Vitamin D-Related Genetic Variations and Nonalcoholic Fatty Liver Disease: A Systematic Review.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
14 Aug 2022
Historique:
received: 07 07 2022
revised: 12 08 2022
accepted: 12 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

Studies have demonstrated the link between vitamin-D-related genetic variations and nonskeletal outcomes. We aimed to identify all available data on the association of vitamin-D-related genetic variations with nonalcoholic fatty liver disease (NAFLD). Potentially eligible studies were identified from Embase and Medline databases from inception to June 2022 using a search strategy that comprised terms for "Vitamin D" and "NAFLD". Eligible studies must report the association between vitamin D-related genetic variations and presence, severity or response to treatment of NAFLD. Data were extracted from each eligible study. A total of 3495 articles were identified. After a systematic review, twelve studies were included. A total of 26 genetic variations were identified. Presence of NAFLD was associated with variations of Multiple vitamin D-related genetic variations were associated with NAFLD, indicating the role of vitamin D in the pathogenesis of NAFLD.

Sections du résumé

BACKGROUND BACKGROUND
Studies have demonstrated the link between vitamin-D-related genetic variations and nonskeletal outcomes. We aimed to identify all available data on the association of vitamin-D-related genetic variations with nonalcoholic fatty liver disease (NAFLD).
METHODS METHODS
Potentially eligible studies were identified from Embase and Medline databases from inception to June 2022 using a search strategy that comprised terms for "Vitamin D" and "NAFLD". Eligible studies must report the association between vitamin D-related genetic variations and presence, severity or response to treatment of NAFLD. Data were extracted from each eligible study.
RESULTS RESULTS
A total of 3495 articles were identified. After a systematic review, twelve studies were included. A total of 26 genetic variations were identified. Presence of NAFLD was associated with variations of
CONCLUSIONS CONCLUSIONS
Multiple vitamin D-related genetic variations were associated with NAFLD, indicating the role of vitamin D in the pathogenesis of NAFLD.

Identifiants

pubmed: 36012386
pii: ijms23169122
doi: 10.3390/ijms23169122
pmc: PMC9409408
pii:
doi:

Substances chimiques

Receptors, Calcitriol 0
Vitamins 0
Vitamin D 1406-16-2
Cytochrome P450 Family 2 EC 1.14.14.1
Cholestanetriol 26-Monooxygenase EC 1.14.15.15
Vitamin D3 24-Hydroxylase EC 1.14.15.16

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Aunchalee Jaroenlapnopparat (A)

Department of Medicine, Mount Auburn Hospital, Beth Israel Lahey Health, Cambridge, MA 02138, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.

Pichatorn Suppakitjanusant (P)

Division of Endocrinology, Metabolism, and Lipids, Emory University School of Medicine, Atlanta, GA 30322, USA.

Ben Ponvilawan (B)

Department of Internal Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA.

Nipith Charoenngam (N)

Department of Medicine, Mount Auburn Hospital, Beth Israel Lahey Health, Cambridge, MA 02138, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.
Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.

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Classifications MeSH