Hypoglycemia is the limiting factor in the glycemic control of diabetes, causing morbidity and death. Recurrent hypoglycemia causes both defective glucose counterregulation and loss of hypoglycemic symptoms during subsequent hypoglycemia, constituting the clinical syndrome of hypoglycemia-associated autonomic failure (HAAF). The mechanisms underlying the signaling of these responses during hypoglycemia and the loss of these responses during HAAF are thought to involve the brain. To date no effective clinical method has shown to reduce the incidence of hypoglycemia without the risk of compromising glycemic control. Thus, a better understanding of the mechanisms underlying the loss of the hypoglycemic responses may help us identify new and innovative therapeutic targets. We hypothesize that there is hierarchical activation of several hypoglycemia-sensitive brain regions that form a functional network in response to declining blood glucose levels, and a potential loss of the connectivity in this network leads to HAAF in individuals with T1DM. With a multidisciplinary approach we will test this hypothesis, using integrated quantitative brain imaging measurements of regional blood flow (ASL-MRI) and functional connectivity (BOLD rs-fMRI) during hyperinsulinemic euglycemic (~90mg/dL) - stepped hypoglycemic (~65-55-45mg/dL) clamps in 20 type 1 diabetic (T1DM) patients with HAAF, 20 T1DM without HAAF and in 20 healthy young adults in a model of HAAF. By determining the changes in BOLD signal during HAAF in DM, we will identify a neuroimaging biomarker that characterizes the effects of HAAF in vivo in T1DM patients to predict outcomes in planned prospective interventional studies.

Public Health Relevance

Low blood sugar, or hypoglycemia, is the most common complication of living with diabetes. Episodes of low blood sugar can limit an individual's ability to achieve good glucose control and can cause death. Previous low blood sugars decrease an individual's symptoms and physical responses to a subsequent low blood sugar episode. It is unclear why this happens, but the brain is believed to regulate this process. Our goal is to use advanced neuroimaging methods to determine how the brain responds to low blood sugars in patients with Type 1 diabetes. Findings from these studies will establish a framework for potential therapeutic strategies to prevent and treat this condition and may lead to the development of neuroimaging biomarkers that could be used to predict outcomes in interventional studies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK101440-01A1
Application #
8886223
Study Section
Clinical and Integrative Diabetes and Obesity Study Section (CIDO)
Program Officer
Teff, Karen L
Project Start
2015-05-15
Project End
2020-03-31
Budget Start
2015-05-15
Budget End
2016-03-31
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Washington University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Lee, John J; Khoury, Nadia; Shackleford, Angela M et al. (2017) Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia. Diabetes 66:2964-2972
Semenkovich, K; Patel, P P; Pollock, A B et al. (2016) Academic abilities and glycaemic control in children and young people with Type 1 diabetes mellitus. Diabet Med 33:668-73