Evidence map›Paper›PMID 29055654›Full record

ArticleJournal of molecular and cellular cardiology2018

Echocardiographic evaluation of diastolic function in mouse models of heart disease.

Moritz Schnelle, Norman Catibog, Min Zhang, Adam A Nabeebaccus, Grace Anderson, Daniel A Richards, Greta Sawyer, Xiaohong Zhang, Karl Toischer, Gerd Hasenfuss and 2 more

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 114 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 2 pooled it
7.5field-weighted citation impact, top 2% 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.

NCT04602338 recruitingnot on this mapstarted 2020, after this paper: background citation

Multimodality Imaging (Cardiovascular Magnetic Resonance Imaging, Echocardiography, and Nuclear Medicine Imaging) in the Screening, Diagnosis and Risk Stratification of Heart Failure With Preserved Ejection Fraction- a Multicenter Study.

Typeobservational_patient_registrySponsorChinese Academy of Medical Sciences, Fuwai HospitalRan2020 to 2028Enrolled1,000ConditionsHeart Failure, Diastolic, Multicenter Study
NCT04603404 recruitingnot on this mapstarted 2019, after this paper: background citation

Multimodality Imaging (Cardiovascular Magnetic Resonance Imaging, Echocardiography, and Nuclear Medicine Imaging) in the Screening, Diagnosis and Risk Stratification of Heart Failure With Preserved Ejection Fraction (HFpEF).

TypeobservationalSponsorChinese Academy of Medical Sciences, Fuwai HospitalRan2019 to 2030Enrolled430ConditionsHeart Failure, Diastolic
3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 2 syntheses or guidelines pooled it, 157 citations in OpenAlex.

  1. Pooled it
  2. Guidelines for measuring cardiac physiology in mice.American journal of physiology. Heart and circulatory physiology · 2018
    Guideline
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  18. Low and High Pressor Doses of Ang II Lead to Two Distinct Phenotypes of Hypertensive Heart Disease in Mice.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2026
    Article
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54 more citing papers are in PubMed but not listed here.

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

12 authors at 1 institution in 1 country.

Moritz SchnelleKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom; Department of Cardiology and Pneumology, University Medical Center Goettingen, Goettingen, Germany.
Norman CatibogKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Min ZhangKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Adam A NabeebaccusKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Grace AndersonKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Daniel A RichardsKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Greta SawyerKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Xiaohong ZhangKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Karl ToischerDepartment of Cardiology and Pneumology, University Medical Center Goettingen, Goettingen, Germany.
Gerd HasenfussDepartment of Cardiology and Pneumology, University Medical Center Goettingen, Goettingen, Germany.
Mark J MonaghanKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom.
Ajay M ShahKing's College London British Heart Foundation Centre of Excellence, Cardiovascular Division, London, United Kingdom. Electronic address: ajay.shah@kcl.ac.uk.
King's College London · GB

Funding

British Heart Foundation CH/1999001/11735British Heart Foundation PG/12/26/29477British Heart Foundation RG/13/11/30384
6 · The paper itself

Abstract

backgroundMouse models of heart disease are extensively employed. The echocardiographic characterization of contractile function is usually focused on systolic function with fewer studies assessing diastolic function. Furthermore, the applicability of diverse echocardiographic parameters of diastolic function that are commonly used in humans has not been extensively evaluated in different pathophysiological models in mice. METHODS AND

resultsWe used high resolution echocardiography to evaluate parameters of diastolic function in mouse models of chronic pressure overload (aortic constriction), volume overload (aorto-caval shunt), heart failure with preserved ejection fraction (HFpEF; DOCA-salt hypertension), and acute sarcoplasmic reticulum dysfunction induced by thapsigargin - all known to exhibit diastolic dysfunction. Left atrial area increased in all three chronic models while mitral E/A was difficult to quantify at high heart rates. Isovolumic relaxation time (IVRT) and Doppler E/E' increased significantly and the peak longitudinal strain rate during early filling (peak reverse longitudinal strain rate) decreased significantly after aortic constriction, with the changes being proportional to the magnitude of hypertrophy. In the HFpEF model, reverse longitudinal strain rate decreased significantly but changes in IVRT and E/E' were non-significant, consistent with less severe dysfunction. With volume overload, there was a significant increase in reverse longitudinal strain rate and decrease in IVRT, indicating a restrictive physiology. Acute thapsigargin treatment caused significant prolongation of IVRT and decrease in reverse longitudinal strain rate.

conclusionThese results indicate that the combined measurement of left atrial area plus reverse longitudinal strain rate and/or IVRT provide an excellent overall assessment of diastolic function in the diseased mouse heart, allowing distinction between different types of pathophysiology.

Indexed as

EchocardiographyAnimalsCardiomegalyDiastoleDisease Models, AnimalHeart DiseasesHeart FailureMice, Inbred C57BLObserver VariationPressureSarcoplasmic Reticulum Calcium-Transporting ATPasesStroke VolumeSystoleThapsigarginSarcoplasmic Reticulum Calcium-Transporting ATPasesThapsigarginDiastolic functionEchocardiographyHypertrophyMouse

Identifiers

PMID29055654
PMCPMC5807035
OpenAlexW2767058951

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.