Falciparum malaria mortality in sub-Saharan Africa in the pretreatment era
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Methods to Investigate the Regulatory Role of Small RNAs and Ribosomal Occupancy of Plasmodium falciparum
Published on: December 4, 2015
James A Watson1, Nicholas J White1, Arjen M Dondorp1
1Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Insights
Sickle-cell trait protects against malaria, leading to high hemoglobin S allele frequencies in Africa. This genetic balance suggests significant childhood mortality from malaria before modern treatments.
Area of Science:
- Genetics
- Epidemiology
- Tropical Medicine
Background:
- Sickle-cell trait offers protection against malaria, a significant health burden in sub-Saharan Africa.
- Balancing selection maintains high frequencies of the sickle-cell allele (hemoglobin S) in malaria-endemic regions.
Purpose of the Study:
- To estimate the historical burden of malaria-attributable childhood mortality in sub-Saharan Africa.
- To understand the impact of sickle-cell trait on population genetics and disease mortality.
Main Methods:
- Utilized population genetic data on hemoglobin S allele frequencies.
- Employed epidemiological modeling to infer mortality rates based on allele frequencies and known protective effects.
Main Results:
- Hemoglobin S allele frequencies range from 15% to 20% in high Plasmodium falciparum transmission areas.
- Estimated childhood mortality attributable to malaria in the pre-treatment era was between 15% and 24%.
Conclusions:
- The prevalence of sickle-cell trait is a direct indicator of historical malaria's severe impact on child survival.
- Understanding this genetic-mortality relationship is crucial for public health strategies in malaria-endemic regions.
Abstract:
Driven by the malaria-protective effect of sickle-cell trait, balancing selection results in hemoglobin S equilibrium allele frequencies of between 15% and 20% in areas of high Plasmodium falciparum transmission in sub-Saharan Africa. From this we estimate that the malaria-attributable childhood mortality in the pretreatment era was between 15% and 24%.
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