Klotho and vitamin D in multiple sclerosis: an Italian study.

Klotho genetic multiple sclerosis vitamin D

Journal

Archives of medical science : AMS
ISSN: 1734-1922
Titre abrégé: Arch Med Sci
Pays: Poland
ID NLM: 101258257

Informations de publication

Date de publication:
2020
Historique:
received: 21 03 2019
accepted: 01 05 2019
entrez: 17 6 2020
pubmed: 17 6 2020
medline: 17 6 2020
Statut: epublish

Résumé

Low vitamin D levels have been recognised as an important risk factor for autoimmune diseases, including multiple sclerosis (MS). MS is a multifactorial disease, the pathogenesis of which contributes both to genetic and environmental factors. Polymorphisms in genes codifying molecules involved in vitamin D homeostasis have been associated with hypovitaminosis D. However, the influence of polymorphisms of Klotho, which codify a protein with a pivotal role in vitamin D metabolism, have never been investigated. The aim of this study was to evaluate the association among genetic variants of Klotho, namely rs1207568 and rs9536314, serum 25(OH)D 107 patients with MS and 133 healthy controls were enrolled in this study. Serum 25(OH)D Allelic and genotypic frequencies did not differ between patients and controls. Concerning rs1207568, we found a trend toward lower serum 25(OH)D Our findings did not identify a role of Klotho in the genetic susceptibility to MS.

Identifiants

pubmed: 32542086
doi: 10.5114/aoms.2019.86969
pii: 37335
pmc: PMC7286339
doi:

Types de publication

Journal Article

Langues

eng

Pagination

842-847

Informations de copyright

Copyright © 2019 Termedia & Banach.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Concetta Scazzone (C)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Luisa Agnello (L)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Bruna Lo Sasso (BL)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Paolo Ragonese (P)

Department of Experimental Biomedicine and Neuroscience, University of Palermo, Palermo, Italy.

Giulia Bivona (G)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Sabrina Realmuto (S)

Department of Experimental Biomedicine and Neuroscience, University of Palermo, Palermo, Italy.

Giorgia Iacolino (G)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Caterina Maria Gambino (CM)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Chiara Bellia (C)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.

Giuseppe Salemi (G)

Department of Experimental Biomedicine and Neuroscience, University of Palermo, Palermo, Italy.

Marcello Ciaccio (M)

Department of Biomedicine, Neuroscience, and Advanced Diagnostics, Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Laboratory Medicine, University of Palermo, Palermo, Italy.
Department of Laboratory Medicine, University-Hospital, Palermo, Italy.

Classifications MeSH