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Biotypes of major depressive disorder: Neuroimaging evidence from resting-state default mode network patterns. | LitMetric

Biotypes of major depressive disorder: Neuroimaging evidence from resting-state default mode network patterns.

Neuroimage Clin

Mental Health Center & Psychiatric Laboratory, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, Sichuan, China; West China Brain Research Centre, West China Hospital, Sichuan University, Chengdu 610041, Sichuan, China. Electronic address:

Published: June 2021

AI Article Synopsis

  • Major depressive disorder (MDD) is complex and can be divided into subtypes based on differences in brain connectivity within the default mode network (DMN), as revealed by a study involving 1,397 participants (690 MDD patients and 707 healthy controls).
  • Researchers used advanced data analysis methods, such as K-means and principal component analysis, to identify two distinct MDD subgroups—hyperDMN MDD (increased connectivity) and hypoDMN MDD (decreased connectivity)—which were consistently observed across multiple trials.
  • The discovery highlights the importance of understanding these neural subtypes, potentially guiding more personalized treatments for individuals with depression based on their specific connectivity patterns.

Article Abstract

Background: Major depressive disorder (MDD) is heterogeneous disorder associated with aberrant functional connectivity within the default mode network (DMN). This study focused on data-driven identification and validation of potential DMN-pattern-based MDD subtypes to parse heterogeneity of the disorder.

Methods: The sample comprised 1397 participants including 690 patients with MDD and 707 healthy controls (HC) registered from multiple sites based on the REST-meta-MDD Project in China. Baseline resting-state functional magnetic resonance imaging (rs-fMRI) data was recorded for each participant. Discriminative features were selected from DMN between patients and HC. Patient subgroups were defined by K-means and principle component analysis in the multi-site datasets and validated in an independent single-site dataset. Statistical significance of resultant clustering were confirmed. Demographic and clinical variables were compared between identified patient subgroups.

Results: Two MDD subgroups with differing functional connectivity profiles of DMN were identified in the multi-site datasets, and relatively stable in different validation samples. The predominant dysfunctional connectivity profiles were detected among superior frontal cortex, ventral medial prefrontal cortex, posterior cingulate cortex and precuneus, whereas one subgroup exhibited increases of connectivity (hyperDMN MDD) and another subgroup showed decreases of connectivity (hypoDMN MDD). The hyperDMN subgroup in the discovery dataset had age-related severity of depressive symptoms. Patient subgroups had comparable demographic and clinical symptom variables.

Conclusions: Findings suggest the existence of two neural subtypes of MDD associated with different dysfunctional DMN connectivity patterns, which may provide useful evidence for parsing heterogeneity of depression and be valuable to inform the search for personalized treatment strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724374PMC
http://dx.doi.org/10.1016/j.nicl.2020.102514DOI Listing

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