Effects of Omega-3 Fatty Acids in Ambient Air Pollution Exposure in Healthy Adults (PISCES)

May 8, 2022 updated by: Haiyan Tong, U.S. EPA Human Studies Facility
This observational study recruits healthy individuals who have been routinely taking high amount (at least 3 g/wk) of dietary eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), and those who don't, and examines the efficacy of dietary EPA and DHA in ameliorating the cardiopulmonary effects of exposure to ambient air pollution.

Study Overview

Status

Completed

Detailed Description

Purpose: To examine the relationship between blood levels of dietary eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and cardiopulmonary responses to environmental air pollution in healthy adults. EPA and DHA are two important omega-3 fatty acids that are mainly found in seafoods and fish oils and associated with beneficial effects to human physiology.

Participants: Healthy 35-55 year-old male and female subjects will be screened for their dietary intake of EPA and DHA. Qualified volunteers will be divided into two groups, group 1: individuals voluntarily taking at least 3 g/wk of EPA and DHA from dietary sources including fish oil supplements and ocean fish/shellfish consumption for a period of at least 6 months prior to enrollment in the study; group 2: individuals who have consumed no more than 1 serving size (4-6 oz)/month of ocean fish/shellfish, or no more than 1 pill/month of fish oil supplement during the 6 month period preceding enrollment.

Procedures (Methods): In this observational panel study, subjects will come to the U.S. EPA Human Studies Facility for up to 5 sessions, each consisting of 2 consecutive visit days. The following endpoints will be collected: blood pressure, heart rate variability measurements, blood biomarkers, endothelial cell function, retinal venule and arteriole diameter, and lung function. Air pollution exposure will be assessed using area-specific air quality data derived from local air monitoring stations interfaced with activity monitoring and GPS tracked location for each subject.

Study Type

Observational

Enrollment (Actual)

62

Contacts and Locations

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

Study Locations

    • North Carolina
      • Chapel Hill, North Carolina, United States, 27514
        • EPA Human Studies Facility

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

25 years to 55 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Healthy 35-55 year-old male and female subjects

Description

Inclusion Criteria:

  • Aged 25-55 years old healthy male and female (19≤BMI≤30).
  • Normal resting ECG. No history of heart arrhythmia.
  • Oxygen saturation greater than 96% at the time of physical exam.
  • Taking at least 3 grams of EPA and DHA from dietary sources including fish oil supplements and ocean fish/shellfish for a 6 months or longer period of time preceding enrollment in the study; or taking no more than 1 serving size (4-6 oz)/month of ocean fish/shellfish, or no more than 1 pill/month of fish oil supplement during the previous 6 months or longer period of time.

Exclusion Criteria:

  • Individuals with a history of acute or chronic cardiovascular disease, such as myocardial infarction.
  • Individuals with a history of chronic respiratory disease, such as COPD and asthma.
  • Individuals with a history of cancer (possible exception for history of non-melanoma skin cancer).
  • Uncontrolled hypertension (≥150 systolic, ≥90 diastolic).
  • Individuals who are diabetic (previously diagnosed or with hemoglobin A1c level >6.4%).
  • Individuals who are currently smoking (including vaping, or using hookah or e cigarettes) or have a smoking history within 1 year of study (defined as more than 1 pk/yr in the past year) or have a greater than/equal to a 5 pack year smoking history.
  • Individuals living with a smoker who smokes inside the house.
  • Individuals who are regularly exposed to high levels of vapors, dust, gases, or fumes.
  • Individuals who do not understand or speak English.
  • Individuals who are taking b-blocker medications.
  • Individuals who are taking statins.
  • Individuals that are unwilling or unable to maintain their current dietary pattern for the whole study.
  • Individuals with bleeding or clotting disorders.
  • Individuals who have active allergies.
  • Individuals who have an allergy to latex, or skin allergy to tape or electrodes.
  • Individuals who are pregnant or attempting to become pregnant.
  • Individuals who have unspecified illnesses, which in the judgment of the investigators might increase the risk associated with clinical procedures will be a basis for exclusion.
  • Individuals who are currently taking anti-depressants.

Temporary exclusion criteria:

  • Individuals who have had recent (within 6 months) abdominal and/or eye surgery, or been diagnosed with any type of hernia, as well as any other contraindications for raised intra-abdominal pressure.
  • Individuals who have had an acute respiratory illness within 4 weeks.

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
Intervention / Treatment
omega-3
individuals voluntarily taking at least 3 g/wk of EPA and DHA from dietary sources including fish oil supplements and ocean fish/shellfish consumption for a period of at least 6 months prior to enrollment in the study
control
individuals who have consumed no more than 1 serving size (4-6 oz)/month of ocean fish/shellfish, or no more than 1 pill/month of fish oil supplement during the 6 month period preceding enrollment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
heart rate variability
Time Frame: Sep. 2016 to Sep 2019
Sep. 2016 to Sep 2019

Secondary Outcome Measures

Outcome Measure
Time Frame
endothelial cell function
Time Frame: Sep. 2016 to Sep 2019
Sep. 2016 to Sep 2019
diameters of retinal arteries and veins
Time Frame: Sep. 2016 to Sep 2019
Sep. 2016 to Sep 2019
pulmonary function indices
Time Frame: Sep. 2016 to Sep 2019
Sep. 2016 to Sep 2019
blood biomarkers
Time Frame: Sep. 2016 to Sep 2019
Sep. 2016 to Sep 2019

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

September 15, 2016

Primary Completion (Actual)

November 15, 2019

Study Completion (Actual)

November 15, 2019

Study Registration Dates

First Submitted

September 28, 2016

First Submitted That Met QC Criteria

September 28, 2016

First Posted (Estimate)

September 30, 2016

Study Record Updates

Last Update Posted (Actual)

May 10, 2022

Last Update Submitted That Met QC Criteria

May 8, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • HSF-001

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.

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