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重度抑郁症中的基因表达。

Gene expression in major depressive disorder.

机构信息

Department of Psychiatry, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.

Department of Biostatistics, University of North Carolina, Chapel Hill, NC, USA.

出版信息

Mol Psychiatry. 2016 Mar;21(3):339-47. doi: 10.1038/mp.2015.57. Epub 2015 May 26.

Abstract

The search for genetic variants underlying major depressive disorder (MDD) has not yet provided firm leads to its underlying molecular biology. A complementary approach is to study gene expression in relation to MDD. We measured gene expression in peripheral blood from 1848 subjects from The Netherlands Study of Depression and Anxiety. Subjects were divided into current MDD (N=882), remitted MDD (N=635) and control (N=331) groups. MDD status and gene expression were measured again 2 years later in 414 subjects. The strongest gene expression differences were between the current MDD and control groups (129 genes at false-discovery rate, FDR<0.1). Gene expression differences across MDD status were largely unrelated to antidepressant use, inflammatory status and blood cell counts. Genes associated with MDD were enriched for interleukin-6 (IL-6)-signaling and natural killer (NK) cell pathways. We identified 13 gene expression clusters with specific clusters enriched for genes involved in NK cell activation (downregulated in current MDD, FDR=5.8 × 10(-5)) and IL-6 pathways (upregulated in current MDD, FDR=3.2 × 10(-3)). Longitudinal analyses largely confirmed results observed in the cross-sectional data. Comparisons of gene expression results to the Psychiatric Genomics Consortium (PGC) MDD genome-wide association study results revealed overlap with DVL3. In conclusion, multiple gene expression associations with MDD were identified and suggest a measurable impact of current MDD state on gene expression. Identified genes and gene clusters are enriched with immune pathways previously associated with the etiology of MDD, in line with the immune suppression and immune activation hypothesis of MDD.

摘要

寻找导致重度抑郁症(MDD)的遗传变异尚未为其潜在的分子生物学提供确凿的线索。另一种方法是研究与 MDD 相关的基因表达。我们测量了来自荷兰抑郁与焦虑研究的 1848 名受试者的外周血中的基因表达。将受试者分为当前 MDD(N=882)、缓解的 MDD(N=635)和对照组(N=331)。在 414 名受试者中,2 年后再次测量 MDD 状态和基因表达。当前 MDD 和对照组之间的基因表达差异最大(假发现率 FDR<0.1 时有 129 个基因)。MDD 状态之间的基因表达差异与抗抑郁药使用、炎症状态和血细胞计数基本无关。与 MDD 相关的基因富集了白细胞介素-6(IL-6)信号和自然杀伤(NK)细胞途径。我们确定了 13 个具有特定基因表达簇的基因表达簇,这些基因簇与 NK 细胞激活相关的基因(当前 MDD 下调,FDR=5.8×10(-5))和 IL-6 途径(当前 MDD 上调,FDR=3.2×10(-3))丰富。纵向分析在很大程度上证实了横断面数据中的结果。将基因表达结果与精神病基因组学联合会(PGC)MDD 全基因组关联研究结果进行比较,结果显示与 DVL3 重叠。总之,确定了与 MDD 相关的多个基因表达关联,并表明当前 MDD 状态对基因表达有可衡量的影响。鉴定的基因和基因簇富含先前与 MDD 病因学相关的免疫途径,符合 MDD 的免疫抑制和免疫激活假说。

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