Genetic polymorphism of angiotensin I-converting enzyme (ACE), but not angiotensin II type I receptor (ATr1), has a gender-specific role in panic disorder

被引:11
作者
Bayoglu, Burcu [1 ]
Cengiz, Mujgan [1 ]
Karacetin, Gul
Uysal, Omer [2 ]
Kocabasoglu, Nese
Bayar, Reha
Balcioglu, Ibrahim
机构
[1] Istanbul Univ, Dept Med Biol, Cerrahpasa Med Fac, Istanbul, Turkey
[2] Bezmialem Vakif Univ, Dept Biostat & Med Informat, Sch Med, Istanbul, Turkey
关键词
ACE; ATr1; gender; genetic polymorphism; panic disorder; INSERTION DELETION POLYMORPHISM; ANXIETY-RELATED BEHAVIOR; SUBSTANCE-P; CONTROL ASSOCIATION; BRAIN ANGIOTENSIN; RELEASE; NEUROTRANSMITTER; SCHIZOPHRENIA; EPIDEMIOLOGY; STRESS;
D O I
10.1111/j.1440-1819.2011.02318.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aims: 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. Methods: 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. Results: 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). Conclusion: 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 (chi(2) = 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.
引用
收藏
页码:130 / 137
页数:8
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