Disrupted subject‐specific gray matter network properties and cognitive dysfunction in type 1 diabetes patients with and without proliferative retinopathy. Issue 3 (23rd December 2015)

• Record Type: Journal Article
• Authors: van Duinkerken, Eelco; Ijzerman, Richard G.; Klein, Martin; Moll, Annette C.; Snoek, Frank J.; Scheltens, Philip; Pouwels, Petra J.W.; Barkhof, Frederik; Diamant, Michaela; Tijms, Betty M.
• Is Part Of: Human brain mapping. Volume 37:Issue 3(2016:Mar.)
• Page Start: 1194
• Page End: 1208
• Publication Date: 2015-12-23
• Subjects: neuroimaging -- graph theory -- cognition -- small worldness -- type 1 diabetes -- microangiopathy; Brain mapping -- Periodicals; 611.81
• DOI: 10.1002/hbm.23096
• Languages: English
• ISSNs: 1065-9471

Abstract

Abstract: Introduction: Type 1 diabetes mellitus (T1DM) patients, especially with concomitant microvascular disease, such as proliferative retinopathy, have an increased risk of cognitive deficits. Local cortical gray matter volume reductions only partially explain these cognitive dysfunctions, possibly because volume reductions do not take into account the complex connectivity structure of the brain. This study aimed to identify gray matter network alterations in relation to cognition in T1DM. Methods : We investigated if subject‐specific structural gray matter network properties, constructed from T1‐weighted MRI scans, were different between T1DM patients with ( n = 51) and without ( n = 53) proliferative retinopathy versus controls ( n = 49), and were associated to cognitive decrements and fractional anisotropy, as measured by voxel‐based TBSS. Global normalized and local (45 bilateral anatomical regions) clustering coefficient and path length were assessed. These network properties measure how the organization of connections in a network differs from that of randomly connected networks. Results : Global gray matter network topology was more randomly organized in both T1DM patient groups versus controls, with the largest effects seen in patients with proliferative retinopathy. Lower local path length values were widely distributed throughout the brain. Lower local clustering was observed in the middle frontal, postcentral, and occipital areas. Complex network topology explained up to 20% of the variance of cognitive decrements, beyond other predictors. Exploratory analyses showed that lower fractional anisotropy was associated with a more random gray matter network organization. Conclusion : T1DM and proliferative retinopathy affect cortical network organization that may consequently contribute to clinically relevant changes in cognitive functioning in these patients. Hum Brain Mapp 37:1194–1208, 2016 . © 2015 Wiley Periodicals, Inc .