Joint resting state and structural networks characterize pediatric bipolar patients compared to healthy controls: a
Xiaoping Yi1, Mingzhao Ma2, Xueying Wang3
1Department of Radiology, Xiangya Hospital, Central South University, Changsha 410008, Hunan, PR China; Clinical Research Center (CRC), Medical Pathology Center (MPC), Cancer Early Detection and Treatment Center (CEDTC) and Translational Medicine Research Center (TMRC), Chongqing University Three Gorges Hospital, Chongqing University, Chongqing 404000, PR China; School of Medicine, Chongqing University, Chongqing 400030, PR China; National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology, Xiangya Hospital, Changsha 410008, Hunan, PR China.
Insights
Pediatric bipolar disorder (PBD) shows distinct brain differences. Functional and structural abnormalities in PBD patients were identified using MRI, offering new insights into neurobiology.
Area of Science:
- Neuroscience
- Psychiatry
- Medical Imaging
Background:
- Pediatric bipolar disorder (PBD) is a severe mental health condition with limited understanding of its neurobiological underpinnings.
- Distinguishing between PBD type I and type II subtypes is challenging, yet crucial for targeted treatment.
- Resting-state functional MRI and structural MRI offer potential biomarkers for PBD.
Purpose of the Study:
- To investigate functional and structural brain abnormalities in pediatric bipolar disorder (PBD) using resting-state functional MRI and structural MRI.
- To compare neurobiological differences between PBD patients and healthy controls (HC).
- To explore variations between PBD type I and type II, and their correlation with depressive symptoms.
Main Methods:
- Utilized transposed Independent Vector Analysis (tIVA), a data fusion unsupervised machine learning approach.
- Analyzed Resting state Regional Homogeneity (ReHo) and grey matter concentration (GMC) data from 58 PBD patients and 21 healthy controls.
- Employed MRI scans to assess brain activity and structure.
Main Results:
- Identified two distinct brain networks differing between PBD patients and HC: one with higher ReHo/GMC in fronto-medial regions (PBD > HC), and another with lower ReHo/GMC in temporo-posterior regions, insula, caudate, and precuneus (PBD < HC).
- Found two networks differentiating PBD type I from type II: an occipito-cerebellar network with increased ReHo/GMC in type I, and a fronto-parietal network with decreased ReHo/GMC in type I.
- Observed a positive correlation between the fronto-medial network abnormalities and depression scores in PBD patients.
Conclusions:
- The study reveals significant functional and structural brain alterations in pediatric bipolar disorder, differentiating it from healthy controls.
- Neurobiological differences exist between PBD type I and type II, suggesting distinct underlying pathophysiology.
- These findings provide novel insights into the neurobiology of PBD and its subtypes, potentially aiding in biomarker development.
Abstract:
Pediatric bipolar disorder (PBD) is a highly debilitating condition, characterized by alternating episodes of mania and depression, with intervening periods of remission. Limited information is available about the functional and structural abnormalities in PBD, particularly when comparing type I with type II subtypes. Resting-state brain activity and structural grey matter, assessed through MRI, may provide insight into the neurobiological biomarkers of this disorder. In this study, Resting state Regional Homogeneity (ReHo) and grey matter concentration (GMC) data of 58 PBD patients, and 21 healthy controls matched for age, gender, education and IQ, were analyzed in a data fusion unsupervised machine learning approach known as transposed Independent Vector Analysis. Two networks significantly differed between BPD and HC. The first network included fronto- medial regions, such as the medial and superior frontal gyrus, the cingulate, and displayed higher ReHo and GMC values in PBD compared to HC. The second network included temporo-posterior regions, as well as the insula, the caudate and the precuneus and displayed lower ReHo and GMC values in PBD compared to HC. Additionally, two networks differ between type-I vs type-II in PBD: an occipito-cerebellar network with increased ReHo and GMC in type-I compared to type-II, and a fronto-parietal network with decreased ReHo and GMC in type-I compared to type-II. Of note, the first network positively correlated with depression scores. These findings shed new light on the functional and structural abnormalities displayed by pediatric bipolar patients.
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