4.3 Article

Epstein-Barr virus antibodies and vitamin D in prospective multiple sclerosis biobank samples

Journal

MULTIPLE SCLEROSIS JOURNAL
Volume 19, Issue 12, Pages 1587-1591

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458513483888

Keywords

Multiple sclerosis; case-control study; risk factors in epidemiology; Epstein-Barr virus (EBV); Epstein-Barr Nuclear Antigen-1 (EBNA-1); vitamin D (25(OH)D)

Funding

  1. Swedish Association of Neurologically Disabled
  2. Department of Clinical Neuroscience at Umea University
  3. Biogen Idec
  4. Sanofi Aventis
  5. Merck Serono
  6. Umea University
  7. Vasterbotten County Council on cooperation in the fields of Medicine, Odontology, and Health (A.L.F.)

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Background: The antibody reactivity against Epstein-Barr nuclear antigen-1 (EBNA-1), and 25-hydroxyvitamin D (25(OH)D) status have been associated with multiple sclerosis (MS) risk. Interaction between these two factors has been proposed. Objectives: The objective of this paper is to examine the association between antibody reactivity against EBNA-1 and five EBNA-1 domains, and the risk of MS, and to examine if these antibodies and 25(OH)D status interact regarding MS risk in prospectively collected blood samples. Methods: Antibody reactivity and 25(OH)D levels were measured using ELISAs in n = 192 MS cases and n = 384 matched controls. The risk of MS was analysed using matched logistic regression. Interaction on the additive scale was assessed. Results: The risk of MS increased across tertiles of antibody reactivity against EBNA-1, domain EBNA-1(402-502), and domain EBNA-1(385-420); p trends < 0.001. In young individuals (below median age at sampling, < 26.4 years), these associations were stronger, and 25(OH)D levels correlated inversely to antibody reactivity against EBNA-1 and the EBNA-1 domains. No statistical interaction was found. Conclusions: We confirm that increased antibody reactivity against EBNA-1 is a risk factor of MS. 25(OH)D status might influence the immune response towards Epstein-Barr virus in young subjects, and thereby modulate MS risk.

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