Journal article
Apolipoprotein E ϵ4 in inclusion body myositis
Annals of Neurolog, Vol.38(6), pp.957-959
1995
Abstract
The genetic predisposition to inclusion body myositis (IBM) is probably multifactorial. The deposition of the β-amyloid protein is a characteristic histological feature of both IBM and Alzheimer's disease (AD). The ϵ4 allele of apolipoprotein E (APO E) has been strongly associated with familial and late-onset AD. We therefore compared the APO E allele frequencies in a group of 14 patients with IBM with those in a group of patients with other inflammatory muscle diseases and in the general population. The frequency of the ϵ4 allele in IBM was increased (0.29) compared with that in patients with other inflammatory muscle diseases (0.15) and the general population (0.13) (p < 0.05). These data suggest that APO E genotype may be one of the factors involved in determining the predisposition to the development of IBM.
Details
- Title
- Apolipoprotein E ϵ4 in inclusion body myositis
- Authors/Creators
- M.J. Garlepp (Author/Creator) - Australian Neuromuscular Research Institute, Australia.H. Tabarias (Author/Creator) - The University of Western AustraliaF.M. van Bockxmeer (Author/Creator) - Royal Perth HospitalP.J. Zilko (Author/Creator) - The University of Western AustraliaB. Laing (Author/Creator) - The University of Western AustraliaF.L. Mastaglia (Author/Creator) - Centre for Neuromuscular and Neurological Disorders
- Publication Details
- Annals of Neurolog, Vol.38(6), pp.957-959
- Publisher
- Wiley
- Identifiers
- 991005544673907891
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
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- 1.52 Neurodegenerative Diseases
- 1.52.57 Alzheimer's Mechanisms
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- Neurosciences
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- Neuroscience & Behavior