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Usefulness of collagen type IV in the detection of significant liver fibrosis in nonalcoholic fatty liver disease.
Stefano, José Tadeu; Guedes, Laura Vilar; de Souza, Arthur Alencar Arrais; Vanni, Denise Siqueira; Alves, Venâncio Avancini Ferreira; Carrilho, Flair José; Largura, Alvaro; Arrese, Marco; Oliveira, Claudia P.
Affiliation
  • Stefano JT; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • Guedes LV; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • de Souza AAA; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • Vanni DS; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • Alves VAF; Department of Pathology (LIM-14), Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • Carrilho FJ; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
  • Largura A; Laboratório Biovel Análises e Pesquisas Clínicas, Cascavel, PR, Brazil; Hospital Universitário do Oeste do Parana (UNIOESTE), Cascavel, PR, Brazil.
  • Arrese M; Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile and Centro de Envejecimiento y Regeneracion (CARE), Departamento de Biologia Celular y Molecular, Facultad de Ciencias Biologicas Pontificia Universidad Catolica de Chile, Santiago, Chil
  • Oliveira CP; Laboratório de Gastroenterologia Clínica e Experimental (LIM-07), Division of Clinical Gastroenterology and Hepatology, Hospital das Clínicas, Department of Gastroenterology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil. Electronic address: cpm@usp.br.
Ann Hepatol ; 20: 100253, 2021.
Article in En | MEDLINE | ID: mdl-32949785
ABSTRACT
INTRODUCTION/

AIMS:

Liver fibrosis assessment is a key issue in the evaluation of nonalcoholic fatty liver disease (NAFLD) patients. In the present study, we aimed to validate a noninvasive marker panel to assess significant and advanced fibrosis in these patients.

METHOD:

126 biopsy-proven NAFLD patients were included. NAFLD diagnosis was based on histological criteria. Fibrosis stages were determined according to NASH-Clinical Research Network criteria. Clinical and laboratorial data were collected during the interval of three months before or after liver biopsy. Histological fibrosis stages were classified as significant fibrosis (F2-F4) and advanced fibrosis (F3-F4). Five serum biomarkers [hyaluronic acid (HA), collagen type IV (cIV), procollagen type III (PC III), laminin (LN) and cholylglycine (CG)] were assessed by chemiluminescence immunoassays.

RESULTS:

Most patients were female (61.61%), mean age 55.7 ±â€¯9.13 years old and mean BMI was 32.1 ±â€¯5.9 kg/m2. Prevalence of diabetes, dyslipidemia, arterial hypertension, and metabolic syndrome was 68.75%, 82.29%, 63.54% and 81.05%, respectively. Patients with cIV above 30 ng/mL had a 5.57-times (IC 1.86-16.69) the chance of having significant fibrosis and 7.61-times (IC 2.27-25.54) the chance of having advanced fibrosis versus patients with values below 30 ng/mL. HA, PC III, LN and CG did not detect the presence of significant and advanced fibrosis. The AUROC of clV for detection of significant (0.718) and advanced fibrosis (0.791) was better than that of other serum biomarkers.

CONCLUSION:

Type 4 collagen could predict the presence of significant and advanced fibrosis in NAFLD patients and it would be a useful tool in routine clinical practice.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Collagen Type IV / Non-alcoholic Fatty Liver Disease / Liver Cirrhosis Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Collagen Type IV / Non-alcoholic Fatty Liver Disease / Liver Cirrhosis Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2021 Type: Article