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Salmon Peptide Fraction: Safety and Cardiometabolic Health (SPF1)

Primary Purpose

Metabolic Syndrome

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Supplement dose 15g/d
Supplement dose 7.5g/d
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Metabolic Syndrome

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • BMI between 25 and 35 kg/m2
  • Waist circumference ≥ 94 cm for men and ≥ 80 cm for women
  • Meet at least one of the following criteria:

Plasma TG > 1.35 mmol/L Fasting glycemia ≥ 5,6 mmol/L and ≤ 6,9 mmol/L HbA1c ≥ 5,7% and ≤ 6.4% Insulin concentration > 42 pmol/L

Exclusion Criteria:

  • Smoker
  • Suffering from any metabolic disorder requiring pharmacological treatment
  • Taking any medications or natural health products affecting glucose metabolism or plasma lipid levels
  • Use of protein supplements, probiotics supplements or antibiotics within the last 3 months
  • Taste aversion for fish/seafood
  • Fish-seafood or casein/milk protein or any non-medicinal ingredients allergy
  • Lactose intolerance
  • Regular alcohol consumption (>2 drinks/d)
  • >5% weight loss over the last 3 months
  • Major surgery within the last 3 months
  • Pregnant and breastfeeding women

Sites / Locations

  • INAF, Université Laval

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

SPF

Comparator

Arm Description

Salmon peptide fraction supplement: powder mixed in water

Casein peptide fraction supplement: powder mixed in water

Outcomes

Primary Outcome Measures

Change in hepatic enzymes using blood sampling
Measure hepatic enzymes aspartate aminotransferase (AST), alanine aminotransferase (ALT) and gamma glutamyl transferase (GGT) to test the safety of SPF
Change in renal function using blood sampling
Measure creatinine to test the safety of SPF
Change in complete blood count using blood sampling
Measure of complete blood count to test th safety of SPF
Adverse event and general acceptability evaluated by questionnaires
To test the safety of SPF

Secondary Outcome Measures

Change in lipid profile
Evaluation of plasma triglycerides (TG), Total cholesterol, LDL, HDL, Apolipoprotein B and free fatty acids
Change in glucose metabolism
Evaluation of blood glucose concentration during a 3h oral glucose tolerance test
Change in insulin secretion
Evaluation of blood insulin and C-peptide concentration during a 3h oral glucose tolerance test
Change in blood pressure
Evaluation of systolic and diastolic blood pressure to test metabolic syndrome risk factors
Change in body mass index
Evaluation of BMI by measuring weight and height to test metabolic risk factors
Change in waist circumference
Measure of waist circumference to test metabolic risk factors

Full Information

First Posted
August 24, 2021
Last Updated
August 4, 2023
Sponsor
Laval University
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1. Study Identification

