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Machado‐joseph disease: Clinical, molecular, and metabolic characterization in chinese kindreds

1997; Wiley; Volume: 41; Issue: 4 Linguagem: Inglês

10.1002/ana.410410407

1531-8249

Bing‐wen Soon, Chung‐Hui Cheng, Ren‐Shyan Liu, Din‐E Shan,

Neurological disorders and treatments

Abstract Machado‐Joseph disease, an autosomal dominant multisystem motor degeneration, has been described mainly in people of Portuguese descent. Our report documents the presence of Machado‐Joseph disease in the Chinese population, based on the specific molecular marker of a CAG repeat array in the 3′ end of the MJD gene. We screened 21 Chinese families with dominant spinocerebellar ataxia. The results showed that Machado‐Joseph disease with CAG expansion accounted for 52% of families with autosomal dominant cerebellar ataxia in this series. The clinical characteristics, besides the well‐documented cerebellar ataxia, dysarthria, nystagmus, corticospinal dysfunctions, a variable degree of facial muscle fasciculation, and proprioceptive loss, included loss of optokinetic nystagmus and autonomic nervous system dysfunction. The CAG repeat number in the MJD gene ranged from 14 to 39 among normal alleles, and from 63 to 81 among MJD alleles. There was a strong inverse correlation (γ = –0.77) between number of CAG repeats and age at symptom onset, accounting for 60% of the variance of age at onset. A strong clinical anticipation of age at onset existed in successive generations. Mild instabilities of expanded CAG repeat numbers during meiotic transmission occurred, with no significant difference according to the gender of the transmitting parent. Finally, brain metabolism in Machado‐Joseph disease, studied with positron emission tomography, was characterized by significant progressive regional hypometabolism in the occipital cortex, as well as the cerebellar hemispheres, vermis, and brainstem.