Cognition and motion dysfunction‐associated brain functional network disruption in diabetic peripheral neuropathy

Author:

Xin Haotian1ORCID,Fu Yajie12ORCID,Wen Hongwei3ORCID,Feng Mengmeng1ORCID,Sui Chaofan4ORCID,Gao Yian4ORCID,Guo Lingfei4ORCID,Liang Changhu14ORCID

Affiliation:

1. Department of Radiology, Shandong Provincial Hospital Shandong University Jinan China

2. Department of Medical Ultrasound The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Medicine and Health Key Laboratory of Abdominal Medical Imaging Jinan China

3. Key Laboratory of Cognition and Personality (Ministry of Education), Faculty of Psychology Southwest University Chongqing China

4. Key Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging Ministry of Education; Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University Jinan China

Abstract

AbstractNeuroimaging studies have demonstrated extensive brain functional alterations in cognitive and motor functional areas in Type 2 diabetes mellitus (T2DM) with diabetic peripheral neuropathy (DPN), suggesting potential alterations in large‐scale brain networks related to DPN and associated cognition and motor dysfunction. In this study, using resting‐state functional connectivity (FC) and graph theory computational approaches, we investigated the topological disruptions of brain functional networks in 28 DPN, 43 T2DM without DPN (NDPN), and 32 healthy controls (HCs) and examined the correlations between altered network topological metrics and cognitive/motor function parameters in T2DM. For global topology, NDPN exhibited a significantly decreased shortest path length compared with HCs, suggesting increased efficient global integration. For regional topology, DPN and NDPN had separated topological reorganization of functional hubs compared with HCs. In addition, DPN showed significantly decreased nodal efficiency (Enodal), mainly in the bilateral superior occipital gyrus (SOG), right cuneus, middle temporal gyrus (MTG), and left inferior parietal gyrus (IPL), compared with NDPN, whereas NDPN showed significantly increased Enodal compared with HCs. Intriguingly, in T2DM patients, the Enodal of the right SOG was significantly negatively correlated with Toronto Clinical Scoring System scores, while the Enodal of the right postcentral gyrus (PoCG) and MTG were significantly positively correlated with Montreal Cognitive Assessment scores. Conclusively, DPN and NDPN patients had segregated disruptions in the brain functional network, which were related to cognition and motion dysfunctions. Our findings provide a theoretical basis for understanding the neurophysiological mechanism of DPN and its effective prevention and treatment in T2DM.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Medical and Health Science and Technology Development Project of Shandong Province

Publisher

Wiley

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