Evidence map›Paper›PMID 34386532›Full record

ReviewFrontiers in cardiovascular medicine2021

The Immune and Inflammatory Basis of Acquired Pediatric Cardiac Disease.

Elysa Jui, Kavya L Singampalli, Kevin Shani, Yao Ning, Jennifer P Connell, Ravi K Birla, Paul L Bollyky, Christopher A Caldarone, Sundeep G Keswani, K Jane Grande-Allen

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
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

10 authors at 5 institutions in 1 country.

Elysa JuiDepartment of Bioengineering, Rice University, Houston, TX, United States.
Kavya L SingampalliDepartment of Bioengineering, Rice University, Houston, TX, United States.
Kevin ShaniJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States.
Yao NingLaboratory for Regenerative Tissue Repair, Division of Pediatric Surgery, Department of Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, United States.
Jennifer P ConnellDepartment of Bioengineering, Rice University, Houston, TX, United States.
Ravi K BirlaLaboratory for Regenerative Tissue Repair, Division of Pediatric Surgery, Department of Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, United States.
Paul L BollykyDivision of Infectious Diseases, Department of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Christopher A CaldaroneDivision of Congenital Heart Surgery, Departments of Surgery and Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, United States.
Sundeep G KeswaniLaboratory for Regenerative Tissue Repair, Division of Pediatric Surgery, Department of Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, United States.
K Jane Grande-AllenDepartment of Bioengineering, Rice University, Houston, TX, United States.
Rice University · USTexas Children's Hospital · USBaylor College of Medicine · USHarvard University · USStanford University · US

Funding

Differential Shear Forces on Endocardial Endothelial Cells Regulate a Fibrotic Spectrum in the Left Ventricular Outflow TractR01HL140305 · NHLBI · RICE UNIVERSITY · PI GRANDE-ALLEN, KATHRYN JANE, KESWANI, SUNDEEP G · 2018 to 2021
$2.2M
NHLBI NIH HHS R01 HL140305
6 · The paper itself

Abstract

Children with acquired heart disease face significant health challenges, including a lifetime of strict medical management, multiple cardiac surgeries, and a high mortality risk. Though the presentation of these conditions is diverse, a unifying factor is the role of immune and inflammatory responses in their development and/or progression. For example, infectious agents have been linked to pediatric cardiovascular disease, leading to a large health burden that disproportionately affects low-income areas. Other implicated mechanisms include antibody targeting of cardiac proteins, infection of cardiac cells, and inflammation-mediated damage to cardiac structures. These changes can alter blood flow patterns, change extracellular matrix composition, and induce cardiac remodeling. Therefore, understanding the relationship between the immune system and cardiovascular disease can inform targeted diagnostic and treatment approaches. In this review, we discuss the current understanding of pediatric immune-associated cardiac diseases, challenges in the field, and areas of research with potential for clinical benefit.

Indexed as

cardiac remodelingimmune responseinflammationpediatric heart diseasepediatric vascular disease

Identifiers

PMID34386532
PMCPMC8353076
OpenAlexW3186811081

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.