| Literature DB >> 25616667 |
An Goris1, Ine Pauwels2, Marte W Gustavsen3, Brechtje van Son4, Kelly Hilven2, Steffan D Bos3, Elisabeth Gulowsen Celius5, Pål Berg-Hansen3, Jan Aarseth6, Kjell-Morten Myhr7, Sandra D'Alfonso8, Nadia Barizzone9, Maurizio A Leone10, Filippo Martinelli Boneschi11, Melissa Sorosina12, Giuseppe Liberatore13, Ingrid Kockum14, Tomas Olsson14, Jan Hillert15, Lars Alfredsson16, Sahl Khalid Bedri15, Bernhard Hemmer17, Dorothea Buck18, Achim Berthele18, Benjamin Knier18, Viola Biberacher18, Vincent van Pesch19, Christian Sindic19, Annette Bang Oturai20, Helle Bach Søndergaard20, Finn Sellebjerg20, Poul Erik H Jensen20, Manuel Comabella21, Xavier Montalban21, Jennifer Pérez-Boza21, Sunny Malhotra21, Jeannette Lechner-Scott22, Simon Broadley23, Mark Slee2, Bruce Taylor24, Allan G Kermode25, Pierre-Antoine Gourraud5, Stephen J Sawcer26, Bettina Kullle Andreassen27, Bénédicte Dubois28, Hanne F Harbo3.
Abstract
Immunological hallmarks of multiple sclerosis include the production of antibodies in the central nervous system, expressed as presence of oligoclonal bands and/or an increased immunoglobulin G index-the level of immunoglobulin G in the cerebrospinal fluid compared to serum. However, the underlying differences between oligoclonal band-positive and -negative patients with multiple sclerosis and reasons for variability in immunoglobulin G index are not known. To identify genetic factors influencing the variation in the antibody levels in the cerebrospinal fluid in multiple sclerosis, we have performed a genome-wide association screen in patients collected from nine countries for two traits, presence or absence of oligoclonal bands (n = 3026) and immunoglobulin G index levels (n = 938), followed by a replication in 3891 additional patients. We replicate previously suggested association signals for oligoclonal band status in the major histocompatibility complex region for the rs9271640*A-rs6457617*G haplotype, correlated with HLA-DRB1*1501, and rs34083746*G, correlated with HLA-DQA1*0301 (P comparing two haplotypes = 8.88 × 10(-16)). Furthermore, we identify a novel association signal of rs9807334, near the ELAC1/SMAD4 genes, for oligoclonal band status (P = 8.45 × 10(-7)). The previously reported association of the immunoglobulin heavy chain locus with immunoglobulin G index reaches strong evidence for association in this data set (P = 3.79 × 10(-37)). We identify two novel associations in the major histocompatibility complex region with immunoglobulin G index: the rs9271640*A-rs6457617*G haplotype (P = 1.59 × 10(-22)), shared with oligoclonal band status, and an additional independent effect of rs6457617*G (P = 3.68 × 10(-6)). Variants identified in this study account for up to 2-fold differences in the odds of being oligoclonal band positive and 7.75% of the variation in immunoglobulin G index. Both traits are associated with clinical features of disease such as female gender, age at onset and severity. This is the largest study population so far investigated for the genetic influence on antibody levels in the cerebrospinal fluid in multiple sclerosis, including 6950 patients. We confirm that genetic factors underlie these antibody levels and identify both the major histocompatibility complex and immunoglobulin heavy chain region as major determinants.Entities:
Keywords: CSF; genetics; immunoglobulin; multiple sclerosis; oligoclonal bands
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Year: 2015 PMID: 25616667 PMCID: PMC4408440 DOI: 10.1093/brain/awu405
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501