Brancati F, Valente E M, Castori M, Vanacore N, Sessa M, Galardi G, Berardelli A, Bentivoglio A R, Defazio G, Girlanda P, Abbruzzese G, Albanese A, Dallapiccola B
Department of Experimental Medicine and Pathology, University La Sapienza, Rome, Italy.
J Neurol Neurosurg Psychiatry. 2003 May;74(5):665-6. doi: 10.1136/jnnp.74.5.665.
Cervical dystonia (CD) is one of the most common forms of primary dystonia. The pathogenesis of the disease is still unknown, although evidence suggests a role for genetic factors. Recently, a polymorphism in the dopamine D5 receptor (DRD5) gene has been associated with the disease in a British population, suggesting that DRD5 is a susceptibility gene for CD. To confirm these data, we performed a case-control study of the microsatellite (CT/GT/GA)(n) at the DRD5 locus in 104 Italian CD patients and 104 healthy controls. The frequency of allele 4 was higher in the CD patients compared to the controls. This resulted in a twofold increased risk of developing the disease. These results provide further evidence of an association between DRD5 and cervical dystonia, supporting the involvement of the dopamine pathway in the pathogenesis of CD.
颈部肌张力障碍(CD)是原发性肌张力障碍最常见的形式之一。尽管有证据表明遗传因素在其中起作用,但该疾病的发病机制仍不清楚。最近,在英国人群中,多巴胺D5受体(DRD5)基因的多态性与该疾病相关,这表明DRD5是CD的一个易感基因。为了证实这些数据,我们对104例意大利CD患者和104名健康对照者进行了DRD5基因座微卫星(CT/GT/GA)(n)的病例对照研究。与对照组相比,CD患者中4号等位基因的频率更高。这导致患该病的风险增加了两倍。这些结果为DRD5与颈部肌张力障碍之间的关联提供了进一步证据,支持多巴胺通路参与CD发病机制。