Evidence map›Paper›PMID 34387124›Full record

ArticleJournal of the American Heart Association2021

Postnatal Right Ventricular Developmental Track Changed by Volume Overload.

Sijuan Sun, Yuqing Hu, Yingying Xiao, Shoubao Wang, Chuan Jiang, Jinfen Liu, Hao Zhang, Haifa Hong, Fen Li, Lincai Ye

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Sijuan SunDepartment of Pediatric Intensive Care Unit Shanghai Children's Medical Center School of Medicine Shanghai Jiao Tong University Shanghai China.
Yuqing HuDepartment of Cardiology, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Yingying XiaoDepartment of Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Shoubao WangDepartment of Plastic and Reconstructive Surgery Shanghai Ninth People's Hospital School of Medicine Shanghai Jiao Tong University Shanghai China.
Chuan JiangDepartment of Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Jinfen LiuDepartment of Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Hao ZhangDepartment of Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Haifa HongShanghai Institute for Pediatric Congenital Heart Disease Shanghai Children's Medical Center School of Medicine Shanghai Jiao Tong University Shanghai China.
Fen LiDepartment of Cardiology, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Lincai YeDepartment of Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine Shanghai Jiao Tong University Shanghai China.
Shanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Current right ventricular (RV) volume overload (VO) is established in adult mice. There are no neonatal mouse VO models and how VO affects postnatal RV development is largely unknown. Methods and Results Neonatal VO was induced by the fistula between abdominal aorta and inferior vena cava on postnatal day 7 and confirmed by abdominal ultrasound, echocardiography, and hematoxylin and eosin staining. The RNA-sequencing results showed that the top 5 most enriched gene ontology terms in normal RV development were energy derivation by oxidation of organic compounds, generation of precursor metabolites and energy, cellular respiration, striated muscle tissue development, and muscle organ development. Under the influence of VO, the top 5 most enriched gene ontology terms were angiogenesis, regulation of cytoskeleton organization, regulation of vasculature development, regulation of mitotic cell cycle, and regulation of the actin filament-based process. The top 3 enriched signaling pathways for the normal RV development were PPAR signaling pathway, citrate cycle (Tricarboxylic acid cycle), and fatty acid degradation. VO changed the signaling pathways to focal adhesion, the PI3K-Akt signaling pathway, and pathways in cancer. The RNA sequencing results were confirmed by the examination of the markers of metabolic and cardiac muscle maturation and the markers of cell cycle and angiogenesis. Conclusions A neonatal mouse VO model was successfully established, and the main processes of postnatal RV development were metabolic and cardiac muscle maturation, and VO changed that to angiogenesis and cell cycle regulation.

Indexed as

TranscriptomeAnimalsAnimals, NewbornAorta, AbdominalArteriovenous Shunt, SurgicalDisease Models, AnimalGene Expression ProfilingGene Expression Regulation, DevelopmentalMaleMiceMice, Inbred C57BLRNA-SeqTime FactorsVena Cava, InferiorVentricular Dysfunction, RightVentricular Function, Rightcardiomyocyteproliferationright ventricleRNA sequencingvolume overload

Identifiers

PMID34387124
PMCPMC8475045
OpenAlexW3187802856

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.