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脑源性神经营养因子rs6265甲硫氨酸等位基因与低家庭凝聚力之间的相互作用与小儿双相情感障碍患者左侧海马体积较小有关。

Interaction between BDNF rs6265 Met allele and low family cohesion is associated with smaller left hippocampal volume in pediatric bipolar disorder.

作者信息

Zeni Cristian Patrick, Mwangi Benson, Cao Bo, Hasan Khader M, Walss-Bass Consuelo, Zunta-Soares Giovana, Soares Jair C

机构信息

Department of Psychiatry and Behavioral Sciences, University of Texas Center of Excellence on Mood Disorders, Houston, TX, USA.

Department of Psychiatry and Behavioral Sciences, University of Texas Center of Excellence on Mood Disorders, Houston, TX, USA.

出版信息

J Affect Disord. 2016 Jan 1;189:94-7. doi: 10.1016/j.jad.2015.09.031. Epub 2015 Sep 25.

Abstract

BACKGROUND

Genetic and environmental factors are implicated in the onset and evolution of pediatric bipolar disorder, and may be associated to structural brain abnormalities. The aim of our study was to assess the impact of the interaction between the Brain-Derived Neurotrophic Factor (BDNF) rs6265 polymorphism and family functioning on hippocampal volumes of children and adolescents with bipolar disorder, and typically-developing controls.

METHODS

We evaluated the family functioning cohesion subscale using the Family Environment Scale-Revised, genotyped the BDNF rs6265 polymorphism, and performed structural brain imaging in 29 children and adolescents with bipolar disorder, and 22 healthy controls.

RESULTS

We did not find significant differences between patients with BD or controls in left or right hippocampus volume (p=0.44, and p=0.71, respectively). However, we detected a significant interaction between low scores on the cohesion subscale and the presence of the Met allele at BNDF on left hippocampal volume of patients with bipolar disorder (F=3.4, p=0.043). None of the factors independently (BDNF Val66Met, cohesion scores) was significantly associated with hippocampal volume differences.

LIMITATIONS

small sample size, cross-sectional study.

CONCLUSIONS

These results may lead to a better understanding of the impact of the interaction between genes and environment factors on brain structures associated to bipolar disorder and its manifestations.

摘要

背景

遗传和环境因素与小儿双相情感障碍的发病及演变有关,可能与脑结构异常相关。我们研究的目的是评估脑源性神经营养因子(BDNF)rs6265多态性与家庭功能的相互作用对双相情感障碍儿童和青少年以及正常发育对照组海马体积的影响。

方法

我们使用修订版家庭环境量表评估家庭功能凝聚性子量表,对BDNF rs6265多态性进行基因分型,并对29名双相情感障碍儿童和青少年以及22名健康对照进行脑结构成像。

结果

我们发现双相情感障碍患者与对照组在左侧或右侧海马体积上没有显著差异(分别为p = 0.44和p = 0.71)。然而,我们检测到凝聚性子量表得分低与双相情感障碍患者左侧海马体积上BDNF存在Met等位基因之间存在显著相互作用(F = 3.4,p = 0.043)。没有一个因素(BDNF Val66Met、凝聚得分)独立地与海马体积差异显著相关。

局限性

样本量小,横断面研究。

结论

这些结果可能有助于更好地理解基因与环境因素之间的相互作用对与双相情感障碍及其表现相关的脑结构的影响。

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本文引用的文献

1
Decreased right hippocampal volumes and neuroprogression markers in adolescents with bipolar disorder.
Neuropsychobiology. 2015;71(3):140-8. doi: 10.1159/000375311. Epub 2015 Apr 25.
2
Treatment moderators of child- and family-focused cognitive-behavioral therapy for pediatric bipolar disorder.
J Am Acad Child Adolesc Psychiatry. 2015 Feb;54(2):116-25. doi: 10.1016/j.jaac.2014.11.007. Epub 2014 Nov 22.
3
BDNF Val66Met genotype interacts with childhood adversity and influences the formation of hippocampal subfields.
Hum Brain Mapp. 2014 Dec;35(12):5776-83. doi: 10.1002/hbm.22584. Epub 2014 Jul 10.
4
BDNF serum levels in subjects developing or not post-traumatic stress disorder after trauma exposure.
Brain Cogn. 2014 Feb;84(1):118-22. doi: 10.1016/j.bandc.2013.11.012. Epub 2013 Dec 21.
5
Negative expressed emotion best discriminates families with bipolar disorder children.
J Affect Disord. 2013 Jun;148(2-3):418-23. doi: 10.1016/j.jad.2012.11.017. Epub 2012 Dec 4.
6
FreeSurfer.
Neuroimage. 2012 Aug 15;62(2):774-81. doi: 10.1016/j.neuroimage.2012.01.021. Epub 2012 Jan 10.
7
The role of BDNF as a mediator of neuroplasticity in bipolar disorder.
Psychiatry Investig. 2010 Dec;7(4):243-50. doi: 10.4306/pi.2010.7.4.243. Epub 2010 Dec 15.
9
A systemic toxicity index developed to assess peripheral changes in mood episodes.
Mol Psychiatry. 2010 Aug;15(8):784-6. doi: 10.1038/mp.2009.112. Epub 2010 Mar 30.

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