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Risk of major adverse liver outcomes among first-degree relatives of individuals with MASLD.
Yang, Wen; Ebrahimi, Fahim; Romeo, Stefano; Holmer, Magnus; Vessby, Johan; Ekstedt, Mattias; Ludvigsson, Jonas F; Shang, Ying; Hagström, Hannes.
Afiliação
  • Yang W; Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.
  • Ebrahimi F; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Romeo S; Department of Gastroenterology and Hepatology, Clarunis University Center for Gastrointestinal and Liver Diseases, Basel, Switzerland.
  • Holmer M; Department of Molecular and Clinical Medicine, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Vessby J; Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.
  • Ekstedt M; Division of Hepatology, Department of Upper GI, Karolinska University Hospital, Stockholm, Sweden.
  • Ludvigsson JF; Department of Medical Sciences, Gastroenterology Research Group, Uppsala University, Uppsala, Sweden.
  • Shang Y; Department of Gastroenterology and Hepatology, Department of Health, Medicine, and Caring Sciences, Linköping University, Linköping, Sweden.
  • Hagström H; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Liver Int ; 44(5): 1253-1264, 2024 May.
Article em En | MEDLINE | ID: mdl-38385564
ABSTRACT
BACKGROUND &

AIMS:

Previous studies have suggested an increased risk of major adverse liver outcomes (MALO) in relatives of patients with metabolic dysfunction-associated steatotic liver disease (MASLD). However, granular and longitudinal evidence is lacking on the future risk of MALO among family members of individuals with MASLD.

METHODS:

We identified 3526 first-degree relatives (FDRs) and 11 079 general population comparators to 1328 patients with MASLD diagnosed between 1974 and 2021, with detailed clinical data, including liver histology in 71% of patients. MALO was defined through diagnostic coding for cirrhosis or its complications. Cox regression models were used to estimate adjusted hazard ratios (aHRs) for MALO among FDRs compared to general population comparators. Cumulative incidence accounting for competing risks was calculated.

RESULTS:

During a median follow-up of 13.4 years, there were 65 (2%, 1.12/1000 person-years) and 225 (2%, 1.26/1000 person-years) MALO events in FDRs and general population comparators respectively. After adjusting for demographic factors and comorbidities, FDRs were at no increased risk of MALO (aHR = 0.99, 95% CI 0.74-1.33). Increased relative rates of MALOs were, however, observed in some subgroups, including parents, although absolute risk estimates were low and comparable to the general population.

CONCLUSIONS:

FDRs of patients with MASLD did not have a higher rate of incident MALO than the general population. Since the absolute risk of MALO in relatives of patients with MASLD was low, these results do not support systematic screening of MASLD-related fibrosis in relatives of patients with MASLD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fígado Gorduroso / Doenças Metabólicas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fígado Gorduroso / Doenças Metabólicas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article