Jeong Dahn, Wong Stanley, Karim Mohammad Ehsanul, Manges Amee R, Makuza Jean Damascene, Bartlett Sofia R, Velásquez García Héctor Alexander, Luster Daryl, Adu Prince Asumadu, Binka Mawuena, Yu Amanda, Krajden Mel, Janjua Naveed Zafar
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.
British Columbia Centre for Disease Control, Vancouver, BC, Canada.
Lancet Reg Health Am. 2023 Dec 29;29:100658. doi: 10.1016/j.lana.2023.100658. eCollection 2024 Jan.
HCV infection is associated with mortality due to extrahepatic manifestations (EHM). Sustained virologic response (SVR) following direct-acting antiviral (DAA) therapy has been linked to decreased all-cause and liver-related mortality. However, evidence regarding the impact of DAA on EHM-related deaths is lacking. This study aimed to assess the impact of DAA and SVR on EHM-related mortality.
The British Columbia Hepatitis Testers Cohort comprises ∼1.7 million people tested for HCV between 1990 and 2015 and is linked with administrative health data. Among individuals diagnosed with HCV by 12/31/2020, those who received at least one DAA treatment were matched to those who never received treatment by the year of their first HCV RNA positive date. We compared three groups: treated & SVR, treated & no-SVR, and untreated; and generated EHM mortality rates and incidence curves. To account for differences in baseline characteristics, we used inverse probability of treatment weights (IPTW). IPTW-weighted multivariable cause-specific Cox regression models were adjusted for competing risk and confounders.
Study population included 12,815 treated (12,287 SVR, 528 no-SVR) and 12,815 untreated individuals (median follow-up 3.4 years, IQR 2.9). The untreated group had the highest EHM mortality rate (30.9 per 1000 person-years [PY], 95% CI 29.2-32.8), followed by the treated & no-SVR group (21.2 per 1000 PY, 95% CI 14.9-30.1), while the treated & SVR group had the lowest EHM mortality rate (7.9 per 1000 PY, 95% CI 7.1-8.7). In the multivariable model, EHM mortality in the treated & SVR group was significantly decreased (adjusted cause-specific hazard ratio [acsHR] 0.20, 95% CI 0.18-0.23). The treated & SVR group had significant reductions in mortality related to each of the EHMs (78-84%).
Treatment of HCV with DAA was associated with significant reductions in EHM-related mortality. These findings emphasize the critical importance of timely diagnosis and treatment of HCV to prevent deaths associated with EHM, and have important implications for clinical practice and public health.
This work was supported by the BC Centre for Disease Control and the Canadian Institutes of Health Research (CIHR) [Grant # NHC-348216, PJT-156066, and PHE-337680]. DJ has received Doctoral Research Award (#201910DF1-435705-64343) from the Canadian Institutes of Health Research (CIHR) and Doctoral fellowship from the Canadian Network on Hepatitis C (CanHepC). CanHepC is funded by a joint initiative of the Canadian Institutes of Health Research (CIHR) (NHC-142832) and the Public Health Agency of Canada (PHAC).
丙型肝炎病毒(HCV)感染与肝外表现(EHM)导致的死亡率相关。直接抗病毒药物(DAA)治疗后的持续病毒学应答(SVR)与全因死亡率和肝脏相关死亡率的降低有关。然而,关于DAA对EHM相关死亡影响的证据尚缺乏。本研究旨在评估DAA和SVR对EHM相关死亡率的影响。
不列颠哥伦比亚省肝炎检测队列包括1990年至2015年间接受HCV检测的约170万人,并与行政卫生数据相关联。在2020年12月31日前被诊断为HCV的个体中,将至少接受过一次DAA治疗的患者与从未接受过治疗的患者按照其首次HCV RNA阳性日期进行匹配。我们比较了三组:治疗后获得SVR组、治疗后未获得SVR组和未治疗组;并生成了EHM死亡率和发病率曲线。为了考虑基线特征的差异,我们使用了治疗权重的逆概率(IPTW)。IPTW加权多变量特定病因Cox回归模型针对竞争风险和混杂因素进行了调整。
研究人群包括12815名接受治疗的患者(12287名获得SVR,528名未获得SVR)和12815名未接受治疗的个体(中位随访时间3.4年,四分位间距2.9)。未治疗组的EHM死亡率最高(每1000人年30.9例,95%置信区间29.2 - 32.8),其次是治疗后未获得SVR组(每1000人年21.2例,95%置信区间14.9 - 30.1),而治疗后获得SVR组的EHM死亡率最低(每1000人年7.9例,95%置信区间7.1 - 8.7)。在多变量模型中,治疗后获得SVR组的EHM死亡率显著降低(调整后的特定病因风险比[acsHR]为0.20,95%置信区间0.18 - 0.23)。治疗后获得SVR组与每种EHM相关的死亡率均显著降低(78 - 84%)。
使用DAA治疗HCV与EHM相关死亡率的显著降低相关。这些发现强调了及时诊断和治疗HCV以预防与EHM相关死亡的至关重要性,并对临床实践和公共卫生具有重要意义。
这项工作得到了不列颠哥伦比亚省疾病控制中心和加拿大卫生研究院(CIHR)的支持[资助编号:NHC - 348216、PJT - 156066和PHE - 337680]。DJ获得了加拿大卫生研究院(CIHR)的博士研究奖(#201910DF1 - 435705 - 64343)以及加拿大丙型肝炎网络(CanHepC)的博士奖学金。CanHepC由加拿大卫生研究院(CIHR)(NHC - 142832)和加拿大公共卫生局(PHAC)的一项联合倡议资助。