Department of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Department of Adults' Infectious Diseases, Medical University of Warsaw, Warsaw, Poland.
PLoS One. 2021 Aug 9;16(8):e0255834. doi: 10.1371/journal.pone.0255834. eCollection 2021.
The life expectancy of people living with HIV (PLWH) remains shorter than that of the general population, despite significant improvement in the recent years. Mortality in HIV-infected individuals may be associated with a higher viral load at of diagnosis, a lower CD4 count, or clinical variables such as sex or route of transmission. This article investigated the role of the HLA-B*5701 varian on mortality among PLWH.
Material for the analysis consist of the data of 2,393 patients for whom the HLA-B*57 variant was known. Those patients were followed under the care of the Infectious Diseases Hospital in Warsaw (n = 1555) and the Clinic of Acquired Immunodeficiency of the Pomeranian Medical University in Szczecin (n = 838). Factors such as age, gender, date of HIV diagnosis, route of transmission, date of death, baseline HIV viral load and baseline CD4 counts, were collected, and end-point cross-sectional analyses were marked at 60, 120, 180 and 240 month of observation.
HLA-B5701 allele was found in 133 (5.5%) analyzed cases. Median age was notably higher for HLA-B5701 positive patients [32.7 (28.3-41.3) vs. 31.6 (26.8-38.3)years p = 0.02]. HLA-B5701 was associated with lower baseline viral load [4.21 (3.5-4.8) vs. 4.79 (4.2-5.3)log copies/ml p<0.001] and higher CD4count [448 (294.5-662) vs. 352 (176-514) cells/μl p<0.001]. There were no association between HLA-B5701 and survival for any given end-point. Higher mortality was associated to male gender, intravenous drug users, lower CD4 count at baseline and higher baseline viral load.
In our study, the presence of HLA-B*5701 allel was not associated with mortality rate of HIV infected patients, irrespective of being associated with both higher baseline CD4 + cell count and lower baseline HIV viral load.
尽管近年来取得了显著进展,但艾滋病毒感染者(PLWH)的预期寿命仍短于普通人群。HIV 感染者的死亡率可能与诊断时更高的病毒载量、更低的 CD4 计数或性别或传播途径等临床变量有关。本文研究了 HLA-B*5701 变体在 PLWH 死亡率中的作用。
分析材料包括 2393 名已知 HLA-B*57 变体的患者的数据。这些患者在华沙传染病医院(n = 1555)和什切青波美拉尼亚医科大学后天免疫诊所(n = 838)接受护理。收集了年龄、性别、HIV 诊断日期、传播途径、死亡日期、基线 HIV 病毒载量和基线 CD4 计数等因素,并在观察的 60、120、180 和 240 个月时进行了终点横断面分析。
在分析的 133 例(5.5%)病例中发现了 HLA-B5701 等位基因。HLA-B5701 阳性患者的中位年龄明显较高[32.7(28.3-41.3)岁 vs. 31.6(26.8-38.3)岁,p = 0.02]。HLA-B5701 与较低的基线病毒载量相关[4.21(3.5-4.8) vs. 4.79(4.2-5.3)log 拷贝/ml,p<0.001]和更高的 CD4 计数[448(294.5-662) vs. 352(176-514)细胞/μl,p<0.001]。在任何给定的终点,HLA-B5701 与生存率之间均无关联。更高的死亡率与男性、静脉吸毒者、较低的基线 CD4 计数和更高的基线病毒载量有关。
在我们的研究中,HLA-B*5701 等位基因的存在与 HIV 感染患者的死亡率无关,无论其是否与较高的基线 CD4+细胞计数和较低的基线 HIV 病毒载量有关。