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N/A N=20 Basic Science

Effect of an Alpha-linolenic Acid-rich Supplement on Ketogenesis and Plasma Fatty Acids

Healthy

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Feb 2019
Primary outcome: Primary: Ketone Production — 217.71; 187.48 µmol/L

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
alpha-linolenic acid-rich supplement (Dietary_supplement)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Université de Sherbrooke
Primary completion
May 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Ketone Production
217.71; 187.48
SECONDARY
Plasma Glucose
4.75; 5.46
SECONDARY
Plasma Triglycerides
0.97; 1.81
SECONDARY
Plasma Free Fatty Acids
0.48; 0.55
SECONDARY
Insulin Concentration in Plasma
10.48; 14.87

Summary

Background: As the main alternative fuel to glucose for the brain, increased plasma ketones could potentially help compensate for brain glucose hypometabolism occurring during aging. The precursor long-chain n-3 polyunsaturated fatty acid (PUFA), α-linolenic acid (ALA), is normally mostly β-oxidized and so could potentially be used to stimulate ketogenesis in humans. Objective: To compare the impact of an ALA-rich supplement on the ketogenic response in young and older healthy adults. Design: Ten young and ten older adults will consume a flaxseed oil supplement providing 2 g/d of ALA for 4 weeks. Plasma ketones, free fatty acids, triglycerides, glucose and insulin will be measured over 6 h during two metabolic study days, one before and one at the end of the supplementation. Hypothesis: ALA-rich supplement for 4 weeks will increase ketone production in both groups.

Eligibility Criteria

Inclusion Criteria

  • aged between 18 and 30 or 65 years and more

Exclusion Criteria

  • non smoker
  • pregnancy or breastfeeding
  • diabetes or insulin resistance
  • uncontrolled thyroid disease, hepatic or renal disease
  • uncontrolled high blood pressure
  • medical treatment influencing lipid or glucide metabolism
  • ongoing or past severe drug or alcohol abuse
  • dementia or psychiatric difficulties or depression
  • chronic immune condition or inflammation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02410161). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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