首页> 美国卫生研究院文献>The Journal of Infectious Diseases >Malaria Parasitemia and Parasite Density in Antiretroviral-Treated HIV-Infected Adults Following Discontinuation of Cotrimoxazole Prophylaxis
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Malaria Parasitemia and Parasite Density in Antiretroviral-Treated HIV-Infected Adults Following Discontinuation of Cotrimoxazole Prophylaxis

机译:终止复方新诺明预防后抗逆转录病毒治疗的HIV感染成人的疟疾寄生虫血症和寄生虫密度

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>Background. Cotrimoxazole (CTX) discontinuation increases malaria incidence in human immunodeficiency virus (HIV)–infected individuals. Rates, quantity, and timing of parasitemia rebound following CTX remain undefined.>Methods. Serial specimens from a trial of HIV-infected individuals receiving antiretroviral treatment (ART) randomized to continue (the CTX arm) or discontinue (the STOP-CTX arm) were examined for malaria parasites by quantitative reverse transcription polymerase chain reaction (PCR). Specimens obtained at enrollment and then quarterly for 12 months and at sick visits were assessed; multiplicity of infection was evaluated by PCR that targeted the polymorphic msp-1/msp-2 alleles.>Results. Among 500 HIV-infected adults receiving ART (median ART duration, 4.5 years), 5% had detectable parasitemia at baseline. After randomization, parasite prevalence increased over time in the STOP-CTX arm, compared with the CTX arm, with values of 4% and <1%, respectively, at month 3, 8% and 2% at month 6, 14% and 2% at month 9, and 22% and 4% at month 12 (P = .0034). The combined mean parasite density at the various time points was higher in the STOP-CTX arm (4.42 vs 3.13 log10 parasites/mL; P < .001). The parasitemia incidence was 42.0 cases per 100 person-years in the STOP-CTX arm and 9.9 cases per 100 person-years in the CTX arm, with an incidence rate ratio of 4.3 (95% confidence interval, 2.7–7.1; P < .001). After enrollment, mixed infections (multiplicity of infection, >1) were only present in the STOP-CTX arm.>Conclusion. Discontinuation of CTX by HIV-infected adults receiving ART resulted in progressive increases in malaria parasitemia prevalence and burden.>Clinical Trials Registration. .
机译:>背景。复方新诺明(CTX)停用会增加人类免疫缺陷病毒(HIV)感染者的疟疾发病率。 CTX后寄生虫反弹的速度,数量和时间尚未确定。>方法。接受抗逆转录病毒治疗(ART)的HIV感染者试验的串行标本被随机分配为继续(CTX组)或中止(通过定量逆转录聚合酶链反应(PCR)检查了疟疾寄生虫(STOP-CTX臂)。评估了入选时,然后每季度12个月以及病假时获得的标本;通过针对多态性msp-1 / msp-2等位基因的PCR评估了感染的多重性。>结果。在接受ART的500例HIV感染成年人中,ART持续时间中位数为4.5年,其中5%可以检出基线为寄生虫血症。随机分组后,与CTX组相比,STOP-CTX组的寄生虫流行率随时间增加,在第3个月时分别为4%和<1%,在第6个月时分别为8%和2%。在第9个月达到%,在第12个月达到22%和4%(P = .0034)。 STOP-CTX组在各个时间点的总平均寄生虫密度较高(4.42 vs 3.13 log10寄生虫/ mL; P <.001)。 STOP-CTX组的寄生虫发病率为每100人年42.0例,CTX组的寄生虫发病率为每100人年9.9例,发生率为4.3(95%置信区间为2.7-7.1; P <。 001)。入选后,仅在STOP-CTX组中出现混合感染(感染的多重性,> 1)。>结论。接受ART的HIV感染成年人停用CTX导致疟疾寄生虫病患病率逐步增加和负担。>临床试验注册。

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