| Literature DB >> 26367100 |
F David Carmona1, Javier Martín1, Miguel A González-Gay2.
Abstract
Giant cell arteritis is a complex immune-mediated disease that involves large blood vessels in individuals older than 50 years. Recent studies have confirmed a strong association of this form of vasculitis with the HLA region, particularly with HLA class II genes. However, other non-HLA loci, such as protein tyrosine phosphatase non-receptor type 22, may also account for the susceptibility to giant cell arteritis. In addition, genetic variants located in genes encoding proinflammatory cytokines seem to influence the phenotypic expression of the disease, including the risk of severe ischemic complications, the presence of polymyalgia rheumatica and the higher incidence of relapses observed in some patients. The identification of putative genetic markers of disease severity could have clear therapeutic implications, as it may allow us to identify patients who are potentially responders to specific treatments.Entities:
Keywords: IFN-γ; IL-6; giant cell arteritis; human leukocyte antigen; polymyalgia rheumatica; protein tyrosine phosphatase non-receptor type 22; relapses; temporal artery biopsy; vascular endothelial growth factor; visual ischemic complications
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Year: 2015 PMID: 26367100 DOI: 10.1586/1744666X.2016.1089173
Source DB: PubMed Journal: Expert Rev Clin Immunol ISSN: 1744-666X Impact factor: 4.473