Association study reveals novel risk loci for sporadic inclusion body myositis

M. Johari, M. Arumilli, J. Palmio, M. Savarese, G. Tasca, M. Mirabella, N. Sandholm, H. Lohi, P. Hackman, B. Udd

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)


Background and purpose: The aim was to identify potential genetic risk factors associated with sporadic inclusion body myositis (sIBM). Methods: An association based case−control approach was utilized on whole exome sequencing data of 30 Finnish sIBM patients and a control cohort (n = 193). A separate Italian cohort of sIBM patients (n = 12) was used for evaluation of the results. Results: Seven single nucleotide polymorphisms were identified in five genes that have a considerably higher observed frequency in Finnish sIBM patients compared to the control population, and the previous association of the genetic human leukocyte antigen region was confirmed. Conclusions: All seven identified variants could individually or in combination increase the susceptibility for sIBM.

Original languageEnglish
Pages (from-to)572-577
Number of pages6
JournalEuropean Journal of Neurology
Issue number4
Publication statusPublished - 1 Apr 2017
Externally publishedYes


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