Intermittent Calorie Restriction, Insulin Resistance, and Biomarkers of Brain Function

NCT ID: NCT02460783

Last Updated: 2024-04-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 129 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-06-22
• Study Completion Date: 2022-12-23

Brief Summary

Background:

• Insulin removes sugar from the blood to use for energy. Insulin resistance means that cells may not respond to insulin normally. It can lead to serious diseases. Researchers want to see how diet affects insulin resistance, weight, and brain chemicals related to Alzheimer s disease.

Objectives:

• To compare two forms of diet and their effects on insulin resistance and the brain.

Eligibility:

• Women ages 55 70 with insulin resistance.

Design:

• This study requires 6 clinic visits over 9 12 weeks. Participants must fast before visits.
• Visit 1, screening:
• Medical history, physical exam, and blood and urine tests.
• Participants will get a wrist device to wear for 4 days.
• Visit 2:
• Weight and waist measurement.
• Blood drawn.
• Questionnaires and thinking tests.
• Lumbar puncture. Skin will be numbed and a needle inserted between bones in the back will remove <TAB>fluid.
• Participants will drink a nutrition shake. Blood will be taken 12 times over 4 <TAB>hours through a thin tube in <TAB>the arm.
• Brain MRI. Participants will lie on a table that slides in and out of a cylinder in a strong magnetic field. <TAB>They will have a coil on their head and may do tasks.
• Participants will get advice about healthy eating and be randomly put in one of 2 groups. One group will get <TAB>nutrition shakes to drink.
• Visits 3 5:
• Weight and waist measurements, vital signs, blood draw, and questionnaires.
• Between visits, participants will get a call or email to check how they are doing.
• Visit 6: Repeat of visit 1.
• Participants will wear the wrist device for 4 more days, have a follow-up contact, then the study is finished.

Detailed Description

Being overweight or obese can cause insulin resistance (IR), which is defined as reduced responsiveness to insulin by the cells of various tissues or organs. IR at midlife increases the risk of developing Alzheimer s disease (AD). We recently discovered novel biomarkers of brain IR (altered Tyr and Ser phosphorylated forms of insulin receptor substrate 1; IRS-1) in plasma exosomes enriched for neuronal origin. Moreover, IR is associated with AD biomarkers including deficits in resting state brain activity and cognitive performance. Calorie restriction is defined as consuming fewer calories than what is considered normal without a lack of nutrients. A certain type of calorie restriction, in which one consumes 500-600 calories a day for two consecutive days, followed by non-restricted eating for 5 days (5-2 CR), has been shown to lower peripheral insulin resistance effectively. Effects of CR and lowering peripheral IR on brain IR and cognition are unknown. The goal of this exploratory pilot study is to provide proof-of-concept that 5-2 CR at midlife can reverse brain IR, lower peripheral IR, improve cognitive performance, and increase brain activation at rest and during tasks. Specifically, we will study the effects of 8 weeks of 5-2 CR versus a control dietary intervention on brain and peripheral IR, memory and executive function, resting state default mode network activity, brain metabolism, and AD biomarkers. Forty overweight to obese women and men (between 55 and 70 years of age) will be randomized 1:1 into 5-2 CR and control groups. In the 5-2 CR group, participants will be offered healthy living dietary counseling at baseline, which they will be instructed to implement for five days/week. For each of the other two consecutive days/week, they will consume two shakes (Boost , CWI Medical), providing a total of 480 Kcal/day. In the control group, participants will be offered healthy living dietary counseling at baseline, which they will be asked to implement for every day of the week. Participants will undergo screening including a history and physical examination, calculation of Body Mass Index (BMI, which must be greater than or equal to 27) and a blood draw for insulin and glucose to determine whether they have insulin resistance. If participants meet eligibility criteria, they will continue with a baseline visit involving anthropometric measures, questionnaires, tests of cognitive function, brain MRI, blood draws for plasma and peripheral blood mononuclear cells, and lumbar puncture for cerebrospinal fluid biomarkers of AD. After 8 weeks, we will collect the same measures. To assess and reinforce compliance with their respective diet, participants will come into the clinic every 2 weeks to discuss compliance, measure their body weight and perform blood draws for measurement of ketones to objectively confirm energy restriction for the 5-2 CR group. We will also contact participants every week to further ensure compliance. To assess the effects of the diets on physical activity, participants will be asked to wear an accelerometer for 96 hours before and after they are on the diet.

