Infectious Diseases Department, Centro Hospitalar de São João and Faculdade de Medicina da Universidade do Porto, Alameda Professor Hernâni Monteiro, 4200-319, Porto, Portugal.
Infectious Diseases Department, Centro Hospitalar de São João and Faculdade de Medicina da Universidade do Porto, Alameda Professor Hernâni Monteiro, 4200-319, Porto, Portugal.
J Microbiol Immunol Infect. 2018 Oct;51(5):593-597. doi: 10.1016/j.jmii.2016.09.003. Epub 2017 Jun 22.
CD4 cell-count has been regarded as the key surrogate marker for prognostic staging and therapeutic monitoring of HIV-infected individuals. Our purpose was to assess the probability of maintaining a CD4 count >200 cells/μL in patients with continuous viral suppression and CD4 cell counts >200 cells/μL.
Retrospective cohort study of HIV-infected patients, treatment naïve, who started antiretroviral therapy between 2007 and 2011. We estimated the probability of maintaining CD4 counts >200 cells/μL during continuous viral suppression using the Kaplan-Meier method. The hazard ratios of a CD4 count <200 cells/μL were estimated and compared using Cox proportional hazards regression.
401 patients were included: 70.1% men; median age 37 years; 98.8% HIV-1 infected. The median duration of continuous viral suppression with CD4 counts >200 cells/μL was 40.5 months. Ninety-three percent of patients maintained CD4 counts ≥200 cells/μL during the period of continuous viral suppression. Compared with those with an initial CD4 count ≥350 cells/μL, patients with initial CD4 count <300 cells/μL had a significantly higher risk of a CD4 count <200 cells/μL. Patients with viral suppression and CD4 counts ≥350 cells/μL had a 97.1% probability of maintaining CD4 cell counts ≥200 cells/μL for 48 months.
The probability of a CD4 count <200 cells/μL in an HIV-infected patient with viral suppression and CD4 ≥350 cells/μL was very low. These data suggests less frequent monitoring of CD4 counts in these patients.
CD4 细胞计数一直被认为是 HIV 感染者预后分期和治疗监测的关键替代标志物。我们的目的是评估在病毒持续抑制和 CD4 细胞计数 >200 个/μL 的情况下,持续病毒抑制的 HIV 感染者保持 CD4 计数 >200 个/μL 的概率。
对 2007 年至 2011 年间开始接受抗逆转录病毒治疗的、未经治疗的 HIV 感染者进行回顾性队列研究。我们使用 Kaplan-Meier 法估计在持续病毒抑制期间保持 CD4 计数 >200 个/μL 的概率。使用 Cox 比例风险回归估计并比较 CD4 计数<200 个/μL 的风险比。
共纳入 401 例患者:70.1%为男性;中位年龄 37 岁;98.8%感染 HIV-1。CD4 计数 >200 个/μL 的持续病毒抑制中位时间为 40.5 个月。93%的患者在持续病毒抑制期间保持 CD4 计数≥200 个/μL。与初始 CD4 计数≥350 个/μL 的患者相比,初始 CD4 计数<300 个/μL 的患者 CD4 计数<200 个/μL 的风险显著更高。病毒抑制且 CD4 计数≥350 个/μL 的患者在 48 个月时保持 CD4 细胞计数≥200 个/μL 的概率为 97.1%。
病毒抑制且 CD4 计数≥350 个/μL 的 HIV 感染者 CD4 计数<200 个/μL 的概率非常低。这些数据表明这些患者 CD4 计数监测的频率可以降低。