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多巴胺D3受体基因DRD3与精神分裂症之间关联的证据。

Evidence for an association between the dopamine D3 receptor gene DRD3 and schizophrenia.

作者信息

Ebstein R P, Macciardi F, Heresco-Levi U, Serretti A, Blaine D, Verga M, Nebamov L, Gur E, Belmaker R H, Avnon M, Lerer B

机构信息

Herzog Hospital, Jerusalem, Israel.

出版信息

Hum Hered. 1997 Jan-Feb;47(1):6-16. doi: 10.1159/000154382.

Abstract

Association of the dopamine D3 receptor gene (DRD3) and schizophrenia was examined in unrelated Israeli and Italian schizophrenic patients and ethnically matched normal control subjects. In the combined sample, there was a significant excess of DRD3 allele 2 among the schizophrenic patients (chi2 = 4.70, d.f. 1, p = 0.03). Comparison of genotype frequencies revealed an excess of the 2-2 genotype in the combined schizophrenic sample (chi2 = 8.30, d.f. 1, p = 0.01) and in the non-Ashkenazi Israeli schizophrenics alone (chi2 = 5.70, d.f. 2, p = 0.05). DRD3 2-2 genotype conferred a significantly increased risk of schizophrenia (chi2 = 8.21, d.f. 1, p = 0.004; OR = 2.87, CI 95% = 1.36-5.76) in the combined sample and in the non-Ashkenazi Israeli schizophrenics (chi2 = 7.22, d.f. 1, p = 0.04; OR = 7.22, CI 95% = 1.04-24.83). In the combined and Italian samples, allele 2 was associated with early age of onset as was the 2-2 genotype in the combined sample and non-Ashkenazi group. The 2-2 genotype was associated with poor response to neuroleptics, particularly in the non-Ashkenazi, Israeli schizophrenics. The possibility that DRD3 or a locus in linkage disequilibrium with it may play a role in the transmission of schizophrenia, is considered in relation to previous positive and negative reports.

摘要

在不相关的以色列和意大利精神分裂症患者以及种族匹配的正常对照受试者中,研究了多巴胺D3受体基因(DRD3)与精神分裂症的关联。在合并样本中,精神分裂症患者中DRD3等位基因2明显过多(卡方值=4.70,自由度1,p=0.03)。基因型频率比较显示,合并的精神分裂症样本(卡方值=8.30,自由度1,p=0.01)以及仅非阿什肯纳兹以色列精神分裂症患者中(卡方值=5.70,自由度2,p=0.05),2-2基因型过多。在合并样本和非阿什肯纳兹以色列精神分裂症患者中,DRD3 2-2基因型使精神分裂症风险显著增加(卡方值=8.21,自由度1,p=0.004;比值比=2.87,95%置信区间=1.36-5.76)(卡方值=7.22,自由度1,p=0.04;比值比=7.22,95%置信区间=1.04-24.83)。在合并样本和意大利样本中,等位基因2与发病年龄早相关,合并样本和非阿什肯纳兹组中的2-2基因型也与发病年龄早相关。2-2基因型与对抗精神病药物反应不佳相关,特别是在非阿什肯纳兹以色列精神分裂症患者中。结合之前的阳性和阴性报告,考虑了DRD3或与其处于连锁不平衡的一个基因座可能在精神分裂症传递中起作用的可能性。

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