Evidence map›Paper›PMID 24875374›Full record

ArticleAmerican journal of epidemiology2014

Variation in the association between colorectal cancer susceptibility loci and colorectal polyps by polyp type.

Andrea N Burnett-Hartman, Polly A Newcomb, Carolyn M Hutter, Ulrike Peters, Michael N Passarelli, Malaika R Schwartz, Melissa P Upton, Lee-Ching Zhu, John D Potter, Karen W Makar

Open access · bronzeAbstract read
In one paragraph

Article in American journal of epidemiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 18 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

10 authors at 1 institution in 1 country.

Andrea N Burnett-Hartman
Polly A Newcomb
Carolyn M Hutter
Ulrike Peters
Michael N Passarelli
Malaika R Schwartz
Melissa P Upton
Lee-Ching Zhu
John D Potter
Karen W Makar
Fred Hutch Cancer Center · US

Funding

Institute of Translational Health SciencesKL2TR000421 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$12.6M
Developing Data-Driven Cancer ResearchersT32CA009168 · NCI · UNIVERSITY OF WASHINGTON · PI STEPHEN M SCHWARTZ, MICHAEL Chiao-An WU · 1985 to 2026
$10.1M
SCREENING MARKERS FOR COLORECTAL CANCERP01CA074184 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STORER, BARRY E. · 1998 to 2002
$4.2M
Colon Cancer Pathways: Hyperplastic Polyps and AdenomasR01CA097325 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2004 to 2009
$2.7M
Training and Research in Colon Cancer SurvivalK05CA152715 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2010 to 2019
$991k
GWAS Identified Colorectal Cancer SNPs and Colorectal Polyp RiskR03CA153323 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2010 to 2011
$173k
NCATS NIH HHS KL2 TR000421NCI NIH HHS K05 CA152715NCI NIH HHS P01 CA074184NCI NIH HHS R01 CA097325NCI NIH HHS R01CA097325NCI NIH HHS R03 CA153323NCI NIH HHS T32 CA009168
6 · The paper itself

Abstract

We conducted a case-control study of the association between subsets of colorectal polyps, including adenomas and serrated polyps, and single-nucleotide polymorphisms (SNPs) related to colorectal cancer through prior genome-wide association studies (GWAS). Participants were enrollees in the Group Health Cooperative (Seattle, Washington) aged 24-79 years who received a colonoscopy from 1998 to 2007, donated a buccal or blood sample, and completed a structured questionnaire. We performed genotyping of 13 colorectal cancer susceptibility SNPs. Polytomous logistic regression models were used to estimate odds ratios and 95% confidence intervals for associations between polyps and the colorectal cancer risk allele for each SNP under a log-additive model. Analyses included 781 controls, 489 cases with adenoma, 401 cases with serrated polyps, and 188 cases with both polyp types. The following SNPs were associated with advanced adenomas: rs10936599, rs10795668, rs16892766, and rs9929218 (P < 0.05). For nonadvanced adenomas and for serrated polyps overall, only rs961253 was statistically significant (P < 0.05). These associations were in the same directions as those in prior colorectal cancer GWAS. No SNP was significantly associated with hyperplastic polyps, and only rs6983267 was significantly associated with sessile serrated polyps, but this association was opposite of that found in colorectal cancer GWAS. Our results suggest that the association between colorectal cancer susceptibility SNPs and colorectal polyps varies by polyp type.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdenomaAdultAgedCase-Control StudiesColonic PolypsColorectal NeoplasmsFemaleGenome-Wide Association StudyGenotypeHumansMaleMiddle AgedSurveys and Questionnairesadenomacolorectal cancercolorectal polypsgenome-wide association studiesserrated polypssingle-nucleotide polymorphisms

Identifiers

PMID24875374
PMCPMC4082340
OpenAlexW2123384433

What OpenQuestion holds

Textmetadata
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.