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Published on: December 4, 2015
Iron deficiency protects against severe Plasmodium falciparum malaria and death in young children
Moses Gwamaka1, Jonathan D Kurtis, Bess E Sorensen
1Mother-Offspring Malaria Studies Project, Seattle Biomedical Research Institute, Washington, USA.
Insights
Iron deficiency (ID) in Tanzanian children was linked to lower malaria risk and mortality. This suggests caution with iron supplementation in malaria-prone regions, as natural iron status impacts malaria outcomes.
Area of Science:
- Pediatric infectious diseases
- Nutritional science
- Global health
Background:
- Iron supplementation's impact on malaria is debated, with potential for increased morbidity.
- The effect of natural iron status variation on malaria risk remains understudied.
Purpose of the Study:
- To investigate the association between iron deficiency (ID) and malaria outcomes in Tanzanian children.
- To evaluate the impact of ID on parasitemia, severe malaria, and mortality.
Main Methods:
- Longitudinal study of 785 Tanzanian children from birth to 3 years in a high malaria transmission area.
- Intensive monitoring for parasitemia and illness, with regular blood smears and plasma iron status assays.
Main Results:
- Iron deficiency (ID) significantly reduced the odds of subsequent parasitemia and severe malaria.
- ID was associated with substantially lower all-cause and malaria-associated mortality.
- Including sick visits, ID markedly decreased parasitemia, hyperparasitemia, and severe malaria prevalence.
Conclusions:
- Physiologic iron status influences malaria risk, indicating potential adverse effects of iron supplementation.
- Interventional studies are needed to explore treating ID alongside malaria control to mitigate risks of iron supplementation.
Background:
Iron supplementation may increase malaria morbidity and mortality, but the effect of naturally occurring variation in iron status on malaria risk is not well studied.
Methods:
A total of 785 Tanzanian children living in an area of intense malaria transmission were enrolled at birth, and intensively monitored for parasitemia and illness including malaria for up to 3 years, with an average of 47 blood smears. We assayed plasma samples collected at routine healthy-child visits, and evaluated the impact of iron deficiency (ID) on future malaria outcomes and mortality.
Results:
ID at routine, well-child visits significantly decreased the odds of subsequent parasitemia (23% decrease, P < .001) and subsequent severe malaria (38% decrease, P = .04). ID was also associated with 60% lower all-cause mortality (P = .04) and 66% lower malaria-associated mortality (P = .11). When sick visits as well as routine healthy-child visits are included in analyses (average of 3 iron status assays/child), ID reduced the prevalence of parasitemia (6.6-fold), hyperparasitemia (24.0-fold), and severe malaria (4.0-fold) at the time of sample collection (all P < .001).
Conclusions:
Malaria risk is influenced by physiologic iron status, and therefore iron supplementation may have adverse effects even among children with ID. Future interventional studies should assess whether treatment for ID coupled with effective malaria control can mitigate the risks of iron supplementation for children in areas of malaria transmission.
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