Stine Jonathan G, Wynter Javelle A, Niccum Blake, Kelly Virginia, Caldwell Stephen H, Shah Neeral L
Division of Gastroenterology & Hepatology, University of Virginia, Charlottesville, Virginia, United States.
Department of Medicine, University of Virginia, Charlottesville, Virginia, United States.
Ann Hepatol. 2017 Mar-Apr;16(2):215-220. doi: 10.5604/16652681.1231581.
The effect of the new direct acting antiviral drugs (DAAs) for chronic hepatitis C (HCV) on glycemic control is unknown.
We conducted a retrospective cohort study of patients who were treated for chronic HCV with direct-acting antiviral medications at a single academic institution between May 2013 and April 2016. Univariate analysis was performed comparing subjects pre- and post-treatment.
One hundred seventy-five consecutive adult patients were treated for chronic HCV and met enrollment criteria. The majority (80.8%) were genotype 1 and overall cohort sustained virologic response at week 12 (SVR12) was 97.8%. Thirty-one (18.5%) had diabetes mellitus (DM); twenty-six had pre- and post-treatment HbA1c values. Of these, 76.9% were male and 61.5% had cirrhosis. Ninety-six percent were prescribed sofosbuvir-based therapy and all but one (96.8%) achieved SVR12. Three patients were started on treatment despite meeting the definition for poorly controlled DM (HbA1c > 9 mg/dL). There was no significant difference when comparing pre-treatment (7.36 mg/dL, 95% CI 6.55-8.16) to post-treatment HbA1c (7.11 mg/dL, 95% CI 6.34-7.88, p = 0.268). Thirty-one percent of subjects required dose escalation or the initiation of insulin based therapy during treatment.
Although chronic HCV is associated with exacerbation of insulin resistance, our results showed HbA1c to be unaffected by eradication of chronic HCV with DAA in diabetic patients with and without cirrhosis. Paradoxically, almost 1/3 of patients required escalation of anti-diabetic therapy during treatment. Long-term studies are warranted to understand the relationship between HCV viral eradication and insulin metabolism.
新型直接作用抗病毒药物(DAA)对慢性丙型肝炎(HCV)患者血糖控制的影响尚不清楚。
我们对2013年5月至2016年4月期间在单一学术机构接受直接作用抗病毒药物治疗慢性HCV的患者进行了一项回顾性队列研究。对治疗前后的受试者进行单因素分析。
175例连续成年患者接受慢性HCV治疗并符合纳入标准。大多数(80.8%)为1型基因型,整个队列在第12周的持续病毒学应答(SVR12)为97.8%。31例(18.5%)患有糖尿病(DM);26例有治疗前后的糖化血红蛋白(HbA1c)值。其中,76.9%为男性,61.5%有肝硬化。96%接受基于索磷布韦的治疗,除1例(96.8%)外均实现SVR12。3例患者尽管符合糖尿病控制不佳的定义(HbA1c>9 mg/dL)仍开始治疗。治疗前(7.36 mg/dL,95%CI 6.55 - 8.16)与治疗后HbA1c(7.11 mg/dL,95%CI 6.34 - 7.88,p = 0.268)比较无显著差异。31%的受试者在治疗期间需要增加剂量或开始胰岛素治疗。
尽管慢性HCV与胰岛素抵抗加剧有关,但我们的结果显示,在有或无肝硬化的糖尿病患者中,DAA根除慢性HCV不会影响HbA1c。矛盾的是,近1/3的患者在治疗期间需要加强抗糖尿病治疗。有必要进行长期研究以了解HCV病毒根除与胰岛素代谢之间的关系。