Prediction of extended high viremia among newly HIV-1-infected persons in sub-Saharan Africa

被引:4
|
作者
Powers, Kimberly A. [1 ]
Price, Matthew A. [2 ,3 ]
Karita, Etienne [4 ]
Kamali, Anatoli [2 ,5 ]
Kilembe, William [6 ,7 ]
Allen, Susan [8 ]
Hunter, Eric [8 ]
Bekker, Linda-Gail [9 ]
Lakhi, Shabir [6 ,7 ]
Inambao, Mubiana [6 ,7 ]
Anzala, Omu [10 ]
Latka, Mary H. [11 ]
Fast, Patricia E. [2 ]
Gilmour, Jill [2 ,12 ]
Sanders, Eduard J. [13 ,14 ,15 ]
机构
[1] Univ N Carolina, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[2] Int AIDS Vaccine Initiat, New York, NY USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Project San Francisco, Kigali, Rwanda
[5] Uganda Virus Res Inst, Uganda Res Unit AIDS, Entebbe, Uganda
[6] Zambia Emory Res Project, Lusaka, Zambia
[7] Zambia Emory Res Project, Copperbelt, Zambia
[8] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[9] Univ Cape Town, Desmond Tutu HIV Ctr, Cape Town, South Africa
[10] Univ Nairobi, KAVI ICR, Nairobi, Kenya
[11] Aurum Inst, Johannesburg, South Africa
[12] Imperial Coll Sci Technol & Med, London, England
[13] Kenya Govt Med Res Ctr, Kilifi, Kenya
[14] Univ Oxford, Headington, England
[15] Univ Amsterdam, Amsterdam, Netherlands
来源
PLOS ONE | 2018年 / 13卷 / 04期
基金
英国惠康基金;
关键词
EARLY HIV-1 INFECTION; ANTIRETROVIRAL THERAPY; VIRAL LOAD; RNA LEVELS; SUBTYPE C; SET-POINT; PROGRESSION; TRANSMISSION; INITIATION; RETENTION;
D O I
10.1371/journal.pone.0192785
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Prompt identification of newly HIV-infected persons, particularly those who are most at risk of extended high viremia (EHV), allows important clinical and transmission prevention benefits. We sought to determine whether EHV could be predicted during early HIV infection (EHI) from clinical, demographic, and laboratory indicators in a large HIV-1 incidence study in Africa. Design Adults acquiring HIV-1 infection were enrolled in an EHI study assessing acute retroviral syndrome (ARS) symptoms and viral dynamics. Methods Estimated date of infection (EDI) was based on a positive plasma viral load or p24 antigen test prior to seroconversion, or the mid-point between negative and positive serological tests. EHV was defined as mean untreated viral load >= 5 log(10) copies/ml 130-330 days post-EDI. We used logistic regression to develop risk score algorithms for predicting EHV based on sex, age, number of ARS symptoms, and CD4 and viral load at diagnosis. Results Models based on the full set of five predictors had excellent performance both in the full population (c-statistic = 0.80) and when confined to persons with each of three HIV-1 subtypes (c-statistic = 0.80-0.83 within subtypes A, C, and D). Reduced models containing only 2-4 predictors performed similarly. In a risk score algorithm based on the final full-population model, predictor scores were one for male sex and enrollment CD4<350 cells/mm(3), and two for having enrollment viral load >4.9 log(10) copies/ml. With a risk score cut-point of two, this algorithm was 85% sensitive (95% CI: 76%-91%) and 61% specific (55%-68%) in predicting EHV. Conclusions Simple risk score algorithms can reliably identify persons with EHI in sub-Saharan Africa who are likely to sustain high viral loads if treatment is delayed. These algorithms may be useful for prioritizing intensified efforts around care linkage and retention, treatment initiation, adherence support, and partner services to optimize clinical and prevention outcomes.
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页数:11
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