Effects of an Omega-3 Fatty Acid-based Supplement on Healthy Ageing

Tolerability and Effects of a New Omega-3 Fatty Acid-based Supplement on Clinical and Biological Markers of Healthy Ageing

The goal of this randomised, double-blind placebo controlled trial is to explore tolerability and the effects of a new omega-3 fatty acid-based supplement on biological and clinical aspects relevant for healthy ageing.

Participants will be asked to take a supplement or a placebo for 6 months, and to attend the clinic a total of 3 times and to perform or submit the following:

• Physical examination
• Muscle function tests
• Cognitive testing
• Questionnaire completion
• Biological samples, including blood, saliva and faeces.

Researchers will compare the results from the group taking the supplement to the results of the group taking a placebo to see if the supplement has an effect on biological and clinical aspects associated with healthy ageing.

Study Overview

• Status: Not yet recruiting
• Conditions: Healthy Aging; Ageing Well
• Intervention / Treatment: Dietary supplement: AvailOm; Dietary supplement: Placebo

Detailed Description

Healthy ageing is the process of developing and maintaining the functional ability that is associated with wellbeing across the life course and comprises mental and physical capacities such as the ability to walk, think, see, hear and remember. These factors are influenced by several factors including diseases, age-related decline in organ function and lifestyle such as diet and physical exercise.

Among dietary factors, omega-3 fatty acids, including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are increasingly recognized as potentially promoting healthy ageing, including benefits to cardiovascular system, as well as muscle function, and brain function. It is also important for brain and eye development. Regular supplementation with EPA and DHA therefore potentially offers a range of health benefits throughout life.

Since humans cannot synthesize omega-3 fatty acids, these are considered essential nutrients and must be incorporated into the diet, with the main source for EPA and DHA incorporation being fish oils and supplementation. Western diets are often deficient in these compounds, therefore, regular supplementation with EPA and DHA potentially delays functional decline in ageing and reduces the incidence / severity of age-related diseases.

Objective/Aims:

Explore tolerability and the effects of the IP on biological and clinical aspects relevant for healthy aging.

Design:

Randomized, double-blind placebo-controlled parallel-group trial for six months.

• Study Type: Interventional
• Enrollment (Estimated): 100
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Dag Aarsland, PhD; Phone Number: +47 51515062; Email: dag.arsland@sus.no

Study Locations

• Norway
  • Stavanger, Norway
    • Stavanger Universitetssjukehus

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Aged 55 or more
• BMI between 25-30,
• Waist-to-hip ratio of at least 0.90 (males) or 0.85 (females)
• Omega-3 index <6

Exclusion Criteria:

• Dementia
• Current clinically significant depression, i.e. major depression or GDS 15 score >7
• Ischemic or haemorrhagic Stroke
• Acute myocardial infarction
• Any form of clinically significant atherosclerotic cardiovascular disease
• Unstable angina pectoris
• Hearth failure in need of treatment
• Diabetes mellitus type 1 or 2
• Clinically relevant kidney diseases that require dialysis, including clinically significant chronic kidney disease
• Liver cirrhosis or active hepatitis B or C
• Cancer of any kind; however, benign tumours are no exclusion criterium
• Clinically relevant inflammatory or autoimmune disorders with history of hospitalisation
• Any form of systemic lupus erythematosus (SLE), rheumatoid arthritis, Colitis ulcerosa, Crohn's disease, Morbus Parkinson, Multiple Sclerosis
• hsCRP > 3.0 mg/L to exclude high risk individuals according to international criteria
• LDL-C > 160mg/dL to exclude individuals with high risk for arterioscleratic coronary disease26
• HBa1C < 6.5% to exclude diabetes
• Fasting Triglycerides >200 mg/dL
• Omega 3 index > 6 % (as they may not show any benefit from supplementation)
• Use of fish oil / omega 3 supplements over the last 6 months
• Fish allergy
• Antibiotic use in the last 24 weeks

