【24h】

Serotonin transporter (5-HTT) gene polymorphism in psychogeriatric patients.

机译:老年精神病患者的5-羟色胺转运蛋白(5-HTT)基因多态性。

获取原文
获取原文并翻译 | 示例
           

摘要

Several studies have attempted to confirm an association between a deletion/insertion polymorphism within the promoter region of the serotonin transporter gene (5-HTT) and Alzheimer's disease independent from the apolipoprotein E (APOE) varepsilon4 status. We examined this deletion/insertion polymorphism of the serotonin transporter gene in a sample of 222 consecutively recruited gerontopsychiatric patients which was divided into four different diagnostic groups: Alzheimer's disease (N=84), mild cognitive impairment (N=29), subjective cognitive complaints (N=49), depression/other psychiatric disorders (N=56) and 118 healthy, non-demented controls. The aim of this approach was to test whether the investigated polymorphism has a high enough selectivity and specificity to distinguish between the different gerontopsychiatric disorders or to differentiate genetically AD from other forms of dementia, respectively. We could not detect any significant differences in the allelic distribution of the deletion/insertion polymorphism of the 5-HTT gene between the four patient subgroups and the control group. This finding indicates that the serotonin transporter does not appear to be a major susceptibility factor in the pathophysiology of Alzheimer's disease and other psychogeriatric disorders.
机译:几项研究试图证实5-羟色胺转运蛋白基因(5-HTT)启动子区域内的缺失/插入多态性与独立于载脂蛋白E(APOE)varepsilon4状态的阿尔茨海默氏病之间的相关性。我们在222名连续入选的老年精神病患者的样本中检查了5-羟色胺转运蛋白基因的这种缺失/插入多态性,该样本分为四个不同的诊断组:阿尔茨海默氏病(N = 84),轻度认知障碍(N = 29),主观认知障碍(N = 49),抑郁症/其他精神疾病(N = 56)和118位健康,无痴呆的对照组。该方法的目的是检验所研究的多态性是否具有足够高的选择性和特异性,以区分不同的老年精神病性疾病或分别将遗传性AD与其他形式的痴呆症区分开。在四个患者亚组和对照组之间,我们无法检测到5-HTT基因缺失/插入多态性的等位基因分布有任何显着差异。该发现表明5-羟色胺转运蛋白似乎不是阿尔茨海默氏病和其他精神病学疾病的病理生理学中的主要易感因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号