Pae Chi-Un, Drago Antonio, Patkar Ashwin A, Jun Tae-Youn, Serretti Alessandro
Department of Psychiatry, The Catholic University of Korea College of Medicine, Seocho-Gu, Seoul 150-713, Republic of Korea.
Eur Neuropsychopharmacol. 2009 Nov;19(11):806-11. doi: 10.1016/j.euroneuro.2009.07.001. Epub 2009 Jul 29.
Suggestive associations have been reported between trace amines and heat shock proteins, and a disrupted pathophysiology that enhances the risk of psychosis and that modifies responses to antipsychotic treatments. Our group previously reported genetic studies on TAAR6 and HSP-70 separately in patients with schizophrenia. In the current study, we investigated possible epistasis between the same set of variations in a sample of 281 patients diagnosed with schizophrenia and 288 healthy controls. We applied the generalized multifactor dimensionality reduction (MDR) method and controlled covariates significantly associated with both diagnosis and treatment efficacy. To the best of our knowledge, epistasis between the present set of variations in schizophrenia has not been tested before. We found significant associations with both the risk of disease and response to treatment. However, the insufficiently balanced accuracy of the applied tests suggests that, despite significantly different genetic variations between cases and controls, these factors have a poor predictive value. Explanations for these findings and possible future directions are also discussed.
已有报道表明痕量胺与热休克蛋白之间存在提示性关联,以及一种破坏的病理生理学,这种病理生理学增加了患精神病的风险,并改变了对抗精神病治疗的反应。我们小组之前分别对精神分裂症患者的TAAR6和HSP - 70进行了基因研究。在当前研究中,我们在281名被诊断为精神分裂症的患者和288名健康对照的样本中,研究了同一组变异之间可能存在的上位性。我们应用了广义多因素降维(MDR)方法,并控制了与诊断和治疗效果均显著相关的协变量。据我们所知,之前尚未对精神分裂症中这组变异之间的上位性进行过测试。我们发现了与疾病风险和治疗反应均有显著关联。然而,所应用测试的平衡准确性不足表明,尽管病例组和对照组之间存在显著不同的基因变异,但这些因素的预测价值较差。本文还讨论了这些发现的解释以及可能的未来研究方向。