Polygenic dissection of major depression clinical heterogeneity.

Polygenic dissection of major depression clinical heterogeneity.
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DOI:
10.1038/mp.2015.86
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发表时间:
2016-04
影响因子:
11
通讯作者:
Penninx BW
Penninx BW
中科院分区:
医学1区
文献类型:
--
作者:
Milaneschi Y;Lamers F;Peyrot WJ;Abdellaoui A;Willemsen G;Hottenga JJ;Jansen R;Mbarek H;Dehghan A;Lu C;CHARGE inflammation working group;Boomsma DI;Penninx BW

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重度抑郁症(MDD)的分子机制在很大程度上尚不清楚。先前遗传学研究的成功有限可能归因于 MDD 的异质性,聚集了生物学上不同的亚型。我们检查了 MDD 的多基因特征和两种常见的临床亚型(典型和非典型),这两种亚型是通过大量已确诊的成人样本的症状特征来定义的。数据来自荷兰抑郁和焦虑研究 (NESDA) 的 1,530 名患者和主要来自荷兰双胞胎登记处 (NTR) 的 1,700 名对照者。 MDD 及其亚型的诊断基于 DSM-IV 症状。 MDD 及其亚型与精神疾病(MDD、双相情感障碍、精神分裂症)和代谢(BMI、C 反应蛋白、甘油三酯)特征的遗传重叠通过大型国际联盟的荟萃分析结果生成的基因组风险评分 (GPRS) 进行评估。还估计了 MDD 和亚型的 SNP 遗传力。 MDD 与精神 GPRS 相关,而 GPRS 与代谢特征没有关联。 MDD 亚型具有不同的多基因特征:典型与精神分裂症 GPRS 密切相关(OR=1.54,p=7.8e-9),而非典型则与 BMI(OR=1.29,p=2.7e-4)和甘油三酯(OR=1.21,p=0.006)GPRS 相关。当仅使用食欲/体重的高度歧视性症状来定义亚型时,也发现了类似的结果。 MDD 的 SNP 遗传率为 32%,食欲/体重降低(典型)和增加(非典型)的亚型分别为 38% 和 43%。总之,MDD 亚型的特点是部分不同的多基因倾向,并且可能代表更同质的表型。解开MDD的异质性可能有助于精神病学领域在寻找抑郁症的分子根源方面取得进展。
The molecular mechanisms underlying Major Depressive Disorder (MDD) are largely unknown. Limited success of previous genetics studies may be attributable to heterogeneity of MDD, aggregating biologically different subtypes. We examined the polygenic features of MDD and two common clinical subtypes (typical and atypical) defined by symptom profiles in a large sample of adults with established diagnoses. Data were from 1,530 patients of the Netherlands Study of Depression and Anxiety (NESDA) and 1,700 controls mainly from the Netherlands Twin Register (NTR). Diagnoses of MDD and its subtypes were based on DSM-IV symptoms. Genetic overlap of MDD and subtypes with psychiatric (MDD, bipolar disorder, schizophrenia) and metabolic (BMI, C-reactive protein, triglycerides) traits was evaluated via genomic profile risk scores (GPRS) generated from meta-analysis results of large international consortia. SNP-heritability of MDD and subtypes was also estimated. MDD was associated with psychiatric GPRS, while no association was found for GPRS of metabolic traits. MDD subtypes had differential polygenic signatures: typical was strongly associated with schizophrenia GPRS (OR=1.54, p=7.8e-9), while atypical was additionally associated with BMI (OR=1.29, p=2.7e-4) and triglycerides (OR=1.21, p=0.006) GPRS. Similar results were found when only the highly discriminatory symptoms of appetite/weight to were used to define subtypes. SNP-heritability was 32% for MDD, 38% and 43% for subtypes with, respectively, decreased (typical) and increased (atypical) appetite/weight. In conclusion, MDD subtypes are characterized by partially distinct polygenic liabilities and may represent more homogeneous phenotypes. Disentangling MDD heterogeneity may help the psychiatric field moving forward in the search for molecular roots of depression.
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发表时间: 2011-02-22
期刊: Circulation
影响因子: 37.8
作者:
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通讯作者: Chasman DI
DOI: 10.1375/183242706779462426
发表时间: 2006-12-01
影响因子: 0.9
作者:
Boomsma, Dorret I.;de Geus, Eco J. C.;Willemsen, Gonneke
通讯作者: Willemsen, Gonneke
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发表时间: 2013-09
期刊: NATURE GENETICS
影响因子: 30.8
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发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者:
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DOI: 10.1016/j.jad.2008.12.004
发表时间: 2009-09-01
影响因子: 6.6
作者:
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通讯作者: Oien, Per Anders