BMC Infectious Diseases | |
Predictors of suboptimal CD4 response among women achieving virologic suppression in a randomized antiretroviral treatment trial, Africa | |
Shahin Lockman5  Michael D Hughes6  Judith Currier2  Robert Salata7  Anthony Ogwu3  Fred Sawe4  Douglas Shaffer4  Kara Wools Kaloustian1  Yu Zheng6  Aida Asmelash3  | |
[1] Indiana University, Indianapolis, USA;University of California, Los Angeles, LA, USA;Botswana Harvard School of Public Health AIDS Initiative Partnership, Gaborone, Botswana;Walter Reed Project, Kericho, Kenya;Brigham and Women’s Hospital, Boston, MA, USA;Harvard School of Public Health, Boston, MA, USA;Case Western Reserve University, Cleveland, OH, USA | |
关键词: CD4; Immune response; HAART; Antiretroviral therapy; HIV; | |
Others : 1127541 DOI : 10.1186/1471-2334-14-331 |
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received in 2013-10-09, accepted in 2014-04-09, 发布年份 2014 | |
【 摘 要 】
Background
A subset of HIV-1 infected patients starting highly active antiretroviral treatment (HAART) experience suboptimal CD4 response (SCR) despite virologic suppression. We studied the rate of and risk factors for SCR among women starting HAART in the ACTG A5208 study conducted in 7 African countries. 741 HAART-naive women with screening CD4 count <200 cells/μL were randomized to start HAART with Tenofovir/Emtricitabine plus either Nevirapine or Lopinavir/Ritonavir.
Methods
This analysis includes the 625 women who remained on-study through 48 weeks without experiencing protocol-defined virologic failure. We defined SCR as < 100 CD4 cells/μL increase from baseline and absolute CD4 cell count < 350 cells/μL, both at 48 weeks after HAART initiation.
Results
The baseline characteristics for the 625 women prior to HAART initiation were: median age 33 years, screening CD4 count 134 cells/μL, and HIV-1 RNA 5.1 log10 copies/mL; 184 (29%) were WHO Stage 3 or 4.
Seventy one (11%) of these 625 women experienced SCR. Baseline factors independently associated with increased odds of SCR included older age, lower HIV-1 RNA, positive Hepatitis B surface antigen, and site location. At 96 weeks, only 6% of the SCR group had CD4 ≥ 350 cells/μL compared with 67% in the non SCR group.
Conclusion
After starting HAART, 11% of women with virologic suppression through 48 weeks experienced SCR. These patients were also less likely to achieve CD4 ≥ 350 cells/μL by 96 weeks. The underlying causes and long term clinical implications of SCR deserve further investigation.
Trial registration
Clinicaltrials.gov Identifier: NCT00089505
【 授权许可】
2014 Asmelash et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
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20150220235626892.pdf | 246KB | download | |
Figure 1. | 38KB | Image | download |
【 图 表 】
Figure 1.
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