Insulin resistance predicts brain amyloid deposition in late middle-aged adults

Alzheimers Dement. 2015 May;11(5):504-510.e1. doi: 10.1016/j.jalz.2014.03.011. Epub 2014 Jul 17.

Abstract

Background: Insulin resistance (IR) increases Alzheimer's disease (AD) risk. IR is related to greater amyloid burden post-mortem and increased deposition within areas affected by early AD. No studies have examined if IR is associated with an in vivo index of amyloid in the human brain in late middle-aged participants at risk for AD.

Methods: Asymptomatic, late middle-aged adults (N = 186) from the Wisconsin Registry for Alzheimer's Prevention underwent [C-11]Pittsburgh compound B (PiB) positron emission tomography. The cross-sectional design tested the interaction between insulin resistance and glycemic status on PiB distribution volume ratio in three regions of interest (frontal, parietal, and temporal).

Results: In participants with normoglycemia but not hyperglycemia, higher insulin resistance corresponded to higher PiB uptake in frontal and temporal areas, reflecting increased amyloid deposition.

Conclusions: This is the first human study to demonstrate that insulin resistance may contribute to amyloid deposition in brain regions affected by AD.

Keywords: Alzheimer's disease; Amyloid; Cognitively normal; Insulin resistance; PiB; Prefrontal.

Publication types

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

MeSH terms

  • Aged
  • Amyloid / metabolism*
  • Aniline Compounds / pharmacokinetics
  • Apolipoproteins E / genetics
  • Body Mass Index
  • Brain / diagnostic imaging
  • Brain / metabolism*
  • Female
  • Humans
  • Hyperglycemia / complications
  • Imaging, Three-Dimensional
  • Insulin Resistance*
  • Magnetic Resonance Imaging
  • Male
  • Mental Status Schedule
  • Middle Aged
  • Positron-Emission Tomography
  • Predictive Value of Tests
  • Thiazoles / pharmacokinetics

Substances

  • 2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole
  • Amyloid
  • Aniline Compounds
  • Apolipoproteins E
  • Thiazoles