Department of Medical Biology, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey.
Psychiatry Clin Neurosci. 2012 Mar;66(2):130-7. doi: 10.1111/j.1440-1819.2011.02318.x.
Angiotensins were shown to have some role in the development of panic disorder (PD). In this study, we aimed to determine the frequency of polymorphisms in two angiotensin-related genes, angiotensin I-converting enzyme (ACE) and angiotensin II type I receptor (ATr1), in a sample of Turkish patients with PD and to evaluate their association with PD development.
Polymerase chain reaction and restriction fragment length polymorphism was used to analyze ATr1 A1166C polymorphism, and only polymerase chain reaction was used to analyze functional ACE insertion/deletion polymorphism in 123 patients with PD and in 169 similarly aged disease-free controls.
There was no significant difference in the genotype distribution between PD patients and controls for each polymorphism (P>0.05). Allele frequency of ACE insertion/deletion was borderline statistically significant between the groups (P=0.055; odds ratio: 1.39; 95% confidence interval: 0.99-1.95), and allele frequency of ATr1 A1166C was not significantly different between the groups (P=0.32; odds ratio: 0.81; 95% confidence interval: 0.53-1.22).
This study suggests that polymorphisms of ACE I/D and ATr1 A1166C are not associated with risk of PD in Turkish patients. However, in ACE insertion/deletion polymorphism, the insertion allele was found to be more frequent in the male subgroup of patients (χ²=4.61, P=0.032) than in controls, suggesting a potential male-specific role of the less active ACE insertion allele in the pathogenesis of PD.
血管紧张素在惊恐障碍(PD)的发展中具有一定作用。本研究旨在确定土耳其 PD 患者中两种血管紧张素相关基因血管紧张素 I 转换酶(ACE)和血管紧张素 II 型 1 型受体(ATr1)的多态性频率,并评估其与 PD 发病的关系。
采用聚合酶链反应和限制性片段长度多态性分析 ATr1 A1166C 多态性,仅采用聚合酶链反应分析 123 例 PD 患者和 169 例年龄匹配无病对照者 ACE 插入/缺失功能多态性。
两种多态性在 PD 患者和对照组之间的基因型分布无显著差异(P>0.05)。ACE 插入/缺失的等位基因频率在两组之间具有边缘统计学意义(P=0.055;比值比:1.39;95%置信区间:0.99-1.95),而 ATr1 A1166C 的等位基因频率在两组之间无显著差异(P=0.32;比值比:0.81;95%置信区间:0.53-1.22)。
本研究提示土耳其 PD 患者 ACE I/D 和 ATr1 A1166C 多态性与 PD 风险无关。然而,在 ACE 插入/缺失多态性中,插入等位基因在患者的男性亚组中(χ²=4.61,P=0.032)比在对照组中更为常见,提示 ACE 插入等位基因在 PD 发病机制中具有潜在的男性特异性作用。