在一个大型的多站点数据集中,从个性化的灰质形态异常中确定了两种亚型的重度抑郁症。

IF 5.5 2区 医学 Q1 PSYCHIATRY
Keke Fang, Baohong Wen, Liang Liu, Ya Tian, Huiting Yang, Shaoqiang Han, Xianfu Sun, Lianjie Niu
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引用次数: 0

摘要

背景:神经影像学研究提供了令人信服的证据,表明重度抑郁症(MDD)与广泛的灰质形态异常有关。然而,显著的个体间变异性使群体水平发现的解释复杂化,突出了调查潜在的重度抑郁症亚型的必要性。方法:在本研究中,我们的目的是根据个体偏离标准灰质体积(gmv)来确定MDD的亚型,这是使用来自健康对照(hc)的规范模型来估计的。我们利用了一个大型的、多站点的高分辨率结构MRI扫描数据集,包括1276名MDD患者和1104名匹配的hc。为了探索所观察到的结构异常的转录和分子机制,我们研究了GMV偏差、转录组相似性(通过相关基因表达[CGE]连接组测量)和神经递质受体/转运体分布之间的关系。结果:我们的研究结果揭示了两种可重复的MDD亚型,每种亚型在研究部位表现出不同的GMV异常模式。亚型1表现为脑区gmv升高,小脑区gmv降低,亚型2表现为脑区gmv降低,小脑区gmv升高。已确定的GMV异常与神经递质受体/转运体分布有不同的相关性。此外,这些异常与转录连接的基因网络有关,表明这两种亚型的遗传基础。值得注意的是,这两种亚型表现出不同的cge疾病中心。结论:本研究确定了两种强大的MDD亚型,为MDD的神经生物学和遗传基础提供了新的见解,并为该疾病的分类学提供了潜在的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two subtypes of major depressive disorder are identified from individualized gray matter morphological abnormalities in a large multi-site dataset.

Background: Neuroimaging studies provide compelling evidence that major depressive disorder (MDD) is associated with widespread gray matter morphological abnormalities. However, significant interindividual variability complicates the interpretation of group-level findings, highlighting the need for investigating potential MDD subtypes.

Methods: In this study, we aimed to identify subtypes of MDD based on individualized deviations from normative gray matter volumes (GMVs), as estimated using a normative model derived from healthy controls (HCs). We leveraged a large, multi-site dataset of high-resolution structural MRI scans, comprising 1,276 MDD patients and 1,104 matched HCs. To explore the transcriptional and molecular mechanisms underlying the observed structural abnormalities, we examined the relationships between GMV deviations, transcriptomic similarities (as measured by the correlated gene expression [CGE] connectome), and the distribution of neurotransmitter receptors/transporters.

Results: Our results revealed two reproducible MDD subtypes, each exhibiting distinct patterns of GMV abnormalities across study sites. Subtype 1 displayed increased GMVs in cerebral regions and decreased GMVs in cerebellar regions, whereas subtype 2 showed the opposite pattern, with decreased GMVs in cerebral regions and increased GMVs in cerebellar areas. The identified GMV abnormalities were differentially associated with neurotransmitter receptor/transporter distributions. Furthermore, these abnormalities were linked to transcriptionally connected gene networks, suggesting genetic underpinnings for both subtypes. Notably, the two subtypes exhibited distinct CGE-informed disease epicenters.

Conclusions: This study identifies two robust MDD subtypes, providing new insights into the neurobiological and genetic bases of MDD and offering a potential advancement in the nosology of the disorder.

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来源期刊
Psychological Medicine
Psychological Medicine 医学-精神病学
CiteScore
11.30
自引率
4.30%
发文量
711
审稿时长
3-6 weeks
期刊介绍: Now in its fifth decade of publication, Psychological Medicine is a leading international journal in the fields of psychiatry, related aspects of psychology and basic sciences. From 2014, there are 16 issues a year, each featuring original articles reporting key research being undertaken worldwide, together with shorter editorials by distinguished scholars and an important book review section. The journal''s success is clearly demonstrated by a consistently high impact factor.
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