Evaluation of the Nutritional Status of Omega-3 Fatty Acids and the Possible Influences of Dietary Patterns and Different Socioeconomic Factors, in a Spanish Population Over 60 Years of Age (OMEGAPRED)

April 8, 2025 updated by: María Dolores Mesa García, Universidad de Granada

Evaluation of the Nutritional Status of Omega-3 Fatty Acids and the Possible Influences of Dietary Patterns and Different Socioeconomic Factors in a Spanish Population Over 60 Years of Age

The long-chain polyunsaturated fatty acids (PUFA) of the n-3 or omega-3 series and, in particular, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), both derived from the essential fatty acid alpha-linolenic acid, are part of all cell membranes and from them derive numerous compounds such as prostaglandins, thromboxanes, leukotrienes, resolvins, protectins and maresins that play numerous biological roles, most notably in the control of body homeostasis, blood coagulation and inflammation. The omega-3 index is a biomarker that reflects the nutritional status of n-3 PUFA, as well as cardiometabolic risk and cardiovascular health. This index is determined as the sum of the percentages in weight of EPA and DHA over the total of fatty acids present in the erythrocyte membranes.

Previous studies carried out in Spain, such as ANIBES, indicate that in adults, and especially in those over 60 years of age, the intake of n-3 PUFA is well below the international recommendations, which is directly related to a low intake of fish, since both EPA and DHA are abundant in oily fish. However, in Spain, the nutritional status of omega-3 PUFA and their possible association with a higher prevalence of cardiometabolic risk is unknown, as well as the relationships with food intake and the cultural and socioeconomic status of the population. Therefore, the main objective of the present study is to evaluate the omega-3 index in the Spanish population over 60 years of age and to establish whether there are differences by sex, as well as in the different Spanish communities. In addition, we will study the possible associations between the omega-3 index and food intake, particularly of fish and omega-3 PUFA-rich supplements, as well as their possible associations with cardiometabolic risk indicators and cultural and socioeconomic conditions of the population.

Determination of the omega-3 index usually requires an invasive venous blood collection followed by processing for separation of erythrocytes and extraction and methylation of their membrane lipids followed by chromatographic analysis. But fatty acids can also be determined on whole blood using less invasive methods, such as obtaining drops of blood with a lancet and depositing them on chromatographic paper impregnated with an antioxidant (dried spots). All this makes sampling much easier, although the result of the omega-3 index has to be corrected because it is affected by the lipid composition present in the plasma. For this reason, this project aims to carry out a validation study between the results of the fatty acid profile obtained in erythrocytes and in whole blood in the Spanish population (medamediantedried spots). In short, the results obtained will be used to calculate regression lines that allow us to evaluate the omega-3 index in erythrocytes in the adult Spanish population from different regions of Spain by means of a minimally invasive methodology. For this purpose, 800 participants aged 60 years or more will be recruited from different regions of Spain, randomized by age and sex for each region; at least 100 of the total number of participants should be frequent consumers of omega-3 supplements; if this figure is not obtained, an active search will be carried out until this number is reached (booster). All of them will be interviewed to complete different questionnaires on cultural and socioeconomic status, history of metabolic disease and cardiovascular health, and questionnaires on frequency of consumption and food intake reminders as established by the European Union. With the help of health personnel from different pharmacies and in mutual agreement with the General Council of Pharmaceutical Associations of Spain, a whole blood sample will be taken by lancet, which will be used to quantify the omega-3 index. For the validation study it will be necessary to obtain whole venous blood extracted by venipuncture from a subsample of 200 participants. This sample will be processed and will be used to determine the fatty acid profile in whole blood and in erythrocytes, which will be related by means of multiple linear and bivariate regression models with the fatty acid profile obtained in the dried spots. Cardiometabolic risk markers will also be determined in these 200 subjects, which will be used to establish relationships with the calculated omega-3 status.

