Effect of Egg Consumption on Cardiometabolic Health in Prediabetic Subjects.

PreDiabetes Clinical Trial

Official title:

A Randomized, Crossover Trial to Assess the Effects of Replacing Commonly Consumed Breakfast Foods With Eggs on Insulin Sensitivity and Other Markers of Cardiometabolic Health in Men and Women at Increased Risk for Type 2 Diabetes Mellitus.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03332927
• Other study ID #: MB-1704
• Status: Completed
• Phase: N/A
• Start date: October 25, 2017
• Est. completion date: August 15, 2018

Study information

• Verified date: July 2019
• Source: Midwest Center for Metabolic and Cardiovascular Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this trial is to assess the effects of whole egg consumption (12 per week), compared to energy-matched typical breakfast control foods, on insulin sensitivity and other markers of metabolic health, including fasting lipoprotein lipid levels and resting blood pressure.

Description:

This is a randomized, crossover study that includes two screening visits and two 4-week test periods separated by a 4-week washout. Subjects will consume two eggs/day (12 eggs/week consumed over 6 days per week, provided as breakfast foods such as burrito-type roll-up, egg sandwich and omelet) or non-egg based control foods (provided as breakfast foods such as English muffins, bagels, ready-to-eat cereal, and flavored muffins). The background diet will be a habitual diet. The nutritional profiles of the egg and control breakfast foods will be designed such that the energy from eggs will be substituted for a mixture of carbohydrate, protein and fat in the control foods.

Study foods will be dispensed with instructions to consume the assigned breakfast food starting on day 1. Subjects will be instructed to consume the breakfast foods in their entirety each day, for the duration of the 28 day test period, and to record daily study food intake. Subjects will receive diet instruction on the incorporation of food substitutions during the test period to maintain habitual energy intake. Compliance will be assessed using the Daily Log intake and number of foods consumed based on returned foods.

An intravenous glucose tolerance test (IVGTT) will be completed at baseline and the end of each treatment period for evaluation of insulin sensitivity. Blood will be collected for a fasting lipid profile (at all visits), glucose and insulin, high-sensitivity C-reactive protein (hs-CRP), vertical auto profile (VAP) for cholesterol carried by lipoprotein fractions (at baseline and end of each treatment period), with additional blood samples collected for storage and archived for possible future analysis of non-genetic indicators of metabolism. Assessments of vital signs and body weight, review of concomitant medication/supplement use and inclusion and exclusion criteria for relevant changes, and evaluation of adverse effects will be performed throughout the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39
• Est. completion date: August 15, 2018
• Est. primary completion date: August 15, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 74 Years

Eligibility

Inclusion Criteria:

1. BMI of =25.0 kg/m2 (=23.0 kg/m2 in Asian Americans) to 39.99 kg/m2.

2. Metabolic syndrome [exhibiting at least 3 out of 5 of these criteria]: waist circumference =102 cm (40 inches) in men or =88 cm (35 inches) in women, TG level =150 mg/dL, HDL-C level <40 mg/dL in men or <50 mg/dL in women, hypertension: =130 systolic and/or /=85 diastolic or on drug therapy for elevated BP, fasting hyperglycemia: 100-125 mg/dL.

3. Prediabetes [exhibiting any of the criteria below at screening]: glycated hemoglobin 5.7-6.4% (inclusive), or fasting capillary glucose of 100-125 mg/dL (inclusive), or a 2-h postprandial glucose of 140-199 mg/dL.

Exclusion Criteria:

1. Atherosclerotic cardiovascular disease including any of the following:

clinical signs of atherosclerosis including peripheral arterial disease, abdominal aortic aneurysm, carotid artery disease [symptomatic (e.g., myocardial infarction, angina, transient ischemic attack or stroke of carotid origin) or >50% stenosis on angiography or ultrasound] or other forms of clinical atherosclerotic disease (e.g., renal artery disease).

2. History or presence of clinically important pulmonary (including uncontrolled asthma), endocrine (including type 1 or 2 diabetes mellitus), chronic inflammatory disease (including irritable bowel disease, lupus, rheumatoid arthritis), hepatic, renal, hematologic, immunologic, neurologic, or biliary disorders.

