Effects of artemisinins on reticulocyte count and relationship to possible embryotoxicity in confirmed and unconfirmed malarial patients
Article first published online: 28 NOV 2011
Copyright © 2011 Wiley-Liss, Inc.
Birth Defects Research Part A: Clinical and Molecular Teratology
Volume 94, Issue 2, pages 61–75, February 2012
How to Cite
Clark, R. L. (2012), Effects of artemisinins on reticulocyte count and relationship to possible embryotoxicity in confirmed and unconfirmed malarial patients. Birth Defects Research Part A: Clinical and Molecular Teratology, 94: 61–75. doi: 10.1002/bdra.22868
- Issue published online: 8 FEB 2012
- Article first published online: 28 NOV 2011
- Manuscript Accepted: 7 SEP 2011
- Manuscript Revised: 1 SEP 2011
- Manuscript Received: 23 JUN 2011
- antimalarial drug;
- unconfirmed malaria
Rat studies suggest that artemisinin-induced decreases in reticulocyte count are a marker for embryotoxicity (in one study, r = 0.82; p < 0.05). In clinical studies, therapeutic doses of artemisinins induced decreases in reticulocyte count that were larger in five of six groups of healthy volunteers (mean decreases of 47–75%) than in 12 groups of patients with malaria (mean decreases of 0–34% and incidences of low reticulocyte count of 0.6–18%). Malaria causes hypoferremia and drug concentrates in infected red cells so, among the explanations for the lesser decreases in patients, is that malaria protects against artemisinin-induced decreases in reticulocyte count by reducing the target tissue levels of active drug and/or ferrous iron which activates the drug to toxic free radicals. The disease could also protect against embryotoxicity in which case pregnant women without malaria would be at greater risk of artemisinin-induced embryotoxicity. Malaria protection against artesunate toxicity has been observed in rats. No artemisinin-induced embryotoxicity has been identified in limited numbers of women with confirmed malaria in the first trimester. However, in large parts of tropical Africa, malaria treatment is based on fever rather than confirmation of parasitemia and many pregnant women without malaria are exposed to antimalarials. No clinical studies have been conducted on uninfected women for whom pregnancy was identified and then an artemisinin was administered subsequently. Testing in rats and/or humans is needed to determine if malaria protects against reticulocytopenia and embryotoxicity and whether the parasite is a more or less sensitive target than the embryo and reticulocyte. Birth Defects Research (Part A), 2012. © 2011 Wiley Periodicals, Inc.