Yang Rongrong, Chen Qianhui, Jiao Fangzhou, Yu Xingxia, Xiong Yong
Department of Infectious Diseases, Zhongnan Hospital of Wuhan University, Donghu Road 169, Wuchang District, Wuhan, 430071, Hubei, China.
Center for AIDS Research, Wuhan University, Wuhan, Hubei, China.
Sci Rep. 2025 Feb 1;15(1):4018. doi: 10.1038/s41598-025-88530-2.
To investigate sex differences in liver disease development and prognosis in individuals with HIV and HBV co-infection. This study comprised 752 HIV/HBV co-infected people who were diagnosed with HIV and started on combination antiretroviral therapy (cART) between January 31st, 2015 and January 31st, 2023. Their clinical data, including CD4 T lymphocyte counts, HBV-DNA, and FIB-4 scores, were tracked once a year. The prognosis was determined during the long-term surveillance period. Risk factors related with the progression of liver diseases were included in both univariable and multivariable logistic regression. Then, sex differences in CD4 T lymphocyte counts, HBV-DNA, FIB-4 scores, changes in liver fibrosis levels, and prognosis were investigated. Multivariable logistic regression analysis identified male as an independent risk factor for liver disease progression. Compared to the male group, the female group had a significantly greater decline of HBV DNA levels at years 1, 2, 3, 3-5, and > 5 post-cART. At each assessment point, the female group showed a significantly greater rise in CD4 T lymphocyte counts than the male group based on their respective baseline values. Furthermore, females had greater CD4 T lymphocyte counts and a lower prevalence of liver cirrhosis than males throughout the study period. Compared to female, higher incidence of end-stage-liver disease (1.190/100 person-years vs 0.714/100 person-years), higher all-cause mortality (0.440/100 person-years vs 0.148/100 person-years) and higher mortality associated with end-stage-liver diseases (0.273/100 person-years vs 0.074/100 person-years) were found in male. Among individuals with HIV and HBV coinfection, males had a worse therapeutic effect of HBV-active therapy and poorer prognosis than females.
为研究人类免疫缺陷病毒(HIV)和乙型肝炎病毒(HBV)合并感染个体在肝脏疾病发生发展及预后方面的性别差异。本研究纳入了752例HIV/HBV合并感染患者,这些患者于2015年1月31日至2023年1月31日期间被诊断为HIV感染并开始接受联合抗逆转录病毒治疗(cART)。每年跟踪他们的临床数据,包括CD4 T淋巴细胞计数、HBV-DNA和FIB-4评分。在长期监测期间确定预后情况。将与肝脏疾病进展相关的危险因素纳入单变量和多变量逻辑回归分析。然后,研究CD4 T淋巴细胞计数、HBV-DNA、FIB-4评分、肝纤维化水平变化及预后方面的性别差异。多变量逻辑回归分析确定男性是肝脏疾病进展的独立危险因素。与男性组相比,女性组在cART后第1年、第2年、第3年、第3至5年以及>5年时HBV DNA水平下降幅度显著更大。在每个评估点,基于各自的基线值,女性组CD4 T淋巴细胞计数的升高幅度均显著大于男性组。此外,在整个研究期间,女性的CD4 T淋巴细胞计数更高,肝硬化患病率更低。与女性相比,男性的终末期肝病发病率更高(1.190/100人年 vs 0.714/100人年)、全因死亡率更高(0.440/100人年 vs 0.148/100人年)以及与终末期肝病相关的死亡率更高(0.273/100人年 vs 0.074/100人年)。在HIV和HBV合并感染个体中,男性的HBV抗病毒治疗效果比女性更差,预后也更差。