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自杀行为作为一种数量性状及其遗传背景。

Suicide behavior as a quantitative trait and its genetic background.

作者信息

Pawlak Joanna, Dmitrzak-Weglarz Monika, Wilkosc Monika, Szczepankiewicz Aleksandra, Leszczynska-Rodziewicz Anna, Zaremba Dorota, Kapelski Pawel, Rajewska-Rager Aleksandra, Hauser Joanna

机构信息

Psychiatric Genetics Unit, Department of Psychiatry, Poznan University of Medical Sciences, Poland.

Psychiatric Genetics Unit, Department of Psychiatry, Poznan University of Medical Sciences, Poland.

出版信息

J Affect Disord. 2016 Dec;206:241-250. doi: 10.1016/j.jad.2016.07.029. Epub 2016 Jul 19.

Abstract

INTRODUCTION

Studies have not given yet a clear answer what is the genetic background of suicidal predisposition. The associations between polymorphisms of the TPH1 and 5-HTTLPR genes and violent suicidal behavior was revealed with the least inconsistencies.

METHOD

We selected 10 "strong candidate genes" and 35 SNPs, SLC6A4 and ACP1 for replication study. We searched associations between precisely described suicidal phenotype in 825 affective patients and polymorphisms of selected neurobiological pathways genes as well as their interactions that constitute suicidal risk.

RESULTS

The results confirm the role of TPH1, TPH2, 5HT2A, CRHR1 and ACP1 variants in the risk of suicidal behavior.

LIMITATIONS

In our study we analyzed limited number of candidate genes and only one of them is linked to lithium mechanism of action. We had no data on pharmacological treatment of investigated patients and its relation to the time of suicide attempt.

CONCLUSION

Our results indicate that polymorphisms of various signaling pathways are involved in the pathogenesis of suicidal behavior. Non-genetic factors are also involved in the risk of suicidal attempts.

摘要

引言

关于自杀易感性的遗传背景,研究尚未给出明确答案。色氨酸羟化酶1(TPH1)基因和5-羟色胺转运体启动子区域(5-HTTLPR)基因的多态性与暴力自杀行为之间的关联,是所有研究中分歧最小的。

方法

我们选择了10个“强候选基因”和35个单核苷酸多态性(SNP),包括溶质载体家族6成员4(SLC6A4)基因和酸性磷酸酶1(ACP1)基因进行重复研究。我们在825名情感障碍患者中,研究精确描述的自杀表型与所选神经生物学通路基因多态性之间的关联,以及它们在构成自杀风险中的相互作用。

结果

结果证实了TPH1、TPH2、5-羟色胺2A受体(5HT2A)、促肾上腺皮质激素释放激素受体1(CRHR1)和ACP1基因变异在自杀行为风险中的作用。

局限性

在我们的研究中,我们分析的候选基因数量有限,且其中只有一个与锂盐的作用机制有关。我们没有关于所研究患者药物治疗情况及其与自杀企图时间关系的数据。

结论

我们的结果表明,各种信号通路的多态性参与了自杀行为的发病机制。非遗传因素也与自杀企图风险有关。

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