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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Hepatitis C Viral Load, Genotype, and Increased Risk of Developing End-Stage Renal Disease: REVEAL-HCV Study
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Hepatitis C Viral Load, Genotype, and Increased Risk of Developing End-Stage Renal Disease: REVEAL-HCV Study

机译:丙型肝炎病毒载荷,基因型和发育末期肾病的风险增加:揭示-HCV研究

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The association between hepatitis C virus (HCV) infection and end-stage renal disease (ESRD) remains controversial without considering the role of HCV viral load and genotype. This study aimed to determine whether HCV RNA level and genotype affect the risk of developing ESRD. Between 1991 and 1992, 19,984 participants aged 30-65 years were enrolled in a community-based prospective cohort study in Taiwan. Chronic HCV infection was defined by detectable HCV viral load. ESRD was determined as the need for chronic dialysis or renal transplantation. Conventional Cox proportional hazard and competing risk models were used to determine the hazard ratio (HR) for ESRD. After a median follow-up of 16.8 years, 204 cases were detected during 319,474 person-years. The incidence rates of ESRD for non-chronically HCV-infected and chronically HCV-infected patients were 60.2 and 194.3 per 100,000 person-years, respectively. The multivariable HR was 2.33 (95% confidence interval [CI] 1.40-3.89) when comparing patients with and without chronic HCV infection. Patients with low and high HCV RNA levels were at higher risk of ESRD than those who were nonchronically HCV-infected (HR, 2.11, 95% CI 1.16-3.86, and HR, 3.06, 95% CI 1.23-7.58; P-trend < 0.001). This association remained robust after taking pre-ESRD death as a competing event for ESRD. Patients with HCV genotype 1 tended to have a higher risk of developing ESRD (HR, 3.60 95% CI 1.83-7.07) compared with nonchronically HCV-infected subjects. Conclusions: This study reveals that chronic HCV infection is associated with an increased risk of developing ESRD and suggests that elevated serum levels of HCV RNA (>167,000 IU/mL) and HCV genotype 1 are strong predictors of ESRD, indicating clinical implications for the management of chronic HCV.
机译:不考虑HCV病毒载荷和基因型的作用,丙型肝炎病毒(HCV)感染与终末期肾病(ESRD)之间的关联仍然存在争议。本研究旨在确定HCV RNA水平和基因型是否影响开发ESRD的风险。 1991年至1992年间,19,984名年龄在30-65岁之间的参与者入学于台湾的社区潜在队列研究。慢性HCV感染由可检测的HCV病毒载量定义。 ESRD被确定为需要慢性透析或肾移植的需要。常规的Cox比例危害和竞争风险模型用于确定ESRD的危险比(HR)。在16.8岁的中位随访后,在319,474人的年度期间检测到204例。非长期HCV感染和慢性HCV感染患者的ESRD的发病率分别为每10万人60.2和194.3岁。在比较患者和不含慢性HCV感染的情况下,多变量的HR为2.33(95%置信区间[CI] 1.40-3.89)。低HCV RNA水平低于ESRD的患者比非同步感染的患者(HR,2.11,95%CI 1.16-3.86和HR,3.06,95%CI 1.23-7.58; P-Trend < 0.001)。在将ESRD预先死亡作为ESRD的竞争事件服用竞争事件后,这种关联仍然强劲。与非HCV感染的受试者相比,HCV基因型1的患者倾向于具有更高的开发ESRD(HR,3.60 95%CI 1.83-7.07)的风险。结论:本研究表明,慢性HCV感染与发育ESRD的风险增加有关,并表明HCV RNA(> 167,000 IU / mL)和HCV基因型1的血清水平升高是ESRD的强预测因子,表明对管理的临床意义慢性HCV。

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