Rev Neurol (Paris). 2001 Jul;157(6-7):633-7.
The prion protein gene was studied in patients with definite or probable Creutzfeldt-Jakob disease (CJD) registered by national CJD units of 6 European countries. The role of genetic factors in CJD was also investigated by comparing the frequencies of a family history of dementia and Parkinson's disease in CJD cases and matched controls. Codon 129 genotype was examined in 337 CJD cases of whom 73.2 p. 100 were homozygous for methionine, 10.9 p. 100 were homozygous for valine and 15.7 p. 100 were heterozygous. The genotype frequencies were not statistically different across countries. Future differences, if any, would constitute a meaningful signal for the surveillance of CJD in Europe. A prion protein gene mutation was found in 14.5 p. 100 of CJD cases; only 40 p. 100 of them had a known family history of CJD. The case-control study showed that positive family histories of dementia and Parkinson's disease were both associated with CJD. Although recall bias is the most likely explanation for this finding, the hypothesis that neurodegenerative diseases might share unknown genetic risk factors can also be considered.
对欧洲6个国家的国家克雅氏病(CJD)监测单位登记的确诊或疑似克雅氏病患者的朊病毒蛋白基因进行了研究。通过比较CJD病例和匹配对照中痴呆症和帕金森病家族史的频率,还对遗传因素在CJD中的作用进行了调查。对337例CJD病例进行了密码子129基因型检测,其中73.2%为蛋氨酸纯合子,10.9%为缬氨酸纯合子,15.7%为杂合子。各国的基因型频率无统计学差异。未来若有差异,将成为欧洲CJD监测的一个有意义的信号。在14.5%的CJD病例中发现了朊病毒蛋白基因突变;其中只有40%有已知的CJD家族史。病例对照研究表明,痴呆症和帕金森病的阳性家族史均与CJD有关。尽管回忆偏倚最有可能解释这一发现,但神经退行性疾病可能共享未知遗传危险因素这一假说也可予以考虑。