Vitamin D, HLA-DRB1 and Epstein-Barr virus antibody levels in a prospective cohort of multiple sclerosis patients.

S Wergeland, K-M Myhr, K I Løken-Amsrud, A G Beiske, K S Bjerve, H Hovdal, R Midgard, S S Kvistad, T Holmøy, T Riise, Ø Torkildsen

Journal: European journal of neurology 2017;23(6):1064-70

PMID: 26998820

Abstract

BACKGROUND AND PURPOSE

Our objective was to study the association between serum levels of anti Epstein-Barr virus nuclear antigen 1 (EBNA-1) antibody and 25-hydroxyvitamin D (25(OH)D) in a prospective cohort of patients with relapsing-remitting multiple sclerosis.

METHOD

The study comprised 90 patients with relapsing-remitting multiple sclerosis, all participants in a randomized clinical trial of ω-3 fatty acids (the OFAMS study). Repeated, paired measurements of serum 25(OH)D and serum EBNA-1 immunoglobulin G (IgG) levels were obtained at baseline and every 6 months for 24 months. The association between serum EBNA-1 IgG and serum 25(OH)D levels was analysed using generalized linear models for hierarchical data.

RESULTS

There was a significant variation in EBNA-1 IgG antibody level between sampling months (Fdf 11 = 1.8, P = 0.043, one-way anova). There was a negative association between EBNA-1 IgG and 25(OH)D [B = -0.230, 95% confidence interval (CI) (-0.440, -0.023), P = 0.030] and a positive association between EBNA-1 IgG and HLA-DRB1*15 positive status [B = 94.7, 95% CI (2.423, 186.9), P = 0.044]. The association between 25(OH)D and EBNA-1 IgG remained significant after adjusting for the patient's age, gender, HLA-DRB1*15, retinol levels and interferon β-1a treatment.

CONCLUSION

Our study demonstrates monthly differences in EBNA-1 IgG levels and an association between EBNA-1 IgG, 25(OH)D levels and HLA-DRB1*15. These results indicate that EBNA-1 IgG serum levels are affected by genetic and environmental factors that also modulate multiple sclerosis risk.

© 2016 EAN.

Address: Department of Neurology, Norwegian Multiple Sclerosis Competence Centre, Haukeland University Hospital, Bergen, Norway.; Department of Clinical Medicine, KG Jebsen MS Research Centre, University of Bergen, Bergen, Norway.; Institute of Clinical Medicine, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway.; Department of Neurology, Innlandet Hospital Trust, Lillehammer, Norway.; Multiple Sclerosis Centre Hakadal, Hakadal, Norway.; Clinic of Laboratory Medicine, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.; Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology, Trondheim, Norway.; Department of Neurology, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.; Department of Neurology, Molde Hospital, Molde, Norway.; Unit for Applied Clinical Research, Norwegian University of Science and Technology, Trondheim, Norway.; Department of Laboratory Medicine, Haukeland University Hospital, Bergen, Norway.; Department of Neurology, Akershus University Hospital, Lørenskog, Norway.; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
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