New developments in genetics of myositis

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New developments in genetics of myositis.

PURPOSE OF REVIEW This article reviews the advances that have been made in our understanding of the genetics of the idiopathic inflammatory myopathies (IIM) in the past 2 years, with a particular focus on polymyositis, dermatomyositis and inclusion body myositis. RECENT FINDINGS Two large human leukocyte antigen (HLA) imputation studies have confirmed a strong association with the 8.1 ancestr...

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Genetics in inclusion body myositis

PURPOSE OF REVIEW To review the advances in our understanding of the genetics of inclusion body myositis (IBM) in the past year. RECENT FINDINGS One large genetic association study focusing on immune-related genes in IBM has refined the association within the human leukocyte antigen (HLA) region to HLA-DRB1 alleles, and identified certain amino acid positions in HLA-DRB1 that may explain this...

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Sporadic inclusion body myositis (IBM) is an acquired muscle disorder associated with ageing, for which there is no effective treatment. Ongoing developments include: genetic studies that may provide insights regarding the pathogenesis of IBM, improved histopathological markers, the description of a new IBM autoantibody, scrutiny of the diagnostic utility of clinical features and biomarkers, th...

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ژورنال

عنوان ژورنال: Current Opinion in Rheumatology

سال: 2016

ISSN: 1040-8711,1531-6963

DOI: 10.1097/bor.0000000000000328