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Genetic correlations between liver fat content, metabolic health, and adiposity distribution in the Fels Longitudinal Study.
Garza, Ariana L; Lee, Miryoung; Blangero, John; Bauer, Cici X; Czerwinski, Stefan A; Choh, Audrey C.
Affiliation
  • Garza AL; UTHealth Houston School of Public Health, Brownsville, TX, United States. Electronic address: ariana.l.garza@uth.tmc.edu.
  • Lee M; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth Houston School of Public Health, Brownsville, TX, United States.
  • Blangero J; South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley, School of Medicine, Brownsville, TX, United States.
  • Bauer CX; Division of Biostatistics, UTHealth Houston School of Public Health, Houston, TX, United States.
  • Czerwinski SA; School of Health and Rehabilitation Sciences, College of Medicine, Ohio State University, Columbus, OH, United States.
  • Choh AC; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth Houston School of Public Health, Brownsville, TX, United States.
Nutr Metab Cardiovasc Dis ; 34(7): 1610-1618, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38555241
ABSTRACT
BACKGROUND AND

AIMS:

Hepatic steatosis is known to be heritable, but its genetic basis is mostly uncharacterized. Steatosis is associated with metabolic and adiposity features; recent studies hypothesize that shared genetic effects between these traits could account for some of the unexplained heritability. This study aimed to quantify these genetic associations in a family-based sample of non-Hispanic white adults. METHODS AND

RESULTS:

704 participants (18-95 years, 55.8% female) from the Fels Longitudinal Study with an MRI assessment of liver fat were included. Quantitative genetic analyses estimated the age- and sex-adjusted heritability of individual traits and the genetic correlations within trait pairs. Mean liver fat was 5.95% (SE = 0.23) and steatosis (liver fat >5.56%) was present in 29.8% of participants. Heritability (h2± SE) of steatosis was 0.72 ± 0.17 (p = 6.80e-6). All other traits including liver enzymes, fasting glucose, HOMA-IR, visceral and subcutaneous adipose tissue (VAT, SAT), body mass index, body fat percent, waist circumference, lipids and blood pressure were also heritable. Significant genetic correlations were found between liver fat and all traits except aspartate aminotransferase (AST), and among most trait pairs. Highest genetic correlations were between liver fat and HOMA-IR (0.85 ± 0.08, p = 1.73e-8), fasting glucose and ALT (0.89 ± 0.26, p = 6.68e-5), and HOMA-IR with waist circumference (0.81 ± 0.12, p = 3.76e-6), body fat percent (0.78 ± 0.12 p = 2.42e-5) and VAT (0.73 ± 0.07, p = 6.37e-8).

CONCLUSIONS:

Common genes may exist between liver fat accumulation, metabolic features and adiposity phenotypes.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetic Predisposition to Disease / Adiposity Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Nutr Metab Cardiovasc Dis Journal subject: ANGIOLOGIA / CARDIOLOGIA / CIENCIAS DA NUTRICAO / METABOLISMO Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetic Predisposition to Disease / Adiposity Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Nutr Metab Cardiovasc Dis Journal subject: ANGIOLOGIA / CARDIOLOGIA / CIENCIAS DA NUTRICAO / METABOLISMO Year: 2024 Document type: Article