Evidence map›Paper›PMID 30756358›Full record

ArticleJournal of cardiovascular translational research2019

Association of Genetic Polymorphisms in the Beta-1 Adrenergic Receptor with Recovery of Left Ventricular Ejection Fraction in Patients with Heart Failure.

Jasmine A Luzum, Joseph D English, Umair S Ahmad, Jessie W Sun, Benjamin D Canan, Wolfgang Sadee, Joseph P Kitzmiller, Philip F Binkley

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of cardiovascular translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Jasmine A LuzumDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI, USA. jluzum@med.umich.edu.ORCID 0000-0003-3639-717X
Joseph D EnglishDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI, USA.
Umair S AhmadHeart and Vascular Institute, Summa Health System, Akron, OH, USA.
Jessie W SunCenter for Pharmacogenomics, Ohio State University College of Medicine, Columbus, OH, USA.
Benjamin D CananDepartment of Physiology and Cell Biology, Ohio State University College of Medicine, Columbus, OH, USA.
Wolfgang SadeeCenter for Pharmacogenomics, Ohio State University College of Medicine, Columbus, OH, USA.
Joseph P KitzmillerDepartment of Biological Chemistry and Pharmacology, Ohio State University College of Medicine, Columbus, OH, USA.
Philip F BinkleyDivision of Cardiovascular Medicine, Department of Internal Medicine, Ohio State University College of Medicine, Columbus, OH, USA.
The Ohio State University · USUniversity of Michigan · USSumma Health System · US

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
NCATS NIH HHS UL1 TR002240NHLBI NIH HHS L30 HL110279
6 · The paper itself

Abstract

Two common genetic polymorphisms in the beta-1 adrenergic receptor (ADRB1 Ser49Gly [rs1801252] and Arg389Gly [rs1801253]) significantly affect receptor function in vitro. The objective of this study was to determine whether ADRB1 Ser49Gly and Arg389Gly are associated with recovery of left ventricular ejection fraction (LVEF) in patients with heart failure. Patients with heart failure and baseline LVEF ≤ 40% were genotyped (n = 98), and retrospective chart review assessed the primary outcome of LVEF recovery to ≥ 40%. Un/adjusted logistic regression models revealed that Ser49Gly, but not Arg389Gly, was significantly associated with LVEF recovery in a dominant genetic model. The adjusted odds ratio for Ser49 was 8.2 (95% CI = 2.1-32.9; p = 0.003), and it was the strongest predictor of LVEF recovery among multiple clinical variables. In conclusion, patients with heart failure and reduced ejection fraction that are homozygous for ADRB1 Ser49 were significantly more likely to experience LVEF recovery than Gly49 carriers.

Indexed as

Polymorphism, GeneticStroke VolumeVentricular Function, LeftAdrenergic beta-1 Receptor AntagonistsAdultAgedFemaleGenetic Association StudiesHeart FailureHeterozygoteHomozygoteHumansMaleMiddle AgedReceptors, Adrenergic, beta-1Recovery of FunctionADRB1 protein, humanAdrenergic beta-1 Receptor AntagonistsReceptors, Adrenergic, beta-1Beta-1 adrenergic receptorBeta-blockerGeneticsHeart failureLeft ventricular ejection fractionPolymorphism

Identifiers

PMID30756358
PMCPMC6690812
OpenAlexW2913676167

What Socratic 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 Socratic graph.