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多巴胺转运体基因功能性可变数目串联重复多态性在伴和不伴先兆偏头痛中的家系关联分析

Family-based association analysis of functional VNTR polymorphisms in the dopamine transporter gene in migraine with and without aura.

作者信息

Karwautz A, Campos de Sousa S, Konrad A, Zesch H-E, Wagner G, Zormann A, Wanner C, Breen G, Ray M, Kienbacher C, Natriashvili S, Collier D A, Wöber C, Wöber-Bingöl C

机构信息

Headache Outpatient Centre, Department of Child and Adolescent Psychiatry, Medical University of Vienna, Vienna, Austria.

出版信息

J Neural Transm (Vienna). 2008;115(1):91-5. doi: 10.1007/s00702-007-0799-0. Epub 2007 Aug 10.

Abstract

Because of the role of dopamine in triggering migraine attacks, genes of the dopamine system are candidates for involvement in migraine. We examined three VNTR polymorphisms in the dopamine transporter, the 5'UTR VNTR, the intron 8 VNTR and the intron 14 VNTR, in a sample of 205 family trios. We used the transmission disequilibirium test (TDT) to examine the transmission of these three markers and their haplotypes to offspring affected by migraine. We found no significant transmission distortion of any marker. Likewise haplotypes of the three markers did not show significant overall or individual association with migraine. Finally we examined migraine with and without aura, and likewise found no association between dopamine transporter VNTRs or their haplotypes and either classification of the disease. We conclude that functional genetic variation in the dopamine transporter does not act as a significant risk factor for migraine.

摘要

由于多巴胺在引发偏头痛发作中所起的作用,多巴胺系统的基因成为偏头痛相关基因的候选对象。我们在一个由205个三联体家庭组成的样本中,检测了多巴胺转运体的三个VNTR多态性,即5'UTR VNTR、内含子8 VNTR和内含子14 VNTR。我们使用传递不平衡检验(TDT)来检测这三个标记及其单倍型向受偏头痛影响的后代的传递情况。我们发现任何标记均无显著的传递扭曲。同样,这三个标记的单倍型与偏头痛之间也未显示出显著的总体或个体关联。最后,我们对有先兆和无先兆偏头痛进行了检测,同样发现多巴胺转运体VNTRs及其单倍型与该疾病的任何一种分类之间均无关联。我们得出结论,多巴胺转运体的功能性基因变异并非偏头痛的显著风险因素。

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