抗逆转录病毒疗法免疫效率低下的艾滋病毒感染者合并症分析

T. V. Balykchinova, A. U. Sabitov, V. V. Zhukov
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摘要

导言。研究表明,抗逆转录病毒疗法(ART)免疫效率低下的患者发生与 HIV 无关的继发性疾病和不良事件的风险很高。本研究旨在评估合并症对 CD4+ 增长的影响以及抗逆转录病毒疗法免疫低效的发生概率。该研究是一项回顾性研究,研究对象包括开始治疗时 CD4+ 细胞数小于 200 cells/µl 的 HIV 感染者。研究分为两组:主要组--抗逆转录病毒疗法免疫效率低下的患者(281人);对照组--抗逆转录病毒疗法免疫反应充分的患者(188人)。结果结核病患者出现免疫功能低下的概率是对照组的 1.7 倍(几率比(OR)-1.7;95 % 置信区间(CI)-1.0-2.9);HCV 感染者的概率是对照组的 1.8 倍(OR-1.8;95 % 置信区间(CI)-2.6-1.2)。主要群体中患心血管疾病的概率高出 2 倍(OR - 2.3;95 % CI - 1.0-5.4)。结核病、丙型肝炎病毒感染和心血管疾病经常出现在主要组患者的合并症结构中。本研究结果显示,合并感染丙型肝炎病毒(HCV)和肺结核的艾滋病病毒感染者出现抗逆转录病毒疗法免疫低效的几率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of Comorbidity in HIV–Infected Patients with Immunological Inefficiency of Antiretroviral Therapy
Introduction. Studies indicate high risks of secondary diseases and adverse events not related to HIV in patients with immunological inefficiency of antiretroviral therapy (ART). The effect of comorbidity on the increase of CD4+ is detected.The aim of the study is assessing the effect of comorbidity on CD4+ growth and the probability of developing immunological inefficiency of ART.Materials and methods. A retrospective study was conducted that included HIV-infected patients with CD4+ at the beginning of treatment <200 cells/µl. Two groups were formed: the main group — patients with immunological inefficiency of ART (281 people); the control group — patients with sufficient immunological response on ART (188 people). Results. The probability of developing immunological inefficiency in patients with tuberculosis was 1.7 times higher (odds ratio (OR) — 1.7; 95 % confidence interval (CI) — 1.0–2.9); in patients with HCV-infection — 1.8 times higher (OR — 1.8; 95 % CI — 2.6–1.2). The probability of cardiovascular disease in the main group was 2 times higher (OR — 2.3; 95 % CI — 1.0–5.4).Discussion. Tuberculosis, HCV-infection and cardiovascular diseases frequently registered in the structure comorbidity in the main group of patients.Conclusion. According to the results of this study, HIV-infected patients with HCV and tuberculosis co-infection have a higher chance of developing immunological inefficiency of ART.
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