Evidence map›Paper›PMID 37883390›Full record

ArticlePloS one2023

Exploring the mechanisms underlying stroke volume variability reduction in a murine model of heart failure with reduced ejection fraction.

Gemma Fernández-Mendoza, Abraham Méndez-Fernández, Hugo J Alves-Figueiredo, Gerardo García-Rivas, Moisés Santillán

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 1 country.

Gemma Fernández-MendozaDepartamento de Física, Escuela Superior de Física y Matemáticas, Instituto Politécnico Nacional, Ciudad de México, México.
Abraham Méndez-FernándezThe Institute for Obesity Research, Tecnologico de Monterrey, Monterrey, NL, Mexico.
Hugo J Alves-FigueiredoCátedra de Cardiología y Medicina Vascular, School of Medicine and Health Sciences, Tecnologico de Monterrey, Monterrey, NL, Mexico.ORCID 0000-0002-0635-6265
Gerardo García-RivasThe Institute for Obesity Research, Tecnologico de Monterrey, Monterrey, NL, Mexico.ORCID 0000-0003-4731-3293
Moisés SantillánUnidad Monterrey, Centro de Investigación y de Estudios Avanzados, Apodaca NL, México.ORCID 0000-0001-8605-7451
Tecnológico de Monterrey · MXCentro de Investigación en Materiales Avanzados · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure with reduced ejection fraction (HFrEF) is accompanied by disregulation of cardiovascular function. Heart rate variability (HRV) is commonly used to assess autonomic dysfunction in HFrEF. However, analysis of stroke volume variability (SVV) may provide additional insights. We examined HRV and SVV in a mouse model of HFrEF. HFrEF mice exhibited reduced stroke volume and ejection fraction versus controls, confirming cardiac contractile dysfunction. HRV was preserved in HFrEF mice. However, SVV was markedly diminished, indicating dissociation between HRV and SVV regulation. Using a mathematical model, we propose that Frank-Starling mechanism abnormalities in HFrEF disrupt SVV independent of HRV. Assessing SVV could thus provide unique insights beyond HRV into cardiovascular control deficits in HFrEF.

Indexed as

Heart FailureVentricular Dysfunction, LeftAnimalsDisease Models, AnimalHeart RateMicePrognosisStroke Volume

Identifiers

PMID37883390
PMCPMC10602350
OpenAlexW4387953138

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.