Association between T-182C, G1287A polymorphism in NET gene and suicidality in major depressive disorder in Chinese patients

被引:3
作者
Cao, Su-Xia [1 ]
Li, Heng-Fen [2 ]
Zhao, Xiao-Feng [2 ]
Pang, Jian-Yue [2 ]
Liu, Qian [2 ]
Xie, Guang-Rong [1 ]
机构
[1] Cent S Univ, Key Lab Psychiat & Mental Hlth Hunan Prov, Xiangya Hosp 2, Mental Hlth Inst,Natl Technol Inst Psychiat, Changsha, Hunan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Psychiat, Zhengzhou, Henan, Peoples R China
关键词
NET; gene polymorphisms; MDD; suicidality; Chinese; NOREPINEPHRINE TRANSPORTER GENE; ANTIDEPRESSANT RESPONSE; SUSCEPTIBILITY; IDENTIFICATION; SEROTONIN;
D O I
10.1080/13651501.2017.1406121
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Previous studies have implicated norepinephrine transporter gene (NET) polymorphisms in the etiology of major depressive disorder (MDD). A functional NET T-182C polymorphism (rs2242446) in the promoter region and a synonymous polymorphisms G1287A in the exon 9 (rs5569) were associated with MDD in different populations. However, few studies have focused on the relationship between these polymorphisms and MDD patients with suicidality. The objective of the present study was to examine whether the two polymorphisms are associated with MDD patients with suicidality in the Han Chinese population.Methods: Two hundred and sixty-three suicidal depressed patients and 241 non-suicidal depressed patients who met DSM-IV criteria for MDD were recruited from our hospital. Three hundred and three unrelated, age- and sex-matched healthy control subjects participated in this case-control study. Suicidality was assessed using Mini International Neuropsychiatric Interview (MINI) and the Hamilton rating scale for depression (HAMD). Genotypes of T-182C polymorphism (rs2242446) and G1287A (rs5569) were screened by polymerase chain reaction.Results: No statistical significant differences between patients and controls were found for any of the analysed polymorphisms, either in the genotype or allele distribution.Conclusions: Our results suggest that the investigated polymorphisms are not major susceptibility factors in the etiology of MDD with suicidality. However, the results must be verified in larger samples and different ethnicities.
引用
收藏
页码:304 / 309
页数:6
相关论文
共 39 条
[2]   Psychiatric diagnoses in 3275 suicides: a meta-analysis [J].
Arsenault-Lapierre, Genevieve ;
Kim, Caroline ;
Turecki, Gustavo .
BMC PSYCHIATRY, 2004, 4 (1)
[3]   REDUCED TYROSINE-HYDROXYLASE IMMUNOREACTIVITY IN LOCUS-CERULEUS OF SUICIDE VICTIMS [J].
BIEGON, A ;
FIELDUST, S .
SYNAPSE, 1992, 10 (01) :79-82
[4]  
Bönisch H, 2006, HANDB EXP PHARM, V175, P485
[5]  
BRUSS M, 1993, HUM GENET, V91, P278
[6]   A Genomewide Linkage Study on Suicidality in Major Depressive Disorder Confirms Evidence for Linkage to 2p12 [J].
Butler, Amy W. ;
Breen, Gerome ;
Tozzi, Federica ;
Craddock, Nick ;
Gill, Mike ;
Korszun, Ania ;
Maier, Wolfgang ;
Middleton, Lefkos T. ;
Mors, Ole ;
Owen, Michael J. ;
Perry, Julia ;
Preisig, Martin ;
Rice, John P. ;
Rietschel, Marcella ;
Jones, Lisa ;
Farmer, Anne E. ;
Lewis, Cathryn M. ;
McGuffin, Peter .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2010, 153B (08) :1465-1473
[7]  
Chang CC, 2007, J PSYCHIATR NEUROSCI, V32, P121
[8]   Unaltered α2-noradrenergic/imidazoline receptors in suicide victims:: a postmortem brain autoradiographic analysis [J].
Gross-Isseroff, R ;
Weizman, A ;
Fieldust, SJ ;
Israeli, M ;
Biegon, A .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2000, 10 (04) :265-271
[9]   Multivariate permutation analysis associates multiple polymorphisms with subphenotypes of major depression [J].
Hahn, M. K. ;
Blackford, J. U. ;
Haman, K. ;
Mazei-Robison, M. ;
English, B. A. ;
Prasad, H. C. ;
Steele, A. ;
Hazelwood, L. ;
Fentress, H. M. ;
Myers, R. ;
Blakely, R. D. ;
Sanders-Bush, E. ;
Shelton, R. .
GENES BRAIN AND BEHAVIOR, 2008, 7 (04) :487-495
[10]   Positive association between T-182C polymorphism in the norepinephrine transporter gene and susceptibility to major depressive disorder in a Japanese population [J].
Inoue, K ;
Itoh, K ;
Yoshida, K ;
Shimizu, T ;
Suzuki, T .
NEUROPSYCHOBIOLOGY, 2004, 50 (04) :301-304