School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, K1G 5Z3, Canada.
College of Osteopathic Medicine, Michigan State University, East Lansing, MI, 48824, USA.
BMC Infect Dis. 2019 Nov 21;19(1):982. doi: 10.1186/s12879-019-4617-8.
Hepatitis B (HBV) and Human Immunodeficiency Virus (HIV) share common risk factors for exposure. Co-infected patients have an increased liver-related mortality risk and may have accelerated HIV progression. The epidemiology and demographic characteristics of HIV-HBV co-infection in Canada remain poorly defined. We compared the demographic and clinical characteristics and factors associated with advanced hepatic fibrosis between HIV and HIV-HBV co-infected patients.
A retrospective cohort analysis was conducted using data from the Canadian Observational Cohort (CANOC) Collaboration, including eight sites from British Columbia, Quebec, and Ontario. Eligible participants were HIV-infected patients who initiated combination ARV between January 1, 2000 and December 14, 2014. Demographic and clinical characteristics were compared between HIV-HBV co-infected and HIV-infected groups using chi-square or Fisher exact tests for categorical variables, and Wilcoxon's Rank Sum test for continuous variables. Liver fibrosis was estimated by the AST to Platelet Ratio Index (APRI).
HBV status and APRI values were available for 2419 cohort participants. 199 (8%) were HBV co-infected. Compared to HIV-infected participants, HIV-HBV co-infected participants were more likely to use injection drugs (28% vs. 21%, p = 0.03) and be HCV-positive (31%, vs. 23%, p = 0.02). HIV-HBV co-infected participants had lower baseline CD4 T cell counts (188 cells/mm, IQR: 120-360) compared to 235 cells/mm in HIV-infected participants (IQR: 85-294) (p = 0.0002) and higher baseline median APRI scores (0.50 vs. 0.37, p < 0.0001). This difference in APRI was no longer clinically significant at follow-up (0.32 vs. 0.30, p = 0.03). HIV-HBV co-infected participants had a higher mortality rate compared to HIV-infected participants (11% vs. 7%, p = 0.02).
The prevalence, demographic and clinical characteristics of the HIV-HBV co-infected population in Canada is described. HIV-HBV co-infected patients have higher mortality, more advanced CD4 T cell depletion, and liver fibrosis that improves in conjunction with ARV therapy. The high prevalence of unknown HBV status demonstrates a need for increased screening among HIV-infected patients in Canada.
乙型肝炎病毒 (HBV) 和人类免疫缺陷病毒 (HIV) 具有共同的暴露风险因素。合并感染的患者具有更高的肝脏相关死亡率风险,并且可能具有加速的 HIV 进展。加拿大 HIV-HBV 合并感染的流行病学和人口统计学特征仍未得到明确界定。我们比较了 HIV 和 HIV-HBV 合并感染患者的人口统计学和临床特征以及与晚期肝纤维化相关的因素。
使用来自加拿大观察队列 (CANOC) 合作的不列颠哥伦比亚省、魁北克省和安大略省的八个地点的数据进行了回顾性队列分析。合格的参与者是在 2000 年 1 月 1 日至 2014 年 12 月 14 日期间开始联合 ARV 治疗的 HIV 感染者。使用卡方检验或 Fisher 精确检验比较 HIV-HBV 合并感染组和 HIV 感染组的人口统计学和临床特征,连续变量采用 Wilcoxon 秩和检验。通过天门冬氨酸转氨酶与血小板比值指数 (APRI) 估计肝纤维化程度。
2419 名队列参与者的 HBV 状态和 APRI 值可用。199 名(8%)为 HBV 合并感染。与 HIV 感染者相比,HIV-HBV 合并感染者更有可能使用注射毒品(28%对 21%,p=0.03)和 HCV 阳性(31%对 23%,p=0.02)。与 HIV 感染者相比,HIV-HBV 合并感染者的基线 CD4 T 细胞计数较低(188 个细胞/mm,IQR:120-360),为 235 个细胞/mm(IQR:85-294)(p=0.0002),基线中位 APRI 评分较高(0.50 对 0.37,p<0.0001)。在随访时,APRI 的这种差异不再具有临床意义(0.32 对 0.30,p=0.03)。与 HIV 感染者相比,HIV-HBV 合并感染者的死亡率较高(11%对 7%,p=0.02)。
描述了加拿大 HIV-HBV 合并感染人群的流行率、人口统计学和临床特征。HIV-HBV 合并感染者死亡率较高,CD4 T 细胞耗竭更为严重,肝纤维化随着 ARV 治疗而改善。大量未知 HBV 状态表明加拿大 HIV 感染者需要增加筛查。