Relationship Between a Vitamin D Genetic Risk Score and Autoantibodies Among First-Degree Relatives of Probands With Rheumatoid Arthritis and Systemic Lupus Erythematosus.

autoantibody negative (aAb-) autoantibody positive (aAb+) genetic risk score (GRS) rheumatoid arthritis (RA) systemic lupus erythematosus (SLE) vitamin D

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 22 02 2022
accepted: 09 05 2022
entrez: 20 6 2022
pubmed: 21 6 2022
medline: 22 6 2022
Statut: epublish

Résumé

Higher 25-hydroxyvitamin D (25(OH)D) levels have been associated with reduced risk for autoimmune diseases and are influenced by vitamin D metabolism genes. We estimated genetically-determined vitamin D levels by calculating a genetic risk score (GRS) and investigated whether the vitamin D GRS was associated with the presence of autoantibodies related to rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) in those at increased risk for developing RA and SLE, respectively. In this cross-sectional study, we selected autoantibody positive (aAb+) and autoantibody negative (aAb-) individuals from the Studies of the Etiologies of Rheumatoid Arthritis (SERA), a cohort study of first-degree relatives (FDRs) of individuals with RA (189 RA aAb+, 181 RA aAb-), and the Lupus Family Registry and Repository (LFRR), a cohort study of FDRs of individuals with SLE (157 SLE aAb+, 185 SLE aAb-). Five SNPs known to be associated with serum 25(OH)D levels were analyzed individually as well as in a GRS: rs4588 ( Both cohorts had similar demographic characteristics, with significantly older and a higher proportion of males in the aAb+ FDRs. The vitamin D GRS was inversely associated with RA aAb+ (OR = 0.85, 95% CI = 0.74-0.99), suggesting a possible protective factor for RA aAb positivity in FDRs of RA probands. The vitamin D GRS was not associated with SLE aAb+ in the LFRR (OR = 1.09, 95% CI = 0.94-1.27). The Genes associated with vitamin D levels may play a protective role in the development of RA aAbs in FDRs of RA probands, perhaps through affecting lifelong vitamin D status. The GRS and the

Identifiants

pubmed: 35720397
doi: 10.3389/fimmu.2022.881332
pmc: PMC9205604
doi:

Substances chimiques

Autoantibodies 0
Vitamins 0
Vitamin D 1406-16-2

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

881332

Subventions

Organisme : NIGMS NIH HHS
ID : U54 GM104938
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR051461
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI144292
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI101981
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR073750
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI101934
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR079369
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR051394
Pays : United States
Organisme : NIAMS NIH HHS
ID : T32 AR007534
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR053483
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI082714
Pays : United States
Organisme : NIGMS NIH HHS
ID : P30 GM103510
Pays : United States

Informations de copyright

Copyright © 2022 Vanderlinden, Bemis, Seifert, Guthridge, Young, Demoruelle, Feser, DeJager, Macwana, Mikuls, O’Dell, Weisman, Buckner, Keating, Gaffney, Kelly, Langefeld, Deane, James, Holers and Norris.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Lauren A Vanderlinden (LA)

Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Elizabeth A Bemis (EA)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Jennifer Seifert (J)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Joel M Guthridge (JM)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Kendra A Young (KA)

Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Mary Kristen Demoruelle (MK)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Marie Feser (M)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Wade DeJager (W)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Susan Macwana (S)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Ted R Mikuls (TR)

Division of Rheumatology and Immunology, University of Nebraska Medical Center and VA Nebraska-Western Iowa Health Care System, Omaha, NE, United States.

James R O'Dell (JR)

Division of Rheumatology and Immunology, University of Nebraska Medical Center and VA Nebraska-Western Iowa Health Care System, Omaha, NE, United States.

Michael H Weisman (MH)

Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, United States.

Jane Buckner (J)

Center for Translational Immunology, Benaroya Research Institute (BRI) at Virginia Mason, Seattle, WA, United States.

Richard M Keating (RM)

Division of Rheumatology, Scripps Health, La Jolla, CA, United States.

Patrick M Gaffney (PM)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Jennifer A Kelly (JA)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Carl D Langefeld (CD)

Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston Salem, NC, United States.
Center for Precision Medicine, Wake Forest School of Medicine, Winston Salem, NC, United States.

Kevin D Deane (KD)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Judith A James (JA)

Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Vernon Michael Holers (VM)

School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Jill M Norris (JM)

Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

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Classifications MeSH