Unique Protocol Identification Number
NCT05025462
Brief Title
Salmon Peptide Fraction: Safety and Cardiometabolic Health
Acronym
SPF1
Official Title
Supplementation With Salmon Peptide Fraction in Overweight-Obese Men and Women: Safety, Cardiometabolic Health Effects and Mechanisms of Action
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall goal of this study is to verify the safety of 15g of salmon peptide fraction (SPF), and to test the effects on metabolic syndrome risk factors of two doses of SPF (7.5g and 15g) in overweight-obese men and women. Transcriptomic, metabolomic and metagenomic approaches will be used to study the physiological effects of SPF and to discover the potential mechanism underlying these effects.
Detailed Description
Increased fish consumption has been suggested to improve the metabolic syndrome (MetS) and to reduce the incidence of type 2 diabetes (T2D) and cardiovascular disease (CVD) in obese subjects. While it is well documented that marine long chain polyunsaturated fatty acids (n-3 PUFA) decrease CVD risk by improving the plasma lipid profile and reducing inflammation, the beneficial effects of n-3 PUFA on glucose homeostasis and insulin sensitivity in humans remains highly controversial. Animal and human studies carried out by the group of investigators over the past 20 years have shown that fish proteins can improve the plasma lipid profile, enhance insulin sensitivity and reduce obesity-linked inflammation. The investigators also reported that a salmon protein hydrolysate reduces body fat and increases insulin sensitivity via its calcitonin content and they observed that protein hydrolysates from salmon and other fish sources reduced inflammation in visceral adipose tissue in rodents. The investigators therefore decided a few years ago to focus on the identification of bioactive peptides from fish proteins to explore the potential of increasing the efficacy of fish muscle protein hydrolysates to prevent/treat the MetS. The investigators hypothesized that it was the peptides produced from gastrointestinal digestion that were responsible for the remarkable bioactive effects of fish proteins on the MetS. The investigators have also confirmed that a small peptides fraction (SPF) from salmon protein markedly reduces the development of T2D and inflammation in a high-fat diet (HFD)-induced, obese, atherosclerosis-prone mouse LDLr knockout (KO). These findings are very promising and suggest that fish protein-derived peptides or amino acids may also explain the beneficial effects of dietary fish intake on the MetS, T2D and CVD. Additional studies are required to validate these observations, delineate the mechanisms, and assess their direct impact in human clinical trials. Subjects will take an oral dose of 15 g of SPF or comparator per day (powder mixed with water) in the first intervention phase (6 weeks), then 7.5 g of SPF or comparator per day (powder mixed with water) in the second intervention phase (6 weeks).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
double blind
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SPF
Arm Type
Experimental
Arm Description
Salmon peptide fraction supplement: powder mixed in water
Arm Title
Comparator
Arm Type
Active Comparator
Arm Description
Casein peptide fraction supplement: powder mixed in water
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplement dose 15g/d
Intervention Description
Supplementation with 15g/day of SPF or Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplement dose 7.5g/d
Intervention Description
Supplementation with 7.5g/d of SPF ou comparator
Primary Outcome Measure Information:
Title
Change in hepatic enzymes using blood sampling
Description
Measure hepatic enzymes aspartate aminotransferase (AST), alanine aminotransferase (ALT) and gamma glutamyl transferase (GGT) to test the safety of SPF
Time Frame
Change between the beginning and the end of the intervention (6 weeks)
Title
Change in renal function using blood sampling
Description
Measure creatinine to test the safety of SPF
Time Frame
Change between the beginning and the end of the intervention (6 weeks)
Title
Change in complete blood count using blood sampling
Description
Measure of complete blood count to test th safety of SPF
Time Frame
Change between the beginning and the end of the intervention (6 weeks)
Title
Adverse event and general acceptability evaluated by questionnaires
Description
To test the safety of SPF
Time Frame
Change between the beginning and the end of the intervention (6 weeks)
Secondary Outcome Measure Information:
Title
Change in lipid profile
Description
Evaluation of plasma triglycerides (TG), Total cholesterol, LDL, HDL, Apolipoprotein B and free fatty acids
Time Frame
Change between the beginning and the end of the intervention (6 weeks)
Title
Change in glucose metabolism
Description
Evaluation of blood glucose concentration during a 3h oral glucose tolerance test
Time Frame
Change between the beginning and th end of the intervention (6 weeks)
Title
Change in insulin secretion
Description
Evaluation of blood insulin and C-peptide concentration during a 3h oral glucose tolerance test
Time Frame
Change between the beginning and th end of the intervention (6 weeks)
Title
Change in blood pressure
Description
Evaluation of systolic and diastolic blood pressure to test metabolic syndrome risk factors
Time Frame
Change between the beginning and th end of the intervention (6 weeks)
Title
Change in body mass index
Description
Evaluation of BMI by measuring weight and height to test metabolic risk factors
Time Frame
Change between the beginning and th end of the intervention (6 weeks)
Title
Change in waist circumference
Description
Measure of waist circumference to test metabolic risk factors
Time Frame
Change between the beginning and th end of the intervention (6 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: BMI between 25 and 35 kg/m2 Waist circumference ≥ 94 cm for men and ≥ 80 cm for women Meet at least one of the following criteria: Plasma TG > 1.35 mmol/L Fasting glycemia ≥ 5,6 mmol/L and ≤ 6,9 mmol/L HbA1c ≥ 5,7% and ≤ 6.4% Insulin concentration > 42 pmol/L Exclusion Criteria: Smoker Suffering from any metabolic disorder requiring pharmacological treatment Taking any medications or natural health products affecting glucose metabolism or plasma lipid levels Use of protein supplements, probiotics supplements or antibiotics within the last 3 months Taste aversion for fish/seafood Fish-seafood or casein/milk protein or any non-medicinal ingredients allergy Lactose intolerance Regular alcohol consumption (>2 drinks/d) >5% weight loss over the last 3 months Major surgery within the last 3 months Pregnant and breastfeeding women
Facility Information:
Facility Name
INAF, Université Laval
City
Québec
ZIP/Postal Code
G1V 0A6
Country
Canada

12. IPD Sharing Statement

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Salmon Peptide Fraction: Safety and Cardiometabolic Health

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