Synergistic effect of 5-HT2A receptor gene and MAOA gene on the negative emotion of patients with depression

被引:15
作者
Guo, Huirong [1 ]
Ren, Yuming [2 ]
Zhao, Ning [3 ]
Wang, Yali [1 ]
Li, Shuying [1 ]
Cui, He [1 ]
Zhang, Sijia [4 ]
Zhang, Jianhua [5 ,6 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[2] Xinxiang Med Univ, Xinxiang, Peoples R China
[3] Henan Prov Peoples Hosp, Zhengzhou, Peoples R China
[4] Peoples Hosp Zhengzhou, Zhengzhou, Peoples R China
[5] Zhengzhou Univ, Dept Biomed Engn, Zhengzhou 450052, Peoples R China
[6] Zhengzhou Univ, Med Engn Technol & Data Min Inst, Zhengzhou 450052, Peoples R China
关键词
5-hydroxytryptamine 2A receptor gene; depression; frontal; functional magnetic resonance imaging; monoamine oxidase A; SEROTONIN SYSTEM; PHARMACOGENETICS; POLYMORPHISM; ASSOCIATION;
D O I
10.1111/cpf.12094
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Objective To analyse the synergistic effect of polymorphism of the tandem repeat sequence u-VNTR of 5-hydroxytryptamine 2A (5-HT2A) receptor gene and monoamine oxidase A (MAOA) gene on the negative emotion in frontal lobe of patients with depression through functional magnetic resonance imaging (fMRI) technique. Methods Functional magnetic resonance imaging scanning was performed for 72 patients with depression and 70 gender, age-matched healthy people with physical examination under negative emotion recognition task. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was adopted to analyse genotype. The superior, middle and inferior gyrus of bilateral frontal lobe was regarded as the brain region of interest, and then the difference of activation intensity in frontal lobe subregion between control groups and patient groups with different genotypes, and the interaction between the two kinds of polymorphism were compared. Results The activation intensity in right frontal middle gyrus of patients with CC genotype increased obviously compared with TT and TC genotype patient groups and TT genotype control group (P<0.01); the activation intensity in right frontal inferior gyrus of patients with CC genotype increased obviously compared with TT and TC genotype patient groups and control groups (P<0.01); the activation intensity in right frontal middle gyrus and left frontal inferior gyrus of patients with MAOA high-activity genotype increased obviously compared with patient and control groups with MAOA low-activity genotype (P<0.01). In sum, there existed synergistic effect of the two genotypes on the activation abnormality of negative emotion recognition in right frontal middle gyrus (F = 6.18, P = 0.029). The negative activation in right frontal middle gyrus of patients with CC+H genotypes increased most obviously (P<0.05). Conclusion The frontal abnormality of patients with depression had certain 5-HT genetic basis, and 5-HT2A receptor CC allele and MAOA-H genotype had synergistic effect on the activity abnormality when recognizing negative emotion in right frontal middle gyrus of patients with depression.
引用
收藏
页码:277 / 281
页数:5
相关论文
共 24 条
[1]
[Anonymous], 2001, CHIN CLASS DIAGN MEN
[2]
[Anonymous], 1994, DIAGN STAT MAN MENT, VFourth, P143
[3]
fMRI responses to emotional faces in children and adolescents at genetic risk for psychiatric illness share some of the features of depression [J].
Barbour, Tracy ;
Pruitt, Patrick ;
Diwadkar, Vaibhav A. .
JOURNAL OF AFFECTIVE DISORDERS, 2012, 136 (03) :276-285
[4]
Brain-derived neurotrophic factor and serotonin transporter gene-linked promoter region genes alter serum levels of brain-derived neurotrophic factor in humans [J].
Bhang, Sooyoung ;
Ahn, Joon-Ho ;
Choi, Sam-Wook .
JOURNAL OF AFFECTIVE DISORDERS, 2011, 128 (03) :299-304
[5]
Serotonergic genes modulate amygdala activity in major depression [J].
Dannlowski, U. ;
Ohrmann, P. ;
Bauer, J. ;
Kugel, H. ;
Baune, B. T. ;
Hohoff, C. ;
Kersting, A. ;
Arolt, V. ;
Heindel, W. ;
Deckert, J. ;
Suslow, T. .
GENES BRAIN AND BEHAVIOR, 2007, 6 (07) :672-676
[6]
Reduced amygdala-prefrontal coupling in major depression: association with MAOA genotype and illness severity [J].
Dannlowski, Udo ;
Ohrmann, Patricia ;
Konrad, Carsten ;
Domschke, Katharina ;
Bauer, Jochen ;
Kugel, Harald ;
Hohoff, Christa ;
Schoening, Sonja ;
Kersting, Anette ;
Baune, Bernhard T. ;
Mortensen, Lena S. ;
Arolt, Volker ;
Zwitserlood, Pienie ;
Deckert, Jurgen ;
Heindel, Walter ;
Suslow, Thomas .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2009, 12 (01) :11-22
[7]
Werneck ALD, 2009, ARQ NEURO-PSIQUIAT, V67, P407, DOI 10.1590/S0004-282X2009000300007
[8]
Gur Raquel E, 2010, Dialogues Clin Neurosci, V12, P333
[9]
Modern neuroimaging in psychiatry: Towards the integration of functional and molecular information [J].
Linden, David ;
Thome, Johannes .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2011, 12 :6-10
[10]
Association of the MAOA promoter uVNTR polymorphism with suicide attempts in patients with major depressive disorder [J].
Lung, For-Wey ;
Tzeng, Dong-Sheng ;
Huang, Mei-Feng ;
Lee, Ming-Been .
BMC MEDICAL GENETICS, 2011, 12