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Familial risk for mood disorder and the personality risk factor, neuroticism, interact in their association with frontolimbic serotonin 2A receptor binding.家族性心境障碍风险与人格风险因素——神经质,共同作用于额眶皮质边缘系统 5-羟色胺 2A 受体结合。
Neuropsychopharmacology. 2010 Apr;35(5):1129-37. doi: 10.1038/npp.2009.218. Epub 2009 Dec 30.
2
Frontolimbic serotonin 2A receptor binding in healthy subjects is associated with personality risk factors for affective disorder.健康受试者的额边缘5-羟色胺2A受体结合与情感障碍的人格危险因素相关。
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3
Gender and the use of hormonal contraception in women are not associated with cerebral cortical 5-HT 2A receptor binding.女性的性别及激素避孕的使用与大脑皮质5-羟色胺2A受体结合无关。
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4
Gender, personality, and serotonin-2A receptor binding in healthy subjects.健康受试者的性别、个性与 5-羟色胺 2A 受体结合。
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Decreased hippocampal 5-HT2A receptor binding in major depressive disorder: in vivo measurement with [18F]altanserin positron emission tomography.重度抑郁症患者海马体5-HT2A受体结合减少:使用[18F]阿坦色林正电子发射断层扫描进行体内测量。
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A nonlinear relationship between cerebral serotonin transporter and 5-HT(2A) receptor binding: an in vivo molecular imaging study in humans.脑内血清素转运体与 5-HT(2A)受体结合的非线性关系:一项人类体内分子影像学研究。
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Low frontal serotonin 2A receptor binding is a state marker for schizophrenia?额叶血清素2A受体结合水平低是精神分裂症的一种状态标志物吗?
Eur Neuropsychopharmacol. 2016 Jul;26(7):1248-50. doi: 10.1016/j.euroneuro.2016.04.008. Epub 2016 May 11.

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Neuroticism predicts the impact of serotonin challenges on fear processing in subgenual anterior cingulate cortex.神经质预测了 5-羟色胺挑战对前扣带回皮质亚区恐惧处理的影响。
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No evidence for a role of the serotonin 4 receptor in five-factor personality traits: A positron emission tomography brain study.5-羟色胺4受体在五因素人格特质中不起作用的证据:一项正电子发射断层扫描脑部研究
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本文引用的文献

1
Brain serotonin 2A receptor binding: relations to body mass index, tobacco and alcohol use.脑血清素2A受体结合:与体重指数、烟草和酒精使用的关系。
Neuroimage. 2009 May 15;46(1):23-30. doi: 10.1016/j.neuroimage.2009.01.050. Epub 2009 Feb 5.
2
Activation of glucocorticoid receptors increases 5-HT2A receptor levels.糖皮质激素受体的激活会增加5-羟色胺2A受体水平。
Exp Neurol. 2009 Jul;218(1):83-91. doi: 10.1016/j.expneurol.2009.04.008. Epub 2009 Apr 18.
3
Effects of chronic citalopram treatment on 5-HT1A and 5-HT2A receptors in group- and isolation-housed mice.慢性西酞普兰治疗对群居和独居小鼠5-HT1A和5-HT2A受体的影响。
Eur J Pharmacol. 2008 Sep 28;593(1-3):49-61. doi: 10.1016/j.ejphar.2008.07.011. Epub 2008 Jul 11.
4
HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression.下丘脑-垂体-肾上腺轴反应性:5-羟色胺转运体基因启动子区多态性、应激与抑郁之间关联的潜在机制
Biol Psychiatry. 2008 May 1;63(9):847-51. doi: 10.1016/j.biopsych.2007.10.008. Epub 2007 Nov 19.
5
Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR).环境压力和性别对抑郁症状与血清素转运体基因连锁多态性区域(5-HTTLPR)之间关联的影响。
Behav Genet. 2008 Jan;38(1):34-43. doi: 10.1007/s10519-007-9172-1. Epub 2007 Oct 23.
6
Frontolimbic serotonin 2A receptor binding in healthy subjects is associated with personality risk factors for affective disorder.健康受试者的额边缘5-羟色胺2A受体结合与情感障碍的人格危险因素相关。
Biol Psychiatry. 2008 Mar 15;63(6):569-76. doi: 10.1016/j.biopsych.2007.07.009. Epub 2007 Sep 19.
7
The moderation by the serotonin transporter gene of environmental adversity in the aetiology of mental illness: review and methodological analysis.血清素转运体基因对精神疾病病因中环境逆境的调节作用:综述与方法学分析
Mol Psychiatry. 2008 Feb;13(2):131-46. doi: 10.1038/sj.mp.4002067. Epub 2007 Aug 14.
8
Personality traits in unaffected twins discordant for affective disorder.情感障碍不一致的未患病双胞胎的人格特质。
Acta Psychiatr Scand. 2007 Jun;115(6):442-50. doi: 10.1111/j.1600-0447.2006.00909.x.
9
A longitudinal study of personality and major depression in a population-based sample of male twins.一项基于人群样本的男性双胞胎人格与重度抑郁症的纵向研究。
Psychol Med. 2007 Aug;37(8):1163-72. doi: 10.1017/S0033291707000244. Epub 2007 Apr 4.
10
Increased waking salivary cortisol levels in young people at familial risk of depression.有抑郁症家族风险的年轻人清醒时唾液皮质醇水平升高。
Am J Psychiatry. 2007 Apr;164(4):617-21. doi: 10.1176/ajp.2007.164.4.617.

