We hypothesize that administration of anti-inflammatory medications such as celecoxib, naprosyn and diclofenac will cause changes in the blood plasma and white blood cells of patients such that they will be less able to efficiently process cholesterol.

Population

Patients age 40-70 who fulfill the ACR criteria for a diagnosis of primary osteoarthritis are considered

Brief Title

Anti-inflammatory Agents and Cholesterol Metabolism

Official Title

Impact of Anti-inflammatory Agents on Cholesterol Metabolism and Atherogenic Potency of Patient Plasma

Brief Summary

We hypothesize that administration of anti-inflammatory medications such as celecoxib,<br /> naprosyn and diclofenac will cause changes in the blood plasma and white blood cells of<br /> patients such that they will be less able to efficiently process cholesterol.

Detailed Description

Drugs that inhibit cyclooxygenase (COX) are frequently administered to relieve pain and
inflammation, but have been associated with cardiovascular (CV) toxicity and an elevated risk
of acute myocardial infarction. We have demonstrated that drugs that inhibit the COX-2
isoform act to interfere with cellular cholesterol movement by suppressing expression of
proteins that facilitate efflux of cholesterol as well as by enhancing expression of
scavenger receptors that mediate cholesterol uptake. We further showed that in cultured THP-1
human macrophages, COX-2 inhibition with drugs (celecoxib, NS398) or by COX-2 RNA silencing
leads to foam cell transformation, a critical component of atherogenesis. Thus, COX-2
inhibitors act in a pro-atherogenic fashion on a series of genes which we have named the
"Cholesterol Metabolic Signature." Alterations in this signature may contribute to heightened
risk of development of atherosclerotic CV disease associated with prolonged use of this drug
class. COX enzyme activity supports cholesterol homeostasis through catalysis of
prostaglandin (PG) production, and we have shown in vitro that specific subsets of these PGs
(PGD2 or PGE2) are sufficient to maintain balance. The aims of this project is: In an
observational study of persons with pharmacologic COX-2 selective inhibition (celecoxib) or
COX-1/2 inhibition (naproxen, diclofenac), document treatment effects on the Cholesterol
Metabolic Signature in isolated subject mononuclear cells and in naïve THP-1
monocytes/macrophages exposed to subject plasma. This will allow detection of variations in
degree of pro-atherogenic response of the Cholesterol Metabolic Signature to COX inhibition
within human patients that may be associated with a higher likelihood of developing CV
sequelae. Understanding the nature of the association between COX inhibition and cholesterol
metabolism, and the extent to which they may promote atherosclerotic CV disease, is of
critical importance in developing analgesic and anti-inflammatory medications with a more
favorable risk profile. The knowledge gained may also improve clinical decision-making by
identifying subsets of patients most vulnerable to adverse CV effects of COX inhibition.

Outcome Measures

Outcome measures are the tests that investigators perform to prove whether or not a treatment being tested in a clinical trial is having any effect.