Evidence map›Paper›PMID 29127239›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2018

A novel method for quantitative myocardial contrast echocardiography in mice.

E Alvarez, N D Dalton, Y Gu, D Smith, A Luong, M Hoshijima, K L Peterson, J Rychak

Abstract readValidation Study
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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.

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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guidelines for measuring cardiac physiology in mice.American journal of physiology. Heart and circulatory physiology · 2018
    Guideline
  2. Mouse Cardiovascular Imaging.Current protocols · 2024
    Review
  3. Article
  4. Article
  5. 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

8 authors.

E AlvarezDepartment of Medicine, University of California , San Diego, California.
N D DaltonDepartment of Medicine, University of California , San Diego, California.
Y GuDepartment of Medicine, University of California , San Diego, California.
D SmithTargeson, Incorporated, San Diego, California.
A LuongTargeson, Incorporated, San Diego, California.
M HoshijimaDepartment of Medicine, University of California , San Diego, California.
K L PetersonDepartment of Medicine, University of California , San Diego, California.
J RychakDepartment of Bioengineering, University of California , San Diego, California.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The small size of the mouse heart frequently imparts technical challenges when applying conventional in vivo imaging methods for assessing heart function. Here, we describe the use of high-frequency ultrasound imaging in conjunction with a size-tuned blood pool contrast agent for quantitatively assessing myocardial perfusion in living mice. A perflurocarbon microbubble formulation exhibiting a narrow size distribution was developed, and echogenicity was assessed at 18 MHz in vitro. Adult mice were subjected to permanent ligation of the left anterior descending artery. Ultrasound imaging was performed on day 7, and a cohort of intact mice was used as a control. Parasternal long-axis cine clips were acquired at 18 MHz before and after contrast administration. Reduced ejection fraction and increased end-systolic volume were observed in infarcted compared with control mice. In control animals, washin of the contrast agent was visible in all myocardial segments. Reduced contrast enhancement was observed in apical-posterolateral regions of all infarcted mice. A novel method for reslicing of the imaging data through the time domain provided a two-dimensional presentation of regional contrast agent washin, enabling convenient identification of locations exhibiting altered perfusion. Myocardial segments exhibiting diminished contractility were observed to have correspondingly low relative myocardial perfusion. The contrast agent formulation and methods demonstrated here provide the basis for simplifying routine in vivo estimation of infarct size in mice and may be particularly useful in longitudinal evaluation of revascularization interventions and assessment of peri-infarct ischemia. NEW & NOTEWORTHY Murine myocardial contrast echocardiography frequently suffers from poor sensitivity to contrast. Here, we formulated a novel size-tuned microbubble contrast agent and validated it for use with ultra-high-frequency ultrasound. A novel data method for evaluating myocardial perfusion based on reslicing the imaging data through the time domain is presented.

Indexed as

AnimalsContrast MediaCoronary CirculationDisease Models, AnimalEchocardiographyImage Interpretation, Computer-AssistedMaleMice, Inbred C57BLMicrobubblesMyocardial ContractionMyocardial InfarctionMyocardial Perfusion ImagingPredictive Value of TestsReproducibility of ResultsTime FactorsContrast Mediahigh-frequency ultrasoundmicrobubblemyocardial contrast echocardiographymyocardial infarction

Identifiers

PMID29127239
PMCPMC5867659

What OpenQuestion holds

Textmetadata
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.