Balmaceda Julia B, Aepfelbacher Julia, Belliveau Olivia, Chaudhury Chloe S, Chairez Cheryl, McLaughlin Mary, Silk Rachel, Gross Chloe, Kattakuzhy Sarah, Rosenthal Elana, Kottilil Shyam, Kleiner David E, Hadigan Colleen
National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Division of Clinical Care and Research, Institute of Human Virology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Antivir Ther. 2019;24(4):451-457. doi: 10.3851/IMP3327.
While acute changes in hepatic fibrosis are recognized shortly after achieving sustained virological response (SVR) using direct-acting antiviral therapies, long-term outcomes for the growing population of successfully treated patients with HCV remain uncertain. The aim of this study is to characterize long-term changes in fibrosis following SVR in patients with and without HIV and to identify potential factors associated with progression or regression of fibrosis.
We completed a prospective longitudinal study of 162 subjects with HCV (34% HIV-coinfected) with pre-treatment fibrosis stage determined by liver biopsy and post-SVR transient elastography. Progression of fibrosis was defined as a two-stage or greater increase in fibrosis, while regression was defined as a two-stage or greater decrease at last follow-up. The median duration of follow-up was 4.1 years.
Fibrosis progression occurred in 4% of subjects while regression occurred in 7% and 89% were stable and did not differ by HIV coinfection. Fibrosis progression was associated with increased body mass index (BMI), hepatic steatosis and smoking pack-years. In a multivariable logistic regression, HIV coinfection (P=0.009), lower steatosis score (P<0.05) and lower smoking pack-years (P=0.0007) were associated with a lower fibrosis score at last follow-up.
We identify potentially important relationships between BMI, hepatic steatosis and smoking, and changes in hepatic fibrosis post-SVR in patients with and without HIV coinfection. Attention to modifiable risk factors such as body weight and smoking may reduce the risk of liver disease progression in the growing population of successfully treated chronic HCV patients.
虽然在使用直接抗病毒疗法实现持续病毒学应答(SVR)后不久就能认识到肝纤维化的急性变化,但对于越来越多成功治疗的丙型肝炎病毒(HCV)患者的长期预后仍不确定。本研究的目的是描述有或无人类免疫缺陷病毒(HIV)感染的患者在SVR后纤维化的长期变化,并确定与纤维化进展或消退相关的潜在因素。
我们完成了一项对162例HCV患者(34%合并HIV感染)的前瞻性纵向研究,通过肝活检确定治疗前纤维化阶段,并在SVR后进行瞬时弹性成像检查。纤维化进展定义为纤维化增加两个阶段或更多,而消退定义为最后一次随访时纤维化减少两个阶段或更多。随访的中位持续时间为4.1年。
4%的受试者出现纤维化进展,7%的受试者出现纤维化消退,89%的受试者纤维化稳定,且合并HIV感染与否无差异。纤维化进展与体重指数(BMI)增加、肝脂肪变性和吸烟包年数有关。在多变量逻辑回归中,合并HIV感染(P = 0.009)、较低的脂肪变性评分(P < 0.05)和较低的吸烟包年数(P = 0.0007)与最后一次随访时较低的纤维化评分相关。
我们确定了BMI、肝脂肪变性和吸烟之间潜在的重要关系,以及有或无HIV合并感染的患者在SVR后肝纤维化的变化。关注体重和吸烟等可改变的危险因素,可能会降低越来越多成功治疗的慢性HCV患者肝病进展的风险。