Epidemiology of sporadic inclusion body myositis

• Published in: Current opinion in rheumatology Vol. 28; no. 6; p. 657
• Main Authors: Molberg, Øyvind, Dobloug, Cecilie
• Format: Journal Article
• Language: English
• Published: United States 01.11.2016
• Subjects: Delayed Diagnosis; Europe - epidemiology; Humans; Myositis, Inclusion Body - diagnosis; Myositis, Inclusion Body - epidemiology; Prevalence; Retrospective Studies; Sjogren's Syndrome - diagnosis; Sjogren's Syndrome - epidemiology
• ISSN: 1531-6963
• DOI: 10.1097/bor.0000000000000327

In this review, we describe recent progress in the clinical epidemiology of sporadic inclusion body myositis (IBM). In a population-based, retrospective study from Norway, performed with a denominator population of 2.6 million; and with cases defined by the 1997 and/or 2011 European Neuro-Muscular Centre Research Diagnostic criteria, the estimated point prevalence of IBM was 3.3/100 000. Mean time from symptom onset to diagnosis was 5.6 years, longer than in earlier studies. The male to female ratio was 3 : 2, and the mean age at diagnosis 67 years, very similar to figures reported this year from a nationwide, Dutch myopathy registry. Coexisting rheumatic diseases were recorded in 25% of Norwegian IBM cases, with Sjøgren's syndrome as the most commonly encountered. Mortality was increased in IBM, with a standardized mortality rate of 1.7, but there was no indication of increased cancer risk. Population-based data indicate that the prevalence of IBM in Europe is higher than expected from previous studies. Diagnostic delay appears to be a persisting problem in IBM; a major challenge with promising new therapies on the horizon.