Study links Celebrex, heart valve calcification after earlier research declared drug safe
A well-known, four-year study found popular arthritis drug Celebrex no more dangerous for the heart than older drugs in its same classification – commonly called NSAIDs. Now, a big-data analysis of patient records at Vanderbilt University has found a link specifically between Celebrex and heart valve calcification.
W. David Merryman, professor of biomedical engineering, Meghan Bowler (Ph.D ’18) started out by testing celecoxib, the active compound in Celebrex, on valve cells in an effort to see if it could double as an aortic stenosis therapy. It made the problem worse.
To confirm their theory about a link between celecoxib and valve calcification, Merryman, who is also a professor of pharmacology, medicine and pediatrics at Vanderbilt, recruited Michael Raddatz, an M.D./Ph.D. student, to analyze more than 8,600 relevant, anonymous patient records from Vanderbilt University Medical Center. Raddatz checked whether there was a link between Celebrex use and aortic valve disease, and, after correcting for other risk factors, discovered that patients who had taken Celebrex had a 20 percent increased prevalence of valve disease.
The 2016 New England Journal of Medicine study that found Celebrex no more damaging than naproxen and ibuprofen only looked at cardiovascular death and nonfatal heart attack or stroke, not valve disease, which affects more than a quarter of the U.S. population older than 65.
“In this study, we’re adding a long-term perspective on celecoxib use,” said Bowler. “Calcification in the aortic valve can take many years. So if you’re at a higher risk for it, you might want to consider taking a different painkiller or rheumatoid arthritis treatment.”
As part of the same study, Bowler and Merryman found dimethyl celecoxib – an inactive form of celecoxib – could potentially slow or stop aortic stenosis. Merryman said he intends to keep testing dimethyl celecoxib for its beneficial effects on heart valve health.
His work was funded by the following grants: NIH R35 (HL135790), NIH R01 (HL115103), NIH T32 (GM007347), NSF CAREER Award (1055384), and NSF Graduate Research Fellowship (2013170175).
by Heidi Hall