HEALTH
Getting a Grip on Pain
cgi.newsweek.com
A new drug may revolutionize arthritis care
By Geoffrey Cowley
Like many arthritis sufferers, 69-year-old Peggie Landvatter faces a daily dilemma. Should she endure the burning pain in her hips and knees--or take her ibuprofen, and transfer the pain to her stomach? "Every time I take something for the arthritis," she says, "it aggravates the ulcer." Nearly a third of America's 40 million arthritis sufferers use drugs like aspirin and ibuprofen to ease their joint pain. Taken in large daily doses, these so-called NSAIDs (nonsteroidal anti-inflammatory drugs) can make daily life bearable--or unbearable. An estimated 107,000 people were hospitalized for NSAID- induced stomach ulcers last year, and 16,500 died of complications from bleeding. But relief may be in sight. Last week advisers to the Food and Drug Administration recommended approval of a new prescription drug called Celebrex. The first in a new class of remedies known as Cox-2 inhibitors, it boasts the same pain-fighting power as other NSAIDs--yet studies suggest it's as easy on the stomach as warm milk. Celebrex could reach the market within the next few months, opening a new era in arthritis care.
To appreciate the beauty of the Cox-2 inhibitors, you need to understand how the older NSAIDs work. Scientists discovered back in the 1970s that the drugs handcuff an enzyme called cyclooxygenase--Cox for short. The body's Cox enzymes normally metabolize a fat called arachidonic acid to generate inflammatory hormones called prostaglandins. When a drug like aspirin knocks Cox out of commission, it stalls the production of prostaglandins, dramatically reducing pain and inflammation. The catch is that prostaglandins do more than make us miserable. While some of them spark inflammatory reactions, others work quietly to maintain the lining of the digestive tract. The question was how to suppress the potential troublemakers while letting the housekeepers go about their work. The answer came in 1991, when scientists isolated two distinct Cox enzymes. Conveniently, one of them (dubbed Cox-1) seemed to govern the housekeeping prostaglandins, while the other (Cox-2) specialized in pain and inflammation. By screening hundreds of drug molecules, researchers led by Dr. Philip Needleman of G.D. Searle & Co. found one that bound selectively to Cox-2. The result was Celebrex.
Because the new drug has 400 times more affinity for Cox-2 than for Cox-1, even large doses have little effect on digestive tissues. When Searle researchers snaked endoscopes into patients' stomachs, they found that 25 percent of those taking traditional NSAIDs harbored small, harmless lesions. The incidence of lesions was just 5 percent among Celebrex users, the same rate seen among patients receiving a placebo. And whereas 2 to 4 percent of prescription NSAID users suffer overt stomach problems, such as bleeding or ulcers, the rate of such events was just 0.2 percent in Searle's studies. Peggie Landvatter, who took part in a three-month Celebrex trial, found that the drug changed her life. "There was no pain or discomfort," she says, referring to her stomach as well as her joints. "I was doing things I'd put off for years."
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