ACE 基因多态性与自杀风险之间的关系

Q2 Medicine
Soudeh ghafouri-fard , Reyhane Eghtedarian , Elham badrlou , Solat eslami , Mohammad taheri , Serge brand
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引用次数: 0

摘要

自杀是一个与多种遗传因素相关的健康问题。一些信号通路的遗传多态性已被证明与自杀行为的病理生理学有关。血管紧张素转换酶(ACE)的变异已被证实会影响某些神经精神疾病和自杀企图的风险。在本研究中,我们评估了伊朗自杀未遂患者(320 名试图用软方法自杀的人和 230 名自杀受害者)和 300 名健康对照者中 ACE rs4646994、rs1799752 和 rs4359 多态性与自杀行为风险之间的关联。采用 tetra-ARMS-PCR 方法对多态性进行基因分型。数据使用 SPSS v.22.0 进行分析。在共显模式下,rs4359与成功自杀有关,TC基因型被确定为风险基因型(OR (95% CI)= 1.86 (1.26-2.75),P值=-0.02)。在显性模型中,与 CC 基因型相比,TT+TC 基因型与更高的成功自杀风险相关(OR (95% CI)= 1.71 (1.18-2.47),P 值=-0.04)。在超显性模型中,与 TC 基因型相比,TT+CC 基因型与较低的风险相关(OR (95% CI)= 0.58 (0.41-0.83),P 值=-0.03)。在共显性、隐性和超显性模型中,rs1799752 与较高的自杀成功风险相关。在共显性模型中,与 DD 基因型相比,ID 基因型增加了风险(OR (95% CI)= 2 (1.37-2.99),P 值=0.003),II 基因型降低了风险(OR (95% CI)= 0.2 (0.09-0.45),P 值<0.0001)。在隐性模型中,与其他基因型的总和相比,II 基因型与较低的风险相关(OR (95% CI)= 0.14 (0.07-0.28),P 值为 0.0001)。rs4646994与成功自杀的风险无关。此外,rs4359 在超显性模型下与自杀未遂风险相关,TT+CC 基因型会降低自杀未遂风险(OR (95% CI)= 0.67 (0.48-0.93),P 值=0.04);rs1799752 在共显和隐性模型下与自杀未遂风险相关,II 基因型会降低自杀未遂风险(OR (95% CI)= 0.53 (0.34-0.83),P 值=0.03)。最后,除隐性模型外,rs4646994 在所有模型中都与自杀未遂风险相关。该 SNP 的 I 等位基因会增加自杀未遂的风险(OR (95% CI)= 1.47 (1.15-1.88),P 值=0.018)。综上所述,ACE1 基因可被视为伊朗人自杀行为的风险位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between ACE gene polymorphisms and risk of suicide

Suicide is a health problem associated with a number of genetic factors. Genetics polymorphisms in several signaling pathways have been shown in the pathophysiology of suicidal behavior. Variants of the angiotensin converting enzyme (ACE) have been demonstrated to affect risk of some neuropsychiatric conditions and suicide attempt. In the current study, we assessed association between ACE rs4646994, rs1799752 and rs4359 polymorphisms and risk of suicide behavior in a population of Iranian patients attempted suicide (320 individuals who attempted suicide with soft methods and 230 suicide victims) and 300 healthy controls. Polymorphisms were genotyped using tetra-ARMS-PCR method. Data was analyzed using SPSS v.22.0. The rs4359 was associated with successful suicide under co-dominant model in a way that TC genotype was identified as a risk genotype (OR (95% CI)= 1.86 (1.26–2.75), P value=-0.02). In dominant model, TT+TC genotypes were associated with higher risk of successful suicide in comparison with CC genotype (OR (95% CI)= 1.71 (1.18–2.47), P value=-0.04). In over-dominant model, TT+CC genotypes were associated with lower risk in comparison with TC genotype (OR (95% CI)= 0.58 (0.41–0.83), P value=-0.03). rs1799752 was associated with higher risk of successful suicide under co-dominant, recessive and over-dominant models. In co-dominant model, while ID genotype increased the risk (OR (95% CI)= 2 (1.37–2.99), P value=0.003), II genotype decreased the risk (OR (95% CI)= 0.2 (0.09–0.45), P value<0.0001) in comparison with DD genotype). In recessive model, II genotype was associated with lower risk in comparison with total sum of the other genotypes (OR (95% CI)= 0.14 (0.07–0.28), P value<0.0001). The rs4646994 was not associated with risk of successful suicide. Besides, rs4359 was associated with risk of suicide attempt under over-dominant model in a way that TT+CC genotypes decreased risk of suicide attempt (OR (95% CI)= 0.67 (0.48–0.93), P value=0.04). rs1799752 was associated with risk of suicide attempt under co-dominant and recessive models in a way that II genotype conferred lower risk of suicide attempt (OR (95% CI)= 0.53 (0.34–0.83), P value=0.03). Finally, rs4646994 was associated with risk of suicide attempt in all models except for recessive model. I allele of this SNP increased risk of suicide attempt (OR (95% CI)= 1.47 (1.15–1.88), P value=0.018). Taken together, ACE1 gene can be considered as a risk locus for suicide behavior among Iranians.

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Biomarkers in Neuropsychiatry
Biomarkers in Neuropsychiatry Medicine-Psychiatry and Mental Health
CiteScore
4.00
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0.00%
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12
审稿时长
7 weeks
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