Aspirin
was formed in 1899 when acetylsalicylic acid was first created. Since then aspirin
has become very a well know drug. It can be used for pain relief, anti-inflammation, as an antipyretic, and as a blood thinner. Now studies are showing that aspirin
is also reducing people’s risk of getting certain cancers. A study was done on
people who had Lynch syndrome, a condition that increases your risk of
colorectal and endometrial cancers. Participants in the study were taking a high
dosage of aspirin and showed a 63% relative risk reduction for developing
colorectal cancers. In June of 2016, a JAMA Oncology study from Harvard showed
that aspirin use of 6 years or longer reduced the risk of colorectal cancer by
19% and gastrointestinal cancer by 15%. The USPSTF currently states that the
people who get the most benefit with the lowest added risk from aspirin are
people ages 50 to 59 who have an elevated risk for cardiovascular disease
(National Cancer Institute, n.d.).
While
aspirin does have some great benefits it also comes with some potentially
harmful side effects. Like many other analgesics, there is a potential risk for
ulcers, gastrointestinal bleeds, and the most concerning is an overall increased
risk of bleeding. Aspirin inhibits the COX enzyme. This blocks prostaglandins,
prostacyclins, and thromboxanes that are normally produced under certain
stimuli such as pain. When thromboxanes specifically are inhibited it causes platelet
aggregation to stop (Undas, Brummel-Ziedins, & Mann, 2007). This is a very
dangerous side effect for some people because if you are unable to clot
bleeding to death becomes a serious concern. I think this opens up the door for
a lot more research and controversy around aspirin. It is a drug capable of
providing some great benefits, but it also has a decent amount of risk carried
along with that. It would be interesting to find out exactly what
mechanistically in aspirin is reducing the risk of cancer and if that could be
isolated. Until then how do weight the risks and benefits of aspirin since it
is impossible to know how many heart attacks and strokes it really prevents?
Who gets to decide whether a drug with the potential to decrease the risk of
heart attacks, strokes, and gastrointestinal cancers should be taken and who
qualifies?
Aspirin to Reduce Cancer Risk. (n.d.).
Retrieved from https://www.cancer.gov/about-cancer/causes-prevention/research/aspirin-cancer-risk.
Connelly, D. (2014, September 26). A history
of aspirin. Retrieved from https://www.pharmaceutical-journal.com/news-and-analysis/infographics/a-history-of-aspirin/20066661.article.
Is
Taking Aspirin Good for Your Heart? (n.d.). Retrieved from https://www.hopkinsmedicine.org/health/wellness-and-prevention/is-taking-aspirin-good-for-your-heart.
Undas,
A., Brummel-Ziedins, K. E., & Mann, K. G. (2007, March 15). Antithrombotic
properties of aspirin and resistance to aspirin: beyond strictly antiplatelet
actions. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1852201/.
The finding that aspirin can be associated with a decreased cancer risk is very cool and important considering its widespread use as a pharmaceutical agent. Other articles support the reduction in cancer risk associated with the use of non-steroidal anti-inflammatory drugs, including aspirin, and further suggest that other diseases such as Alzheimer’s can be reduced with these drugs (Flower, 2003). As mentioned above, Aspirin inhibits the COX pathway and more specifically aspirin inhibits both the COX 1 and COX 2 pathways (Flower, 2003). Even though the exact mechanism is unknown, the reductions in disease rates appear to be specifically associated with the COX 2 pathway (Flower, 2003). While aspirin works in reducing the COX 2 pathway, it also blocks the COX 1 pathway. Finding inhibitors specific to the COX 2 pathway could greatly reduce the negative effects of prolonged aspirin use and simultaneously keep the positive benefits that help reduce cancer and other diseases.
ReplyDeleteFlower, R. (2003). What are all the things that aspirin does? BMJ : British Medical Journal, 327(7415), 572–573. https://doi.org/10.1136/bmj.327.7415.572