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[精神分裂症中多巴胺D2受体基因141C插入/缺失多态性无关联]

[No association of 141C-ins/del polymorphism in the D2 dopamine receptor gene in schizophrenia].

作者信息

Rohrmeier Thomas, Putzhammer Albert, Sartor Heino, Knapp Michael, Albus Margot, Borrmann-Hassenbach Margitta, Lichtermann Dirk, Wildenauer Dieter, Schwab Sibylle, Maier Wolfgang, Klein Helmfried E, Eichhammer Peter

机构信息

Klinik und Poliklinik für Psychiatrie und Psychotherapie der Universität Regensburg am Bezirksklinikum, Franz-Josef-Strauss-Allee 11, 93042 Regensburg.

出版信息

Psychiatr Prax. 2003 May;30 Suppl 2:S212-5.

Abstract

Recently, a putative functional polymorphism (-141C Ins/Del) in the 5'-flanking region of the dopamine D2 receptor was found. An association of the Ins allele with schizophrenia has been described in a Japanese sample. In the present study this association was examined in a German schizophrenia patient population. In a family based approach 190 German family trios were analyzed for the -141C Ins/Del genotype. Using the transmission disequilibrium test (TDT) we found no evidence for an association of the Ins allele with schizophrenia (TDT = 0.152, P = 0.696). In parallel, we performed an independent case control study with 268 schizophrenic patients and 244 controls. Again, we did not detect an overrepresentation of the Ins allele in patients (P = 0.124). Thus, our data do not support the hypothesis that the -141C Ins variant plays a major role in predisposition to schizophrenia. To confirm our conclusion further preferentially family based studies are needed.

摘要

最近,在多巴胺D2受体5'侧翼区域发现了一个假定的功能性多态性(-141C Ins/Del)。在一个日本样本中,已报道Ins等位基因与精神分裂症有关联。在本研究中,在德国精神分裂症患者群体中对这种关联进行了检测。采用基于家系的方法,对190个德国家系三联体进行了-141C Ins/Del基因型分析。使用传递不平衡检验(TDT),我们未发现Ins等位基因与精神分裂症有关联的证据(TDT = 0.152,P = 0.696)。同时,我们对268例精神分裂症患者和244例对照进行了一项独立的病例对照研究。同样,我们未检测到患者中Ins等位基因的过度表达(P = 0.124)。因此,我们的数据不支持-141C Ins变异在精神分裂症易感性中起主要作用这一假设。为进一步证实我们的结论,优先需要进行基于家系的研究。

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