Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis

被引:109
作者
Needham, Merrilee [1 ]
Corbett, Alastair [2 ]
Day, Timothy [3 ]
Christiansen, Frank [4 ]
Fabian, Vicki [5 ]
Mastaglia, Frank L.
机构
[1] Univ Western Australia, Australian Neuromuscular Res Inst, Ctr Neuromuscular & Neurol Disorders, Queen Elizabeth II Med Ctr, Perth, WA 6009, Australia
[2] Concord Repatriat Gen Hosp, Dept Neurol, Sydney, NSW, Australia
[3] Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia
[4] Royal Perth Hosp, Dept Immunol, Perth, WA, Australia
[5] Royal Perth Hosp, Dept Anat Pathol, Sect Neuropathol, Perth, WA, Australia
基金
英国医学研究理事会;
关键词
Inclusion body myositis; Diagnosis; HLA-DR3; Prevalence;
D O I
10.1016/j.jocn.2008.01.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The prevalence of sporadic inclusion body myositis (sIBM) is variable in different populations and ethnic groups. A previous survey in Western Australia in 2000 found a prevalence of 9.3 per million population. We have now performed a follow-up survey to determine whether there has since been any change in prevalence. The current prevalence was found to be 14.9 per million population, with a prevalence of 51.3 per million population in people over 50 years of age. This is the highest reported prevalence of sIBM and correlates with a high frequency of HLA-DR3 and the 8.1 major histocompatibility complex ancestral haplotype in this population. Review of a combined cohort of 57 sIBM cases from three Australian centres revealed a high rate of initial misdiagnosis and a mean time to diagnosis of 5.2 years, which suggests that even the latest prevalence figure may be an underestimate, and emphasising the need to increase the level of awareness of the condition among the medical community. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1350 / 1353
页数:4
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