Your browser doesn't support javascript.
loading
Development and validation of pFIB scores for exclusion of significant liver fibrosis in pediatric MASLD.
Lefere, Sander; Mosca, Antonella; Hudert, Christian; Dupont, Ellen; Fitzpatrick, Emer; Kyrana, Eirini; Dhawan, Anil; Kalveram, Laura; Pietrobattista, Andrea; Geerts, Anja; De Bruyne, Ruth.
Afiliação
  • Lefere S; Hepatology Research Unit, Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
  • Mosca A; Liver Research Center Ghent, Ghent University Hospital, Ghent, Belgium.
  • Hudert C; Hepatogastroenterology, Nutrition, Digestive Endoscopy and Liver Transplant Unit, Bambino Gesù Children's Hospital, Rome, Italy.
  • Dupont E; Department of Pediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Fitzpatrick E; Zeepreventorium, De Haan, Belgium.
  • Kyrana E; Paediatric Liver, GI and Nutrition Centre, King's College Hospital, London, UK.
  • Dhawan A; Department of Gastroenterology, Hepatology and Nutrition, Children's Health Ireland and University College Dublin, Ireland.
  • Kalveram L; Institute of Liver Studies, King's College Hospital, London, UK.
  • Pietrobattista A; Paediatric Liver, GI and Nutrition Centre, King's College Hospital, London, UK.
  • Geerts A; Department of Pediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • De Bruyne R; Hepatogastroenterology, Nutrition, Digestive Endoscopy and Liver Transplant Unit, Bambino Gesù Children's Hospital, Rome, Italy.
Hepatology ; 2024 Jul 19.
Article em En | MEDLINE | ID: mdl-39028885
ABSTRACT
BACKGROUND

AIMS:

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most prevalent pediatric liver disease, yet accurate risk scores for referral of children/adolescents with suspected clinically significant liver fibrosis are currently lacking. APPROACH

RESULTS:

Clinical and biochemical variables were collected in a prospective cohort of 327 children and adolescents with severe obesity, in whom liver fibrosis was evaluated by transient elastography. Logistic regression was performed to establish continuous (pFIB-c) and simplified (pFIB-6) diagnostic scores that accurately exclude significant (≥F2) fibrosis. Performance for each was compared to established non-invasive fibrosis scores. These scores were validated in elastography (n=504) and multiple biopsy-proven MASLD (n=261) cohorts. Patient sex, ethnicity, weight z-score, HOMA-IR index, ALT, and presence of hypertension were included in the scores. The pFIB-c and pFIB-6 exhibited good discriminatory capacity (c-statistic of 0.839 and 0.826), outperforming existing indices. Negative predictive values (NPV) were >90% for both scores in the derivation and elastography validation cohorts. Performance in the histological cohorts varied (AUROCs for the pFIB-c between 0.710 and 0.770), as the scores were less accurate when applied to populations in tertiary referral centers characterized by a high prevalence of significant fibrosis and high ALT levels.

CONCLUSIONS:

Analyzing several cohorts totaling approximately 1100 children and adolescents, we developed novel risk scores incorporating readily available clinical variables. In accordance with the aim of excluding pediatric MASLD-associated fibrosis, the scores performed better in non-selected cohorts of children and adolescents living with obesity than in patients referred to tertiary liver units.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hepatology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hepatology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica