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Mortality outcomes in individuals with MASLD versus MASLD and increased alcohol intake
Indexado
WoS WOS:001296461800001
Scopus SCOPUS_ID:85201976854
DOI 10.1111/JGH.16726
Año 2024
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Background and Aim Metabolic dysfunction-associated steatotic liver disease (MASLD) has become a leading cause of chronic liver disease worldwide. A new entity termed MetALD has also been described and is defined as individuals with MASLD and increased alcohol intake. However, the natural history of MetALD compared with MASLD is unknown. We aimed to compare longitudinal outcomes in patients with MASLD versus MetALD. Methods This study was performed using data from the National Health and Nutrition Examination Survey from 2011 to 2018. MASLD patients (defined by the United States Fatty Liver Index > 30) who met cardiometabolic criteria including body mass index (BMI) > 25 (BMI > 23 in Asians), hypertension, diabetes mellitus, dyslipidemia, and hypertriglyceridemia were included. MetALD was defined as MASLD with increased alcohol intake (3-6 standard drinks per day in males; 2-5 standard drinks per day in females). A comparison of overall, cardiovascular, cancer-related, and other causes of mortality in patients with MASLD versus MetALD was performed. Results A total of 2838 individuals with MASLD and 2557 individuals with MetALD were included with a median follow-up time of 56 months. MetALD patients were at increased risk of cancer-related mortality compared with patients with MASLD (hazard ratio 1.32; 95% confidence interval 1.14-1.53; P < 0.01). However, there was no significant difference in overall, cardiovascular, and other causes of mortality. Conclusions Patients with MetALD were at higher risk for cancer-related mortality than MASLD. Close attention to regular cancer surveillance and accurate classification of alcohol consumption in individuals with diagnosed MASLD is warranted to help improve patient care and outcome.

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Disciplinas de Investigación



WOS
Gastroenterology & Hepatology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Aboona, Majd B. - UNIV ARIZONA - Estados Unidos
University of Arizona College of Medicine – Phoenix - Estados Unidos
2 Danpanichkul, Pojsakorn - TEXAS TECH UNIV - Estados Unidos
Chiang Mai Univ - Tailandia
Faculty of Medicine, Chiang Mai University - Tailandia
TTUHSC School of Medicine - Estados Unidos
3 Chen, Vincent L. - Univ Michigan Hlth Syst - Estados Unidos
University of Michigan Medical School - Estados Unidos
4 Rangan, Pooja - UNIV ARIZONA - Estados Unidos
University of Arizona College of Medicine – Phoenix - Estados Unidos
5 Kim, Donghee - Stanford Univ - Estados Unidos
Stanford University School of Medicine - Estados Unidos
6 Alkhouri, Naim - Arizona Liver Inst - Estados Unidos
Arizona Liver Health - Estados Unidos
7 Fallon, Michael B. - UNIV ARIZONA - Estados Unidos
Banner Univ - Estados Unidos
Banner - University Medical Center Phoenix - Estados Unidos
University of Arizona College of Medicine – Phoenix - Estados Unidos
8 Noureddin, Mazen Hombre Houston Res Inst - Estados Unidos
Houston Methodist Hosp - Estados Unidos
Houston Methodist Hospital - Estados Unidos
9 Arab, Juanpablo Hombre Virginia Commonwealth Univ - Estados Unidos
Pontificia Universidad Católica de Chile - Chile
Escuela de Medicina - Chile
TTUHSC School of Medicine - Estados Unidos
VCU School of Medicine - Estados Unidos
10 Wijarnpreecha, Karn - UNIV ARIZONA - Estados Unidos
Banner Univ - Estados Unidos
Banner - University Medical Center Phoenix - Estados Unidos
University of Arizona College of Medicine – Phoenix - Estados Unidos

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Financiamiento



Fuente
National Institute of Diabetes and Digestive and Kidney Diseases
NIDDK

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Agradecimientos



Agradecimiento
Vincent L Chen was supported in part by NIDDK (K08 DK132312).
: Vincent L Chen was supported in part by NIDDK (K08 DK132312). Financial support

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