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Huntington's disease is a multi-system disorder
被引:45
|作者:
Mielcarek, Michal
[1
]
机构:
[1] Imperial Coll London, Dept Life Sci, London, England
基金:
欧洲研究理事会;
关键词:
cardiomyopathy;
Huntington's disease;
neurodegeneration;
peripheral tissue pathology;
skeletal muscle atrophy;
triplet repeat disorder;
D O I:
10.1080/21675511.2015.1058464
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Huntington's disease (HD) is one of the most common non-curable rare diseases and is characterized by choreic movements, psychiatric symptoms, and slowly progressive dementia. HD is inherited as an autosomal dominant disorder with complete penetrance. Although brain pathology has become a hallmark of HD, there is a critical mass of new studies suggesting peripheral tissue pathology as an important factor in disease progression. In particular, recently published studies about skeletal muscle malfunction and HD-related cardiomyopathy in HD mouse models strongly suggest their important roles, leading to upcoming preclinical and clinical trials. One might conclude that therapeutic approaches in HD should not be restricted only to the brain pathology but instead major efforts should also be made to understand the cross-talk between diseased tissues like the CNS-Heart or CNS-skeletal muscle axes.
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