Evidence map›Paper›PMID 22703928›Full record

ArticleJournal of the American College of Cardiology2012

Adrenergic-pathway gene variants influence beta-blocker-related outcomes after acute coronary syndrome in a race-specific manner.

Sharon Cresci, Gerald W Dorn, Philip G Jones, Amber L Beitelshees, Allie Y Li, Petra A Lenzini, Michael A Province, John A Spertus, David E Lanfear

Abstract read
In one paragraph

Article in Journal of the American College of Cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. βGenetic testing and molecular biomarkers · 2019
    Pooled it
  2. Effect of Beta-Blocker Dose on Survival After Acute Myocardial Infarction.Journal of the American College of Cardiology · 2015
    Trial
  3. Trial
  4. Observational
  5. Article
  6. Associations betweenCardiology research and practice · 2022
    Article
  7. Article
  8. Article
  9. Observational
  10. Observational
  11. Article
  12. Practical Pharmacogenomic Approaches to Heart Failure Therapeutics.Current treatment options in cardiovascular medicine · 2016
    Review
  13. Review
  14. CHRNA5 variant predicts smoking cessation in patients with acute myocardial infarction.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2014
    Article
  15. Observational
  16. Observational
  17. Article
  18. Review
  19. Highlights of the year in JACC 2012.Journal of the American College of Cardiology · 2013
    Review
  20. Review
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

9 authors at 4 institutions in 1 country.

Sharon CresciDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Gerald W Dorn
Philip G Jones
Amber L Beitelshees
Allie Y Li
Petra A Lenzini
Michael A Province
John A Spertus
David E Lanfear
Washington University in St. Louis · USSaint Luke's Hospital · USHenry Ford Hospital · USUniversity of Maryland, Baltimore · US

Funding

SCCOR in Cardiac Dysfunction and DiseaseP50HL077113 · NHLBI · WASHINGTON UNIVERSITY · PI SPERTUS, JOHN A · 2005 to 2009
$13.4M
Genomic variants associated with angina and health status outcome after MIR01NR013396 · NINR · WASHINGTON UNIVERSITY · PI CRESCI, SHARON · 2011 to 2019
$4.5M
Impact of Race and Genetic Factors on Beta-blocker Effectiveness in Heart FailureR01HL103871 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E · 2011 to 2015
$3.5M
Pharmacogenetics of the B-type Natriuretic Peptide PathwayK23HL085124 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E · 2008 to 2012
$632k
NHLBI NIH HHS HL085124NHLBI NIH HHS HL103871NHLBI NIH HHS K23 HL085124NHLBI NIH HHS P50 HL077113NHLBI NIH HHS R01 HL103871NINR NIH HHS NR013396NINR NIH HHS R01 NR013396
6 · The paper itself

Abstract

objectivesOvercoming racial differences in acute coronary syndrome (ACS) outcomes is a strategic goal for U.S. health care. Genetic polymorphisms in the adrenergic pathway seem to explain some outcome differences by race in other cardiovascular diseases treated with β-adrenergic receptor blockade (BB). Whether these genetic variants are associated with survival among ACS patients treated with BB, and if this differs by race, is unknown.

backgroundβ-adrenergic receptor blockade after ACS is a measure of quality care, but the effectiveness across racial groups is less clear.

methodsA prospective cohort of 2,673 ACS patients (2,072 Caucasian; 601 African-American) discharged on BB from 22 U.S. hospitals were followed for 2 years. Subjects were genotyped for polymorphisms in ADRB1, ADRB2, ADRA2C, and GRK5. We used proportional hazards regression to model the effect of genotype on mortality, stratified by race and adjusted for baseline factors.

resultsThe overall 2-year mortality rate was 7.5% for Caucasians and 16.7% for African Americans. The prognosis associated with different genotypes in these BB-treated patients differed by race. In Caucasians, ADRA2C 322-325 deletion carriers had significantly lower mortality as compared with homozygous individuals lacking the deletion (hazard ratio: 0.46; confidence interval [CI]: 0.21 to 0.99; p = 0.047; race × genotype interaction p = 0.053). In African Americans, the ADRB2 16R allele was associated with significantly increased mortality (hazard ratio for RG vs. GG: 2.10; CI: 1.14 to 3.86; RR vs. GG: 2.65; CI: 1.38 to 5.08; p = 0.013; race × genotype interaction p = 0.096).

conclusionsAdrenergic pathway polymorphisms are associated with mortality in ACS patients receiving BB in a race-specific manner. Understanding the mechanism by which different genes impact post-ACS mortality differently in Caucasians and African Americans might illuminate opportunities to improve BB therapy in these groups.

Indexed as

Polymorphism, GeneticAcute Coronary SyndromeAdrenergic beta-AntagonistsAdultAgedAngina, UnstableBlack or African AmericanCohort StudiesConfounding Factors, EpidemiologicFemaleGene DeletionG-Protein-Coupled Receptor Kinase 5HomozygoteHumansKaplan-Meier EstimateMaleADRA2C protein, humanADRB1 protein, humanADRB2 protein, humanAdrenergic beta-AntagonistsG-Protein-Coupled Receptor Kinase 5GRK5 protein, humanReceptors, Adrenergic, alpha-2Receptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2

Identifiers

PMID22703928
PMCPMC3678950
OpenAlexW1972742428

What OpenQuestion holds

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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.