Evidence map›Paper›PMID 25618792›Full record

ArticleCancer causes & control : CCC2015

Blood lipids and colorectal polyps: testing an etiologic hypothesis using phenotypic measurements and Mendelian randomization.

Michael N Passarelli, Polly A Newcomb, Karen W Makar, Andrea N Burnett-Hartman, John D Potter, Melissa P Upton, Lee-Ching Zhu, Michael E Rosenfeld, Stephen M Schwartz, Carolyn M Rutter

Abstract read
In one paragraph

Article in Cancer causes & control : CCC, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Michael N PassarelliPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, M4-B402, Seattle, WA, 98109, USA.
Polly A Newcomb
Karen W Makar
Andrea N Burnett-Hartman
John D Potter
Melissa P Upton
Lee-Ching Zhu
Michael E Rosenfeld
Stephen M Schwartz
Carolyn M Rutter

Funding

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 POTTER, JOHN D · 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
Lipid genotypes, phenotypes, and colorectal adenomas: Elucidating mechanismsR03CA171014 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2012 to 2013
$171k
NCI NIH HHS K05 CA152715NCI NIH HHS K05CA152715NCI NIH HHS P01 CA074184NCI NIH HHS P01CA074184NCI NIH HHS R01 CA097325NCI NIH HHS R01CA097325NCI NIH HHS R03 CA171014NCI NIH HHS R03CA171014NCI NIH HHS T32 CA009168NCI NIH HHS T32CA009168
6 · The paper itself

Abstract

purposeStudies linking cholesterol levels to the development of colorectal neoplasia are inconsistent, and Mendelian randomization has been suggested as a way to help avoid problems with confounding and reverse causation.

methodsWe genotyped individuals who received a colonoscopy at Group Health (1998-2007) for 96 of 102 single-nucleotide polymorphisms identified by the Global Lipids Genetics Consortium. Participants included 139 advanced adenoma cases, 518 non-advanced adenoma cases, 380 non-adenomatous polyp cases, and 754 polyp-free controls. All had at least one available pre-colonoscopy lipid measurement from electronic records maintained by Group Health.

resultsAdvanced adenoma cases were more likely than controls to have higher pre-colonoscopy zenith low-density lipoprotein (LDL), triglycerides (TG), and total cholesterol (TC) (odds ratio, OR per 20 mg/dL LDL increase: 1.16, 95 % confidence interval, CI 1.03-1.30; per 40 mg/dL TG increase: 1.09, 1.03-1.16; and per 20 mg/dL TC increase: 1.09, 1.02-1.18). For these traits, genotype-polyp ORs using weighted allele scores were not statistically significant (OR per increase in score scaled to a 20 mg/dL LDL increase: 1.17, 0.78-1.75; a 40 mg/dL TG increase: 1.12, 0.91-1.38; a 20 mg/dL TC increase: 0.99, 0.71-1.38).

conclusionsCholesterol levels may be associated with advanced adenomas, but larger studies are warranted to determine whether this association can be attributed to genetics.

Indexed as

Polymorphism, Single NucleotideAdenomaAdultAgedBiopsyCholesterolColonic PolypsColonoscopyColorectal NeoplasmsFemaleGenotypeHumansLipidsMaleMendelian Randomization AnalysisMiddle AgedCholesterolLipidsTriglycerides

Identifiers

PMID25618792
PMCPMC4334709

What OpenQuestion holds

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Registered trials

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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.