Evidence map›Paper›PMID 23743396›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2013

Diastolic chamber properties of the left ventricle assessed by global fitting of pressure-volume data: improving the gold standard of diastolic function.

Javier Bermejo, Raquel Yotti, Candelas Pérez del Villar, Juan C del Álamo, Daniel Rodríguez-Pérez, Pablo Martínez-Legazpi, Yolanda Benito, J Carlos Antoranz, M Mar Desco, Ana González-Mansilla and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04739215 (Effects of Sodium-Glucose Cotransporter 2 Inhibition on the Mechanisms of Cardiac Damage in the Diabetic Patient With Heart Failure With Preserved Ejection Fraction), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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.

NCT04739215 phase4unknown statusstarted 2021, after this paper: background citation

Effects of Sodium-Glucose Cotransporter 2 Inhibition on the Mechanisms of Cardiac Damage in the Diabetic Patient With Heart Failure With Preserved Ejection Fraction

Ran2021Enrolled62Registered outcomes10Posted comparisons0ConditionsDiabetes Mellitus, Type 2, Heart Failure With Preserved Ejection FractionArmsDapagliflozin 10 MG [Farxiga], Placebo
PMID 26378978PMID 21329845PMID 28402411other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

13 authors.

Javier BermejoDepartment of Cardiology, Hospital General Universitario Gregorio Marañón, and the Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain. javbermejo@jet.es
Raquel Yotti
Candelas Pérez del Villar
Juan C del Álamo
Daniel Rodríguez-Pérez
Pablo Martínez-Legazpi
Yolanda Benito
J Carlos Antoranz
M Mar Desco
Ana González-Mansilla
Alicia Barrio
Jaime Elízaga
Francisco Fernández-Avilés

Funding

Characterization of intraventricular filling vortices in the clinical settingR21HL108268 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEL ALAMO, JUAN CARLOS, KAHN, ANDREW · 2011 to 2012
$415k
NHLBI NIH HHS 1R21 HL-108268-01
6 · The paper itself

Abstract

In cardiovascular research, relaxation and stiffness are calculated from pressure-volume (PV) curves by separately fitting the data during the isovolumic and end-diastolic phases (end-diastolic PV relationship), respectively. This method is limited because it assumes uncoupled active and passive properties during these phases, it penalizes statistical power, and it cannot account for elastic restoring forces. We aimed to improve this analysis by implementing a method based on global optimization of all PV diastolic data. In 1,000 Monte Carlo experiments, the optimization algorithm recovered entered parameters of diastolic properties below and above the equilibrium volume (intraclass correlation coefficients = 0.99). Inotropic modulation experiments in 26 pigs modified passive pressure generated by restoring forces due to changes in the operative and/or equilibrium volumes. Volume overload and coronary microembolization caused incomplete relaxation at end diastole (active pressure > 0.5 mmHg), rendering the end-diastolic PV relationship method ill-posed. In 28 patients undergoing PV cardiac catheterization, the new algorithm reduced the confidence intervals of stiffness parameters by one-fifth. The Jacobian matrix allowed visualizing the contribution of each property to instantaneous diastolic pressure on a per-patient basis. The algorithm allowed estimating stiffness from single-beat PV data (derivative of left ventricular pressure with respect to volume at end-diastolic volume intraclass correlation coefficient = 0.65, error = 0.07 ± 0.24 mmHg/ml). Thus, in clinical and preclinical research, global optimization algorithms provide the most complete, accurate, and reproducible assessment of global left ventricular diastolic chamber properties from PV data. Using global optimization, we were able to fully uncouple relaxation and passive PV curves for the first time in the intact heart.

Indexed as

AlgorithmsAnimalsBlood PressureCardiac CatheterizationCardiac VolumeDiastoleHeartHeart VentriclesHumansStroke VolumeSwineVentricular Function, Leftdiastolediastolic functiondiastolic stiffnesshemodynamicsleft ventriclemechanical propertiespressurerelaxation

Identifiers

PMID23743396
PMCPMC3742944

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.