Sustained virological response halts fibrosis progression: A long-term follow-up study of people with chronic hepatitis C infection

被引:14
作者
Mei, Swee Lin G. Chen Yi [1 ,2 ]
Thompson, Alexander J. [1 ,2 ]
Christensen, Britt [1 ]
Cunningham, Georgina [1 ]
McDonald, Lucy [1 ]
Bell, Sally [1 ,2 ]
Iser, David [1 ]
Nguyen, Tin [1 ]
Desmond, Paul V. [1 ,2 ]
机构
[1] St Vincents Hosp, Dept Gastroenterol, Melbourne, Australia
[2] Univ Melbourne, Dept Med, Melbourne, Australia
关键词
VIRUS-INFECTION; LIVER FIBROSIS; TRANSIENT ELASTOGRAPHY; NONINVASIVE ASSESSMENT; STIFFNESS; CIRRHOSIS; ALCOHOL; BIOPSY; IMPACT; EPIDEMIOLOGY;
D O I
10.1371/journal.pone.0185609
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background/Aims Long-term follow-up studies validating the clinical benefit of sustained virological response (SVR) in people with chronic hepatitis C (CHC) infection are lacking. Our aim was to identify rates and predictors of liver fibrosis progression in a large, well characterized cohort of CHC patients in whom paired liver fibrosis assessments were performed more than 10 years apart. Methods CHC patients who had undergone a baseline liver biopsy pre-2004 and a follow up liver fibrosis assessment more than 10 years later (biopsy or liver stiffness measurement (LSM) using transient elastography [FibroScan]) were identified. Subjects who had undergone a baseline liver biopsy but had no follow up fibrosis assessment were recalled for LSM. Fibrosis was categorised as mild-moderate (METAVIR F0-2 / LSM result of <= 9.5 kPa) or advanced (METAVIR F3-4/LSM >9.5 kPa). The primary objective was to assess the association between SVR and the rate of liver fibrosis progression over at least 10 years, defined as an increase from mild-moderate fibrosis at baseline liver biopsy (METAVIR F0-2) to advanced fibrosis at follow-up liver fibrosis assessment. Results 131 subjects were included in this analysis: 69% male, 82% Caucasian, 60% G1 HCV, 25% G3 HCV. The median age at F/U fibrosis staging was 57 (IQR 54-62) years with median estimated duration of infection 33-years (IQR 29-38). At F/U, liver fibrosis assessment was performed by LSM in 86% and liver biopsy in 14%. The median period between fibrosis assessments was 14-years (IQR 12-17). 109 (83%) participants had received interferon-based antiviral therapy. 40% attained SVR. At F/U, there was a significant increase in the proportion of subjects with advanced liver fibrosis: 27% at baseline vs. 46% at F/U (p = 0.002). The prevalence of advanced fibrosis did not change among subjects who attained SVR, 30% at B/L vs 25% at F/U (p = 0.343). However, advanced fibrosis became more common at F/U among subjects with persistent viremia: 10% at B/L vs 31% at F/U (p = 0.0001). SVR was independently associated with protection from liver fibrosis progression after adjustment for other variables including baseline ALT (p = 0.011), duration of HCV infection and mode of acquisition. Conclusion HCV eradication is associated with lower rates of liver fibrosis progression. The data support early treatment to prevent long-term liver complications of HCV infection.
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页数:12
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