Evidence map›Paper›PMID 25329201›Full record

Trial reportAnnals of internal medicine2014

Genetic and environmental risk assessment and colorectal cancer screening in an average-risk population: a randomized trial.

David S Weinberg, Ronald E Myers, Eileen Keenan, Karen Ruth, Randa Sifri, Barry Ziring, Eric Ross, Sharon L Manne

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Annals of internal medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 5 pooled it
5.4field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 5 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Colonic neoplasia and celiac disease: A systematic review.World journal of gastroenterology · 2025
    Pooled it
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  4. Multigene panels in prostate cancer risk assessment: a systematic review.Genetics in medicine : official journal of the American College of Medical Genetics · 2016
    Pooled it
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  18. Investigation ofOncoTargets and therapy · 2016
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

David S Weinberg
Ronald E Myers
Eileen Keenan
Karen Ruth
Randa Sifri
Barry Ziring
Eric Ross
Sharon L Manne
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
Gene-Environmental Risk Assessment and CRC ScreeningR01CA112230 · NCI · FOX CHASE CANCER CENTER · PI WEINBERG, DAVID S · 2006 to 2011
$3.4M
NCI NIH HHS P30 CA006927NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA112230NCI NIH HHS R01CA112230
6 · The paper itself

Abstract

backgroundNew methods are needed to improve health behaviors, such as adherence to colorectal cancer (CRC) screening. Personalized genetic information to guide medical decisions is increasingly available. Whether such information motivates behavioral change is unknown.

objectiveTo determine whether individualized genetic and environmental risk assessment (GERA) of CRC susceptibility improves adherence to screening in average-risk persons.

design2-group, randomized, controlled trial. (ClinicalTrials.gov: NCT0087360).

setting4 medical school-affiliated primary care practices.

participants783 participants at average risk for CRC who were not adherent to screening at study entry.

interventionParticipants were randomly assigned to usual care or GERA, which evaluated methylenetetrahydrofolate reductase polymorphisms and serum folate levels. On the basis of prespecified combinations of polymorphisms and serum folate levels, GERA recipients were told that they were at elevated or average risk for CRC. MEASUREMENTS: The primary outcome was CRC screening within 6 months of study entry.

resultsOverall screening rates for CRC did not statistically significant differ between the usual care (35.7%) and GERA (33.1%) groups. After adjustment for baseline participant factors, the odds ratio for screening completion for GERA versus usual care was 0.88 (95% CI, 0.64 to 1.22). Within the GERA group, screening rates did not significantly differ between average-risk (38.1%) and elevated-risk (26.9%) participants. Odds ratios for elevated- versus average-risk participants remained nonsignificant after adjustment for covariates (odds ratio, 0.75 [CI, 0.39 to 1.42]). LIMITATION: Only 1 personalized genetic and environmental interaction and 1 health behavior (CRC screening) were assessed.

conclusionIn average-risk persons, CRC screening uptake was not positively associated with feedback from a single personalized GERA. Additional studies will be required to evaluate whether other approaches to providing GERA affect screening utilization differently. These findings raise concern about the effectiveness of moderately predictive assessment of genetic risk to promote favorable health care behavior. PRIMARY FUNDING SOURCE: National Institutes of Health.

Indexed as

Genetic Predisposition to DiseasePatient ComplianceRisk AssessmentAgedColorectal NeoplasmsEarly Detection of CancerFemaleFolic AcidGenetic TestingHumansMaleMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedPolymorphism, GeneticPrecision MedicineRiskFolic AcidMethylenetetrahydrofolate Reductase (NADPH2)

Identifiers

PMID25329201
PMCPMC4412019
OpenAlexW1990725932

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.