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大麻素受体基因()多态性与惊恐障碍的关联。

Association of cannabinoid receptor genes () polymorphisms and panic disorder.

机构信息

Clinical Pharmacology Unit and Neuropharmacology on Pain and Functional Diversity (NED), Department of Health of Alicante - General Hospital, ISABIAL, Alicante, Spain.

Neuroscience Institute, Alicante, Miguel Hernández University, San Juan de Alicante, Spain.

出版信息

Anxiety Stress Coping. 2020 May;33(3):256-265. doi: 10.1080/10615806.2020.1732358. Epub 2020 Mar 2.

Abstract

Panic disorder (PD) is an anxiety disorder characterized by recurrent and unexpected panic attacks along with sudden onset of apprehension, fear or terror. The endocannabinoid system (ECS) has a role in stress recovery, regulating anxiety. The aim of this study was to analyze potential genetic alterations in key ECS targets in patients suffering from panic disorders. We analyzed single nucleotide polymorphisms (SNPs) of the cannabinoid receptors () and the endocannabinoid hydrolytic enzyme fatty acid amide hydrolase () genes in 164 Spanish PD patients and 320 matched controls. No significant differences were observed in the SNPs of the and genes tested. However, when analyzing genotype-by-sex interaction at A592G (rs2501431) and C315T (rs2501432) in the gene, the presence of the G-allele in males was associated with a protective haplotype. Genotyping analysis revealed that variants in confer vulnerability to PD, with a significantly increased risk associated with the G-allele (rs12720071) and C-allele (rs806368). This finding was consistent when analyzing genotype-by-sex interaction, where females presented a greater PD risk. Polymorphisms at the gene may be a risk factor for PD contributing to sex-specific dysfunction in females.

摘要

惊恐障碍(PD)是一种以反复和意外的惊恐发作以及突然出现的忧虑、恐惧或恐惧为特征的焦虑障碍。内源性大麻素系统(ECS)在应激恢复中起作用,调节焦虑。本研究旨在分析患有惊恐障碍的患者中关键 ECS 靶标潜在的遗传改变。我们分析了 164 名西班牙 PD 患者和 320 名匹配对照的大麻素受体()和内源性大麻素水解酶脂肪酸酰胺水解酶()基因的单核苷酸多态性(SNP)。在测试的和基因的 SNP 中未观察到显著差异。然而,当分析基因中的 A592G(rs2501431)和 C315T(rs2501432)的基因型-性别相互作用时,男性中 G-等位基因的存在与保护性单倍型相关。基因分型分析显示,基因中的变异易患 PD,G-等位基因(rs12720071)和 C-等位基因(rs806368)与风险显著增加相关。当分析基因型-性别相互作用时,这一发现是一致的,女性表现出更高的 PD 风险。基因的多态性可能是 PD 的一个风险因素,导致女性特定的功能障碍。

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