Evidence map›Paper›PMID 35348004›Full record

ReviewJournal of the American Heart Association2022

Epigenetics in Congenital Heart Disease.

Guanglei Wang, Bingbing Wang, Peixin Yang

Open access · goldAbstract readReview
In one paragraph

Review in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
5.6field-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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 70 citations in OpenAlex.

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  18. Role of circulating microRNAs in tetralogy of Fallot.Postepy w kardiologii interwencyjnej = Advances in interventional cardiology · 2025
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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

3 authors at 1 institution in 1 country.

Guanglei WangDepartment of Obstetrics, Gynecology, & Reproductive Sciences University of Maryland School of Medicine Baltimore MD.
Bingbing WangDepartment of Obstetrics, Gynecology, & Reproductive Sciences University of Maryland School of Medicine Baltimore MD.
Peixin YangDepartment of Obstetrics, Gynecology, & Reproductive Sciences University of Maryland School of Medicine Baltimore MD.ORCID 0000-0002-2104-0699
University of Maryland, Baltimore · US

Funding

Characterization of the Cardiac Progenitor Cell Exosomes for Optimal TherapeuticsR01HL141922 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY · 2019 to 2022
$2.8M
Hyperglycemia of Maternal Diabetes Induces Cardiac Isl1 Positive Progenitor Dysfunction Leading to Heart DefectsR01HL153141 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY, YANG, PEIXIN · 2020 to 2023
$2.5M
MicroRNA-Suppressed Mitochondrial Fusion in Mediating the Teratogenicity of Maternal Diabetes Leading to Heart DefectsR01HL134368 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, JIAN-YING, YANG, PEIXIN · 2017 to 2020
$2.4M
Cellular Stress-Induced Gene Dysregulation in Heart Defects Formation of Diabetic PregnancyR01HL151108 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI YANG, PEIXIN · 2020 to 2023
$2.4M
The Role of C-Kit Positive Cardiac Progenitors in Maternal Diabetes-Induced Heart Defects and the Therapeutic Values of These CellsR01HL139060 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY, YANG, PEIXIN · 2017 to 2020
$2.4M
Maternal Diabetes-Suppressed Vascular Signaling Induces Vasculopathy and Neural Tube DefectsR01HL131737 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI YANG, PEIXIN · 2016 to 2019
$2.1M
BLRD VA I01 BX000332NHLBI NIH HHS R01 HL131737NHLBI NIH HHS R01 HL134368NHLBI NIH HHS R01 HL139060NHLBI NIH HHS R01 HL141922NHLBI NIH HHS R01 HL151108NHLBI NIH HHS R01 HL153141
6 · The paper itself

Abstract

Embryonic heart development is an intricate process that mainly involves morphogens, transcription factors, and cardiac genes. The precise spatiotemporal expression of these genes during different developmental stages underlies normal heart development. Thus, mutation or aberrant expression of these genes may lead to congenital heart disease (CHD). However, evidence demonstrates that the mutation of genes accounts for only a small portion of CHD cases, whereas the aberrant expression regulated by epigenetic modification plays a predominant role in the pathogenesis of CHD. In this review, we provide essential knowledge on the aberrant epigenetic modification involved in the pathogenesis of CHD. Then, we discuss recent advances in the identification of novel epigenetic biomarkers. Last, we highlight the epigenetic roles in some adverse intrauterine environment-related CHD, which may help the prevention, diagnosis, and treatment of these kinds of CHD.

Indexed as

Heart Defects, CongenitalEpigenesis, GeneticEpigenomicsHeartHumansMutationbiomarkerscardiac developmentcongenital heart diseaseepigenetics

Identifiers

PMID35348004
PMCPMC9075469
OpenAlexW4220801281

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.