The resting perfusion pattern associates with functional decline in type 2 diabetes

Neurobiol Aging. 2017 Dec:60:192-202. doi: 10.1016/j.neurobiolaging.2017.09.004. Epub 2017 Sep 14.

Abstract

We investigated the relationships between cerebral blood flow (CBF), cognitive, and mobility decline in type 2 diabetes mellitus (T2DM) over a 2-year period. Seventy-three participants (41 T2DM and 32 controls) were evaluated using volumetric CBF with arterial spin labeling perfusion magnetic resonance imaging at baseline and at the 2-year follow-up. Regions with significant CBF differences between T2DM participants and controls at baseline were detected using voxel-wise analysis. Correlation analysis was performed to investigate the association between regional CBF and cognitive or mobility performance over the 2-year span. Compared to controls, participants with T2DM had decreased CBF in the resting-state default mode, visual, and cerebellum networks. Greater decrease in longitudinal CBF values at these regions over a 2-year span was associated with worse gait, memory and executive functions, and higher baseline insulin resistance and worse baseline cognitive performance. In T2DM, impairment of resting regional perfusion is closely related to worse cognitive and mobility performance. Insulin resistance may further contribute to regional perfusion deficit in T2DM.

Keywords: Arterial spin labeling MRI; Cerebral blood flow; Cognitive impairment; Insulin resistance; Type 2 diabetes mellitus; Voxel-based analyses.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cerebrovascular Circulation / physiology*
  • Cognition / physiology*
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Diabetes Mellitus, Type 2 / psychology*
  • Executive Function / physiology
  • Female
  • Gait / physiology
  • Humans
  • Insulin Resistance / physiology
  • Male
  • Memory / physiology
  • Middle Aged
  • Motor Activity / physiology*
  • Rest / physiology*
  • Time Factors