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多巴胺D5受体基因多态性与帕金森病患者左旋多巴诱发的运动波动风险

Dopamine D5 receptor gene polymorphism and the risk of levodopa-induced motor fluctuations in patients with Parkinson's disease.

作者信息

Wang J, Liu Z L, Chen B

机构信息

Department of Neurology, The First Affiliated Hospital, Sun Yat-Sen University of Medical Sciences, 510080, Guangzhou, China.

出版信息

Neurosci Lett. 2001 Jul 27;308(1):21-4. doi: 10.1016/s0304-3940(01)01971-1.

Abstract

Motor fluctuations are the most common complication of levodopa therapy for Parkinson's disease (PD). Genetic factors could play a role in determining the occurrence of motor fluctuations. To investigate whether dopamine receptor D5 (DRD5) T978C polymorphism is associated with the risk of developing motor fluctuations in PD, we studied this polymorphism in a case-control study of 120 subjects with sporadic PD and 110 control subjects. We found that the overall allelic and genotypic frequencies did not differ significantly between patients with PD and control subjects (all P>0.7), and between motor fluctuators (n=50) and non-motor fluctuators (n=50) (all P>0.8). It suggests that DRD5 T978C polymorphism is not associated with the susceptibility to PD, nor with the risk of developing motor fluctuations in PD. Therefore, other polymorphisms that alter the expression of the dopamine receptors should be further studied.

摘要

运动波动是帕金森病(PD)左旋多巴治疗最常见的并发症。遗传因素可能在决定运动波动的发生中起作用。为了研究多巴胺受体D5(DRD5)T978C多态性是否与PD发生运动波动的风险相关,我们在一项病例对照研究中对120例散发性PD患者和110例对照者研究了这种多态性。我们发现,PD患者与对照者之间的总体等位基因和基因型频率没有显著差异(所有P>0.7),运动波动者(n=50)与非运动波动者(n=50)之间也是如此(所有P>0.8)。这表明DRD5 T978C多态性与PD易感性无关,也与PD发生运动波动的风险无关。因此,应进一步研究其他改变多巴胺受体表达的多态性。

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