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Among simple non-invasive scores, Pro-C3 and ADAPT best exclude advanced fibrosis in Asian patients with MAFLD.
Tang, Liang-Jie; Ma, Hong-Lei; Eslam, Mohammed; Wong, Grace Lai-Hung; Zhu, Pei-Wu; Chen, Sui-Dan; Leeming, Diana Julie; Karsdal, Morten; Li, Gang; Huang, Ou-Yang; Leung, Howard Ho-Wai; Zhou, Yu-Jie; Feng, Qian; Jiang, Pei; Gao, Li-Mei; Byrne, Christopher D; Targher, Giovanni; George, Jacob; Wong, Vincent Wai-Sun; Zheng, Ming-Hua.
Afiliación
  • Tang LJ; MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Ma HL; MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Eslam M; Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital, Westmead, and University of Sydney, Sydney, Australia.
  • Wong GL; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong, China.
  • Zhu PW; Department of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Chen SD; Department of Pathology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Leeming DJ; Nordic Bioscience Biomarkers and Research A/S, Herlev, Denmark.
  • Karsdal M; Nordic Bioscience Biomarkers and Research A/S, Herlev, Denmark.
  • Li G; MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Huang OY; MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Leung HH; Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China.
  • Zhou YJ; Division of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Institute of Digestive Disease, Shanghai, China.
  • Feng Q; Department of Gastroenterology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Jiang P; Fosun Diagnostics (Shanghai) Co., Ltd, Shanghai, China.
  • Gao LM; Fosun Diagnostics (Shanghai) Co., Ltd, Shanghai, China.
  • Byrne CD; Southampton National Institute for Health Research Biomedical Research Centre, University Hospital Southampton, Southampton General Hospital, Southampton, UK.
  • Targher G; Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata of Verona, Verona, Italy.
  • George J; Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital, Westmead, and University of Sydney, Sydney, Australia.
  • Wong VW; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong, China. Electronic address: wongv@cuhk.edu.hk.
  • Zheng MH; MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China; Institute of Hepatology, Wenzhou Medical University, Wenzhou, China; Key Laboratory of Diagnosis and Treatment for the Development of Chronic Liver Disease in Zhejiang Provin
Metabolism ; 128: 154958, 2022 03.
Article en En | MEDLINE | ID: mdl-34958817
ABSTRACT

BACKGROUND:

With metabolic dysfunction-associated fatty liver disease (MAFLD) incidence and prevalence increasing, it is necessary to identify patients with advanced fibrosis (F3-F4 stages). We evaluated the performance of new biomarkers and algorithms for diagnosing advanced fibrosis in an Asian population.

METHODS:

Data from two Asian cohorts (including 851 biopsy-proven MAFLD [578 from Wenzhou, 273 from Hong Kong]) were studied. The association between N-terminal propeptide of type 3 collagen (PRO-C3) and the histologic stage of liver fibrosis was analyzed by multivariable linear regression. The area under the receiver operating characteristic curve (AUROC) was used to test the diagnostic performance of serum PRO-C3 and the ADAPT score for advanced fibrosis and compared them to other established non-invasive tests.

RESULTS:

Serum PRO-C3 levels increased progressively across liver fibrosis stages and correlated with advanced fibrosis (P < 0.001). The ADAPT score had an AUROC of 0.865 (95% confidence interval 0.829-0.901) for advanced fibrosis; the accuracy, sensitivity and negative predictive values were 81.4%, 82.2% and 96.1%, respectively. This result was better compared to that of PRO-C3 alone or other non-invasive fibrosis biomarkers (aspartate aminotransferase-to-platelet ratio index, Fibrosis-4, BARD, and NAFLD fibrosis score). In subgroup analyses (including sex, age, diabetes, NAFLD activity score, body mass index or serum alanine aminotransferase levels), the ADAPT score had good diagnostic performance.

CONCLUSION:

PRO-C3 and the ADAPT score reliably exclude advanced fibrosis in MAFLD patients and reduce the need for liver biopsy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Metabolism Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Metabolism Año: 2022 Tipo del documento: Article País de afiliación: China