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Genes, Omega-3 Fatty Acids and Cardiovascular Disease Risk Factors

Genes, Omega-3 Fatty Acids and Cardiovascular Disease Risk Factors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01343342
Acronym
FAS
Enrollment
200
Registered
2011-04-28
Start date
2009-10-01
Completion date
2029-03-01
Last updated
2026-09-03

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

Conditions

Cardiovascular Disease

Keywords

omega-3, PUFA, fatty acids, cardiovascular disease, gene expression

Brief summary

The main purpose of this study is to examine whether n-3 PUFA-induced changes in metabolic risk factors are influenced by genetic variations within genes acting as fatty acids sensors.

Detailed description

The main purpose of this study is to examine whether n-3 PUFA-induced changes in metabolic risk factors are influenced by genetic variations within genes acting as fatty acids sensors. To do so, the metabolic risk factor response to an n-e PUFA supplementation will be compared in carriers and non-carriers of polymorphism within genes acting as fatty acids sensors.

Interventions

DIETARY_SUPPLEMENTn-3 PUFA supplementation

3g per day of n-3 PUFA supplementation (1.9g EPA, 1.1g DHA). 5 capsules per day (1g fish oil each, 5g of fish oil/day)

Sponsors

Laval University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy men and women aged between 18 to 50 years; * having a BMI between 25 and 40kg/m2; * plasma triglycerides levels \<4.0 mmol/L; * non-smokers; * free of any thyroid or metabolic disorders requiring treatment such as diabetes, hypertension, severe dyslipidemia, and coronary heart disease.

Exclusion criteria

* subjects taking medication for hyperlipidemia, hypertension, diabetes or taking anticoagulant or n-3 PUFA supplementation; * having a taste aversion for fish, fish allergy or regular alcohol drinker; * body mass index \> 40kg/m2; * pregnant or nursing women.

Design outcomes

Primary

MeasureTime frame
Change in blood lipids (Total cholesterol, HDL-Cholesterol, Triglycerides)Before and after a 6-weeks supplementation

Secondary

MeasureTime frame
Change in blood pressureBefore and after a 6-weeks supplementation
Change in anthropometric measures (waist and hip girth)Before and after a 6-weeks supplementation
Change in plasma glycemia and insulin levelsBefore and after a 6-weeks supplementation
Change in gene expression levelsBefore and after a 6-weeks supplementation

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORMarie-Claude Vohl, Ph.D.

Institute of Nutraceutical and Functional Foods (INAF), Laval University

Outcome results

None listed

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