Malaria Parasitemia and Parasite Density in Antiretroviral-Treated HIV-Infected Adults Following Discontinuation of Cotrimoxazole Prophylaxis

被引:10
|
作者
Ottichilo, Ronald K. [1 ,2 ]
Polyak, Christina S. [3 ,4 ]
Guyah, Bernard [2 ]
Singa, Benson [5 ]
Nyataya, Josphat [1 ]
Yuhas, Krista [6 ]
John-Stewart, Grace [4 ,6 ,7 ,8 ]
Waitumbi, John N. [1 ]
机构
[1] Kenya Govt Med Res Ctr, Walter Reed Army Inst Res, US Army Med Res Directorate Kenya, Kisumu, Kenya
[2] Maseno Univ, Dept Med Immunol, Kisumu, Kenya
[3] Kenya Govt Med Res Ctr, Nairobi, Kenya
[4] Walter Reed Army Inst Res, Henry Jackson Fdn, US Mil HIV Res Program, Bethesda, MD USA
[5] Univ Washington, Dept Med, Seattle, WA USA
[6] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[7] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[8] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2017年 / 215卷 / 01期
基金
美国国家卫生研究院;
关键词
HIV; malaria; cotrimoxazole; parasitemia; antiretroviral treatment; adults; TRIMETHOPRIM-SULFAMETHOXAZOLE; DIHYDROPTEROATE SYNTHASE; STREPTOCOCCUS-PNEUMONIAE; DIHYDROFOLATE-REDUCTASE; HIV-1-INFECTED ADULTS; COTE-DIVOIRE; PLASMODIUM; FALCIPARUM; RESISTANCE; UGANDA;
D O I
10.1093/infdis/jiw495
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 log(10) 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.
引用
收藏
页码:88 / 94
页数:7
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