Resting-State Brain Functional Connectivity Is Altered in Type 2 Diabetes

Author:

Musen Gail12,Jacobson Alan M.123,Bolo Nicolas R.245,Simonson Donald C.67,Shenton Martha E.28910,McCartney Richard L.1,Flores Veronica L.1,Hoogenboom Wouter S.19

Affiliation:

1. Research Division, Joslin Diabetes Center, Boston, Massachusetts

2. Department of Psychiatry, Harvard Medical School, Boston, Massachusetts

3. Winthrop University Hospital, Mineola, New York

4. Department of Psychiatry, Beth Israel Deaconess Medical Center, Boston, Massachusetts

5. Brain Imaging Center, McLean Hospital, Belmont, Massachusetts

6. Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women’s Hospital, Boston, Massachusetts

7. Department of Medicine, Harvard Medical School, Boston, Massachusetts

8. Departments of Psychiatry, Psychiatry and Behavioral Science Imaging,, Brigham and Women’s Hospital, Boston, Massachusetts

9. Psychiatry Neuroimaging Laboratory, Brigham and Women’s Hospital, Boston, Massachusetts

10. Clinical Neuroscience Division, Laboratory of Neuroscience, VA Boston Healthcare System, Harvard Medical School, Brockton, Massachusetts

Abstract

Type 2 diabetes mellitus (T2DM) is a risk factor for Alzheimer disease (AD). Populations at risk for AD show altered brain activity in the default mode network (DMN) before cognitive dysfunction. We evaluated this brain pattern in T2DM patients. We compared T2DM patients (n = 10, age = 56 ± 2.2 years, fasting plasma glucose [FPG] = 8.4 ± 1.3 mmol/L, HbA1c = 7.5 ± 0.54%) with nondiabetic age-matched control subjects (n = 11, age = 54 ± 1.8 years, FPG = 4.8 ± 0.2 mmol/L) using resting-state functional magnetic resonance imaging to evaluate functional connectivity strength among DMN regions. We also evaluated hippocampal volume, cognition, and insulin sensitivity by homeostasis model assessment of insulin resistance (HOMA-IR). Control subjects showed stronger correlations versus T2DM patients in the DMN between the seed (posterior cingulate) and bilateral middle temporal gyrus (β = 0.67 vs. 0.43), the right inferior and left medial frontal gyri (β = 0.75 vs. 0.54), and the left thalamus (β = 0.59 vs. 0.37), respectively, with no group differences in cognition or hippocampal size. In T2DM patients, HOMA-IR was inversely correlated with functional connectivity in the right inferior frontal gyrus and precuneus. T2DM patients showed reduced functional connectivity in the DMN compared with control subjects, which was associated with insulin resistance in selected brain regions, but there were no group effects of brain structure or cognition.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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