Li J, Zhang T, Gordon S C, Rupp L B, Trudeau S, Holmberg S D, Moorman A C, Spradling P R, Teshale E H, Boscarino J A, Schmidt M A, Daida Y G, Lu M
Department of Public Health Sciences, Henry Ford Health System, Detroit, MI, USA.
Division of Gastroenterology and Hepatology, Henry Ford Health System, Detroit, MI, USA.
J Viral Hepat. 2018 Aug;25(8):952-958. doi: 10.1111/jvh.12887. Epub 2018 Mar 15.
Data regarding the impact of hepatitis C (HCV) therapy on incidence of type 2 diabetes mellitus are limited. We used the data from the longitudinal Chronic Hepatitis Cohort Study-drawn from four large US health systems-to investigate how response to HCV treatment impacts the risk of subsequent diabetes. Among HCV patients without a history of type 2 diabetes mellitus or hepatitis B, we investigated the incidence of type 2 diabetes from 12 weeks post-HCV treatment through December 2015. Cox proportional hazards models were used to test the effect of treatment status (sustained virologic response [SVR] or treatment failure) and baseline risk factors on the development of diabetes, considering any possible risk factor-by-SVR interactions, and death as a competing risk. Among 5127 patients with an average follow-up of 3.7 years, diabetes incidence was significantly lower among patients who achieved SVR (231/3748; 6.2%) than among patients with treatment failure (299/1379; 21.7%; adjusted hazard ratio [aHR] = 0.79; 95% CI: 0.65-0.96). Risk of diabetes was higher among African American and Asian American patients than White patients (aHR = 1.82 and 1.75, respectively; P < .05), and among Hispanic patients than non-Hispanics (aHR = 1.86). Patients with BMI ≥ 30 and 25-30 (demonstrated higher risk of diabetes aHR = 3.62 and 1.72, respectively; P < .05) than those with BMI < 25; patients with cirrhosis at baseline had higher risk than those without cirrhosis (aHR = 1.47). Among a large US cohort of patients treated for HCV, patients who achieved SVR demonstrated a substantially lower risk for the development of type 2 diabetes mellitus than patients with treatment failure.
关于丙型肝炎(HCV)治疗对2型糖尿病发病率影响的数据有限。我们使用了来自美国四个大型医疗系统的纵向慢性丙型肝炎队列研究的数据,以调查对HCV治疗的反应如何影响后续患糖尿病的风险。在没有2型糖尿病或乙型肝炎病史的HCV患者中,我们调查了从HCV治疗后12周直至2015年12月的2型糖尿病发病率。使用Cox比例风险模型来测试治疗状态(持续病毒学应答[SVR]或治疗失败)和基线风险因素对糖尿病发生的影响,同时考虑任何可能的风险因素与SVR的相互作用,并将死亡作为竞争风险。在平均随访3.7年的5127名患者中,实现SVR的患者糖尿病发病率(231/3748;6.2%)显著低于治疗失败的患者(299/1379;21.7%;调整后风险比[aHR]=0.79;95%可信区间:0.65-0.96)。非裔美国人和亚裔美国人患者患糖尿病的风险高于白人患者(aHR分别为1.82和1.75;P<0.05),西班牙裔患者高于非西班牙裔患者(aHR=1.86)。体重指数(BMI)≥30和25-30的患者患糖尿病的风险(aHR分别为3.62和1.72;P<0.05)高于BMI<25的患者;基线时有肝硬化的患者风险高于无肝硬化的患者(aHR=1.47)。在美国一大群接受HCV治疗的患者中,实现SVR的患者发生2型糖尿病的风险明显低于治疗失败的患者。