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: AvailOm; Availom capsules will be administered orally in a dose of 5 capsules/day per individum for a total of 6 months.	Dietary supplement: AvailOm; 5 capsules taken once daily with main meal
Placebo Comparator: Placebo; Placebo capsules matching AvailOm will be administered orally in a dose of 5 capsules/day per individum for a total of 6 months.	Dietary supplement: Placebo; 5 capsules taken once daily with main meal

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effects of Availom on DNA methylation	Effects of Availom on DNA methylation will be measured by a novel saliva-based method and correlated with the individual's genotype. EPIC (850k) chip platform for DNA methylation patterns will be used to measure these changes.	6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effects of Availom on inflammation	Blood will be analysed for markers of inflammation (CRP and cytokines; eg TNFa, IL6), using commercially available immunoassays all measurements will be in pg/ml.	6 months
Effects of Availom on plasma lipids	Changes in plasma lipids will be measured; Omega-3 fatty acids and their metabolites, especially eicosanoids, resolvins D1, EPA/DHA levels, LDL-cholesterol. Commercially available immunoassays will be used. The unit of measurement for all measures will be pg/ml.	6 months
Effects of Availom on in vitro neurogenesis markers	Serum obtained from participants at baseline and end point visit will be used to treat hippocampal progenitor cells in an established in vitro model of hippocampal neurogenesis, developed by the Thuret lab at KCL. This will be an entirely in vitro experiment using only the serum samples from this trial's participants. Following cell culture and immunocytochemistry, this assay provides information on the neurogenic potential of each individual. Neurogenic potential is measured as percentage cells positive for SOX2/ NESTIN/ KI67/ CC3 /DCX and MAP2. The values obtained from cells treated with endpoint samples will be compared to values obtained from cells treated with baseline samples for each individual to control for inter-individual differences allowing us to use this set up to establish if 6 months of availom can alter an individuals neurogenic potential.	6 months
Effects of Availom on brain-derived neurotrophic factor	Levels of BDNF has been shown to be a reliable index as biomarker for assessing the effectiveness of Omega-3 supplements in improving brain function.	6 months
Effect of Availom on microbiome changes	DNA will be extracted from stool samples provided by study subjects and the microbial composition determined following next-generation sequencing to assess the effect of Availom on microbial composition.	6 months
Investigate potential moderators of the effect of Availom on microbial composition	Microbiome data obtained in outcome 7 will be analysed and correlated to (meta)data collected to identify key species linked to gut health.	6 months
Effects of Availom on cognition as measured by use of MoCA	As measured by Montreal Cognitive Assessment (MoCA). MOCA scores range between 0 and 30 points, with a higher score indicating higer cognitive function.	6 months
Effects of Availom on cognition as measured by use of CERAD	As measured by the word list memory test from the Consortium to establish a registry for Alzheimer's disease (CERAD) neuropsychological battery. The same list is presented in a different order three times and the participant is asked to recall as many words as possible. The maximum number of correct responses is 10 for each trial with a maximum score of 30.	6 months
Effects of Availom on muscle function as asessed by TUG	As measured by the Timed Up and Go test (TUG)	6 months
Effects of Availom on muscle function as assessed by grip strength	As measured by testing grip strength with a dynamometer	6 months
Effects of genotype on association between Availom and genotype	Genotype of saliva samples will be analysed using Ilumina Infinium Global Screening Array the effect of different genotypes will be assessed as a potential moderators of the association between availom and DNA methylation	6 months

Collaborators and Investigators

• Sponsor: Helse Stavanger HF
• Collaborators: Evonik Industries AG
• Investigators: Principal Investigator: Dag Aarsland, PhD, Helse Stavanger HF

Study record dates

Study Major Dates

• Study Start (Estimated): December 1, 2023
• Primary Completion (Estimated): September 1, 2024
• Study Completion (Estimated): December 31, 2025

Study Registration Dates

• First Submitted: September 7, 2023
• First Submitted That Met QC Criteria: November 20, 2023
• First Posted (Actual): November 29, 2023

Study Record Updates

• Last Update Posted (Actual): November 29, 2023
• Last Update Submitted That Met QC Criteria: November 20, 2023
• Last Verified: August 1, 2023

More Information

Terms related to this study

• Other Study ID Numbers: AvailOm

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No