Angiotensin I converting enzyme gene polymorphisms and risk of psychiatric disorders

被引:0
作者
Mohammadarian Akbari
Reyhane Eghtedarian
Bashdar Mahmud Hussen
Solat Eslami
Mohammad Taheri
Soudeh Ghafouri-Fard
机构
[1] Loghman Hakim Hospital,Skull Base Research Center
[2] Shahid Beheshti University of Medical Sciences,Phytochemistry Research Center
[3] Shahid Beheshti University of Medical Sciences,Department of Pharmacognosy, College of Pharmacy
[4] Hawler Medical University,Dietary Supplements and Probiotic Research Center
[5] Alborz University of Medical Sciences,Department of Medical Biotechnology, School of Medicine
[6] Alborz University of Medical Sciences,Department of Medical Genetics, School of Medicine
[7] Men’s Health and Reproductive Health Research Center,undefined
[8] Shahid Beheshti University of Medical Sciences,undefined
[9] Shahid Beheshti University of Medical Sciences,undefined
来源
BMC Psychiatry | / 22卷
关键词
ACE; Polymorphism; Bipolar disorder; Schizophrenia; Obsessive–compulsive disorder;
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摘要
Angiotensin-converting enzyme (ACE) as an important enzyme in the renin-angiotensin system facilitates biogenesis of the functionally active product angiotensin II from angiotensin I. ACE gene contains a number of functional polymorphisms which modulate activity of the encoded protein. In the current case–control study, we appraised the association between the rs4359 and rs1799752 polymorphisms and risk of bipolar disorder (type I and type II; BPDI and BPDII), schizophrenia (SCZ) and obsessive–compulsive disorder (OCD). The rs4359 was associated with risk of OCD, BPDI and BPDII in co-dominant and dominant models. The rs1799752 was associated with all assessed psychiatric conditions in four inheritance models except for BPDII whose association was not significant in recessive model. The I allele of rs1799752 was associated with OCD (adjusted FDR q-Value = 4.04E-04), SCZ (adjusted FDR q-Value = 6.00E-06), BPDI (adjusted FDR q-Value = 8.40E-03) and BPDII (adjusted FDR q-Value = 6.00E-06). The effective T allele of rs4359 showed a significant association with disease risk for BPDII group. The estimated haplotypes of these polymorphisms have been distributed differently among patients and controls. Taken together, ACE polymorphisms can be regarded as risk factors for a variety of psychiatric disorders.
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