Effects of Fish Oil and Red Wine on Oxidative Stress Biomarkers



Status:Active, not recruiting
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:21 - 60
Updated:2/14/2019
Start Date:May 2008
End Date:November 2026

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Effects of Fish Oil and Red Wine on Oxidative Stress Biomarkers: a Randomized Double-blinded Trial on the Modulation of the Eicosanoid and Isoprostane Pathways in Healthy Subjects by Omega-3 Polyunsaturated Fatty Acids and Red Wine.

The American Heart Association and the American College of Cardiology (AHA/ACC) recently
encouraged "increased consumption of omega-3 fatty acids in the form of fish or capsule form
(1 g/day) for risk reduction" and stated that "for treatment of elevated triglycerides,
higher doses are usually necessary for risk reduction" (Smith SC et al. Circulation
2006;113:2363-72). These recommendations are based on conflicting evidence about the efficacy
of the omega-3 treatment with data derived from single randomized trials or non-randomized
studies (Smith SC et al. Circulation 2006;113:2363-72). Much effort has been undertaken to
elucidate the role of omega-3 fatty acids in the development of cardiovascular disease, but
even recent meta-analyses deliver no clear picture; they either favor (Mozaffarian D Jama
2006;296:1885-99) or reject (Hooper L Bmj 2006;332:752-60) the hypothesis of cardioprotective
effects of omega-3 FAs.

The objective of the clinical study is to study the effects of fish oil on blood and urinary
markers of inflammation and cell stress. By using different permutations of high-dose
supplementation of omega-3 and omega-6 fatty acids versus different alimentary omega-3 fish
doses and grain alcohol versus different kinds of red wine, this trial will study how omega-3
fatty acids, ethanol and red wine constituents modulate biomarkers of inflammation and cell
stress.

This clinical study comprises several parts:

Part 1: Single-arm open oral administration of ethanol in n=40 healthy participants.

Part 1.1: Single-arm open oral administration of fish oil capsules and ethanol in n=12
healthy participants.

Part 2a: Randomized double-blind oral administration of fish oil or safflower oil capsules
and ethanol in n=44 healthy participants.

Part 2b: Randomized double-blind oral administration of fish foods or control diet and open
oral administration of ethanol in n=40 healthy participants.

Part 3: Randomized double-blind oral administration of fish foods or control diet and red
wine beverages in n=40 healthy participants.

Inclusion Criteria:

- Age between 21 - 60,

- Subjects must be in good health as based on medical history, physical examination,
vital signs, and laboratory tests.

- All Subjects have to adhere to the following criteria:

- Must be non-smoking volunteers (both male and non-pregnant females) due to a
significant influence of smoking and overweight on the outcome measures of lipid
peroxidation,

- Must be of normal weight with a body mass index (BMI) ≤ 25. The correlation between
the BMI number and body fatness is fairly strong; however it varies by sex, race, and
age. These variations include the following examples: At the same BMI, women tend to
have more body fat than men; at the same BMI, older people, on average, tend to have
more body fat than younger adults; highly trained athletes may have a high BMI because
of increased muscularity rather than increased body fatness; source at
http://www.cdc.gov/healthyweight/assessing/bmi/adult_BMI/index.html. Therefore,
subjects with a BMI > 25 can be enrolled at the discretion of the PI in writing.

- Female subjects of child bearing potential must be using a medically acceptable method
of contraception (oral contraception, depo-provera injection, IUD, condom with
spermicide, diaphragm, cervical cap, progestin implant, abstinence, tubal ligation,
oophorectomy, TAH) throughout the entire study period. All female subjects must
consent to a urine pregnancy test at screening and just prior to the start of each
treatment phase of the study (first study visit, every ethanol administration visit,
at first visit of fish oil administration), and during the third week of fish oil
administration. All pregnancy tests must be negative at all time points.

- Male subjects must be surgically sterile and/or agree to use condoms throughout the
duration of the study.

- Persons who consume vitamin supplements are required to undergo a "washout period" of
≥ five weeks without supplement prior to study enrollment (in analogy to Block G, et
al. Am J Epidemiol 2002; 156: 274)

- Urine ethanol assessment indicating abstinence.

Exclusion Criteria:

- Female subjects who are pregnant or nursing a child.

- Subjects, who have received an experimental drug, used an experimental medical device
within 30 days prior to screening, or who gave a blood donation of ≥ one pint within 8
weeks prior to screening.

- Subjects with any coagulation, bleeding or blood disorders.

- Subjects with nutritional inefficiencies in Fe, Zn, Cu, Mg (according to 61)

- Subjects who are sensitive or allergic to fish, fish oil or fish-containing products.

- Subjects with any evidence of cancer or history of significant cardiovascular disease
(including stroke or TIA), renal, hepatic, respiratory, endocrine, metabolic,
hematopoietic or neurological disorder.

- Subjects with a systolic blood pressure above 160 or a diastolic blood pressure above
95,

- Subjects with any evidence of GI disorders that could interfere with fat absorption

- Subjects with an intention to lose weight during their participation in the trial

- Subjects with any abnormal laboratory value or physical finding that according to the
investigator may interfere with interpretation of the study results, be indicative of
an underlying disease state, or compromise the safety of a potential subject. Subjects
who have had a history of drug or alcohol abuse within the last 6 months.

- Carbohydrate-deficient transferrin > 6% indicating chronic alcohol abuse

- Complete abstinence from alcohol

- Intake of more than three alcoholic drinks per day

- Subjects with a history of cancer, including skin cancer
We found this trial at
1
site
Philadelphia, Pennsylvania 19104
Principal Investigator: Garret A FitzGerald, M.D.
Phone: 215-662-4652
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mi
from
Philadelphia, PA
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