Impact of Microscopic and Submicroscopic Parasitemia During Pregnancy on Placental Malaria in a High-Transmission Setting in Uganda. (19th March 2019)

• Record Type: Journal Article
• Authors: Briggs, Jessica; Ategeka, John; Kajubi, Richard; Ochieng, Teddy; Kakuru, Abel; Ssemanda, Cephus; Wasswa, Razack; Jagannathan, Prasanna; Greenhouse, Bryan; Rodriguez-Barraquer, Isabel; Kamya, Moses; Dorsey, Grant
• Is Part Of: Journal of infectious diseases. Volume 220:Number 3(2019)
• Page Start: 457
• Page End: 466
• Publication Date: 2019-03-19
• Subjects: placental malaria -- submicroscopic parasitemia -- microscopic parasitemia -- asymptomatic malaria infection -- intermittent preventive treatment during pregnancy -- dihydroartemisinin-piperaquine; Communicable diseases -- Periodicals; Diseases -- Causes and theories of causation -- Periodicals; Medicine -- Periodicals; Communicable Diseases -- Periodicals; Electronic journals; 616.9
• DOI: 10.1093/infdis/jiz130
• Languages: English
• ISSNs: 0022-1899

Abstract

Abstract : In pregnant women assessed for parasitemia every 28 days, the risk of placental malaria increased in a dose-response relationship with both increasing frequency and density of parasitemia; however, even women with only submicroscopic parasitemia were at risk for placental malaria. Abstract: Background: Placental malaria is a major cause of adverse birth outcomes. However, data are limited on the relationships between longitudinal measures of parasitemia during pregnancy and placental malaria. Methods: Data came from 637 women enrolled in a randomized controlled trial of intermittent preventive treatment of malaria in pregnancy (IPTp) from Uganda. Plasmodium falciparum parasitemia was assessed using microscopy and ultrasensitive quantitative PCR at intervals of 28 days from 12 to 20 weeks gestation through delivery. Multivariate analysis was used to measure associations between characteristics of parasitemia during pregnancy and the risk of placental malaria based on histopathology. Results: Overall risk of placental malaria was 44.6%. None of the 34 women without parasitemia detected during pregnancy had evidence of placental malaria. Increasing proportion of interval assessments with parasitemia and higher parasite densities were independently associated with an increased risk of placental malaria. Higher gravidity and more effective IPTp were associated with a decreased risk of placental malaria. Women with parasitemia only detected before the third trimester still had an increased risk of placental malaria. Conclusions: The frequency, density, and timing of parasitemia are all important risk factors for placental malaria. Interventions should target the prevention of all levels of parasitemia throughout pregnancy.