Abnormal dynamics of resting-state functional activity and couplings in postpartum depression with and without anxiety. (17th February 2022)

• Record Type: Journal Article
• Authors: Cheng, Bochao; Wang, Xiuli; Roberts, Neil; Zhou, Yushan; Wang, Song; Deng, Pengcheng; Meng, Yajing; Deng, Wei; Wang, Jiaojian
• Is Part Of: Cerebral cortex. Volume 32:Number 24(2022)
• Page Start: 5597
• Page End: 5608
• Publication Date: 2022-02-17
• Subjects: dynamic amplitude of low-frequency fluctuation -- dynamic functional connectivity -- postpartum depression -- postpartum depression with anxiety -- resting-state fMRI; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhac038
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: Postpartum depression (PPD) and PPD comorbid with anxiety (PPD-A) are highly prevalent and severe mental health problems in postnatal women. PPD and PPD-A share similar pathopsychological features, leading to ongoing debates regarding the diagnostic and neurobiological uniqueness. This paper aims to delineate common and disorder-specific neural underpinnings and potential treatment targets for PPD and PPD-A by characterizing functional dynamics with resting-state functional magnetic resonance imaging in 138 participants (45 first-episode, treatment-naïve PPD; 31 PDD-A patients; and 62 healthy postnatal women [HPW]). PPD-A group showed specifically increased dynamic amplitude of low-frequency fluctuation in the subgenual anterior cingulate cortex (sgACC) and increased dynamic functional connectivity (dFC) between the sgACC and superior temporal sulcus. PPD group exhibited specifically increased static FC (sFC) between the sgACC and ventral anterior insula. Common disrupted sFC between the sgACC and middle temporal gyrus was found in both PPD and PPD-A patients. Interestingly, dynamic changes in dFC between the sgACC and superior temporal gyrus could differentiate PPD, PPD-A, and HPW. Our study presents initial evidence on specifically abnormal functional dynamics of limbic, emotion regulation, and social cognition systems in patients with PDD and PPD-A, which may facilitate understanding neurophysiological mechanisms, diagnosis, and treatment for PPD and PPD-A.