Effects of Omega-3 Fatty Acids in Ambient Air Pollution Exposure in Healthy Adults
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 35 - 55 |
Updated: | 10/28/2017 |
Start Date: | September 2016 |
End Date: | September 2019 |
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.
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.
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.
(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.
Inclusion Criteria:
- Aged 35-55 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.
We found this trial at
1
site
Chapel Hill, North Carolina 27599
Principal Investigator: Haiyan Tong, MD, PhD
Phone: 919-966-6217
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