Skip to content

The Effects of Western Diet Patterns on Plasma Inflammatory and Cardio Metabolic Health Signatures in Middle-aged Adults

The Effects of Western Diet Patterns on Plasma Inflammatory and Cardio Metabolic Health Signatures in Middle-aged Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04275843
Enrollment
21
Registered
2020-02-19
Start date
2020-10-01
Completion date
2021-12-21
Last updated
2022-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Diet

Brief summary

The Western diet pattern or standard American diet is a modern dietary pattern that is characterized by high intakes of meat, pre-packaged foods, fried foods, high-fat dairy products, eggs, refined grains etc. When considering the role of saturated fat, it may be prudent to advise limiting all foods that contain saturated fats, including unprocessed/minimally processed meat, eggs, whole dairy in addition to processed, pre-packaged foods; however, this reductionist approach fails to take into account the food matrix and overall diet in which these nutrients are consumed. Epidemiological evidence suggests that increased modern, pre-packaged food consumption is a major risk factor for metabolic disease by promoting inflammation. Based on these data, the investigators hypothesize that the pro-atherogenic effect of the Western diet is caused by the pro-inflammatory effects of consuming large amounts of modern ultra-processed foods, and that consumption of a similar amount of fat from minimally processed beef, poultry, dairy, eggs, as part of an unprocessed diet will positively impact inflammatory markers and lipoprotein profiles of study participants when compared to a diet rich in modern ultra-processed foods.

Interventions

DIETARY_SUPPLEMENTTraditional Diet

Consuming an traditional whole foods based diet for 4 weeks.

DIETARY_SUPPLEMENTModern Diet

Consuming an processed formulation of the traditional diet for 4 weeks.

Sponsors

North Dakota Beef Commission
CollaboratorUNKNOWN
Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

As this is feeding study with two very much different diets, participants and investigators were not blinded. The Core facilities that are analyzing de-identified coded samples and remain blinded to treatments.

Eligibility

Sex/Gender
ALL
Age
35 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Age ≥35 and ≤60 years; * BMI ≥25 and ≤35 kg/m2; * Weight stable in last 3 months (Loss or gain \<4%); * Consistent physical activity levels; * Hemoglobin A1C (HbA1C) ≤6.4%; * Fasting insulin; \<15 µU/mL; * Fasting plasma glucose concentration \<126 mg/dl; * Willingness to eat the food provided in this study; * Subjects must be able to speak and understand English to participate in this study * Own a smartphone or other mobile device capable of downloading the Garmin Connect app.

Exclusion criteria

* Diagnoses of active malignancy, congestive heart failure, diabetes mellitus, chronic obstructive pulmonary disease, thyroid disease or other metabolic disorders that influence metabolism; * Evidence of impaired kidney function (Estimated glomerular filtration rate \[eGFR\] \<44 mL/min; * Regular use of medication that interferes with the measurement of study outcomes as determined by the study team (e.g., NSAIDs, corticosteroids); * Consuming \>14 drinks per week of \>4 drinks per night twice/week for male; \>7 drinks per week or \>3 drinks per night twice/week for female; * Use of cigarettes (or other tobacco products) or use of any other (recreational) drug in last 3 months; * Engaged in high-level competitive exercise (e.g., marathons, triathlons, cycling, weight-lifting competitions etc.) * Self-reported sleep duration \<5 hours per night; * Any inflammatory diseases (e.g. asthma, autoimmune diseases, coeliac disease, glomerulonephritis, hepatitis, inflammatory bowel disease, arthritis); * Use of antibiotics in last 30 days; * Pregnant or lactating women; * Eating disorders (e.g., anorexia nervosa, bulimia nervosa, binge eating disorders etc.) * Psychological disorders (e.g., clinical depression, bipolar disorders etc.); * Strict dietary patterns (e.g., vegan, carnivore, kosher, low-carb etc.); * History of stomach or bowel resection (other than appendectomy), gastric bypass or other bariatric weight loss procedure effecting absorption; * Persons who are not able to grant voluntary informed consent; * Persons who are unable or unwilling to follow the study protocol or who, for any reason, the research team considers not an appropriate candidate for this study, including non-compliance with screening appointments or study visits.

Design outcomes

Primary

MeasureTime frameDescription
Change in plasma interleukin-6 levelsBaseline, up to 4 weeks.Plasma interleukin-6 levels will be measured before and after each diet
Change in plasma c-reactive protein levelsBaseline, up to 4 weeks.Plasma c-reactive protein levels levels will be measured before and after each diet
Change in plasma acylcarnitine profilesBaseline, up to 4 weeks.Plasma acylcarnitines profiles levels will be measured before and after each diet

Secondary

MeasureTime frameDescription
Change in gut microbiota communitiesBaseline, up to 4 weeks.Bifidobacterium, Faecalibacterium prausnitzii, Anerostipes, Roseburia
Energy expenditureup to 4 weeks.Measured by the doubly labeled water method during the last week of each diet
Change in NeuroinflammationBaseline, up to 4 weeks.Neurofilament light (NfL), glial fibrillary acidic protein (GFAP), Aß42 and p-tau will be measured before and after each diet

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026