Investigating Age-dependent Effects of Egg Intake on HDL and Immune Profiles

NCT ID: NCT06086795

Last Updated: 2025-08-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-23

Study Completion Date

2026-06-30

Brief Summary

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The goal of this intervention study is to determine whether consumption of different fractions of chicken eggs, including egg whites, egg yolks, and whole eggs, confer different changes in markers of HDL function and T cell profiles in younger vs. older men and women. The study will address the following objectives:

* Objective 1: Determine if daily consumption of egg fractions differentially alter HDL profiles across age groups.
* Objective 2: Determine if daily consumption of egg fractions differentially alter immune cell profiles across age groups.

Participants will be asked to consume egg whites, egg yolks, and whole eggs on a daily basis for 4-weeks each, and avoid eating eggs for a total of 8 weeks at different points in the study. Participants will additionally be provided guidance on following a generally healthy diet, and will be asked to complete surveys about dietary intake and physical activity, as well as provide blood samples throughout the course of the study.

Researchers will compare whether daily consumption of egg whites, egg yolks, and whole eggs differentially alter markers of HDL function and T cell profiles in younger vs. older adults.

Detailed Description

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Conditions

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Lipoproteins Inflammatory Response

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Egg whites

3 large egg equivalent of liquid egg whites per day for 4 weeks

Group Type ACTIVE_COMPARATOR

Egg whites

Intervention Type OTHER

3 large egg equivalent of egg whites per day for 4 weeks

Egg yolks

3 large egg equivalent of liquid egg yolks per day for 4 weeks

Group Type EXPERIMENTAL

Egg yolks

Intervention Type OTHER

3 large egg equivalent of egg yolks per day for 4 weeks

Whole eggs

3 large whole eggs per day for 4 weeks

Group Type EXPERIMENTAL

Whole eggs

Intervention Type OTHER

3 large whole eggs per day for 4 weeks

Interventions

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Whole eggs

3 large whole eggs per day for 4 weeks

Intervention Type OTHER

Egg yolks

3 large egg equivalent of egg yolks per day for 4 weeks

Intervention Type OTHER

Egg whites

3 large egg equivalent of egg whites per day for 4 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18-30 years old, or 50-75 years old (at time of screening)
* Body mass index (BMI) \< 30 kg/m2
* Willing to consume whole eggs, egg whites, or egg yolks on a daily basis during study periods, and refrain from eating eggs during other study periods

Exclusion Criteria

* \< 18 years old; 31-49 years old; \> 75 years old
* BMI ≥ 30 kg/m2 or body weight \< 110 pounds
* Weight changes \> 10% over the last 4 weeks
* Self-reported history of diabetes, heart disease, stroke, renal or liver disease, cancer, eating disorders, certain severe and/or relapsing/remitting autoimmune, inflammatory, or metabolic diseases, chronic infections, scleroderma, blood clotting disorders, intravenous drug use, or current pregnancy or lactation
* Allergy or intolerance to eggs, egg components, or egg products
* Implanted medical device (e.g., pacemaker) or other health condition that would prevent measurement of body composition by bioelectrical impedance
* Highly elevated fasting lipid and glucose levels (triglyceride levels higher than 500 mg/dL, fasting glucose higher than 126 mg/dL), or total cholesterol \< 120 mg/dL and HDL-cholesterol \< 15 mg/dL
* Currently taking lipid-lowering medications (e.g. statins, fibrates), anti-inflammatory medications (e.g., NSAIDs, corticosteroids), or medications that primarily affect blood clotting (e.g., warfarin)
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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American Egg Board

OTHER

Sponsor Role collaborator

University of Connecticut

OTHER

Sponsor Role lead

Responsible Party

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Catherine Andersen

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Catherine J Andersen, PhD, RDN

Role: PRINCIPAL_INVESTIGATOR

University of Connecticut

Locations

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University of Connecticut

Storrs, Connecticut, United States

Site Status

Countries

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United States

Other Identifiers

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AG221113

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

H22-0174

Identifier Type: -

Identifier Source: org_study_id

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