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Effects of Ketosis on Brain Function in Patients With T1DM

Not Applicable
Recruiting
Conditions
Type1diabetes
Interventions
Other: Standard carbohydrate diet
Other: Very low carbohydrate diet
Registration Number
NCT04219709
Lead Sponsor
Boston Children's Hospital
Brief Summary

The scientific goal of this study is to examine the effects of a ketogenic diet on hypoglycemia tolerance and brain function in people with type 1 diabetes mellitus (T1D) and to clarify the mechanistic role of ketones in this process. Glycemic management of T1D is typified by alternating periods of hyper- and hypo-glycemia. Because brain metabolism under usual conditions depends on glucose, acute hypoglycemia leads to immediate complications including impaired cognitive function and a counter-regulatory hormone response. Recurrent hypoglycemia is associated with functional and structural changes in the brain and contributes to the cognitive decline observed in individuals with diabetes. The state of nutritional ketosis (as it occurs during fasting or when following a ketogenic \[very low carbohydrate\] diet) may protect against these acute and chronic complications. As the body relies on fat metabolism, ketone bodies build up and provide an alternative fuel for the brain. Studies during hypoglycemia have shown better cognitive function and less hypoglycemia symptoms in the setting of nutritional ketosis or with ketone administration. This physiological benefit may have special relevance for people with T1D who experience hypoglycemia frequently. To date, no mechanistic studies have examined brain effects of nutritional ketosis in T1D; nor have any trials explored the potential relevance of this for diabetes care.

Detailed Description

To test the hypothesis that a ketogenic diet increases hypoglycemia tolerance and improves brain function and cognitive performance during hypoglycemia, the researchers propose a randomized mechanistic study using insulin infusions and neuroimaging. The study will leverage an existing randomized controlled trial (RCT) in 32 young adults with T1D who will receive a ketogenic vs a standard carbohydrate diet for 12 weeks. Researchers will conduct a euglycemic-hypoglycemic insulin clamp using a continuous infusion of insulin, along with a glucose infusion that is adjusted to keep blood glucose levels normal (90 mg/dL), followed by a slow drop to hypoglycemia (50 mg/dL). Researchers will assess activation and connectivity of relevant brain areas by magnetic resonance imaging (MRI). Using continuous imaging during the gradual glycemic descent from 90 mg/dL to 50 mg/dL, the researchers will establish the glycemic threshold at which the hypothalamus becomes activated. Using a combination of MRI modalities, they will assess brain activation and connectivity changes during hypoglycemia versus euglycemia, both during rest and in relation to a cognitive task. Brain findings will be integrated with physiologic (blood levels of glucose, ketones, free fatty acids, counter-regulatory hormones) and behavioral (reaction time, cognitive task performance, hypoglycemia symptoms scale) parameters. In additional studies, researchers will give an oral ketone drink to raise blood ketone levels in participants in the standard carbohydrate diet arm. They will perform the same insulin infusion and MRI investigations to clarify the mechanistic role of ketones in mediating brain activation patterns. Comparison will be between nutritional vs no ketosis, exogenous vs no ketosis, and nutritional vs exogenous ketosis.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Males and females with T1D for at least 1 year
  • Age 18 to 40 years
  • Tanner stage ≥ IV
  • BMI 18.5-35 kg/m2
  • Stable glycemic control (HbA1c 6.5-9%)
  • Use of a continuous glucose monitor (CGM)
  • Use of an insulin pump
  • Attendance of at least 1 diabetes care visit over the past 12 months (including virtual)
Exclusion Criteria
  • Ketoacidosis or severe hypoglycemia with seizure or coma in the past 6 months

  • Dietary restrictions or intolerances that are incompatible with the planned food deliveries, e.g. celiac disease, gastroparesis, certain food allergies

  • Following a weight-loss or otherwise restrictive diet

  • Vigorous exercise >2 hours on >3 days a week

  • History of an eating disorder or at risk for eating disorder, assessed by the Eating Disorders Diagnostic Scale (EDDS)

  • Major medical illness or use of medications other than insulin and metformin that could interfere with metabolic or glycemic variables

  • Significant psychiatric illness

  • Smoking, use of recreational drugs, or excessive alcohol consumption

  • Pregnancy or breastfeeding

  • Anemia

  • For participants who undergo MRI:

    1. Standard MRI exclusion criteria
    2. Irregular menses
    3. Use of psychotropic medication other than SSRIs or other mild antidepressant or anxiety medications (unless these medications are safe to be held for several days to allow for the acquisition of MRI data).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard dietStandard carbohydrate dietDietary Intervention, food delivery
Very low carbohydrate dietVery low carbohydrate dietDietary Intervention, food delivery
Primary Outcome Measures
NameTimeMethod
Glycemic threshold for hypothalamic activationDiet week 5-12

The blood glucose level at which hypothalamic activation is detected by continuous BOLD functional MRI during a 40 min glycemic descent from 90 to 50 mg/dL

Secondary Outcome Measures
NameTimeMethod
Response time changes during hypoglycemiaDiet week 5-12

Response time to a working-memory cognitive task (n-back) will be measured during hypoglycemia and compared to the response time in euglycemia

Blood glucose level at which participant reports symptoms of hypoglycemia.Diet week 5-12

Participants will be instructed to push a response button when they first notice any symptoms of hypoglycemia during the glycemic descent phase.

Functional connectivity changes in brain areas related to cognition during hypoglycemiaDiet week 5-12

Functional connectivity activation will be measured using resting state functional MRI during euglycemia and hypoglycemia and differences will be reported

Cognitive performance during hypoglycemiaDiet week 5-12

Response accuracy of a cognitive task (n-back) during hypoglycemia compared to euglycemia will be reported

Hypoglycemia symptomsDiet week 5-12

A Hypoglycemia Symptoms Scale comprising 6 autonomic/neurogenic (sweating, palpitations, trembling, weakness, nausea, and hunger) and 5 neuroglycopenic (drowsiness, confusion, difficulty concentrating, lightheadedness, and headache) symptoms will be used to assess each symptom on a 0-4 scale (higher scores indicate more symptoms) during euglycemia and hypoglycemia. Average scores for hypoglycemia symptoms overall, autonomic/neurogenic symptoms, and neuroglycopenic symptoms will be reported for each time point.

Task-related brain activation changes during hypoglycemia in brain areas related to cognitionDiet week 5-12

Task-related brain activation will be measured during a working memory task (n-back) by BOLD during euglycemia and hypoglycemia and differences will be reported

Resting brain activation changes in brain areas related to cognition during hypoglycemiaDiet week 5-12

Resting brain activation will be measured by arterial spin labeling (ASL) during euglycemia and hypoglycemia and differences will be reported

Trial Locations

Locations (1)

Boston Childrens Hospital

🇺🇸

Boston, Massachusetts, United States

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