» Articles » PMID: 26445546

Emerging Therapeutic Options for Sporadic Inclusion Body Myositis

Overview
Publisher Dove Medical Press
Date 2015 Oct 8
PMID 26445546
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Sporadic inclusion body myositis is the most common inflammatory muscle disorder preferentially affecting males over the age of 40 years. Progressive muscle weakness of the finger flexors and quadriceps muscles results in loss of independence with activities of daily living and eventual wheelchair dependence. Initial signs of disease are often overlooked and can lead to mis- or delayed diagnosis. The underlying cause of disease is unknown, and disease progression appears refractory to available treatment options. This review discusses the clinical presentation of inclusion body myositis and the current efforts in diagnosis, and focuses on the current state of research for both nonpharmacological and pharmacological treatment options for this patient group.

Citing Articles

Whole-body-electro-myostimulation for the care of inclusion body myositis-A case report.

Freitag N, Dragutinovic B, Notbohm H, Filipovic A, Schiffer T, Bloch W Clin Case Rep. 2024; 12(11):e9539.

PMID: 39479585 PMC: 11522995. DOI: 10.1002/ccr3.9539.


A cross-sectional study of hand function in inclusion body myositis: Implications for functional rating scale.

Lin A, Clapp M, Karanja E, Dooley K, Weihl C, Wang L Neuromuscul Disord. 2020; 30(3):200-206.

PMID: 32057637 PMC: 9724478. DOI: 10.1016/j.nmd.2019.12.002.


Multicenter questionnaire survey for sporadic inclusion body myositis in Japan.

Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata K, Inamori Y Orphanet J Rare Dis. 2016; 11(1):146.

PMID: 27821140 PMC: 5100251. DOI: 10.1186/s13023-016-0524-x.

References
1.
Brady S, Squier W, Hilton-Jones D . Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features. J Neurol Neurosurg Psychiatry. 2013; 84(11):1240-6. DOI: 10.1136/jnnp-2013-305690. View

2.
Eriksson M, Lindberg C . Hand function in 45 patients with sporadic inclusion body myositis. Occup Ther Int. 2012; 19(2):108-16. DOI: 10.1002/oti.1325. View

3.
Chahin N, Engel A . Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM. Neurology. 2007; 70(6):418-24. DOI: 10.1212/01.wnl.0000277527.69388.fe. View

4.
Cox F, Titulaer M, Sont J, Wintzen A, Verschuuren J, Badrising U . A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities. Brain. 2011; 134(Pt 11):3167-75. DOI: 10.1093/brain/awr217. View

5.
Benveniste O, Guiguet M, Freebody J, Dubourg O, Squier W, Maisonobe T . Long-term observational study of sporadic inclusion body myositis. Brain. 2011; 134(Pt 11):3176-84. DOI: 10.1093/brain/awr213. View