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糖尿病性神经病变中因果性中枢神经网络重塑:一项磁共振成像与功能磁共振成像整合研究

Causal Central Network Remodeling in Diabetic Neuropathy: An Integrated MR-fMRI Study.

作者信息

Li Xiya, Gao Ling

机构信息

Department of Endocrinology and Metabolism, Renmin Hospital, Wuhan University, Wuhan, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2025 Aug 9;18:2753-2765. doi: 10.2147/DMSO.S525219. eCollection 2025.

Abstract

PURPOSE

Diabetic peripheral neuropathy (DPN) is traditionally viewed as a peripheral disorder, yet emerging evidence implicates central nervous system (CNS) network dysfunction in its pathogenesis, though causal mechanisms remain incompletely understood.

METHODS

Bidirectional two-sample Mendelian randomization (MR) analysis examined causal relationships between Resting-State Functional Magnetic Resonance Imaging (rs-fMRI) phenotypes (n=34,691) and DPN (n=96,474). For validation, amplitude of low-frequency fluctuation (ALFF) and functional connectivity (FC) analyses were conducted using rs-fMRI scans from DPN patients (n=16), diabetic controls without DPN (NDPN, n=24), and healthy controls (HC, n=20).

RESULTS

Bidirectional MR demonstrated that: (a) reduced default mode-visual network connectivity causally elevates DPN risk (OR=0.61, P=0.04); (b) DPN promotes subcortical-cerebellar hyperconnectivity (OR=1.04, P=0.01). DPN patients exhibited significantly higher age, triglyceride levels, pain scores, and cognitive impairment relative to comparison groups (all P<0.001). Neuroimaging identified increased ALFF in the left superior frontal gyrus (LSFG) (AUC=0.79, P<0.05), which correlated positively with disease duration, accompanied by decoupled FC with the lingual gyrus but enhanced FC with the precuneus.

CONCLUSION

This study establishes DPN as a CNS-periphery integrated network disorder: genetic drivers disrupt default mode-visual integration, while compensatory subcortical-cerebellar hyperconnectivity stabilizes motor function via adaptive mechanisms. The LSFG emerges as a neuroadaptive hub, where elevated ALFF and connectivity reorganization (↓lingual gyrus/↑precuneus) reflect dynamic rebalancing between impaired basic vision and enhanced visuospatial processing. These findings redefine DPN pathogenesis beyond pure peripheral neurodegeneration, providing a theoretical foundation for early detection and circuit-targeted neuromodulation therapies.

摘要

目的

糖尿病周围神经病变(DPN)传统上被视为一种周围性疾病,但新出现的证据表明中枢神经系统(CNS)网络功能障碍参与其发病机制,尽管因果机制仍未完全明确。

方法

双向两样本孟德尔随机化(MR)分析研究了静息态功能磁共振成像(rs-fMRI)表型(n = 34,691)与DPN(n = 96,474)之间的因果关系。为进行验证,使用来自DPN患者(n = 16)、无DPN的糖尿病对照(NDPN,n = 24)和健康对照(HC,n = 20)的rs-fMRI扫描进行低频振幅(ALFF)和功能连接(FC)分析。

结果

双向MR表明:(a)默认模式-视觉网络连接性降低会因果性地增加DPN风险(OR = 0.61,P = 0.04);(b)DPN会促进皮质下-小脑高连接性(OR = 1.04,P = 0.01)。与对照组相比,DPN患者的年龄、甘油三酯水平、疼痛评分和认知障碍显著更高(均P < 0.001)。神经影像学检查发现左侧额上回(LSFG)的ALFF增加(AUC = 0.79,P < 0.05),其与病程呈正相关,同时与舌回的FC解耦,但与楔前叶的FC增强。

结论

本研究将DPN确立为一种中枢神经系统-外周整合网络疾病:基因驱动因素破坏默认模式-视觉整合,而代偿性皮质下-小脑高连接性通过适应性机制稳定运动功能。LSFG成为一个神经适应性枢纽,其中升高的ALFF和连接性重组(舌回↓/楔前叶↑)反映了受损的基本视觉与增强的视觉空间处理之间的动态重新平衡。这些发现重新定义了DPN的发病机制,超越了单纯的外周神经退行性变,为早期检测和针对神经回路的神经调节治疗提供了理论基础。

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