Evidence map›Paper›PMID 29739794›Full record

Observational studyJournal of the American Heart Association2018

Race and Beta-Blocker Survival Benefit in Patients With Heart Failure: An Investigation of Self-Reported Race and Proportion of African Genetic Ancestry.

Jasmine A Luzum, Edward Peterson, Jia Li, Ruicong She, Hongsheng Gui, Bin Liu, John A Spertus, Yigal M Pinto, L Keoki Williams, Hani N Sabbah and 1 more

Open access · goldAbstract readComparative StudyObservational Study
In one paragraph

Observational study in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 pooled it
1.7field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Common Variants onCirculation. Heart failure · 2023
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Social Inequalities in Non-ischemic Cardiomyopathies.Frontiers in cardiovascular medicine · 2022
    Review
  13. Observational
  14. Article
  15. Article
  16. 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

11 authors at 4 institutions in 2 countries.

Jasmine A LuzumDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI.
Edward PetersonDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI.
Jia LiDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI.
Ruicong SheDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI.
Hongsheng GuiCenter for Health Policy and Health Services Research, Henry Ford Health System, Detroit, MI.
Bin LiuDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI.
John A SpertusSaint Luke's Mid America Heart Institute/UMKC, Kansas City, MO.
Yigal M PintoDepartment of Cardiology, University of Amsterdam, Amsterdam, The Netherlands.
L Keoki WilliamsCenter for Health Policy and Health Services Research, Henry Ford Health System, Detroit, MI.
Hani N SabbahHeart and Vascular Institute, Henry Ford Health System, Detroit, MI.
David E LanfearCenter for Health Policy and Health Services Research, Henry Ford Health System, Detroit, MI dlanfea1@hfhs.org.
Henry Ford Health System · USSaint Luke's Hospital · USUniversity of Amsterdam · NLUniversity of Michigan–Ann Arbor · US

Funding

Substrate Selection and Oxidative Stress in Heart FailureP01HL074237 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI HOPPEL, CHARLES LESLIE · 2003 to 2013
$19.9M
PHARMACOGENOMICS OF INHALED CORTICOSTEROID RESPONSIVENESS IN PATIENTS WITH ASTHMAR01AI079139 · NIAID · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2009 to 2013
$3.9M
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
Leveraging electronic medical records to perform large-scale diabetes pharmacogenomics among ancestrally diverse patient populationsR01DK113003 · NIDDK · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2017 to 2021
$3.2M
Plasma Metabolomics and Myocardial Energetics in Heart FailureR01HL132154 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E, SABBAH, HANI N · 2017 to 2020
$3.1M
Combined Transcriptomics and Genomics to Find Asthma Genes in Admixed PopulationsR01HL118267 · NHLBI · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2014 to 2017
$2.9M
VALIDATION OF ADHERENCE DATA--USE IN CLINICAL PRACTICER01DK064695 · NIDDK · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2003 to 2010
$2.7M
Precision Medicine for Heart Failure: The Role of Genomics in the Efficacy and Racial Disparity of Cornerstone PharmacotherapyK08HL146990 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUZUM, JASMINE A · 2019 to 2023
$772k
NHLBI NIH HHS K08 HL146990NHLBI NIH HHS L30 HL110279NHLBI NIH HHS P01 HL074237NHLBI NIH HHS R01 HL103871NHLBI NIH HHS R01 HL118267NHLBI NIH HHS R01 HL132154NIAID NIH HHS R01 AI079139NIDDK NIH HHS R01 DK064695NIDDK NIH HHS R01 DK113003
6 · The paper itself

Abstract

backgroundIt remains unclear whether beta-blockade is similarly effective in black patients with heart failure and reduced ejection fraction as in white patients, but self-reported race is a complex social construct with both biological and environmental components. The objective of this study was to compare the reduction in mortality associated with beta-blocker exposure in heart failure and reduced ejection fraction patients by both self-reported race and by proportion African genetic ancestry. METHODS AND

resultsInsured patients with heart failure and reduced ejection fraction (n=1122) were included in a prospective registry at Henry Ford Health System. This included 575 self-reported blacks (129 deaths, 22%) and 547 self-reported whites (126 deaths, 23%) followed for a median 3.0 years. Beta-blocker exposure (BBexp) was calculated from pharmacy claims, and the proportion of African genetic ancestry was determined from genome-wide array data. Time-dependent Cox proportional hazards regression was used to separately test the association of BBexp with all-cause mortality by self-reported race or by proportion of African genetic ancestry. Both sets of models were evaluated unadjusted and then adjusted for baseline risk factors and beta-blocker propensity score. BBexp effect estimates were protective and of similar magnitude both by self-reported race and by African genetic ancestry (adjusted hazard ratio=0.56 in blacks and adjusted hazard ratio=0.48 in whites). The tests for interactions with BBexp for both self-reported race and for African genetic ancestry were not statistically significant in any model (

conclusionsAmong black and white patients with heart failure and reduced ejection fraction, reduction in all-cause mortality associated with BBexp was similar, regardless of self-reported race or proportion African genetic ancestry.

Indexed as

Self ReportAdrenergic beta-AntagonistsAgedAged, 80 and overBlack or African AmericanFemaleHeart FailureHumansMaleMichiganMiddle AgedPedigreePharmacogeneticsProspective StudiesProtective FactorsRisk AssessmentAdrenergic beta-Antagonistsancestrybeta‐blockerdisparitygeneticsgenomicsheart failurepharmacogeneticspharmacogenomicsrace

Identifiers

PMID29739794
PMCPMC6015313
OpenAlexW2800915477

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.