Evidence map›Paper›PMID 36863704›Full record

ArticleAging2023

Identification MNS1, FRZB, OGN, LUM, SERP1NA3 and FCN3 as the potential immune-related key genes involved in ischaemic cardiomyopathy by random forest and nomogram.

Peng-Fei Zheng, Fen Liu, Zhao-Fen Zheng, Hong-Wei Pan, Zheng-Yu Liu

Open access · hybridFull text read
In one paragraph

Article in Aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 10 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

5 authors at 2 institutions in 1 country.

Peng-Fei ZhengCardiology Department, Hunan Provincial People’s Hospital, Furong, Changsha 410000, Hunan, China.
Fen LiuInstitute of Cardiovascular Epidemiology, Hunan Provincial People’s Hospital, Furong, Changsha 410000, Hunan, China.
Zhao-Fen ZhengCardiology Department, Hunan Provincial People’s Hospital, Furong, Changsha 410000, Hunan, China.
Hong-Wei PanCardiology Department, Hunan Provincial People’s Hospital, Furong, Changsha 410000, Hunan, China.
Zheng-Yu LiuCardiology Department, Hunan Provincial People’s Hospital, Furong, Changsha 410000, Hunan, China.
Hunan Provincial People's Hospital · CNHunan Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune molecular mechanisms involved in ischaemic cardiomyopathy (ICM) have not been fully elucidated. The current study aimed to elucidate the immune cell infiltration pattern of the ICM and identify key immune-related genes that participate in the pathologic process of the ICM. The differentially expressed genes (DEGs) were identified from two datasets (GSE42955 combined with GSE57338) and the top 8 key DEGs related to ICM were screened using random forest and used to construct the nomogram model. Moreover, the "CIBERSORT" software package was used to determine the proportion of infiltrating immune cells in the ICM. A total of 39 DEGs (18 upregulated and 21 downregulated) were identified in the current study. Four upregulated DEGs, including

Indexed as

CardiomyopathiesMyocardial IschemiaComputational BiologyHumansIntercellular Signaling Peptides and ProteinsLectinsNomogramsRandom ForestFCN3 protein, humanIntercellular Signaling Peptides and ProteinsLectinsOGN protein, humanbioinformatics analysisimmune cell infiltratesimmune-related genesischaemic cardiomyopathyrandom forest

Identifiers

PMID36863704
PMCPMC10042686
OpenAlexW4322762134

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read20
table measurements read1
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.