
    1. The Zinc Investigators’ Collaborative Group. Prevention of diarrhoea and pneumonia by zinc supplementation in children in developing countries :pooled analysis of randomized controlled trialsZinc investigators’ collaborative group. J Pediatr. 1999;135:689–697. doi: 10.1016/S0022-3476(99)70086-7.
    1. Rahman MM, Vermund SH, Wahed MA, Fuchs GJ, Baqui AH, Alvarez JO. Simultaneous zinc and vitamin A supplements in Bangladeshi children: randomised double blind controlled trial. BMJ. 2001;323:314–318. doi: 10.1136/bmj.323.7308.314.
    1. Gupta DN, Mondal SK, Ghosh S, Rajendran K, Sur D, Manna B. Impact of zinc supplementation on diarrhoeal morbidity in rural children of West Bengal, India. Acta Pediatr. 2003;92:531–536. doi: 10.1111/j.1651-2227.2003.tb02501.x.
    1. Lo NB, Aaron GL, Hess SY, Dossou NI, Guiro AT, Wade S, Brown KH. Plasma zinc concentration responds to zinc supplementation, but non zinc fortification, in young children in Senegal. Am J Clin Nutr. 2011;93:1348–1355. doi: 10.3945/ajcn.111.012278.
    1. Walker CF, Black RE. Zinc and the risk for infectious disease. Annu Rev Nut. 2004;24:255–275. doi: 10.1146/annurev.nutr.23.011702.073054.

Source: PubMed

3
S'abonner