3. Known allergy, sensitivity, or intolerance to any ingredients in the study foods.

4. Uncontrolled hypertension

5. Recent history of cancer in the prior 5 years, except for non-melanoma skin cancer.

6. Recent change in body weight of ±4.5 kg.

7. Unstable use of any antihypertensive medication.

8. Recent use of any medications intended to alter the lipid profile [e.g. bile acid sequestrants, cholesterol absorption inhibitor, fibrates, niacin (drug form), omega-3-ethyl ester drugs, and/or proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors], weight-loss drugs, systemic corticosteroid drugs, medications known to influence carbohydrate (CHO) metabolism [e.g. adrenergic receptor blockers, thiazide diuretics, hypoglycemic medications], and/or anti-psychotics.

9. Recent use of foods or dietary supplements that might influence lipid metabolism [e.g. omega-3 fatty acid supplements (e.g., fish or algal oils) or fortified foods, sterol/stanol products; dietary supplements (red rice yeast supplements; garlic supplements; soy isoflavone supplements; niacin or its analogues at doses >400 mg/d], inconsistent use of Metamucil® or viscous fiber-containing supplements

10. Use of antibiotics within 5 days of screening.

11. Pregnant, planning to be pregnant during the study period, lactating, or of childbearing potential and unwilling to commit to the use of a medically approved form of contraception throughout the study period.

12. Extreme dietary habits (e.g., vegan or very low carbohydrate diet).

13. Current or recent history or strong potential, for drug or alcohol abuse.

14. History of a diagnosed eating disorder (e.g., anorexia or bulimia nervosa).

15. Recent exposure to any non-registered drug product.

Related Conditions & MeSH terms

• PreDiabetes
• Prediabetic State

Intervention

Other:
• Egg based breakfast foods
Two eggs/day, 6 days per week provided as breakfast foods such as burrito-type roll-up, egg sandwich and omelet.
• Non-egg based breakfast foods
Non-egg based control foods provided as breakfast foods 6 days per week such as waffles, ready-to-eat cereal, fruits and cheeses.

Locations

Country	Name	City	State
United States	Great Lakes Clinical Trials	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
Midwest Center for Metabolic and Cardiovascular Research

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Insulin sensitivity index (IV-SI) from short (40 min) IVGTT.	Percent change or change from baseline to end of each treatment condition	Up to 40 minutes - measured at baseline and end of each treatment period.
Secondary	Disposition index [acute insulin response to intravenous glucose (AIRg) x IV-SI]	Percent change (or change) from baseline to the end of each treatment period.	Up to 40 minutes - measured at baseline and end of each treatment period.
Secondary	Glucose fractional disappearance rate from t = 10-40 min (Kg)	Percent change (or change) from baseline to the end of each treatment period.	Up to 40 minutes - measured at baseline and end of each treatment period.
Secondary	Homeostasis model assessments of insulin sensitivity (HOMA%S)	Percent change (or change) from baseline to the end of each treatment period.	Up to 29 days for each treatment period
Secondary	Beta-cell function (HOMA%B)	Percent change (or change) from baseline to the end of each treatment period.	Up to 29 days for each treatment period
Secondary	Percent change in Total cholesterol (TC)	Percent change in TC from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Percent change in low-density lipoprotein cholesterol (LDL-C)	Percent change in LDL-C from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Percent change in high-density lipoprotein cholesterol (HDL-C)	Percent change in HDL-C from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Percent change in non-HDL-C	Percent change in non-HDL-C from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Percent change in TC/HDL-C ratio	Percent change in TC/HDL-C ratio from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Percent change in Triglycerides (TG)	Percent change in TG from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Seated, resting systolic and diastolic blood pressure (BP)	Percent change in seated, resting systolic and diastolic BP (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period
Secondary	Vertical Auto-Profile (VAP) analysis of cholesterol carried by lipoproteins and lipoprotein subfractions.	Percent change in VAP analysed cholesterol in lipoproteins and lipoprotein subfractions from baseline (average of the values from one screening visit and the baseline visit) to the end of each test condition (average of the values at 3-week and 4-week visits of each test period)	Up to 29 days for each treatment period