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汉族人群中去甲肾上腺素转运体基因多态性与双相情感障碍的关联研究

Association study of the norepinephrine transporter gene polymorphisms and bipolar disorder in Han Chinese population.

作者信息

Chang Chuan-Chia, Lu Ru-Band, Ma Kuo-Hsing, Chang Hsin-An, Chen Chih-Lun, Huang Cheng-Chang, Lin Wei-Wen, Huang San-Yuan

机构信息

Department of Psychiatry, Tri-Service General Hospital, National Defense Medical Center, Taipei, ROC, Taiwan.

出版信息

World J Biol Psychiatry. 2007;8(3):188-95. doi: 10.1080/15622970601136195.

Abstract

Many studies have indicated that the norepinephrine transporter (NET) may play an important role in the mechanisms underlying affective disorders. Thus, the genes of the NET (SLC6A2) are good candidates for research on bipolar disorder (BPD). This study examined whether the NET gene is a susceptibility factor for the BPD in Han Chinese. A promoter -182 T/C polymorphism (rs 2242446) and the exonic polymorphism 1287 G/A (rs 5569) of the NET gene were analysed using a polymerase chain reaction (PCR)-based method in 261 BPD patients and 245 unrelated, age- and gender-matched controls. Furthermore, to reduce the clinical heterogeneity, we also carried out analysis in clinical subgroups of bipolar patients defined according to type I and type II BPD, presence or absence of family history of major affective disorders and the age at onset of BPD. No significant difference was found between either bipolar patients or its more homogeneous subgroups and healthy controls in the genotype and allele frequencies for the investigated NET polymorphisms. Our results suggest that the investigated polymorphisms of NET are not major risk factors responsible for predisposition to BPD or its clinical subtypes in Han Chinese. However, replication studies with larger different ethnic samples are needed.

摘要

许多研究表明,去甲肾上腺素转运体(NET)可能在情感障碍的潜在机制中发挥重要作用。因此,NET基因(SLC6A2)是双相情感障碍(BPD)研究的良好候选基因。本研究探讨NET基因是否为汉族人群中BPD的易感因素。采用聚合酶链反应(PCR)方法,对261例BPD患者和245例年龄、性别匹配的无亲缘关系对照者的NET基因启动子-182 T/C多态性(rs 2242446)和外显子多态性1287 G/A(rs 5569)进行分析。此外,为了减少临床异质性,我们还对根据I型和II型BPD、是否存在主要情感障碍家族史以及BPD发病年龄定义的双相情感障碍患者临床亚组进行了分析。在所研究的NET多态性的基因型和等位基因频率方面,双相情感障碍患者及其更具同质性的亚组与健康对照之间均未发现显著差异。我们的结果表明,所研究的NET多态性不是汉族人群中BPD或其临床亚型易感性的主要危险因素。然而,需要在更大的不同种族样本中进行重复研究。

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