[No authors listed]
Malaria in pregnancy causes adverse birth outcomes due to sequestration of Plasmodium falciparum-infected erythrocytes in the placenta. Angiopoietins are critical regulators of vascular development and formation of placental villous vasculature. Angiopoietin-1 and Angiopoietin-2 concentrations were measured in peripheral and placental plasma samples from 70 malaria-infected and 216 control women using commercially available DuoSet ELISA development kit. Angiopoietins increased in placental plasma (ANG1-5833.5âpg/ml and ANG2-9580.6âpg/ml) as compared to peripheral plasma (ANG1-2293.1âpg/ml and ANG2-1198.9âpg/ml, p < 0.0001). The concentration of placental and peripheral ANG1 (6099.23âpg/ml and 2320.5âpg/ml) was significantly lower (5013.5âpg/ml, 2208.5âpg/ml), and ANG2 (9553.3âpg/ml, 1180.92âpg/ml) was significantly higher (9664.6âpg/ml, 1254.4âpg/ml) in malaria-positive cases as compared to malaria-negative (p < 0.0001). The association of dysregulated angiopoietins in malaria with adverse birth outcomes showed that the peripheral and placental ANG1 concentration was lower and ANG2 concentration was higher in low-birth-weight baby and stillbirth birth outcome as compared to normal deliveries among malaria-positive group. Therefore, ANG1 and ANG2 could be considered a biomarker for adverse outcome during malaria in pregnancy.
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