PRO-C3 is a predictor of clinical outcomes in distinct cohorts of patients with advanced liver disease

被引:7
|
作者
Nielsen, Mette J. [1 ]
Dolman, Grace E. [2 ]
Harris, Rebecca [2 ]
Frederiksen, Peder
Chalmers, Jane [2 ,3 ]
Grove, Jane I. [2 ]
Irving, William L. [2 ,4 ]
Karsdal, Morten A. [1 ]
Patel, Keyur [5 ]
Leeming, Diana Julie
Guha, Indra Neil [2 ,3 ,6 ]
机构
[1] Nord Biosci, Herlev, Denmark
[2] Univ Nottingham, Nottingham Univ Hosp NHS Trust, Natl Inst Hlth Res NIHR Nottingham Biomed Res Ctr, Nottingham, England
[3] Univ Nottingham, Nottingham Digest Dis Ctr, Sch Med, Nottingham, England
[4] Univ Nottingham, Sch Life Sci, Nottingham, England
[5] Univ Toronto Hlth Network, Div Gastroenterol & Hepatol, Toronto, ON, Canada
[6] Univ Nottingham, Nottingham Univ Hosp NHS Trust, NIHR Nottingham Biomed Res Ctr, Derby Rd, Nottingham, England
关键词
Cirrhosis; Biomarker; Outcome; Extracellular matrix; HEPATITIS-C; EXTRACELLULAR-MATRIX; FIBROSIS; PROGRESSION; MARKERS; BIOMARKERS; PROGNOSIS; CIRRHOSIS; RISK;
D O I
10.1016/j.jhepr.2023.100743
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Fibroblast activity is a key feature of fibrosis progression and organ function loss, leading to liver-related complications and mortality. The fibrogenesis marker, PRO-C3, has been shown to have prognostic significance in relation to fibrosis progression and as a treatment efficacy marker. We investigated whether PRO-C3 was prognostic for clinical outcome and mortality in two distinct cohorts of compensated cirrhosis. Methods: Cohort 1 was a rapid fibrosis progression cohort including 104 patients with HCV and biopsy-proven Ishak fibrosis stage >-3 without prior clinical events. Cohort 2 was a prospective cohort including 172 patients with compensated cirrhosis of mixed aetiology. Patients were assessed for clinical outcomes. PRO-C3 was assessed in serum at baseline in cohorts 1 and 2, and compared with model for end-stage liver disease and albumin-bilirubin (ALBI) scores. Results: In cohort 1, a 2-fold increase in PRO-C3 was associated with 2.7-fold increased hazard of liver-related events (95% CI 1.6-4.6), whereas a one unit increase in ALBI score was associated with a 6.5-fold increased hazard (95% CI 2.9-14.6). In cohort 2, a 2-fold increase in PRO-C3 was associated with a 2.7-fold increased hazard (95% CI 1.8-3.9), whereas a one unit increase in ALBI score was associated with a 6.3-fold increased hazard (95% CI 3.0-13.2). A multivariable Cox regression analysis identified PRO-C3 and ALBI as being independently associated with the hazard of liver-related outcomes. Conclusions: PRO-C3 and ALBI were independent prognostic factors for predicting liver-related clinical outcomes. Understanding the dynamic range of PRO-C3 might enhance its use for both drug development and clinical practice. Impact and Implications: We tested novel proteins of liver scarring (PRO-C3) in two groups of liver patients with advanced disease to see if they could predict clinical events. We found that this marker and an established test called ALBI were both independently associated with future liver-related clinical outcomes. & COPY; 2023 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:8
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