Oral Docosahexanoic Acid Supplementation in Cystic Fibrosis

The study design will be a single-center, randomized, placebo-controlled, cross-over trial.
After informed consent has been obtained, 18 eligible subjects with pancreatic insufficient
cystic fibrosis will be enrolled in the study. Participants will take part in two 4 week
study sessions, each separated by a 4 week washout period. One session will involve
treatment with placebo and the other two sessions will provide treatment with approximately
25mg and 35 mg of DHA/kg of body weight. The patients will be assigned to each of the
treatment sessions in random order, as described above. The DHA source will be provided by
Martek Biosciences Corporation, Columbia, MD, USA in the form of a chewable capsule
containing 200 mg of DHA. The placebos will be identical to the DHA supplement but will not
contain the active ingredient, DHA. Subjects will be instructed to take the study capsules
in addition to their normal doses of pancreatic enzymes with meals and to maintain their
usual diets. Blood, urine, and exhaled breath condensate samples will be collected at
baseline and after completion of each of the study periods. Patients will be screened and
enrolled when they present to clinic for their routine check-up. The subjects have routine
blood work at their annual check-ups, and when possible will have an additional tube of
blood saved for the baseline fatty acid profiles so as to avoid unnecessary blood draws.
Following each study period, blood draw, urine collection, and exhaled breath condensate
(EBC) will be collected at the Vanderbilt Clinical Research Center. The patients will also
be given the supply of DHA and placebo (for the entire study) at time of enrollment. The
order in which they take the supplement or the placebo will be determined using a
randomization table.

Inclusion Criteria:

- Diagnosis of Cystic Fibrosis based on sweat chloride value > 60 mEq/L or genotyping

- Pancreatic insufficiency, defined by requirement for treatment with exogenous
pancreatic enzymes

- FEV 1 > 40

- Less than 3 pulmonary exacerbations in the last year (as diagnosed by pulmonary
attending physician)

- Age greater than 6 years

- Capability of performing pulmonary function tests

- Ability to swallow gel capsule

- Ability to comply with medication use, study visits, and study procedures

- Written informed consent obtained from subject or study subject's legal
representative

Exclusion Criteria:

- Presence of severe CF-related liver disease, including SGOT or SGPT>3 times the
normal limits, history of biliary cirrhosis, or portal hypertension

- Severe pulmonary disease, as defined by FEV1 < 40%

- Elevated serum creatinine or BUN

- Pregnancy

- PT >1.5 time normal

- Diabetes mellitus

- Daily use of NSAIDs or other anticoagulants

- History of fish allergy

- Use of ticlopidine, clopidogrel, dipyridamole

- Use of glucocorticoids

- History of lung transplant or currently on lung transplantation list

- Presence of a condition or abnormality that in the opinion of the investigator would
compromise the safety of the subject or the quality of the data