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HMG CoA reductase inhibitors, NSAIDs and risk of glioma
Jennifer S Ferris1, Lucie McCoy, Alfred I Neugut
1Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Abstract:
3-Hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase inhibitors (statins) have shown inverse associations with cancer risks, but the results have been inconsistent. As there are no previous published data in brain tumors, we conducted a case-control study to investigate statin therapy and risk of glioma. We further evaluated the use of nonsteriodal anti-inflammatory drugs (NSAIDs) and risk of these tumors. We recruited newly diagnosed glioma cases and frequency matched controls at Columbia University and the University of California San Francisco. Standardized questions on statins and NSAIDs were used at both institutions. Intakes of these drugs were defined as >6 months of at least twice weekly use versus less than this amount or never use. From July 2007 to January 2010, we recruited a total of 517 cases and 400 controls. Simvastatin and lovastatin showed significant inverse associations with glioma (odds ratio [OR] = 0.49, 95% confidence interval [CI] 0.30, 0.81 and OR = 0.47, 95% CI 0.24, 0.93, respectively). For NSAIDs, aspirin use was also inversely related to glioma risk (OR = 0.68, 95% CI 0.49, 0.96). Both statins and NSAIDs showed significant inverse trends between the duration of drug use and glioma risk (trend tests p = 0.03 and p = 0.02, respectively), and drug intake for >120 months demonstrated the most significant associations for both types of medication. The inverse association between statin therapy and risk of glioma supports the roles of Ras/Rho GTPases or inflammatory cytokines in gliomagenesis, and a similar relationship between NSAIDs and glioma highlights the importance of cyclo-oxygenase 2 in glioma pathogenesis.
Insights
Statins and NSAIDs, including aspirin, may reduce glioma risk. Longer use of these drugs showed stronger inverse associations with glioma development, suggesting a role in brain tumor pathogenesis.
Area of Science:
- Neuro-oncology
- Pharmacology
- Epidemiology
Background:
- Statins (HMG CoA reductase inhibitors) show inconsistent associations with cancer risk.
- Limited data exists on statin use and brain tumor risk, specifically glioma.
- Nonsteroidal anti-inflammatory drugs (NSAIDs) are also investigated for their potential role in cancer prevention.
Purpose of the Study:
- To investigate the association between statin therapy and glioma risk.
- To evaluate the association between NSAID use and glioma risk.
- To explore the impact of drug usage duration on glioma risk.
Main Methods:
- A case-control study was conducted with newly diagnosed glioma cases and frequency-matched controls.
- Data on statin and NSAID use (defined as >6 months, ≥twice weekly) were collected.
- 517 cases and 400 controls were recruited between July 2007 and January 2010.
Main Results:
- Simvastatin and lovastatin use were associated with significantly reduced glioma risk (OR=0.49, OR=0.47).
- Aspirin use was also inversely related to glioma risk (OR=0.68).
- Significant inverse trends in glioma risk were observed with longer duration of statin and NSAID use (p=0.03, p=0.02).
Conclusions:
- Statin therapy is associated with a reduced risk of glioma, potentially through pathways involving Ras/Rho GTPases or inflammatory cytokines.
- NSAID use, particularly aspirin, is also linked to lower glioma risk, highlighting the role of cyclo-oxygenase 2 in glioma pathogenesis.
- Extended use of both statins and NSAIDs demonstrated the most significant risk reduction for glioma.
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