Evidence map›Paper›PMID 33758249›Full record

ArticleScientific reports2021

Gestational intermittent hyperoxia rescues murine genetic congenital heart disease in part.

Cassandra F Doll, Natalia J Pereira, Mustafa S Hashimi, Tabor J Grindrod, Fariz F Alkassis, Lawrence X Cai, Una Milovanovic, Adriana I Sandino, Hideko Kasahara

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
0.1field-weighted citation impact, top 58% 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, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Genetic and Environmental Contributors To Congenital Heart Disease.Current treatment options in cardiovascular medicine · 2025
    Review
  4. 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

9 authors at 2 institutions in 2 countries.

Cassandra F Doll *Department of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Natalia J Pereira *Department of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Mustafa S Hashimi *Department of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Tabor J GrindrodDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Fariz F AlkassisDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Lawrence X CaiDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Una MilovanovicDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Adriana I SandinoDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA.
Hideko KasaharaDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Rd. M543, Gainesville, FL, 32610-0274, USA. hkasahar@ufl.edu.
University of Florida · USFlorida College · US

Funding

Engineering Tissue Mimics to Investigate Congenital Heart DiseaseR21HD090608 · NICHD · UNIVERSITY OF FLORIDA · PI KASAHARA, HIDEKO, SCHMIDT, CHRISTINE E · 2017 to 2018
$407k
NICHD NIH HHS R21 HD090608
6 · The paper itself

Abstract

Cardiac development is a dynamic process, temporally and spatially. When disturbed, it leads to congenital cardiac anomalies that affect approximately 1% of live births. Genetic variants in several loci lead to anomalies, with the transcription factor NKX2-5 being one of the largest. However, there are also non-genetic factors that influence cardiac malformations. We examined the hypothesis that hyperoxia may be beneficial and can rescue genetic cardiac anomalies induced by an Nkx2-5 mutation. Intermittent mild hyperoxia (40% PO

Indexed as

AnimalsFemaleFetal HeartHeart Septal Defects, VentricularHomeobox Protein Nkx-2.5Hyperbaric OxygenationMiceMutationHomeobox Protein Nkx-2.5Nkx2-5 protein, mouse

Identifiers

PMID33758249
PMCPMC7988122
OpenAlexW3139231306

What OpenQuestion holds

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LicenceCC BY
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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.