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Estimated)

800

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: María D Mesa García, PhD
  • Phone Number: 607505068
  • Email: mdmesa@ugr.es

Study Contact Backup

  • Name: Carolina T Gómez Llorente, PhD
  • Phone Number: +34686458391
  • Email: gomezll@ugr.es

Study Locations

      • Granada, Spain, 18016
        • Recruiting
        • Avd del Conocimiento 19
        • Contact:
          • Carolina Gómez Llorente, PhD
        • Contact:
          • Estefanía Sánchez Rodríguez, PhD
          • Phone Number: +34677113815
          • Email: estefaniasr@ugr.es
        • Contact:
          • María D Mesa García, PhD
          • Phone Number: +34607505068
          • Email: mdmesa@ugr.es
        • Contact:
          • María D Ruiz López, PhD
        • Contact:
          • Ángel Gil Hernández, PhD
        • Contact:
          • Reyes Artacho, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

800 volunteers in total, men and women from 37 locations in Spain distributed in 8 different areas (Nielsen Areas) covering the eastern, eastern, eastern, southern, southern, central, northwestern, northern and metropolitan areas of Madrid and Barcelona in Spain.

These 800 participants will be randomized according to sex and the territory to which they belong, into three age groups: one group will be between 60 and 70 years old, another group will be between 71 and 80 years old, and the third will be made up of people over 80 years old. In addition, 100 of these subjects must be regular consumers of omega-3 supplements.

Description

Inclusion Criteria:

  • Older than 60 years of age

Exclusion Criteria: Diseases that affect nutritional status

  • Gastrointestinal diseases that affect the absorption of nutrites
  • Cancer
  • Chronic kidney disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Validation cohort
Healthy people (n=200) over 60 year of age that will be bleeded for the validation of the dry spot methodology
Exploratory cohort
Healthy people (n=600) over 60 year of age that will be study with the dry spot methodology

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
omega-3 index
Time Frame: At the time of enrollement
The omega-3 index measure the presence of omega-3 fatty acids in the erythrocyte membrane
At the time of enrollement

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nutritional assesment
Time Frame: At the time of enrollement
Food frecuency questionarie
At the time of enrollement
Physical activity assesment
Time Frame: At the time of enrollement
Physical activity questionaries
At the time of enrollement
Socioeconomic assesment
Time Frame: At the time of enrollement
Socioeconomic questionaries
At the time of enrollement
DNA genotyping
Time Frame: At the time of enrollement
Specific genes related to lipid metabolism and cardiovascular risk will be genotiped only in the validation cohort
At the time of enrollement
Plasma triacylglycerides
Time Frame: At the time of enrollement
Plasma triacylglycerides only in the validation cohort
At the time of enrollement
Plasma cholesterol
Time Frame: At the time of enrollement
Plasma Total cholesterol, HDL-Cholesterol, LDL-cholesterol only in the validation cohort
At the time of enrollement
Plasma glucose
Time Frame: At the time of enrollement
Plasma glucose levels only in the validation cohort
At the time of enrollement
Plasma insulin
Time Frame: At the time of enrollement
Plasma insulin levels only in the validation cohort
At the time of enrollement

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Estefanía Sánchez Rodríguez, PhD, Universidad de Granada

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 19, 2025

Primary Completion (Estimated)

April 30, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

March 31, 2025

First Submitted That Met QC Criteria

March 31, 2025

First Posted (Actual)

April 8, 2025

Study Record Updates

Last Update Posted (Actual)

April 11, 2025

Last Update Submitted That Met QC Criteria

April 8, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • OMEGAPRED (PIP-0265-2024)
  • PIP-0265-2024 (Other Identifier: Junta de Andalucía)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

all collected anonimous IPD

IPD Sharing Time Frame

Beginning 1 year after publication with no end date

IPD Sharing Access Criteria

A proposal that describes planned analyses must be submitted, and a data sharing agreement must be signed. Researcher will contact the IP of tthe present project (estefaniasr@ugr.es), explain the proposal. She will send them an agreement document to be submitted.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Fatty Acids, Omega-3

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