Martinello M, Grebely J, Petoumenos K, Gane E, Hellard M, Shaw D, Sasadeusz J, Applegate T L, Dore G J, Matthews G V
Viral Hepatitis Clinical Research Program, Kirby Institute, UNSW Australia, Sydney, NSW, Australia.
Auckland Hospital, Auckland, New Zealand.
J Viral Hepat. 2017 May;24(5):359-370. doi: 10.1111/jvh.12666. Epub 2017 Jan 23.
One challenge to HCV elimination through therapeutic intervention is reinfection. The aim of this analysis was to calculate the incidence of HCV reinfection among both HIV-positive and HIV-negative individuals treated for recent HCV infection (estimated infection duration <18 months). Individuals with recent HCV infection who achieved an end-of-treatment response in four open-label studies between 2004 and 2015 in Australia and New Zealand were assessed for HCV reinfection, confirmed by sequencing of the Core-E2 and/or NS5B regions. Reinfection incidence was calculated using person-time of observation. Exact Poisson regression analysis was used to assess factors associated with HCV reinfection. The cohort at risk for reinfection (n=120; 83% male; median age 36 years) was composed of HIV-positive men-who-have-sex-with-men (53%) and people who inject drugs (current 49%, ever 69%). Total follow-up time at risk was 135 person-years (median 1.08 years, range 0.17, 2.53). Ten cases of HCV reinfection were identified, for an incidence of 7.4 per 100 py (95% CI 4.0, 13.8). Reinfection incidence was significantly higher among participants who reported injection drug use at end of or post-treatment, irrespective of HIV status (15.5 per 100 py, 95% CI 7.8, 31.1). In adjusted analysis, factors associated with reinfection were older age (aIRR 5.3, 95% CI 1.15, 51.5, P=.042) and injection drug use at end of or post-treatment (aIRR 7.9, 95% CI 1.6, 77.2, P=.008). High reinfection incidence following treatment for recent HCV infection in individuals with ongoing risk behaviour emphasizes the need for post-treatment surveillance, harm reduction strategies and education in at-risk populations.
通过治疗干预消除丙型肝炎病毒(HCV)面临的一个挑战是再次感染。本分析的目的是计算在接受近期HCV感染治疗(估计感染持续时间<18个月)的HIV阳性和HIV阴性个体中HCV再次感染的发生率。对2004年至2015年期间在澳大利亚和新西兰进行的四项开放标签研究中实现治疗结束反应的近期HCV感染个体进行了HCV再次感染评估,通过对核心-E2和/或NS5B区域进行测序来确认。使用观察人时计算再次感染发生率。采用精确泊松回归分析来评估与HCV再次感染相关的因素。有再次感染风险的队列(n = 120;83%为男性;中位年龄36岁)由男男性行为的HIV阳性者(53%)和注射毒品者(目前占49%,曾经占69%)组成。总的风险随访时间为135人年(中位1.08年,范围0.17至2.53年)。确定了10例HCV再次感染病例,发生率为每100人年7.4例(95%可信区间4.0至13.8)。在治疗结束时或治疗后报告注射毒品使用的参与者中,无论HIV状态如何,再次感染发生率显著更高(每100人年15.5例,95%可信区间7.8至31.1)。在多因素分析中,与再次感染相关的因素是年龄较大(调整后发病率比[aIRR]为5.3,95%可信区间1.15至51.5,P = 0.042)以及治疗结束时或治疗后注射毒品使用(aIRR为7.9,95%可信区间1.6至77.2,P = 0.008)。对于有持续风险行为的个体,近期HCV感染治疗后较高的再次感染发生率强调了在高危人群中进行治疗后监测、减少伤害策略和教育的必要性。