Conditions

Alzheimer's Disease; Obesity; Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

5-2 CR

Healthy living diet for 5 days/week; Calorie Restriction (480 Kcal in the form of a shake) for 2 days/week.

Group Type: EXPERIMENTAL

Boost (R) 5-2 diet

Intervention Type: OTHER

Regular diet for 5 days/week; Calorie Restriction (480 Kcal in the form of a shake) for 2 days/week. Supplement providing 240 Kcal per shake. Participant takes 2 shakes per calorie restriction day.

Healthy Living Diet

Healthy living diet for 7 days/week

Group Type: ACTIVE_COMPARATOR

Healthy Living Diet

Intervention Type: OTHER

Counseling and educational material on diet portion, consistency

Interventions

Boost (R) 5-2 diet

Regular diet for 5 days/week; Calorie Restriction (480 Kcal in the form of a shake) for 2 days/week. Supplement providing 240 Kcal per shake. Participant takes 2 shakes per calorie restriction day.

Intervention Type: OTHER

Healthy Living Diet

Counseling and educational material on diet portion, consistency

Intervention Type: OTHER

Other Intervention Names

5-2 Intermittent Fasting (IF)

Eligibility Criteria

Inclusion Criteria

• BMI greater than or equal to 27; in addition, weight less than or equal to 350 lbs (weight limit for MRI scanner);
• Age of 55-70 years;
• HOMA-IR greater than or equal to 1.8;
• MMSE greater than or equal to 26

EXCLUSION CRITEIRA:

• History of clinically significant cardiovascular disease for the purpose of this study, such as chronic heart failure, coronary disease, cardiomyopathy, clinically significant cardiac valvular disease or clinically significant peripheral vascular disease. Cardiovascular conditions that are clinically non-significant for the purpose of this study, such as controlled hypertension, minor EKG abnormalities, mitral valve prolapse or benign murmurs are permissible;
• History of clinically significant stroke or other neurological disease of the central nervous system;
• History of substance abuse in the past 6 months or positive urine drug screen;
• History of clinically significant endocrine disorders (common mild endocrine disorders, such as untreated subclinical hypothyroidism with TSH < 10 mU/l or successfully treated hypothyroidism may be allowed);
• History of eating disorders, significant GI disorders or malabsorption disorders;
• History of type 2 diabetes; and/or use of anti-diabetes medications or insulin; and/or type 2 diabetes diagnosed during the screening visit based on fasting glucose > 125 mg/dL;
• History of hypoglycemia; and/or a fasting glucose < 70 mg/dL during the screening visit.
• Current use of systemic corticosteroids;
• Positive screening tests for HIV, HCV or HBV;
• Hematocrit less than 35% or hemoglobin less than 11 mg/dL;
• ALT or AST > 1.5 times the upper normal limit;
• Contraindications for MRI (pacemakers, ferrous metal implants or shrapnel in or around the head, etc.).
• Contraindications to LP, such as Coumadin, coagulopathy (international normalized ratio, or INR > 1.5; prothrombin time (PT), partial prothrombin time (PTT) > 1.5 x upper normal limit). Aspirin 81 mg qd is allowed. Aspirin up to 325 mg qd is allowed, if withheld for 7 days prior to the LP.
• Pregnancy or nursing.
• Refusal to consent to genetic testing for APOE.

• Minimum Eligible Age: 55 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute on Aging (NIA)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dimitrios I Kapogiannis, M.D.

Role: PRINCIPAL_INVESTIGATOR

National Institute on Aging (NIA)

Locations

National Institute of Aging, Clinical Research Unit

Baltimore, Maryland, United States

Countries

United States

References

Kapogiannis D, Manolopoulos A, Mullins R, Avgerinos K, Delgado-Peraza F, Mustapic M, Nogueras-Ortiz C, Yao PJ, Pucha KA, Brooks J, Chen Q, Haas SS, Ge R, Hartnell LM, Cookson MR, Egan JM, Frangou S, Mattson MP. Brain responses to intermittent fasting and the healthy living diet in older adults. Cell Metab. 2024 Aug 6;36(8):1668-1678.e5. doi: 10.1016/j.cmet.2024.05.017. Epub 2024 Jun 19.

Reference Type: DERIVED

PMID: 38901423 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Related Links

https://clinicalstudies.info.nih.gov/cgi/detail.cgi?B_2015-AG-0123.html

NIH Clinical Center Detailed Web Page

Other Identifiers

15-AG-0123

Identifier Type: -

Identifier Source: secondary_id

150123

Identifier Type: -

Identifier Source: org_study_id