Study2018Open access

Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis

Langer-Gould A, Lucas RM, Xiang AH, Wu J, Chen LH, Gonzales E, Haraszti S, Smith JB, Quach H, Barcellos LF

Nutrients · 24 citations

How it was studied

Design
Case-control study (classified by our AI screen)
Studied in
People
Main outcome
Clinical events such as disease or death

Who paid for it

Funding
Independent funding
Government
National Institute of Neurological Disorders and Stroke
Government
NINDS NIH HHS
Government
National Institues of Health
Grants
National Institute of Neurological Disorders and Stroke (R01NS075308)

Based on 3 listed funder(s) and full-text disclosure statement.

Publication

Published
2018-02-07 · Nutrients · vol. 10 · issue 2 · p. 184
Publisher
Multidisciplinary Digital Publishing Institute
Cited
36 citations · more than 94% of similar papers · 3.8× the field average
Impact
Top 10% most cited in its field
References
32 works
Access
Open access (journal) · CC-BY
Research areas
Vitamin D Research Studies · Multiple Sclerosis Research Studies · Psoriasis: Treatment and Pathogenesis
Keywords
Vitamin D and neurology, Vitamin D-binding protein, Multiple sclerosis, Allele, Medicine, Genotype, vitamin D deficiency, Haplotype, Internal medicine, Lower risk, Sun exposure, Calcitriol receptor, Endocrinology, Demography, Immunology, Genetics, Gene, Biology, Confidence interval
MeSH
humans, multiple sclerosis, vitamin d, vitamin d-binding protein, risk factors, sunlight, genotype, polymorphism, genetic, adult, middle aged, female, male, hispanic or latino, white people, black or african american

10 authors

From US, AU

  • Annette Magdalene Langer-Gould · correspondingLos Angeles Medical Center
  • Robyn Marjorie LucasAustralian National University
  • Anny H. XiangKaiser Permanente
  • Jun WuKaiser Permanente
  • Lie ChenKaiser Permanente
  • Edlin G. GonzalesKaiser Permanente

Abstract

Blacks have different dominant polymorphisms in the vitamin D-binding protein (DBP) gene that result in higher bioavailable vitamin D than whites. This study tested whether the lack of association between 25-hydroxyvitamin D (25OHD) and multiple sclerosis (MS) risk in blacks and Hispanics is due to differences in these common polymorphisms (rs7041, rs4588). We recruited incident MS cases and controls (blacks 116 cases/131 controls; Hispanics 183/197; whites 247/267) from Kaiser Permanente Southern California. AA is the dominant rs7041 genotype in blacks (70.0%) whereas C is the dominant allele in whites (79.0% AC/CC) and Hispanics (77.1%). Higher 25OHD levels were associated with a lower risk of MS in whites who carried at least one copy of the C allele but not AA carriers. No association was found in Hispanics or blacks regardless of genotype. Higher ultraviolet radiation exposure was associated with a lower risk of MS in blacks (OR = 0.06), Hispanics and whites who carried at least one copy of the C allele but not in others. Racial/ethnic variations in bioavailable vitamin D do not explain the lack of association between 25OHD and MS in blacks and Hispanics. These findings further challenge the biological plausibility of vitamin D deficiency as causal for MS.

Abstract via Europe PMC. Copyright remains with the authors or publisher (CC BY).

Community trust

Loading…

How much do you trust this study's findings?

0 · not at all10 · completely

Comments

Sign in to rate, comment on or flag this study.Sign in

Something wrong here?

Flag this study if its information, labels or funding look wrong. An editor reviews every flag.

Sign in to rate, comment on or flag this study.Sign in

Educational information about published research. Not medical advice, and not a recommendation to start or stop anything.