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自杀分析中的分子遗传学

Molecular genetics in the analysis of suicide.

作者信息

Souery Daniel, Oswald Pierre, Linkowski Paul, Mendlewicz Julien

机构信息

Department of Psychiatry, University Clinics of Brussels, Erasme Hospital, Université Libre de Bruxelles, Belgium.

出版信息

Ann Med. 2003;35(3):191-6. doi: 10.1080/07853890310008242.

DOI:10.1080/07853890310008242
PMID:12822741
Abstract

Each year, one million people die of suicide. Among the different identified risk factors, genetic factors seem to be part of a multidimensional behavior, including psychiatric, psychosocial, biological factors and physical illness. Family studies have provided evidence for familial transmission in suicide, confirmed in twin and adoption studies. At a molecular level, serotonin seems to be one of the key neurotransmitters implicated in suicidal behavior. Therefore, genes coding for proteins involved in serotonergic neurotransmission have been extensively studied in case-control association studies on suicide. Major findings concern Tryptophan hydroxylase (TPH) gene, particularly in violent suicidal behavior. Though they may seem contradictory, studies on Serotonin transporter (5-HTT), Monaomine oxidase (MAOA), Serotonin 2A and 2C receptors (5-HT2A and 5-HT2C) and Tyrosine hydroxylase (TH) genes are promising. In spite of those observations having some limitations, it appears that genetic factors are a serious risk factor, besides environmental aspects of suicidal behavior.

摘要

每年有100万人死于自杀。在已确定的不同风险因素中,遗传因素似乎是多维行为的一部分,包括精神、心理社会、生物因素和身体疾病。家族研究为自杀的家族遗传提供了证据,这在双胞胎和收养研究中得到了证实。在分子水平上,血清素似乎是与自杀行为有关的关键神经递质之一。因此,在自杀的病例对照关联研究中,对编码参与血清素能神经传递的蛋白质的基因进行了广泛研究。主要发现涉及色氨酸羟化酶(TPH)基因,特别是在暴力自杀行为方面。尽管这些研究结果可能看似相互矛盾,但对血清素转运体(5-HTT)、单胺氧化酶(MAOA)、血清素2A和2C受体(5-HT2A和5-HT2C)以及酪氨酸羟化酶(TH)基因的研究很有前景。尽管这些观察结果存在一些局限性,但除了自杀行为的环境因素外,遗传因素似乎也是一个严重的风险因素。

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