Almond Consumption and Glycemia

Sponsor
Purdue University (Other)
Overall Status
Completed
CT.gov ID
NCT03236116
Collaborator
Almond Board of California (Other)
75
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2
41
25
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Study Details

Study Description

Brief Summary

This study will examine the effects of almonds consumed by adults with different body fat distributions on indices of carbohydrate and lipid metabolism.

Condition or Disease Intervention/Treatment Phase
  • Other: Almonds
  • Other: Control (no nuts)
N/A

Detailed Description

There is considerable evidence supporting a causal role for truncal visceral fat depots in glucose dysregulation. Individuals with large visceral fat depots have impaired suppression of free fatty acid release in response to insulin, elevated triglycerides and low concentrations of high density lipoprotein cholesterol. The high free fatty acid concentration may induce insulin resistance in the muscle and liver. There is more recent evidence that truncal subcutaneous fat depots are also problematic, though this literature is mixed. In contrast, gluteo-femoral fat depots have not been implicated in insulin resistance and dysregulation of carbohydrate metabolism. Failure to account for differences in the contributions of these depots will add noise to measurements of dietary interventions to mitigate glucose dysregulation. Previous studies have reported evidence indicating acute and chronic consumption of almonds improves glycemia. Acute effects are important indicators of health benefit, but longer-term trials, ones permitting identification of the effects of a dietary intervention on HbA1c, are more telling and clinically relevant. To more definitively establish the association between almond consumption and improved carbohydrate metabolism, we propose a six-month trial that contrasts the effects of almond consumption at optimal times of the day versus consumption of low nutrient dense snack foods on indices of carbohydrate metabolism, food intake and appetite in adults characterized by three distinct fat depots.

Participants will consume either almonds, or no nuts every day for 6 months. At baseline, participants will be weighed and undergo a DEXA scan to determine body fat composition and will be assigned a group. Blood will also be collected fasted and at stipulated times in response to a meal tolerance test to measure insulin, glucose, C-peptide, HbA1c, lipid panel, gut peptides, and compliance to the diet. Participants will be given links to complete appetite ratings and record food intake. Participants will report to the lab every two weeks to be weighed, and get a resupply of almonds (if in the almond group). At the two-week mark on months 2 and 4, participants will be weighed, blood will be taken to assess compliance to the diet, and links will be given to complete appetite ratings and record food intake. At month 6, all measurements from baseline will be repeated.

Study Design

Study Type:
Interventional
Actual Enrollment :
75 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Almond Consumption and Glycemia
Actual Study Start Date :
Aug 1, 2017
Actual Primary Completion Date :
Mar 20, 2020
Actual Study Completion Date :
Dec 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Almond Group

Participants will consumed almonds every day for 6 months, but will not be allowed to consume any other nuts or nut products.

Other: Almonds
Participants will consume almonds everyday for 6 months.

Experimental: Control Group

Participants will continue with their normal eating routine for 6 months, but will not be allowed to consume any nuts or nut products.

Other: Control (no nuts)
Participants will not be permited to consume any nuts for 6 months.

Outcome Measures

Primary Outcome Measures

  1. HbA1c [Baseline]

    HbA1c.

  2. fasting glucose [Baseline]

    fasting glucose,

  3. fasting triglycerides [Baseline]

    fasting triglycerides

  4. Change in Body weight [Every two weeks for 6 months.]

    Body weight

  5. Body composition [Baseline]

    Body composition

  6. GLP-1 [Baseline]

    GLP-1

  7. Change in HbA1c [6 months]

    HbA1c.

  8. Change in fasting glucose [6 months]

    fasting glucose

  9. fasting triglycerides [6 months]

    fasting triglycerides

  10. Change in Body composition [6 months]

    Body composition

  11. Change in GLP-1 [6 months]

    GLP-1

  12. fasting insulin [Baseline]

    fasting insulin

  13. total cholesterol [Baseline]

    total cholesterol

  14. LDL-cholesterol [Baseline]

    LDL-cholesterol

  15. HDL-cholesterol [Baseline]

    HDL-cholesterol

  16. GIP [Baseline]

    GIP

  17. change in fasting insulin [6 months]

    fasting insulin

  18. change in total cholesterol [6 months]

    total cholesterol

  19. change in LDL-cholesterol [6 months]

    LDL-cholesterol

  20. change in HDL-cholesterol [6 months]

    HDL-cholesterol

  21. change in GIP [6 months]

    GIP

  22. C-peptide [baseline]

  23. C-peptide [6 months]

  24. Homa-IR [baseline]

  25. Homa-IR [6 months]

  26. Homa-Percent Beta [Baseline]

  27. Homa-Percent Beta [6 months]

Secondary Outcome Measures

  1. Diet Quality [Three days (two non-consecutive week days and one weekend day) at baseline, month 2, 4, and 6.]

    Determine the effect of substituting a wholesome snack food (almonds) for more traditional, less nutrient dense, snack foods on total diet quality. Food intake will be measured by the ASA-24 for three days (two non-consecutive week days and one weekend day) at baseline, month 2, 4, and 6.

  2. Compliance [Baseline, month 2, 4, and 6.]

    Demonstrate the utility of a novel, sensitive approach to document compliance with a prescription to ingest almonds on a daily basis for six months.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Meeting one of the following body fat distribution criteria determined by DEXA: 1. High visceral fat 2. High gluteo-femoral fat 3. High truncal subcutaneous fat

  • 18-60 years

  • no nut allergies

Exclusion Criteria:
  • Not meeting one of the body fat distribution criteria

  • allergic to nuts

Contacts and Locations

Locations

Site City State Country Postal Code
1 Indiana University School of Medicine Indianapolis Indiana United States 46202
2 Purdue University West Lafayette Indiana United States 47907
3 Purdue University West Lafayette Indiana United States 47909

Sponsors and Collaborators

  • Purdue University
  • Almond Board of California

Investigators

  • Principal Investigator: Richard D Mattes, PhD, Purdue University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Richard Mattes, Professor, Nutrition Sciences, Purdue University
ClinicalTrials.gov Identifier:
NCT03236116
Other Study ID Numbers:
  • 055-047
First Posted:
Aug 1, 2017
Last Update Posted:
Jan 7, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 7, 2021