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促胆囊收缩素原基因多态性与 HPA 轴失调、症状严重程度和抗抑郁治疗反应的性别特异性关联。

Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response.

机构信息

Max Planck Institute of Psychiatry, München, Germany.

出版信息

Neuropsychopharmacology. 2010 Jun;35(7):1583-92. doi: 10.1038/npp.2010.30. Epub 2010 Mar 17.

Abstract

Galanin (GAL) is an estrogen-inducible neuropeptide, highly expressed in brain regions reported to be involved in regulation of mood and anxiety. GAL possibly has a direct modulatory effect on hypothalamic-pituitary-adrenal (HPA)-axis regulation. Recent data from pharmacological and genetic studies indicate a significant function of GAL in stress-related disorders. By using a tag SNP approach covering the locus encoding preprogalanin (PPGAL), earlier findings of female-specific associations of polymorphisms in this locus with panic disorder were expanded to a larger sample of 268 outpatients with anxiety disorders (ADs). Within a larger sample of 541 inpatients with major depressive disorder (MDD), we then tested associations of one PPGAL tag SNP with specific depression symptom clusters and HPA-axis activity assessed by the combined dexamethasone-suppression/CRH-stimulation test both at inpatient admission and discharge (n=298). Gender specificity as well as dependence of the association on levels of circulating estrogens was analyzed. Genotyping revealed high linkage disequilibrium in the promoter area of the PPGAL gene, which includes several estrogen-response elements. Confirming earlier results, rs948854, tagging this promoter region, was associated with more severe anxiety pathology in female AD patients, but not in males. In premenopausal female MDD patients, the same allele of rs948854 was associated with more severe vegetative but not cognitive depressive symptoms at discharge and worse treatment response on antidepressant medication. Furthermore, this allele was associated with higher HPA-axis activity at admission. No significant case-control associations could be observed. However, because of power limitations of both patient samples, small effects cannot be excluded. The reported associations in independent samples of AD and MDD support an estrogen-dependent function of GAL in pathophysiology of anxiety and depression, affecting response to antidepressant treatment.

摘要

甘丙肽(GAL)是一种雌激素诱导的神经肽,在报道参与调节情绪和焦虑的大脑区域中高度表达。GAL 可能对下丘脑-垂体-肾上腺(HPA)轴调节有直接的调节作用。最近的药理学和遗传学研究数据表明,GAL 在应激相关疾病中具有重要功能。通过使用覆盖编码前甘丙肽(PPGAL)基因座的标签 SNP 方法,该基因座中多态性与惊恐障碍的女性特异性关联的早期发现扩展到了一个更大的 268 名焦虑障碍(AD)门诊患者样本。在一个更大的 541 名住院的重度抑郁症(MDD)患者样本中,我们随后测试了一个 PPGAL 标签 SNP 与特定抑郁症状群和 HPA 轴活性的关联,该 HPA 轴活性通过联合地塞米松抑制/CRH 刺激试验在住院入院和出院时评估(n=298)。分析了性别特异性以及关联对循环雌激素水平的依赖性。基因分型显示 PPGAL 基因启动子区域的高度连锁不平衡,该区域包含几个雌激素反应元件。证实了早期的结果,rs948854 标记了这个启动子区域,与女性 AD 患者更严重的焦虑病理相关,但与男性无关。在绝经前的女性 MDD 患者中,rs948854 的相同等位基因与出院时更严重的植物性但不是认知性抑郁症状相关,并且抗抑郁药物治疗的反应更差。此外,该等位基因与入院时更高的 HPA 轴活性相关。未观察到显著的病例对照关联。然而,由于两个患者样本的效力限制,不能排除小效应。在 AD 和 MDD 的独立样本中报告的关联支持 GAL 在焦虑和抑郁的病理生理学中的雌激素依赖性功能,影响抗抑郁治疗的反应。

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