Literature DB >> 25152387

Clinical features of Japanese patients with inclusion body myositis.

Hiroko Hori1, Satoshi Yamashita2, Nozomu Tawara1, Tomoo Hirahara1, Kensuke Kawakami1, Tomo Nishikami1, Yasushi Maeda1, Yukio Ando1.   

Abstract

BACKGROUND: The incidence of sporadic inclusion body myositis (sIBM) has been much lower in Japanese than in Western populations. Because of a few reports on Asian populations, it is unclear whether the clinical characteristics of sIBM are identical in Caucasian and Japanese patients.
METHODS: We compared 18 patients with sIBM, divided into 3 groups by age-of-onset, with previous cohort studies. We calculated the ΔIBM functional rating scale/time duration (ΔIBMFRS/Δtime) as an index of functional disability progression. Patients' electrophysiology was analyzed in relation to their clinical characteristics.
RESULTS: The cohort was 83.3% male and showed uniform initial muscle weakness in the lower and/or upper limbs. An older age-at-onset was associated with a more rapid progression, and patients with a longer duration frequently showed F-wave abnormalities and findings of chronic denervation.
CONCLUSIONS: The clinical characteristics of sIBM were relatively homogeneous beyond the ethnic differences. Aging might be a synergistic factor for the progression of sIBM pathology.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chronic denervation; Clinical characteristics; F-wave abnormality; Japanese cases; Motor neuron disease; Sporadic inclusion body myositis

Mesh:

Year:  2014        PMID: 25152387     DOI: 10.1016/j.jns.2014.08.009

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  1 in total

Review 1.  Myositis Mimics.

Authors:  E Harlan Michelle; Andrew L Mammen
Journal:  Curr Rheumatol Rep       Date:  2015-10       Impact factor: 4.592

  1 in total

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