Type 2 Diabetes and Biomarkers of Brain Structure, Perfusion, Metabolism, and Function in Late Mid-Life: A Multimodal Discordant Twin Study

Author:

Karayiannis Christopher C.12,Srikanth Velandai234,Beare Richard235,Mehta Hemal67,Gillies Mark7,Phan Thanh G.8,Xu Zheng Yang69,Chen Christine1011,Moran Chris2341213

Affiliation:

1. Department of Medicine, Peninsula Health, Melbourne, Australia

2. Peninsula Clinical School, Central Clinical School, Monash University, Melbourne, Australia

3. National Centre for Healthy Ageing, Melbourne, Australia

4. Department of Geriatric Medicine, Peninsula Health, Melbourne, Australia

5. Developmental Imaging, Murdoch Children’s Research Institute, Melbourne, Australia

6. Royal Free London NHS Foundation Trust, London, UK

7. Macular Research Group, University of Sydney, Sydney, Australia

8. Stroke and Ageing Research Centre, School of Clinical Sciences, Monash University, Melbourne, Australia

9. UCL Medical School, London, UK

10. Ophthalmology Department, Monash Health, Melbourne, Australia

11. Department of Surgery, School of Clinical Sciences, Monash University, Melbourne, Australia

12. Department of Aged Care, Alfred Health, Melbourne, Australia

13. School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia

Abstract

Background: Type 2 diabetes (T2D) is associated with an increased risk of dementia and early features may become evident even in mid-life. Characterizing these early features comprehensively requires multiple measurement modalities and careful selection of participants with and without T2D. Objective: We conducted a cross-sectional multimodal imaging study of T2D-discordant twins in late mid-life to provide insights into underlying mechanisms. Methods: Measurements included computerized cognitive battery, brain MRI (including arterial spin labelling, diffusion tensor, resting state functional), fluorodeoxyglucose (FDG)-PET, and retinal optical coherence tomography. Results: There were 23 pairs, mean age 63.7 (±6.1) years. In global analyses, T2D was associated with poorer attention (β= –0.45, p <0.001) and with reduced FDG uptake (β= –5.04, p = 0.02), but not with cortical thickness (p = 0.71), total brain volume (p = 0.51), fractional anisotropy (p = 0.15), mean diffusivity (p = 0.34), or resting state activity (p = 0.4). Higher FDG uptake was associated with better attention (β= 3.19, p = 0.01) but not with other cognitive domains. In regional analyses, T2D was associated with lower accumbens volume (β= –44, p = 0.0004) which was in turn associated with poorer attention. Conclusion: T2D-related brain dysfunction in mid-life manifests as attentional loss accompanied by evidence of subtle neurodegeneration and global reduction in cerebral metabolism, in the absence of overt cerebrovascular disease.

Publisher

IOS Press

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