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Absence of Association Between Sickle Trait Hemoglobin and Placental Malaria Outcomes
Jaymin C Patel1, Victor Mwapasa2, Linda Kalilani2
1Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi; Department of Community Health, College of Medicine, Blantyre, Malawi; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom; Division of Infectious Diseases and International Health and Duke Global Health Institute, Duke University Medical Center, Durham, North Carolina jaymin.patel@unc.edu.
Insights
Sickle trait (HbAS) does not protect against placental malaria (PM) or low birth weight (LBW) in Malawian women. This study found no association between HbAS and reduced risk of P. falciparum infection or adverse birth outcomes.
Area of Science:
- Malaria research
- Hematology
- Obstetrics
Background:
- Sickle trait (HbAS) is known to protect children against severe falciparum malaria.
- Placental malaria (PM) is a significant cause of adverse birth outcomes, including low birth weight (LBW).
- The binding of Plasmodium-infected red blood cells (iRBCs) to ligands is crucial in PM pathogenesis.
Purpose of the Study:
- To investigate whether sickle trait (HbAS) is associated with a reduced risk of placental malaria (PM) and low birth weight (LBW) in pregnant women.
- To evaluate the protective effect of HbAS against P. falciparum infection in placental and peripheral blood.
- To assess the association of HbAS with histological evidence of PM and infant birth weight.
Main Methods:
- A study was conducted on 850 delivering women in southern Malawi.
- Parasite detection utilized polymerase chain reaction (PCR) in placental and peripheral blood.
- Placentae were histologically scored for evidence of PM.
Main Results:
- The prevalence of HbAS was 3.7%, and 11.2% of infants were LBW.
- HbAS was not associated with a reduced prevalence of P. falciparum in placental or peripheral blood.
- No significant association was found between HbAS and histological PM or LBW, with similar mean birth weights observed for HbAS and non-HbAS mothers.
Conclusions:
- Sickle trait (HbAS) did not confer protection against placental malaria (PM) in this Malawian cohort.
- HbAS was not associated with a reduced risk of low birth weight (LBW) or P. falciparum infection.
- The findings suggest HbAS does not protect against PM or its adverse effects in pregnant women.
Abstract:
Heterozygous hemoglobin S (HbAS), or sickle trait, protects children from life-threatening falciparum malaria, potentially by attenuating binding of Plasmodium-infected red blood cells (iRBCs) to extracellular ligands. Such binding is central to the pathogenesis of placental malaria (PM). We hypothesized that HbAS would be associated with reduced risks of PM and low birth weight (LBW). We tested this hypothesis in 850 delivering women in southern Malawi. Parasites were detected by polymerase chain reaction in placental and peripheral blood, and placentae were scored histologically for PM. The prevalence of HbAS was 3.7%, and 11.2% of infants were LBW (< 2,500 g). The prevalence of Plasmodium falciparum was 12.7% in placental and 8.5% in peripheral blood; 24.4% of placentae demonstrated histological evidence of P. falciparum HbAS was not associated with reduced prevalence of P. falciparum in placental (odds ratio [OR]: 1.27, 95% confidence interval [CI]: 0.50-3.23, P = 0.61) or peripheral blood (OR: 2.53, 95% CI: 1.08-2.54, P = 0.03), prevalence of histological PM (OR: 0.97, 95% CI: 0.40-2.34, P = 0.95), or prevalence of LBW (OR: 0.82, 95% CI: 0.24-2.73, P = 0.74). Mean (standard deviation) birth weights of infants born to HbAS (2,947 g [563]) and, homozygous hemoglobin A (2,991 g [465]) mothers were similar. Across a range of parasitologic, clinical, and histologic outcomes, HbAS did not confer protection from PM or its adverse effects.
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