包括BDNF在内的关键区域在人类精神病理和肥胖中的高度渗透改变。

Carl Ernst, Christian R Marshall, Yiping Shen, Kay Metcalfe, Jill Rosenfeld, Jennelle C Hodge, Alcy Torres, Ian Blumenthal, Colby Chiang, Vamsee Pillalamarri, Liam Crapper, Alpha B Diallo, Douglas Ruderfer, Shahrin Pereira, Pamela Sklar, Shaun Purcell, Robert S Wildin, Anne C Spencer, Bradley F Quade, David J Harris, Emanuelle Lemyre, Bai-Lin Wu, Dimitri J Stavropoulos, Michael T Geraghty, Lisa G Shaffer, Cynthia C Morton, Stephen W Scherer, James F Gusella, Michael E Talkowski
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引用次数: 24

摘要

基于病例报告或涉及大型结构异常的研究,脑源性神经营养因子(BDNF)被怀疑是精神疾病的致病因素。目的探讨BDNF在人精神病理中的作用。设计病例对照研究。来自7个分子诊断中心的基于微阵列的比较基因组杂交数据,包括38550名受影响的受试者和28705名未受影响的受试者。患者:受试者到诊断筛选中心进行基于微阵列的比较基因组杂交,以诊断身体或认知障碍。主要结果测量基因组拷贝数的增加和减少。结果:我们报告了5例精神病理和包括BDNF在内的关键区域基因组缺失的患者。在没有发育异常的对照组或诊断病例中,定义的关键区域从未中断。结论BDNF区域的半合子性与焦虑、行为和情绪障碍等多种精神表型有关。
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Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity.

CONTEXT Brain-derived neurotrophic factor (BDNF) is suspected of being a causative factor in psychiatric disorders based on case reports or studies involving large structural anomalies. OBJECTIVE To determine the involvement of BDNF in human psychopathology. DESIGN Case-control study. SETTING Microarray-based comparative genomic hybridization data from 7 molecular diagnostic centers including 38 550 affected subjects and 28 705 unaffected subjects. PATIENTS Subjects referred to diagnostic screening centers for microarray-based comparative genomic hybridization for physical or cognitive impairment. MAIN OUTCOME MEASURES Genomic copy number gains and losses. RESULTS We report 5 individuals with psychopathology and genomic deletion of a critical region including BDNF. The defined critical region was never disrupted in control subjects or diagnostic cases without developmental abnormalities. CONCLUSION Hemizygosity of the BDNF region contributes to variable psychiatric phenotypes including anxiety, behavioral, and mood disorders.

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Archives of general psychiatry
Archives of general psychiatry 医学-精神病学
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