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尽管 CD4+ 计数 > 500 个/立方毫米的参与者开始抗逆转录病毒治疗时病毒已得到抑制,但仍存在 CD4+ 计数恢复不佳的风险因素:来自战略时机抗逆转录病毒治疗(START)试验的结果。

Risk Factors for Low CD4+ Count Recovery Despite Viral Suppression Among Participants Initiating Antiretroviral Treatment With CD4+ Counts > 500 Cells/mm3: Findings From the Strategic Timing of AntiRetroviral Therapy (START) Trial.

机构信息

University of Minnesota, Minneapolis, MN.

Hennepin Healthcare Research Institute, Minneapolis, MN.

出版信息

J Acquir Immune Defic Syndr. 2019 May 1;81(1):10-17. doi: 10.1097/QAI.0000000000001967.

Abstract

BACKGROUND

Low CD4 recovery among HIV-positive individuals who achieve virologic suppression is common but has not been studied among individuals initiating treatment at CD4 counts of >500 cells/mm.

SETTING

United States, Africa, Asia, Europe and Israel, Australia, Latin America.

METHODS

Among participants randomized to immediate antiretroviral therapy (ART) in the Strategic Timing of AntiRetroviral Therapy trial, low CD4 recovery was defined as a CD4 increase of <50 cells/mm from baseline after 8 months despite viral load of ≤200 copies/mL. Risk factors for low recovery were investigated with logistic regression.

RESULTS

Low CD4 recovery was observed in 39.7% of participants. Male sex [odds ratio (OR), 1.53; P = 0.007], lower screening CD4 cell counts (OR, 1.09 per 100 fewer cells/mm; P = 0.004), higher baseline CD8 cell counts (OR, 1.05 per 100 more cells/mm; P < 0.001), and lower HIV RNA levels (OR, 1.93 per log10 decrease; P < 0.001) were associated with low CD4 recovery. D-dimer had a quadratic association with low CD4 recovery, with lowest odds occurring at 0.32 μg/mL. At lower HIV RNA levels, the odds of low CD4 recovery were elevated across the levels of screening CD4 count; but at higher HIV RNA levels, the odds of low CD4 recovery were higher among those with lower vs. higher screening CD4.

CONCLUSIONS

Low CD4 recovery is frequent among participants starting ART at high CD4 counts. Risk factors include male sex, lower screening CD4 cell counts, higher CD8 cell counts, and lower HIV RNA levels. More follow-up is required to determine the impact of low CD4 recovery on clinical outcomes.

摘要

背景

在达到病毒学抑制的 HIV 阳性个体中,CD4 恢复较低是常见的,但在 CD4 计数 >500 个细胞/mm 的个体开始治疗时,尚未对此进行研究。

地点

美国、非洲、亚洲、欧洲和以色列、澳大利亚、拉丁美洲。

方法

在 Strategic Timing of AntiRetroviral Therapy 试验中,随机接受立即抗逆转录病毒治疗(ART)的参与者中,低 CD4 恢复定义为尽管病毒载量 ≤200 拷贝/mL,但在 8 个月后,从基线时的 CD4 增加 <50 个细胞/mm。使用逻辑回归调查低恢复的风险因素。

结果

低 CD4 恢复见于 39.7%的参与者。男性(比值比 [OR],1.53;P = 0.007)、较低的筛查 CD4 细胞计数(OR,每减少 100 个细胞/mm 增加 1.09;P = 0.004)、较高的基线 CD8 细胞计数(OR,每增加 100 个细胞/mm 增加 1.05;P < 0.001)和较低的 HIV RNA 水平(OR,每 log10 减少增加 1.93;P < 0.001)与低 CD4 恢复相关。D-二聚体与低 CD4 恢复呈二次关联,最低比值出现在 0.32μg/mL。在较低的 HIV RNA 水平下,随着筛查 CD4 计数的降低,低 CD4 恢复的可能性升高;但在较高的 HIV RNA 水平下,低 CD4 恢复的可能性在筛查 CD4 计数较低的患者中更高。

结论

在 CD4 计数较高的患者开始 ART 时,低 CD4 恢复很常见。风险因素包括男性、较低的筛查 CD4 细胞计数、较高的 CD8 细胞计数和较低的 HIV RNA 水平。需要更多的随访来确定低 CD4 恢复对临床结局的影响。

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