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. 2018 Sep 14;68(11):1807–1814. doi: 10.1093/cid/ciy791

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© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 1. — The effect of iron status on subsequent malaria. A, Scatter plots of iron biomarkers stratified by no subsequent malaria or one or more subsequent malaria episodes. Horizontal line indicates mean while vertical line indicates standard deviation. P value was derived from Poisson regression model. B, Adjusted incidence rate ratios for the effect of iron biomarkers on subsequent malaria episodes. Circle marker indicates overall, diamond Kenya and square Uganda. Labels indicate incidence rate ratio and 95% confidence intervals. Poisson regression models were adjusted for age, sex, parasitemia, inflammation, length of follow-up and study site. Maximum length of follow-up was 6 months. Abbreviations: sTfR, soluble transferrin receptor; TSAT, transferrin saturation.