Evidence map›Paper›PMID 26310667›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance2015

Left ventricular mechanical dysfunction in diet-induced obese mice is exacerbated during inotropic stress: a cine DENSE cardiovascular magnetic resonance study.

Christopher M Haggerty, Andrea C Mattingly, Sage P Kramer, Cassi M Binkley, Linyuan Jing, Jonathan D Suever, David K Powell, Richard J Charnigo, Frederick H Epstein, Brandon K Fornwalt

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Diagnostic imaging in the management of patients with metabolic syndrome.Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  7. Review of Journal of Cardiovascular Magnetic Resonance (JCMR) 2015-2016 and transition of the JCMR office to Boston.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2017
    Review
  8. Rad-deletion Phenocopies Tonic Sympathetic Stimulation of the Heart.Journal of cardiovascular translational research · 2016
    Article
  9. Review of Journal of Cardiovascular Magnetic Resonance 2015.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2016
    Review
  10. Cardiovascular magnetic resonance detects the progression of impaired myocardial perfusion reserve and increased left-ventricular mass in mice fed a high-fat diet.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2016
    Article
  11. Article
  12. Time course of cardiometabolic alterations in a high fat high sucrose diet mice model and improvement after GLP-1 analog treatment using multimodal cardiovascular magnetic resonance.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2015
    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

10 authors at 2 institutions in 1 country.

Christopher M HaggertySaha Cardiovascular Research Center, University of Kentucky, Lexington, KY, USA. chaggerty3@gatech.edu.
Andrea C MattinglySaha Cardiovascular Research Center, University of Kentucky, Lexington, KY, USA. acma242@g.uky.edu.
Sage P KramerCollege of Medicine, University of Kentucky, Lexington, KY, USA. s.kramer@uky.edu.
Cassi M BinkleyDepartment of Physiology, University of Kentucky, Lexington, KY, USA. cassi.binkley@uky.edu.
Linyuan JingSaha Cardiovascular Research Center, University of Kentucky, Lexington, KY, USA. ljing@geisinger.edu.
Jonathan D SueverSaha Cardiovascular Research Center, University of Kentucky, Lexington, KY, USA. jdsuever@geisinger.edu.
David K PowellDepartment of Biomedical Engineering, University of Kentucky, Lexington, KY, USA. david.k.powell@uky.edu.
Richard J CharnigoDepartment of Biostatistics, University of Kentucky, Lexington, KY, USA. rjcharn2@aol.com.
Frederick H EpsteinDepartments of Biomedical Engineering and Radiology, University of Virginia, Charlottesville, VA, USA. FHE6B@hscmail.mcc.virginia.edu.
Brandon K FornwaltSaha Cardiovascular Research Center, University of Kentucky, Lexington, KY, USA. bkf@gatech.edu.
University of Kentucky · USUniversity of Virginia · US

Funding

The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI FINLIN, BRIAN S · 2012 to 2017
$13.7M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
MRI of Myocardial Function in Post-Infarct Knockout MiceR01EB001763 · NIBIB · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI EPSTEIN, FREDERICK H · 2003 to 2020
$5.4M
A High-Field Small Animal MR Imager for Biomedical ResearchS10RR029541 · NCRR · UNIVERSITY OF KENTUCKY · PI SMITH, CHARLES DENNIS · 2010 to 2010
$3.1M
Clinical Scholars In Cardiovascular ScienceT32HL091812 · NHLBI · UNIVERSITY OF KENTUCKY · PI SMYTH, SUSAN S. · 2008 to 2018
$2.3M
Aortic Wall Distensibility in the Growth and Rupture of Abdominal Aortic AneurysmF32HL123215 · NHLBI · UNIVERSITY OF KENTUCKY · PI HAGGERTY, CHRISTOPHER M · 2014 to 2014
$52k
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1TR000117NCRR NIH HHS S10 RR029541NHLBI NIH HHS F32 HL123215NHLBI NIH HHS T32 HL091812NHLBI NIH HHS T32 HL123215NHLBI NIH HHS T32 HL91812NIBIB NIH HHS R01 EB001763NIGMS NIH HHS P20 GM103527
6 · The paper itself

Abstract

backgroundObesity is a risk factor for cardiovascular disease. There is evidence of impaired left ventricular (LV) function associated with obesity, which may relate to cardiovascular mortality, but some studies have reported no dysfunction. Ventricular function data are generally acquired under resting conditions, which could mask subtle differences and potentially contribute to these contradictory findings. Furthermore, abnormal ventricular mechanics (strains, strain rates, and torsion) may manifest prior to global changes in cardiac function (i.e., ejection fraction) and may therefore represent more sensitive markers of cardiovascular disease. This study evaluated LV mechanics under both resting and stress conditions with the hypothesis that the LV mechanical dysfunction associated with obesity is exacerbated with stress and manifested at earlier stages of disease compared to baseline.

methodsC57BL/6J mice were randomized to a high-fat or control diet (60 %, 10 % kcal from fat, respectively) for varying time intervals (n = 7 - 10 subjects per group per time point, 100 total; 4 - 55 weeks on diet). LV mechanics were quantified under baseline (resting) and/or stress conditions (40 μg/kg/min continuous infusion of dobutamine) using cine displacement encoding with stimulated echoes (DENSE) with 7.4 ms temporal resolution on a 7 T Bruker ClinScan. Peak strain, systolic strain rates, and torsion were quantified. A linear mixed model was used with Benjamini-Hochberg adjustments for multiple comparisons.

resultsReductions in LV peak longitudinal strain at baseline were first observed in the obese group after 42 weeks, with no differences in systolic strain rates or torsion. Conversely, reductions in longitudinal strain and circumferential and radial strain rates were seen under inotropic stress conditions after only 22 weeks on diet. Furthermore, stress cardiovascular magnetic resonance (CMR) evaluation revealed supranormal values of LV radial strain and torsion in the obese group early on diet, followed by later deficits.

conclusionsDifferences in left ventricular mechanics in obese mice are exacerbated under stress conditions. Stress CMR demonstrated a broader array of mechanical dysfunction and revealed these differences at earlier time points. Thus, it may be important to evaluate cardiac function in the setting of obesity under stress conditions to fully elucidate the presence of ventricular dysfunction.

Indexed as

Diet, High-FatMagnetic Resonance Imaging, CineStress, PhysiologicalAnimalsBiomechanical PhenomenaCardiotonic AgentsDisease Models, AnimalDobutamineInfusions, IntravenousLinear ModelsMaleMice, Inbred C57BLMyocardial ContractionObesityPredictive Value of TestsRisk FactorsCardiotonic AgentsDobutamine

Identifiers

PMID26310667
PMCPMC4551701
OpenAlexW2097689917

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.