| Literature DB >> 23726763 |
Wei Qiu1, Kym Pham, Ian James, David Nolan, Allison Castley, Frank T Christiansen, Petra Czarniak, Yuebei Luo, Jingshan Wu, Michael Garlepp, Steve Wilton, William M Carroll, Frank L Mastaglia, Allan G Kermode.
Abstract
Non-Human Leukocyte Antigen (HLA) genes have concomitant, although modest, effects on multiple sclerosis (MS) susceptibility; however findings have varied in different populations. Here we present the results of an association study of 16 single nucleotide polymorphisms (SNPs) in 10 non-HLA genes (IL7R, IL2RA, CLEC-16A, TYK2, CD58, IRF5, STAT3, CTLA-4, APOE, ICAM-1) in a Western Australian cohort of 350 MS patients and 498 population control subjects. Our results indicate that in this population, SNPs in IL7R, TYK2, IRF5 and APOE have modifying effects on MS susceptibility. We also found evidence of interactive protective effects between polymorphisms in the IL7R/CD58, CLEC-16A/CTLA-4, and TYK2/IRF5 genes, which in some instances are restricted within HLA- or gender-defined groups.Entities:
Keywords: APOE; Apolipoprotein E; C-type lectin domain family 16; CLEC-16A; CTLA-4; Cytotoxic T-lymphocyte antigen 4; HLA; ICAM-1; IL2RA; IL7R; IRF5; Intercellular adhesion molecule 1; Interferon regulatory factor 5; Interleukin 2 receptor a; Interleukin 7 receptor; Multiple sclerosis; Non-HLA genes; STAT3; Signal transducer and activator of transcription 3; Single nucleotide polymorphisms; TYK2; Tyrosine kinase 2
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Year: 2013 PMID： 23726763 DOI： 10.1016/j.jneuroim.2013.04.022
Source DB: PubMed Journal: J Neuroimmunol ISSN： 0165-5728 Impact factor: 3.478