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亨廷顿舞蹈病发病年龄与IT-15中三核苷酸重复序列长度之间的相关性。

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

作者信息

Stine O C, Pleasant N, Franz M L, Abbott M H, Folstein S E, Ross C A

机构信息

Department of Psychiatry, Johns Hopkins School of Medicine, Baltimore, MD 21287.

出版信息

Hum Mol Genet. 1993 Oct;2(10):1547-9. doi: 10.1093/hmg/2.10.1547.

Abstract

Huntington's disease (HD) is an autosomal dominant disorder with a variable age of onset that is influenced by the sex of the affected parent. The recent recognition that HD is caused by an expanded triplet repeat suggests the possibility that the onset age may be predicted by the length of the repeat. This hypothesis was tested by assaying the length of the repeat in 114 individuals who were clinically diagnosed with HD and had a known onset age. Every individual had an expanded allele. The range was from 36 to 82 repeats (mean = 48.4 +/- 9.51) and larger than the normal range (6 to 31). The size of the expanded allele was correlated with the age of onset (r = -0.65 p < .0001). Despite the highly significant correlation, the repeat size explains less than half of the variance in onset age. Furthermore, the age of onset cannot be predicted from the size of the triplet repeat, particularly if the number of repeats is in the smaller end of the expanded range. If the repeat is < or = 50 triplets, the amount of variation in the age of onset explained by the length of the triplet repeat is less than 10%. As an illustration, the onset age of individuals with 39 repeats ranges from 30 to 65 years old. The sex of the affected parent had no effect in our sample beyond the effect of the length of the repeat. Affected offspring of affected fathers had longer repeats and a larger variance in allele size than offspring of affected mothers, perhaps reflecting greater instability in paternal transmission.

摘要

亨廷顿舞蹈症(HD)是一种常染色体显性疾病,发病年龄各异,且受患病亲本的性别影响。最近认识到HD是由三联体重复序列扩增引起的,这表明发病年龄可能由重复序列的长度预测。通过检测114名临床诊断为HD且已知发病年龄的个体的重复序列长度来验证这一假设。每个个体都有一个扩增的等位基因。范围是36至82个重复序列(平均值 = 48.4 +/- 9.51),大于正常范围(6至31)。扩增等位基因的大小与发病年龄相关(r = -0.65,p <.0001)。尽管相关性非常显著,但重复序列大小解释的发病年龄方差不到一半。此外,不能从三联体重复序列的大小预测发病年龄,特别是如果重复序列数量处于扩增范围的较小端。如果重复序列≤50个三联体,三联体重复序列长度解释的发病年龄变异量不到10%。例如,具有39个重复序列的个体的发病年龄范围为30至65岁。在我们的样本中,除了重复序列长度的影响外,患病亲本的性别没有影响。患病父亲的患病后代比患病母亲的后代具有更长的重复序列和更大的等位基因大小方差,这可能反映了父系传递中更大的不稳定性。

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