Department of Psychiatry, The Catholic University of Korea College of Medicine, Republic of Korea.
Neurosci Lett. 2009 Nov 20;465(3):257-61. doi: 10.1016/j.neulet.2009.09.025. Epub 2009 Sep 17.
We report on the impact of a set of variations located in the HSP-70 (heat shock protein 70) and TAAR6 (trace amine associated receptors 6 gene) in a sample of bipolar patients. Holding a diagnosis of BPD was the first outcome measure. Response to pharmacotreatment in bipolar patients was the secondary outcome measure. One hundred seventy-one bipolar patients and 288 controls were enrolled for the study. Patients were administered HAM-D, YMRS and CGI at baseline and discharge by independent psychiatrists blind to genotypes. As a result, homozygosis at rs2075799 (HSP-70) was found to be more represented in controls than in cases (p=0.000009). The investigated variations did not show impact on treatment outcome. This study provides preliminary evidence that HSP-70 may play a role in the disrupted mechanisms that lead to BPD. Further confirmatory analyses in this direction are mandatory.
我们报告了一组位于 HSP-70(热休克蛋白 70)和 TAAR6(痕量胺相关受体 6 基因)中的变异对一组双相情感障碍患者样本的影响。双相情感障碍的诊断是第一个结果衡量标准。双相情感障碍患者的药物治疗反应是第二个结果衡量标准。171 名双相情感障碍患者和 288 名对照者被纳入该研究。由独立的、对基因型不知情的精神科医生在基线和出院时对患者进行 HAM-D、YMRS 和 CGI 评估。结果发现,rs2075799(HSP-70)的纯合子在对照组中的比例高于病例组(p=0.000009)。所研究的变异对治疗结果没有影响。这项研究提供了初步证据,表明 HSP-70 可能在导致 BPD 的失调机制中发挥作用。有必要在这一方向上进行进一步的验证性分析。