Evidence map›Paper›PMID 24889828›Full record

ArticleHuman genetics2014

Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.

Christine M Lusk, Greg Dyson, Andrew G Clark, Christie M Ballantyne, Ruth Frikke-Schmidt, Anne Tybjærg-Hansen, Eric Boerwinkle, Charles F Sing

Abstract read
In one paragraph

Article in Human genetics, 2014. 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
2.1field-weighted citation impact, top 13% 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, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Implementing genome-driven personalized cardiology in clinical practice.Journal of molecular and cellular cardiology · 2018
    Review
  6. Interactions betweenOncotarget · 2017
    Article
  7. Transdisciplinary approaches enhance the production of translational knowledge.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  8. Article
  9. Review
  10. Article
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 5 institutions in 2 countries.

Christine M LuskDepartment of Human Genetics, University of Michigan, 1241 E. Catherine St., Ann Arbor, MI, 48109, USA, luskc@karmanos.org.
Greg Dyson
Andrew G Clark
Christie M Ballantyne
Ruth Frikke-Schmidt
Anne Tybjærg-Hansen
Eric Boerwinkle
Charles F Sing
Baylor College of Medicine · USUniversity of Copenhagen · DKUniversity of Michigan–Ann Arbor · USCornell University · USWayne State University · US

Funding

Variable DNA sites predicting interindividual variation in health measuresP50GM065509 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SING, CHARLES · 2001 to 2011
$27.5M
Modeling DNA Diversity in Reverse Cholesterol TransportR01HL072810 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A. · 2003 to 2012
$9.6M
Modeling DNA Diversity in Reverse Cholesterol TransportR01HL072905 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SING, CHARLES · 2003 to 2012
$5.3M
Modeling DNA Diversity in Reverse Cholestrol TransportR01HL072904 · NHLBI · CORNELL UNIVERSITY ITHACA · PI CLARK, ANDREW G · 2003 to 2012
$2.9M
NHLBI NIH HHS R01 HL072810NHLBI NIH HHS R01-HL072810NHLBI NIH HHS R01 HL072904NHLBI NIH HHS R01-HL072904NHLBI NIH HHS R01 HL072905NHLBI NIH HHS R01-HL072905NIGMS NIH HHS P50 GM065509NIGMS NIH HHS P50-GM065509
6 · The paper itself

Abstract

Markers of the chromosome 9p21 region are regarded as the strongest and most reliably significant genome-wide association study (GWAS) signals for Coronary heart disease (CHD) risk; this was recently confirmed by the CARDIoGRAMplusC4D Consortium meta-analysis. However, while these associations are significant at the population level, they may not be clinically relevant predictors of risk for all individuals. We describe here the results of a study designed to address the question: What is the contribution of context defined by traditional risk factors in determining the utility of DNA sequence variations marking the 9p21 region for explaining variation in CHD risk? We analyzed a sample of 7,589 (3,869 females and 3,720 males) European American participants of the Atherosclerosis Risk in Communities study. We confirmed CHD-SNP genotype associations for two 9p21 region marker SNPs previously identified by the CARDIoGRAMplusC4D Consortium study, of which ARIC was a part. We then tested each marker SNP genotype effect on prediction of CHD within sub-groups of the ARIC sample defined by traditional CHD risk factors by applying a novel multi-model strategy, PRIM. We observed that the effects of SNP genotypes in the 9p21 region were strongest in a sub-group of hypertensives. We subsequently validated the effect of the region in an independent sample from the Copenhagen City Heart Study. Our study suggests that marker SNPs identified as predictors of CHD risk in large population based GWAS may have their greatest utility in explaining risk of disease in particular sub-groups characterized by biological and environmental effects measured by the traditional CHD risk factors.

Indexed as

Polymorphism, Single NucleotideAtherosclerosisChromosomes, Human, Pair 9Cohort StudiesCoronary Artery DiseaseFemaleGene-Environment InteractionGenetic MarkersGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMaleMarylandMiddle AgedMinnesotaGenetic Markers

Identifiers

PMID24889828
PMCPMC4164053
OpenAlexW1984499236

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.