Infectious Diseases Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.
Clin Infect Dis. 2023 Jun 8;76(11):2027-2037. doi: 10.1093/cid/ciad177.
We assessed whether low CD4 count and high viral load (VL) affect the response to currently preferred ART. We performed a systematic review of randomized, controlled clinical trials that analyzed preferred first-line ART and a subgroup analysis by CD4 count (≤ or >200 CD4/μL) or VL (≤ or >100 000 copies/mL). We computed the odds ratio (OR) of treatment failure (TF) for each subgroup and individual treatment arm. Patients with ≤200 CD4 cells or VL ≥100 000 copies/mL showed an increased likelihood of TF at 48 weeks: OR, 1.94; 95% confidence interval (CI): 1.45-2.61 and OR, 1.75; 95% CI: 1.30-2.35, respectively. A similar increase in the risk of TF was observed at 96 weeks. There was no significant heterogeneity regarding integrase strand transfer inhibitor or nucleoside reverse transcriptase inhibitor backbone. Our results show that CD4 <200 cells/μL and VL ≥100,000 copies/mL impair ART efficacy in all preferred regimens.
我们评估了低 CD4 计数和高病毒载量(VL)是否会影响目前首选的 ART 治疗反应。我们进行了一项系统评价,纳入了分析首选一线 ART 的随机对照临床试验,并按 CD4 计数(≤200 CD4/μL 或>200 CD4/μL)或 VL(≤100000 拷贝/mL 或>100000 拷贝/mL)进行亚组分析。我们计算了每个亚组和每个治疗臂治疗失败(TF)的比值比(OR)。CD4 计数≤200 个细胞或 VL≥100000 拷贝/mL 的患者在 48 周时 TF 的可能性增加:OR,1.94;95%置信区间(CI):1.45-2.61 和 OR,1.75;95%CI:1.30-2.35。在 96 周时,TF 风险也出现了类似的增加。在整合酶抑制剂或核苷逆转录酶抑制剂骨架方面,没有显著的异质性。我们的研究结果表明,CD4<200 个细胞/μL 和 VL≥100000 拷贝/mL 会损害所有首选方案中的 ART 疗效。