Usefulness of collagen type IV in the detection of significant liver fibrosis in nonalcoholic fatty liver disease.
Keywords: Nonalcoholic fatty liver diseaseserum biomarkerLiver fibrosisType 4 collagen
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 ± 9.13 years old and mean BMI was 32.1 ± 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.
Más información
Título de la Revista: | ANNALS OF HEPATOLOGY |
Volumen: | 20 |
Editorial: | MEXICAN ASSOC HEPATOLOGY |
Fecha de publicación: | 2021 |
Página de inicio: | 100253 |
Idioma: | ingles |
DOI: |
10.1016/j.aohep.2020.08.070 |
Notas: | ISI |