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Clinical Trials/NCT05915390
NCT05915390
Completed
Not Applicable

Effects of Walnuts on Innate, Acquired and Gut Immunity in Older Adults With Overweight: A Randomized Controlled Trial

Loma Linda University1 site in 1 country52 target enrollmentStarted: June 27, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
1
Primary Endpoint
changes in lymphocyte activity

Overview

Brief Summary

The main objective of the study is to determine if eating walnuts enhances immune function, in older free-living men and postmenopausal women with overweight.

Detailed Description

The main objectives of our proposed study are to determine the effect of walnut consumption on innate, acquired, and gut immunity by assessing whether the ingestion of walnuts enhances immune function, in older free-living men and postmenopausal women with overweight. To accomplish these objectives, a randomized controlled, parallel design study is proposed with two groups consuming their habitual diet, but with one (Walnut group) receiving 15% of their total energy as walnuts and the other (Control group) abstaining from eating any walnuts and limited amounts of other tree nuts and peanuts (up to <1 serving/wk).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

The investigator and outcome assessor will not be aware which participant is in what arm. The participant and the care provider will know about the treatment allocation

Eligibility Criteria

Ages
55 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Older men and post-menopausal women aged 55-75 years
  • Have a BMI of 25-32
  • Being able to commute to Loma Linda University.
  • Not taking medication or supplements that affect immunity

Exclusion Criteria

  • Intolerance or allergy to walnuts
  • Regular intake of walnuts and/or other nuts (\>3 ounces per week).
  • Immune system insufficiency or disease.
  • Using immune boosting supplements.
  • Exposure to antibiotics and corticoids immediately prior to the study.
  • Participants with uncontrolled chronic diseases, and relevant psychiatric illness, including major depression will not be included in study
  • Flu vaccination or Covid booster within past 6 months

Outcomes

Primary Outcomes

changes in lymphocyte activity

Time Frame: baseline to 12 weeks

The production of lymphocytes will be measured in the supernatant using Enzyme linked immunosorbent assay (ELISA)

changes in cytokine production

Time Frame: baseline to 12 weeks

The cytokines produced due to lymphocyte activity will be measured in the supernatant using Enzyme linked immunosorbent assay (ELISA)

changes in serum inflammatory cytokine concentration

Time Frame: baseline to 12 weeks

changes in the concentrations of the inflammatory cytokines will be performed on serum using enzyme-linked immunoassay (ELISA) will include hs-CRP, interleukin (IL)-1β, IL-6, TNF-α, IL-10, and IL-4.

changes in diversity of immune-modulating and butyrate -producing gut bacteria in feces

Time Frame: baseline to 12 weeks

DNA extraction from stool samples will be performed using QIAamp DNA Stool Mini kits.69 The QIIME (Quantitative Insights Into Microbial Ecology) software will be used to analyze 16S rRNA gene sequences and determine the effect of the intervention on microbial diversity at the phylum, genus, and operational taxonomic unit levels.

Changes in concentration of Immunoglobulin A in feces

Time Frame: baseline to 12 weeks

changes in Immunoglobulin A will be determined using high performance liquid chromatography-mass spectrometry (HPLC-MS)

changes in lymphocyte populations

Time Frame: baseline to 12 weeks

Immunophenotyping will be performed by flow cytometry to measure the number of T helper, T cytotoxic, Naïve and memory cells and B cells

Changes in concentration of Calprotectin in feces

Time Frame: baseline to 12 weeks

changes in Calprotectin will be determined using high performance liquid chromatography-mass spectrometry (HPLC-MS)

Changes in concentration of small chain fatty in feces

Time Frame: baseline to 12 weeks

changes in Small chain fatty acids will be determined using high performance liquid chromatography-mass spectrometry (HPLC-MS)

Secondary Outcomes

  • changes in upper respiratory infection questionnaire score(baseline to 12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Joan Sabate,DrPH, MD

Professor Nutrition and Epidemiology

Loma Linda University

Study Sites (1)

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