Genotype-by-Environment Interactions in Nonalcoholic Fatty Liver Disease and Chronic Illness among Mexican Americans: The Role of Acculturation Stress.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
01 Aug 2024
Historique:
received: 24 05 2024
revised: 23 07 2024
accepted: 30 07 2024
medline: 1 9 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: epublish

Résumé

This study examines the complex interplay of genetic and environmental interactions that shape chronic illness risk. Evidence is mounting for the role of genetic expression and the immune response in the pathogenesis of chronic disease. In the Rio Grande Valley of south Texas, where 90% of the population is Mexican American, chronic illnesses (including obesity, diabetes, nonalcoholic liver disease, and depression) are reaching epidemic proportions. This study leverages an ongoing family study of the genetic determinants of risk for obesity, diabetes, hypertension, hyperlipidemia, and depression in a Mexican American population. Data collected included blood pressure, BMI, hepatic transaminases, HbA1c, depression (BDI-II), acculturation/marginalization (ARSMA-II), and liver health as assessed by elastography. Heritability and genotype-by-environment (G×E) interactions were analyzed, focusing on the marginalization/separation measure of the ARSMA-II. Significant heritabilities were found for traits such as HbA1c (h

Identifiants

pubmed: 39202366
pii: genes15081006
doi: 10.3390/genes15081006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Knapp Community Care Foundation
ID : 00000

Auteurs

Eron G Manusov (EG)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Vincent P Diego (VP)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Marcio Almeida (M)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

David Ortiz (D)

School of Medicine, University of Texas Rio Grande Valley, Edinburg, TX 78539, USA.

Joanne E Curran (JE)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Jacob Galan (J)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Ana C Leandro (AC)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Sandra Laston (S)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

John Blangero (J)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

Sarah Williams-Blangero (S)

Department of Human Genetics, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.
South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX 78520, USA.

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Classifications MeSH