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Randomized Controlled Trial
. 2011 Nov;8(11):e1001125.
doi: 10.1371/journal.pmed.1001125. Epub 2011 Nov 22.

Effect of supplementation with zinc and other micronutrients on malaria in Tanzanian children: a randomised trial

Affiliations
Randomized Controlled Trial

Effect of supplementation with zinc and other micronutrients on malaria in Tanzanian children: a randomised trial

Jacobien Veenemans et al. PLoS Med. 2011 Nov.

Abstract

Background: It is uncertain to what extent oral supplementation with zinc can reduce episodes of malaria in endemic areas. Protection may depend on other nutrients. We measured the effect of supplementation with zinc and other nutrients on malaria rates.

Methods and findings: In a 2×2 factorial trial, 612 rural Tanzanian children aged 6-60 months in an area with intense malaria transmission and with height-for-age z-score≤-1.5 SD were randomized to receive daily oral supplementation with either zinc alone (10 mg), multi-nutrients without zinc, multi-nutrients with zinc, or placebo. Intervention group was indicated by colour code, but neither participants, researchers, nor field staff knew who received what intervention. Those with Plasmodium infection at baseline were treated with artemether-lumefantrine. The primary outcome, an episode of malaria, was assessed among children reported sick at a primary care clinic, and pre-defined as current Plasmodium infection with an inflammatory response, shown by axillary temperature ≥37.5°C or whole blood C-reactive protein concentration ≥ 8 mg/L. Nutritional indicators were assessed at baseline and at 251 days (median; 95% reference range: 191-296 days). In the primary intention-to-treat analysis, we adjusted for pre-specified baseline factors, using Cox regression models that accounted for multiple episodes per child. 592 children completed the study. The primary analysis included 1,572 malaria episodes during 526 child-years of observation (median follow-up: 331 days). Malaria incidence in groups receiving zinc, multi-nutrients without zinc, multi-nutrients with zinc and placebo was 2.89/child-year, 2.95/child-year, 3.26/child-year, and 2.87/child-year, respectively. There was no evidence that multi-nutrients influenced the effect of zinc (or vice versa). Neither zinc nor multi-nutrients influenced malaria rates (marginal analysis; adjusted HR, 95% CI: 1.04, 0.93-1.18 and 1.10, 0.97-1.24 respectively). The prevalence of zinc deficiency (plasma zinc concentration <9.9 µmol/L) was high at baseline (67% overall; 60% in those without inflammation) and strongly reduced by zinc supplementation.

Conclusions: We found no evidence from this trial that zinc supplementation protected against malaria.

Trial registration: ClinicalTrials.gov NCT00623857

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Flow chart of study recruitment and follow-up.
Compliance was measured as the proportion of children who consumed >95% of scheduled supplements.
Figure 2
Figure 2. Effect of zinc (panel A) or multi-nutrients (panel B) on time to first malaria episode.
Marginal group comparisons (Kaplan-Meier analysis), with p-values obtained by Tarone-Ware test. Values below each panel indicates the number of children at risk.
Figure 3
Figure 3. Effect of multi-nutrient supplementation on malaria rates, by iron status and age class.
Malaria with case definition as pre-defined in the analysis plan. Values on the right indicate crude hazard ratios (95% CIs); p-values for differences in intervention effects between subgroups (with age class entered on an ordinal scale). Initial iron status was defined as iron-deficient (black diamond; plasma ferritin concentration <12 µg/L, n = 111) or iron replete (white diamond; plasma ferritin concentration ≥12 µg/L, without inflammation; n = 312). In the analysis, we excluded children in whom iron status was uncertain (plasma ferritin concentration ≥12 µg/L, with inflammation); hence analyses are restricted to 423 subjects. Adjustment for distance between homestead and dispensary, height-for-age z-scores, mosquito net use, and Plasmodium infection at baseline led to similar estimates (unpublished data).
Figure 4
Figure 4. Effect of multi-nutrients on haemoglobin concentration at the second survey, by iron status and age class.
Top: haemoglobin concentrations, by supplementation group. Bottom: effects of multi-nutrients on haemoglobin concentrations. Left: By initial iron status. Right: By age class. Line bars indicate 95% CIs (only upper half of the interval indicated in top panel). Analysis based on 598 children. All estimates are adjusted for standardized haemoglobin concentrations at baseline. p-Values indicate interaction between age class or iron status and intervention effects on haemoglobin concentration.
Figure 5
Figure 5. Effect of multi-nutrients on haemoglobin concentration during the first malaria episode, by iron status and age class.
Top: haemoglobin concentrations, by supplementation group. Bottom: effects of multi-nutrients on haemoglobin concentrations. (A and B) By initial iron status. C and D) By age class. Line bars indicate 95% CIs (only upper half of the interval indicated in top panel). Analysis is based on 507 episodes. All estimates are adjusted for standardized haemoglobin concentrations at baseline. Further adjustment for time between start of intervention and episode led to virtually identical estimates. p-Values indicate interaction between age class or iron status and intervention effects on haemoglobin concentration.

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