家族性心境障碍风险与人格风险因素——神经质,共同作用于额眶皮质边缘系统 5-羟色胺 2A 受体结合。

Familial risk for mood disorder and the personality risk factor, neuroticism, interact in their association with frontolimbic serotonin 2A receptor binding.

机构信息

Neurobiology Research Unit and Center for Integrated Molecular Brain Imaging, Denmark.

出版信息

Neuropsychopharmacology. 2010 Apr;35(5):1129-37. doi: 10.1038/npp.2009.218. Epub 2009 Dec 30.

DOI:10.1038/npp.2009.218
PMID:20043006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3055406/
Abstract

Life stress is a robust risk factor for later development of mood disorders, particularly for individuals at familial risk. Likewise, scoring high on the personality trait neuroticism is associated with an increased risk for mood disorders. Neuroticism partly reflects stress vulnerability and is positively correlated to frontolimbic serotonin 2A (5-HT(2A)) receptor binding. Here, we investigate whether neuroticism interacts with familial risk in relation to frontolimbic 5-HT(2A) receptor binding. Twenty-one healthy twins with a co-twin history of mood disorder and 16 healthy twins without a co-twin history of mood disorder were included. They answered self-report personality questionnaires and underwent [(18)F]altanserin positron emission tomography. We found a significant interaction between neuroticism and familial risk in predicting the frontolimbic 5-HT(2A) receptor binding (p=0.026) in an analysis adjusting for age and body mass index. Within the high-risk group only, neuroticism and frontolimbic 5-HT(2A) receptor binding was positively associated (p=0.0037). In conclusion, our data indicate that familial risk and neuroticism interact in their relation to frontolimbic 5-HT(2A) receptor binding. These findings point at a plausible neurobiological link between genetic and personality risk factors and vulnerability to developing mood disorders. It contributes to our understanding of why some people at high risk develop mood disorders while others do not. We speculate that an increased stress reactivity in individuals at high familial risk for mood disorders might enhance the effect of neuroticism in shaping the impact of potential environmental stress and thereby influence serotonergic neurotransmission.

摘要

生活压力是情绪障碍后期发展的一个强有力的风险因素,尤其是对于有家族风险的个体。同样,神经质人格特质得分高与情绪障碍的风险增加有关。神经质在一定程度上反映了压力易感性,与额眶皮质 5-羟色胺 2A(5-HT2A)受体结合呈正相关。在这里,我们研究神经质是否与家族风险相互作用,与额眶皮质 5-HT2A 受体结合有关。纳入了 21 名有同卵双胞胎心境障碍病史的健康双胞胎和 16 名无同卵双胞胎心境障碍病史的健康双胞胎。他们回答了自我报告的人格问卷,并接受了 [(18)F]altanserin 正电子发射断层扫描。我们发现,在调整年龄和体重指数后,神经质和家族风险在预测额眶皮质 5-HT2A 受体结合方面存在显著的交互作用(p=0.026)。仅在高风险组中,神经质和额眶皮质 5-HT2A 受体结合呈正相关(p=0.0037)。总之,我们的数据表明,家族风险和神经质在与额眶皮质 5-HT2A 受体结合的关系中相互作用。这些发现表明遗传和人格风险因素与易患情绪障碍之间存在合理的神经生物学联系。它有助于我们理解为什么一些处于高风险的人会发展出情绪障碍,而另一些人则不会。我们推测,情绪障碍高家族风险个体的应激反应增加可能会增强神经质在塑造潜在环境应激影响方面的作用,从而影响 5-羟色胺能神经传递。