首页> 美国卫生研究院文献>Journal of Medical Genetics >The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.
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The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.

机译:tRNA(Gln)4336线粒体DNA变异不是高外显眼突变易突变易患痴呆年龄75岁。

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摘要

The genetic factors that predispose to Alzheimer's disease (AD) are heterogeneous. Two recent reports have suggested that a mitochondrial DNA mutation within the tRNAGln gene, located at position 4336, may be a risk factor for AD, as it was found in 10/256 (3.9%) cases with AD confirmed by necropsy. Although low prevalences of this mutation were detected in non-demented subjects in both of these studies, the controls were not carefully matched with the AD cases. We have investigated the frequency of this mutation in two community based elderly cohorts in Cambridgeshire, who have participated in longitudinal studies of cognitive function. The 4336 mitochondrial mutation was detected in 8/ 443 people examined. These people were found to be non-demented at ages 74, 81, 84, 86, 89, 90, 91, and 102 years, in contrast to the previously described cases whose onset of dementia occurred between 60 and 76 years (mean 68). Accordingly, we believe that this mitochondrial variant is not a high penetrance mutation which predisposes to dementia before the age of 76 years.
机译:易患阿尔茨海默氏病(AD)的遗传因素是异质的。最近的两项报道表明,位于尸体确诊的10/256(3.9%)例AD中发现,位于4336位的tRNAGln基因内的线粒体DNA突变可能是AD的危险因素。尽管在这两项研究中均未痴呆的受试者中检测到此突变的患病率较低,但对照并未与AD病例仔细匹配。我们在剑桥郡的两个社区老年队列研究了这种突变的频率,他们参加了认知功能的纵向研究。在检查的8/443人中检测到4336线粒体突变。发现这些人在74、81、84、86、89、90、91和102岁时没有痴呆,而之前描述的痴呆发作在60到76岁之间的病例则相反(平均68岁) 。因此,我们认为该线粒体变体不是高外显率突变,其易患76岁之前的痴呆症。

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