Evidence map›Paper›PMID 20190279›Full record

ArticleCirculation. Cardiovascular imaging2010

Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining.

Karl Degenhardt, Alexander C Wright, Debra Horng, Arun Padmanabhan, Jonathan A Epstein

Open access · greenAbstract read
In one paragraph

Article in Circulation. Cardiovascular imaging, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

152 citing papers in PubMed, 1 synthesis or guideline pooled it, 273 citations in OpenAlex.

  1. Pooled it
  2. Proteomic study for the prediction ofHistochemistry and cell biology · 2026
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92 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Karl DegenhardtDepartment of Cell and Developmental Biology, Penn Cardiovascular Institute, University of Pennsylvania, Philadelphia, PA 19104, USA. degenhardt@email.chop.edu
Alexander C Wright
Debra Horng
Arun Padmanabhan
Jonathan A Epstein
University of Pennsylvania · US

Funding

Training in Molecular Therapeutics for Pediatric CardiologyT32HL007915 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Robert J Levy, JOSEPH W ROSSANO · 1999 to 2026
$13.4M
WNT SIGNALING AND LUNG VASCULAR DEVELOPMENTP01HL075215 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI KAHN, MARK L · 2004 to 2008
$10.5M
QUANTITATIVE TECHNIQUES FOR MR AND CT MICROIMAGINGK25EB001427 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI WRIGHT, ALEXANDER C · 2003 to 2007
$601k
NHLBI NIH HHS P01 HL075215NHLBI NIH HHS P01HL075215NHLBI NIH HHS T32 HL007915NHLBI NIH HHS T32HL007915NIBIB NIH HHS EB001427NIBIB NIH HHS K25 EB001427
6 · The paper itself

Abstract

backgroundMicrocomputed tomography (micro-CT) has been used extensively in research to generate high-resolution 3D images of calcified tissues in small animals nondestructively. It has been especially useful for the characterization of skeletal mutations but limited in its utility for the analysis of soft tissue such as the cardiovascular system. Visualization of the cardiovascular system has been largely restricted to structures that can be filled with radiopaque intravascular contrast agents in adult animals. Recent ex vivo studies using osmium tetroxide, iodinated contrast agents, inorganic iodine, and phosphotungstic acid have demonstrated the ability to stain soft tissues differentially, allowing for high intertissue contrast in micro-CT images. In the present study, we demonstrate the application of this technology for visualization of cardiovascular structures in developing mouse embryos using Lugol solution (aqueous potassium iodide plus iodine). METHODS AND

resultsWe show the optimization of this method to obtain ex vivo micro-CT images of embryonic and neonatal mice with excellent soft-tissue contrast. We demonstrate the utility of this method to visualize key structures during cardiovascular development at various stages of embryogenesis. Our method benefits from the ease of sample preparation, low toxicity, and low cost. Furthermore, we show how multiple cardiac defects can be demonstrated by micro-CT in a single specimen with a known genetic lesion. Indeed, a previously undescribed cardiac venous abnormality is revealed in a PlexinD1 mutant mouse.

conclusionsMicro-CT of iodine-stained tissue is a valuable technique for the characterization of cardiovascular development and defects in mouse models of congenital heart disease.

Indexed as

IodidesAnimalsAnimals, NewbornCardiovascular SystemColoring AgentsDisease Models, AnimalHeartHeart Defects, CongenitalImaging, Three-DimensionalMicePhenotypeRadiographic Image EnhancementX-Ray MicrotomographyColoring AgentsIodidesLugol's solution

Identifiers

PMID20190279
PMCPMC3059892
OpenAlexW2044528153

What OpenQuestion holds

Textmetadata
LicenceTDM
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.