Aberrant modular segregation of brain networks in female patients with bulimia nervosa

Author:

Lan Zhihui1,Zhu Lin‐lin1,Wu Yan‐kun1,Yang Jing‐jing2,Li Ji‐tao1,Zeng Ya‐wei3,Li Ke3,Kong Qing‐mei1,Su Yun‐Ai1,Si Tianmei1ORCID

Affiliation:

1. Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University) National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital) Beijing China

2. School of Mental Health Wenzhou Medical University Wenzhou Zhejiang China

3. Department of Radiology PLA Strategic support Force Characteristic Medical Center Beijing China

Abstract

AbstractObjectiveBulimia nervosa (BN) is an eating disorder associated with the dysfunction of intrinsic brain networks. However, whether the network disruptions in BN patients manifest as dysconnectivity or imbalances of network modular segregation remains unclear.MethodWe collected data from 41 women with BN and 41 matched healthy control (HC) women. We performed graph theory analysis based on resting‐state functional magnetic resonance imaging (RS‐fMRI) data; then, we computed the participation coefficient (PC) among brain modules to characterize the modular segregation for the BN and HC groups. The number of intra‐ and inter‐modular connections was calculated to explain the PC changes. Additionally, we examined the potential associations of the measures mentioned above with clinical variables within the BN group.ResultsCompared with the HC group, the BN group showed significantly decreased PC in the fronto‐parietal network (FPN), cingulo‐opercular network (CON), and cerebellum (Cere). Additionally, the number of intra‐modular connections of the default mode network (DMN) and the number of the inter‐modular connections between the DMN and CON, FPN and Cere, and CON and Cere in the BN group were lower than those in the HC group. The nodal level analysis showed that the BN group had a decreased PC of the anterior prefrontal cortex (aPFC), dorsal frontal cortex (dFC), inferior parietal lobule (IPL), thalamus, and angular gyrus. Further, these metrics were significantly correlated with clinical variables in the BN group.DiscussionThese findings may provide novel insights to capture atypical topologies associated with pathophysiology mechanisms and clinical symptoms underlying BN.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Psychiatry and Mental health

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