Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD, USA,
Pac Symp Biocomput. 2022;27:133-143. doi: 10.1142/9789811250477_0013.
Big Data neuroimaging collaborations including Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) integrated worldwide data to identify regional brain deficits in major depressive disorder (MDD). We evaluated the sensitivity of translating ENIGMA-defined MDD deficit patterns to the individual level. We treated ENIGMA MDD deficit patterns as a vector to gauge the similarity between individual and MDD patterns by calculating ENIGMA dot product (EDP). We analyzed the sensitivity and specificity of EDP in separating subjects with (1) subclinical depressive symptoms without a diagnosis of MDD, (2) single episode MDD, (3) recurrent MDD, and (4) controls free of neuropsychiatric disorders. We compared EDP to the Quantile Regression Index (QRI; a linear alternative to the brain age metric) and the global gray matter thickness and subcortical volumes and fractional anisotropy (FA) of water diffusion. We performed this analysis in a large epidemiological sample of UK Biobank (UKBB) participants (N=17,053/19,265 M/F). Group-average increases in depressive symptoms from controls to recurrent MDD was mirrored by EDP (r2=0.85), followed by FA (r2=0.81) and QRI (r2=0.56). Subjects with MDD showed worse performance on cognitive tests than controls with deficits observed for 3 out of 9 cognitive tests administered by the UKBB. We calculated correlations of EDP and other brain indices with measures of cognitive performance in controls. The correlation pattern between EDP and cognition in controls was similar (r2=0.75) to the pattern of cognitive differences in MDD. This suggests that the elevation in EDP, even in controls, is associated with cognitive performance - specifically in the MDD-affected domains. That specificity was missing for QRI, FA or other brain imaging indices. In summary, translating anatomically informed meta-analytic indices of similarity using a linear vector approach led to better sensitivity to depressive symptoms and cognitive patterns than whole-brain imaging measurements or an index of accelerated aging.
大数据神经影像学合作,包括通过元分析增强神经影像学遗传学(ENIGMA),整合了全球数据,以确定重度抑郁症(MDD)的区域性大脑缺陷。我们评估了将 ENIGMA 定义的 MDD 缺陷模式转化为个体水平的敏感性。我们将 ENIGMA MDD 缺陷模式视为矢量,通过计算 ENIGMA 点积(EDP)来衡量个体与 MDD 模式之间的相似性。我们分析了 EDP 在区分以下受试者方面的敏感性和特异性:(1)没有 MDD 诊断的亚临床抑郁症状,(2)单次发作 MDD,(3)复发性 MDD,和(4)无神经精神障碍的对照。我们将 EDP 与定量回归指数(QRI;大脑年龄指标的线性替代物)以及全脑灰质厚度和皮质下体积以及水扩散的各向异性分数(FA)进行了比较。我们在英国生物库(UKBB)参与者的大型流行病学样本中进行了此分析(N=17053/19265M/F)。从对照组到复发性 MDD,抑郁症状的平均增加与 EDP 相匹配(r2=0.85),其次是 FA(r2=0.81)和 QRI(r2=0.56)。与对照组相比,MDD 患者在认知测试中的表现更差,在 UKBB 进行的 9 项认知测试中有 3 项观察到缺陷。我们计算了 EDP 和其他大脑指标与对照组认知表现的相关性。在对照组中,EDP 与认知之间的相关模式(r2=0.75)与 MDD 中认知差异的模式相似。这表明,即使在对照组中,EDP 的升高也与认知表现相关-特别是在受 MDD 影响的领域。而 QRI、FA 或其他大脑成像指标则没有这种特异性。总之,使用线性向量方法翻译解剖学上相似的元分析指标,与全脑成像测量或加速老化指数相比,对抑郁症状和认知模式的敏感性更高。