Udd Bjarne
Department of Neurology, Tampere University Hospital and Vasa Central Hospital, University of Tampere Medical Scool, Finland.
Biochim Biophys Acta. 2007 Feb;1772(2):145-58. doi: 10.1016/j.bbadis.2006.08.005. Epub 2006 Aug 18.
During the last 10 years several muscular dystrophies within the group of distal myopathies have been clarified as to the molecular genetic cause of the disease. Currently, the next steps are carried out to identify the molecular pathogenesis downstream of the gene defects. Some early ideas on what is going on in the muscle cells based on the defect proteins are emerging. However, in no single distal muscular dystrophy these efforts have yet reached the point where direct trials for therapy would have been launched, and in many distal dystrophies the causative gene is still lacking. When comparing the gene defects in the distal dystrophies with the more common proximal muscular dystrophies such as dystrophinopathies or limb-girdle muscular dystrophies, there is a striking difference: the genes for distal dystrophies encode sarcomere proteins whereas the genes for proximal dystrophies more often encode sarcolemmal proteins.
在过去十年中,远端肌病组中的几种肌肉营养不良症在疾病的分子遗传原因方面已得到阐明。目前,正在采取后续步骤来确定基因缺陷下游的分子发病机制。基于缺陷蛋白,一些关于肌肉细胞中正在发生什么的早期观点正在浮现。然而,在任何一种远端肌肉营养不良症中,这些努力都尚未达到可以开展直接治疗试验的阶段,而且在许多远端肌营养不良症中,致病基因仍然未知。当将远端肌营养不良症中的基因缺陷与更常见的近端肌肉营养不良症(如肌营养不良症或肢带型肌肉营养不良症)进行比较时,存在一个显著差异:远端肌营养不良症的基因编码肌节蛋白,而近端肌营养不良症的基因更常编码肌膜蛋白。