Generalizable stratification based on thalamo-somatomotor functional connectivity predicts responses to antidepressants in patients with depression.

IF 10.1 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yuto Kashiwagi, Tomoki Tokuda, Yuji Takahara, Yukiko Masaki, Yuki Sakai, Junichiro Yoshimoto, Ayumu Yamashita, Toshinori Yoshioka, Koichi Ogawa, Go Okada, Yasumasa Okamoto, Mitsuo Kawato, Okito Yamashita
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Abstract

Major depressive disorder (MDD) is diagnosed based on signs and symptoms without relying on physical, biological, or cognitive tests. Patients with MDD exhibit a wide range of complex symptoms, and diverse underlying neurobiological backgrounds have been assumed. If biomarkers can stratify patients with MDD into biologically homogeneous subtypes, personalized precision medicine would be within reach. Some studies have used resting-state functional connectivity (rs-FC) to stratify and predict treatment responses for MDD subtypes. However, few studies have demonstrated the reproducibility (i.e., generalizability) of stratification biomarkers in independent validation cohorts. Lack of generalizability may be due to inherent measurement and sampling biases in functional magnetic resonance imaging (fMRI) data and overfitting to discovery cohorts. To address this problem, we previously constructed a multisite, multidisorder fMRI database from thousands of participants, proposed a hierarchical supervised-unsupervised learning strategy, and developed generalizable diagnostic biomarkers of MDD via supervised learning. Using unsupervised learning, we constructed here stratification biomarkers for patients with MDD based on subsets of the top-ranked rs-FCs in MDD diagnostic biomarkers. We utilized two multisite datasets, constructed stratification biomarkers, and identified the most stable biomarker. The identified biomarker was based on several rs-FCs between the thalamus and postcentral gyrus. MDD subtypes stratified by this biomarker showed significantly different responsiveness to treatment with a selective serotonin reuptake inhibitor. By narrowing down the feature dimensions, we avoided overfitting to the training data and successfully constructed a generalizable stratification biomarker. This biomarker might have the potential to facilitate personalized precision medicine for patients with MDD.

基于丘脑-躯体运动功能连通性的可概括分层预测抑郁症患者对抗抑郁药的反应。
重度抑郁症(MDD)的诊断是基于体征和症状,而不依赖于身体、生物或认知测试。重度抑郁症患者表现出广泛的复杂症状,并且假定其潜在的神经生物学背景多种多样。如果生物标志物可以将重度抑郁症患者划分为生物学上同质的亚型,个性化的精准医疗将触手可及。一些研究已经使用静息状态功能连接(rs-FC)来分层和预测MDD亚型的治疗反应。然而,很少有研究证明了分层生物标志物在独立验证队列中的可重复性(即普遍性)。缺乏通用性可能是由于功能磁共振成像(fMRI)数据固有的测量和抽样偏差以及对发现队列的过度拟合。为了解决这个问题,我们之前从数千名参与者中构建了一个多站点、多障碍的fMRI数据库,提出了一种分层监督-无监督学习策略,并通过监督学习开发了可推广的MDD诊断生物标志物。使用无监督学习,我们基于MDD诊断生物标志物中排名最高的rs- fc子集构建了MDD患者的分层生物标志物。我们利用两个多位点数据集,构建了分层生物标志物,并确定了最稳定的生物标志物。所鉴定的生物标志物是基于丘脑和中央后回之间的几个rs- fc。通过该生物标志物分层的MDD亚型对选择性5 -羟色胺再摄取抑制剂的治疗表现出显著不同的反应性。通过缩小特征维度,我们避免了与训练数据的过拟合,并成功构建了一个可推广的分层生物标志物。这种生物标志物可能有潜力为重度抑郁症患者提供个性化的精准医疗。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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