Affiliation:
1. Center for Global Health and Diseases, Case Western Reserve University, Cleveland, Ohio
2. Division of Vector Borne Diseases, Nairobi, Kenya
3. Department of Veteran's Affairs Medical Center, Cleveland, Ohio
Abstract
ABSTRACT
Real-time quantitative PCR (RTQ-PCR) provides a quick, accurate, and reproducible quantification of parasites. However, the value of RTQ-PCR for predicting clinical outcomes of malaria is unknown. Here, we compared RTQ-PCR to microscopy of blood smears, nested PCR (nPCR), and parasite circulating-antigen (CAg) assays for detection of
Plasmodium falciparum
in pregnant Kenyan women and their infants and related these findings to parity and birth weights in their newborns (
n
= 554). nPCR was the most sensitive assay for detection of malaria in pregnancy, followed in decreasing order of sensitivity by RTQ-PCR, CAg assays, and blood smears. RTQ-PCR detected a higher frequency of malaria infection (46%) in maternal peripheral blood in primiparous than in multiparous women (35%;
P
< 0.001), with a >12-fold difference in parasite burden (geometric mean = 25,870 versus 2,143 amplicons/μl blood;
P
< 0.0001). Similarly, the presence of placental malaria determined by RTQ-PCR was approximately twofold higher in primiparous versus multiparous women (21% versus 13%;
P
< 0.01). The presence and intensity of malaria infection in pregnant women estimated by RTQ-PCR strongly correlated with low-birth-weight babies, especially in those with high amplicon numbers. RTQ-PCR identified malaria-infected women, missed by blood smear, who were at risk for having underweight offspring. By contrast, malaria detected by nPCR and CAg assay showed a much weaker association with parity or low birth weight. Thus, RTQ-PCR provides an estimate of parasite burden that is more sensitive than blood smear and is predictive of clinical outcomes of malaria infection in pregnant women and newborns.
Publisher
American Society for Microbiology
Cited by
61 articles.
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