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October 27, 2016Journal of Investigative Medicine12 citations

Does Aspirin Use Reduce the Risk for Cancer?

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UIUsman IqbalHYHsuan‐Chia YangWJWen‐Shan Jian

Key Result

Aspirin use was associated with a reduced overall cancer risk (adjusted OR 0.95; 95% CI 0.94 to 0.96), specifically for colorectal and digestive system cancers.

Study Design

Type

Case-Control (n=3,008,665)

Structured PICO

Does aspirin use reduce the risk for cancer in the Taiwanese population?

P
Population
601,733 patients diagnosed with cancer and 2,406,932 matched controls (matched for age, sex, and index date) from the Taiwan NHI database (2001-2011)
I
Intervention
Aspirin use
C
Comparator
No aspirin use
O
Outcome
Overall cancer riskhard clinical

Aspirin use is associated with a small but statistically significant reduction in overall, colorectal, and digestive system cancer risk in a large Taiwanese cohort.

Main Result

Effect estimate: AOR 0.95 (95% CI 0.94 to 0.96)

Abstract

Recently, studies have reported that aspirin has chemopreventive properties. In this study, we used the Taiwan NHI database, which covers a population of 23 million (99.99%) Taiwanese from 2001 to 2011. This was a case-control study which identified 601,733 patients using ICD-9-CM codes who were diagnosed with cancer. Each case with 4 eligible controls was matched for age, sex, and index date and adjusted for confounding factors. The observed overall cancer risk (adjusted OR (AOR), 0.95; 95% CI 0.94 to 0.96) reduced with aspirin use, specifically, colorectal (AOR, 0.97; 95% CI 0.94 to 0.99) and digestive system (AOR, 0.96; 95% CI 0.94 to 0.98) cancers. Findings from the Asian population would contribute to the discussion on aspirin's safety profile.

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Cite This Study

Iqbal et al. (2016) conducted a case-control in Cancer (n=3,008,665). Aspirin vs. No aspirin use (matched controls) was evaluated on Overall cancer risk (AOR 0.95, 95% CI 0.94 to 0.96). Aspirin use was associated with a reduced overall cancer risk (adjusted OR 0.95; 95% CI 0.94 to 0.96), specifically for colorectal and digestive system cancers.

synapsesocial.com/papers/6a164f4ef9339c53aa8eba85https://doi.org/10.1136/jim-2016-000275
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