Evidence map›Paper›PMID 21764857›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2011

Nonsteroidal anti-inflammatory drug use and risk of adenomatous and hyperplastic polyps.

Harvey J Murff, Martha J Shrubsole, Zhi Chen, Walter E Smalley, Heidi Chen, Yu Shyr, Reid M Ness, Wei Zheng

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Harvey J MurffDivision of General Internal Medicine and Public Health, Vanderbilt University Medical Center, Nashville, TN, USA. harvey.j.murff@vanderbilt.edu
Martha J Shrubsole
Zhi Chen
Walter E Smalley
Heidi Chen
Yu Shyr
Reid M Ness
Wei Zheng
Geriatric Research Education and Clinical Center · USVanderbilt-Ingram Cancer CenterVanderbilt University Medical Center · USVA Tennessee Valley Healthcare System · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
Understanding and Controlling p120 Dysfunction in CRCP50CA095103 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2002 to 2017
$33.6M
Tumor Markers and Recurrent Adenomas: A Follow-up StudyR01CA097386 · NCI · VANDERBILT UNIVERSITY · PI ZHENG, WEI · 2002 to 2006
$3.6M
Long-Chain Fatty Acids, Oxidative Stress and Colorectal Neoplasm RiskR01CA143288 · NCI · VANDERBILT UNIVERSITY · PI MURFF, HARVEY J. · 2010 to 2013
$1.0M
Mechanisms and Management of Familial Colon CancerK07CA114029 · NCI · VANDERBILT UNIVERSITY · PI MURFF, HARVEY J. · 2006 to 2010
$651k
NCI NIH HHS K07 CA114029NCI NIH HHS K07CA114029NCI NIH HHS P30 CA068485NCI NIH HHS P30 CA 68485NCI NIH HHS P50 CA095103NCI NIH HHS P50CA95103NCI NIH HHS R01 CA097386NCI NIH HHS R01 CA143288NCI NIH HHS R01CA143288NCI NIH HHS R01CA97386
6 · The paper itself

Abstract

Adenomatous polyps are known precursor lesions for colorectal cancer and some hyperplastic polyps also have malignant potential. The use of aspirin and nonsteroidal anti-inflammatory drugs (NSAID) is associated with a reduced risk of adenomatous polyps; however, less evidence exists with regard to NSAID use and hyperplastic polyp risk. We conducted a colonoscopy-based case-control study including 2,028 polyp cases (1,529 adenomatous and 499 hyperplastic) and 3,431 polyp-free controls. Multivariate logistic regression models were constructed to derived adjusted ORs and 95% CIs as the measure of the association between NSAID use and polyp risk. Use of baby aspirin, regular aspirin, and nonaspirin NSAIDs, were associated with a reduced risk of adenomatous polyps (OR = 0.79, 95% CI: 0.66-0.93, OR = 0.73, 95% CI: 0.58-0.90, and OR = 0.67, 95% CI: 0.53-0.86, respectively). Baby aspirin was also associated with a reduced risk of hyperplastic polyps (OR = 0.74, 0.56-0.97). Although a dose response was seen with adenoma risk and regular use of any NSAIDs (less than 7 doses per week, 7 doses per week, and greater than 7 doses per week), a dose response was not seen with hyperplastic polyps. We found no evidence of interaction between NSAID dose and duration and polyp risk. The use of any NSAID regardless of type was associated with a reduced risk of adenomatous polyps; however, regular aspirin and COX-2 inhibitors use was not associated with hyperplastic polyp risk.

Indexed as

AdenomaAdenomatous PolypsAdultAgedAnti-Inflammatory Agents, Non-SteroidalCase-Control StudiesColonic PolypsColonoscopyFemaleHumansHyperplasiaMaleMiddle AgedPrognosisRisk FactorsAnti-Inflammatory Agents, Non-Steroidal

Identifiers

PMID21764857
PMCPMC3203989
OpenAlexW2115304388

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.