With the advancement of medical technology, COX inhibitors have become one of the indispensable drugs in daily life, especially in the treatment of inflammation, pain and other chronic diseases. However, in recent years, more and more studies have begun to reveal the complex relationship between COX inhibitors and cardiovascular risk, causing people to doubt their safety.
COX (cyclooxygenase) is an important enzyme responsible for converting arachidonic acid into prostaglandins, molecules that play a key role in regulating inflammatory responses and other physiological processes. There are two main isoforms of COX: COX-1 and COX-2. Generally speaking, COX-1 plays a role in maintaining the integrity of the gastrointestinal mucosa and renal function in normal physiology, while COX-2 is usually expressed more strongly during inflammation.
Drugs that inhibit COX can provide relief from inflammation and pain. Nonsteroidal anti-inflammatory drugs (NSAIDs) such as aspirin and ibuprofen work by inhibiting COX.
Based on their selectivity, COX inhibitors can be divided into traditional NSAIDs and selective COX-2 inhibitors. Traditional NSAIDs generally have an inhibitory effect on all types of COX, which leads to significant side effects on the digestive system, common of which include peptic ulcers and stomach discomfort. Selective COX-2 inhibitors such as celecoxib and etoricoxib are favored because of their lower gastrointestinal adverse reactions.
Although COX-2 inhibitors can reduce gastrointestinal discomfort, studies suggest they may increase the risk of cardiovascular events. A 2006 analysis found that selective COX-2 inhibitors were associated with an increased risk of myocardial infarction. Although this result was disputed in the 2016 PRECISION trial, which showed that celecoxib had a lower incidence of cardiovascular death and other major cardiovascular events than ibuprofen and naproxen, these results do not necessarily reduce the vigilance for cardiovascular risk.
It is worth noting that some traditional NSAIDs such as difluchlorothiazide and ibuprofen are also associated with increased cardiovascular risk when used in high doses.
In search of safer alternatives, many studies have turned to natural COX inhibitors. Certain plant ingredients, such as shiitake mushrooms and fish oil, have been found to inhibit COX activity without causing cardiovascular risks. These natural substances not only provide anti-inflammatory effects, but also have positive effects on cardiovascular health.
Currently, research on COX inhibitors is still ongoing, and the use of drugs should be based on individual circumstances. Although COX inhibitors play an irreplaceable role in the treatment of inflammation and pain, vigilance against cardiovascular risks remains a challenge that the medical community and patients need to overcome. In the future, can we find a solution that can effectively control pain while ensuring cardiovascular health?