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血管紧张素I转换酶插入/缺失基因功能多态性与人类惊恐障碍之间不存在关联。

Lack of association between angiotensin I-converting enzyme insertion/deletion gene functional polymorphism and panic disorder in humans.

作者信息

Shimizu Eiji, Hashimoto Kenji, Kobayashi Keisuke, Mitsumori Makoto, Ohgake Shintaro, Koizumi Hiroki, Okamura Naoe, Koike Kaori, Kumakiri Chikara, Nakazato Michiko, Komatsu Naoya, Iyo Masaomi

机构信息

Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.

出版信息

Neurosci Lett. 2004 Jun 3;363(1):81-3. doi: 10.1016/j.neulet.2004.03.050.

Abstract

Family and twin studies have indicated that genes influence susceptibility to panic disorder, but the genes involved remain unknown. The neuropeptide angiotensin II has been found to be involved in anxiety and regulation of respiration which are important in the pathophysiology of panic attacks. Assuming that angiotensins may be candidate genes in panic disorder, we analyzed the association between panic disorder and angiotensin I-converting enzyme (ACE) insertion (I)/deletion (D) gene functional polymorphism. We recruited 101 patients with panic disorder diagnosed according to DSM-IV criteria, and 184 control subjects in the study. No significant differences in the frequency of the genotype or allele in the polymorphism between patient and control groups were found (genotype, chi(2)=0.56, d.f.=2, P=0.77; allele, chi(2)=0.074, d.f.=1, P=0.78). This study suggests that the ACE I/D gene polymorphism is not directly associated with panic disorder in our Japanese patient group.

摘要

家族研究和双生子研究表明,基因会影响惊恐障碍的易感性,但具体涉及哪些基因仍不清楚。人们发现神经肽血管紧张素II与焦虑及呼吸调节有关,而这两者在惊恐发作的病理生理过程中很重要。假设血管紧张素可能是惊恐障碍的候选基因,我们分析了惊恐障碍与血管紧张素转换酶(ACE)插入(I)/缺失(D)基因功能多态性之间的关联。我们招募了101名根据《精神疾病诊断与统计手册》第四版标准诊断为惊恐障碍的患者以及184名对照受试者参与本研究。在患者组和对照组之间,未发现该多态性的基因型或等位基因频率存在显著差异(基因型,χ² = 0.56,自由度 = 2,P = 0.77;等位基因,χ² = 0.074,自由度 = 1,P = 0.78)。本研究表明,在我们的日本患者组中,ACE I/D基因多态性与惊恐障碍无直接关联。

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