van Welzen Berend J, Smit Colette, Boyd Anders, Lieveld Faydra I, Mudrikova Tania, Reiss Peter, Brouwer Annemarie E, Hoepelman Andy I M, Arends Joop E
Department of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.
Stichting HIV Monitoring, Amsterdam, the Netherlands.
Open Forum Infect Dis. 2020 Jun 25;7(7):ofaa226. doi: 10.1093/ofid/ofaa226. eCollection 2020 Jul.
The development of efficacious combination antiretroviral therapy (cART) has led to a dramatic decrease in mortality in HIV-positive patients. Specific data on the impact in HIV/hepatitis B virus (HBV)-coinfected patients are lacking. In this study, all-cause and cause-specific mortality risks stratified per era of diagnosis are investigated.
Data were analyzed from HIV/HBV-coinfected patients enrolled in the ATHENA cohort between January 1, 1998, and December 31, 2017. Risk for (cause-specific) mortality was calculated using Cox proportional hazard regression analysis, comparing patients diagnosed before 2003 with those diagnosed ≥2003. Risk factors for all-cause and liver-related mortality were also assessed using Cox proportional hazard regression analysis.
A total of 1301 HIV/HBV-coinfected patients were included (14 882 person-years of follow-up). One-hundred ninety-eight patients (15%) died during follow-up. The adjusted hazard ratio (aHR) for all-cause mortality in patients diagnosed in or after 2003 was 0.50 (95% CI, 0.35-0.72) relative to patients diagnosed before 2003. Similar risk reduction was observed for liver-related (aHR, 0.29; 95% CI, 0.11-0.75) and AIDS-related mortality (aHR, 0.44; 95% CI, 0.22-0.87). Use of a tenofovir-containing regimen was independently associated with a reduced risk of all-cause and liver-related mortality. Prior exposure to didanosine/stavudine was strongly associated with liver-related mortality. Ten percent of the population used only lamivudine as treatment for HBV.
All-cause, liver-related, and AIDS-related mortality risk in HIV/HBV-coinfected patients has markedly decreased over the years, coinciding with the introduction of tenofovir. Tenofovir-containing regimens, in absence of major contraindications, should be strongly encouraged in this population.
有效的联合抗逆转录病毒疗法(cART)的发展已导致HIV阳性患者的死亡率大幅下降。目前缺乏关于HIV/乙型肝炎病毒(HBV)合并感染患者受影响的具体数据。在本研究中,我们调查了按诊断时代分层的全因死亡率和特定病因死亡率风险。
分析了1998年1月1日至2017年12月31日期间纳入ATHENA队列的HIV/HBV合并感染患者的数据。使用Cox比例风险回归分析计算(特定病因)死亡率风险,将2003年前诊断的患者与2003年及以后诊断的患者进行比较。还使用Cox比例风险回归分析评估了全因死亡率和肝脏相关死亡率的危险因素。
共纳入1301例HIV/HBV合并感染患者(随访14882人年)。198例患者(15%)在随访期间死亡。与2003年前诊断的患者相比,2003年及以后诊断的患者全因死亡率的调整后风险比(aHR)为0.50(95%CI,0.35-0.72)。肝脏相关死亡率(aHR,0.29;95%CI,0.11-0.75)和艾滋病相关死亡率(aHR,0.44;95%CI,0.22-0.87)也观察到类似的风险降低。使用含替诺福韦的方案与全因死亡率和肝脏相关死亡率风险降低独立相关。先前使用去羟肌苷/司他夫定与肝脏相关死亡率密切相关。10%的人群仅使用拉米夫定治疗HBV。
多年来,HIV/HBV合并感染患者的全因死亡率、肝脏相关死亡率和艾滋病相关死亡率风险显著下降,这与替诺福韦的引入相吻合。在该人群中,若无重大禁忌证,应强烈鼓励使用含替诺福韦的方案。