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Neuroanatomical maps of psychosis onset: voxel-wise meta-analysis of antipsychotic-naive VBM studies.神经解剖学图谱的精神病发病:抗精神病药初治 VBM 研究的体素水平荟萃分析。
Schizophr Bull. 2012 Nov;38(6):1297-307. doi: 10.1093/schbul/sbr134. Epub 2011 Nov 10.
2
A meta-analysis of whole-brain diffusion tensor imaging studies in bipolar disorder.双相障碍全脑弥散张量成像研究的荟萃分析。
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Dec 1;35(8):1820-6. doi: 10.1016/j.pnpbp.2011.05.009. Epub 2011 May 23.
3
Neuroanatomy of vulnerability to psychosis: a voxel-based meta-analysis.精神分裂症易感性的神经解剖学:基于体素的荟萃分析。
Neurosci Biobehav Rev. 2011 Apr;35(5):1175-85. doi: 10.1016/j.neubiorev.2010.12.005. Epub 2010 Dec 17.
4
The impact of general intellectual ability and white matter volume on the functional outcome of patients with Bipolar Disorder and their relatives.一般智力和白质体积对双相情感障碍患者及其亲属的功能预后的影响。
J Affect Disord. 2011 May;130(3):413-20. doi: 10.1016/j.jad.2010.10.048. Epub 2010 Nov 26.
5
Altered development of white matter in youth at high familial risk for bipolar disorder: a diffusion tensor imaging study.青少年期家族性双相障碍高风险人群的脑白质发育改变:一项弥散张量成像研究。
J Am Acad Child Adolesc Psychiatry. 2010 Dec;49(12):1249-59, 1259.e1. doi: 10.1016/j.jaac.2010.09.007. Epub 2010 Oct 29.
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Genetic and environmental influences on focal brain density in bipolar disorder.双相障碍患者大脑局部密度的遗传和环境影响。
Brain. 2010 Oct;133(10):3080-92. doi: 10.1093/brain/awq236. Epub 2010 Sep 12.
7
A comprehensive review and model of putative prodromal features of bipolar affective disorder.双相情感障碍前驱症状的综合述评和模型。
Psychol Med. 2011 Aug;41(8):1567-77. doi: 10.1017/S0033291710001790. Epub 2010 Sep 14.
8
A preliminary evaluation of the validity of at-risk criteria for bipolar disorders in help-seeking adolescents and young adults.求助青少年和年轻成人中双相障碍风险标准有效性的初步评估。
J Affect Disord. 2010 Dec;127(1-3):316-20. doi: 10.1016/j.jad.2010.06.016. Epub 2010 Jul 8.
9
Exaggerated neural response to emotional faces in patients with bipolar disorder and their first-degree relatives.双相障碍患者及其一级亲属对情绪面孔的过度神经反应。
Neuroimage. 2010 Oct 15;53(1):58-64. doi: 10.1016/j.neuroimage.2010.05.069. Epub 2010 Jun 8.
10
White matter hyperintensities in affected and unaffected late teenage and early adulthood offspring of bipolar parents: a two-center high-risk study.双相父母的晚期青少年和成年早期受影响和未受影响子女的脑白质高信号:一项双中心高危研究。
J Psychiatr Res. 2011 Jan;45(1):76-82. doi: 10.1016/j.jpsychires.2010.04.019. Epub 2010 May 20.

绘制双相障碍易感性图谱:神经影像学研究的系统综述和荟萃分析。

Mapping vulnerability to bipolar disorder: a systematic review and meta-analysis of neuroimaging studies.

机构信息

Institute of Psychiatry, Department of Psychosis Studies, King's College London, London, United Kingdom.

出版信息

J Psychiatry Neurosci. 2012 May;37(3):170-84. doi: 10.1503/jpn.110061.

DOI:10.1503/jpn.110061
PMID:22297067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3341409/
Abstract

BACKGROUND

Although early interventions in individuals with bipolar disorder may reduce the associated personal and economic burden, the neurobiologic markers of enhanced risk are unknown.

METHODS

Neuroimaging studies involving individuals at enhanced genetic risk for bipolar disorder (HR) were included in a systematic review. We then performed a region of interest (ROI) analysis and a whole-brain meta-analysis combined with a formal effect-sizes meta-analysis in a subset of studies.

RESULTS

There were 37 studies included in our systematic review. The overall sample for the systematic review included 1258 controls and 996 HR individuals. No significant differences were detected between HR individuals and controls in the selected ROIs: striatum, amygdala, hippocampus, pituitary and frontal lobe. The HR group showed increased grey matter volume compared with patients with established bipolar disorder. The HR individuals showed increased neural response in the left superior frontal gyrus, medial frontal gyrus and left insula compared with controls, independent from the functional magnetic resonance imaging task used. There were no publication biases. Sensitivity analysis confirmed the robustness of these results.

LIMITATIONS

As the included studies were cross-sectional, it remains to be determined whether the observed neurofunctional and structural alterations represent risk factors that can be clinically used in preventive interventions for prodromal bipolar disorder.

CONCLUSION

Accumulating structural and functional imaging evidence supports the existence of neurobiologic trait abnormalities in individuals at genetic risk for bipolar disorder at various scales of investigation.

摘要

背景

尽管早期干预双相情感障碍患者可能会降低相关的个人和经济负担,但增强风险的神经生物学标志物尚不清楚。

方法

系统综述中纳入了具有双相情感障碍增强遗传风险的个体的神经影像学研究。然后,我们在一部分研究中进行了感兴趣区域(ROI)分析和全脑荟萃分析,并结合了正式的效应大小荟萃分析。

结果

我们的系统综述共纳入 37 项研究。系统综述的总体样本包括 1258 名对照和 996 名 HR 个体。在选定的 ROI 中,HR 个体与对照组之间未检测到显著差异:纹状体、杏仁核、海马体、垂体和额叶。与已确诊的双相情感障碍患者相比,HR 组的灰质体积增加。与对照组相比,HR 个体在左侧额上回、内侧额回和左侧脑岛表现出更高的神经反应,而与所使用的功能磁共振成像任务无关。没有发现发表偏倚。敏感性分析证实了这些结果的稳健性。

局限性

由于纳入的研究是横断面的,因此仍需要确定观察到的神经功能和结构改变是否代表可以在前驱期双相情感障碍的预防性干预中临床应用的风险因素。

结论

越来越多的结构和功能影像学证据支持在各种研究规模上,具有双相情感障碍遗传风险的个体存在神经生物学特征异常。