Evidence map›Paper›PMID 31487691›Full record

ArticleAging2019

TPM2 as a potential predictive biomarker for atherosclerosis.

Ling-Bing Meng, Meng-Jie Shan, Yong Qiu, Ruomei Qi, Ze-Mou Yu, Peng Guo, Chen-Yi Di, Tao Gong

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.6field-weighted citation impact, top 6% 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, 70 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

8 authors at 5 institutions in 1 country.

Ling-Bing MengNeurology Department, Beijing Hospital, National Center of Gerontology, Beijing 100730, P. R. China.
Meng-Jie ShanGraduate School, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P. R. China.
Yong QiuAnesthesiology Department, Beijing Hospital, National Center of Gerontology, Beijing 100730, P. R. China.
Ruomei QiThe MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing 100730, P. R. China.
Ze-Mou YuDepartment of Neurology, Peking University First Hospital, Beijing 100034, P. R. China.
Peng GuoDepartment of Orthopedics, The Fourth Hospital of Hebei Medical University, Shijiazhuang Development Zone, Hebei 050011, P.R. China.
Chen-Yi DiSchool of Basic Medicine, Peking University, Beijing 100191, P. R. China.
Tao GongNeurology Department, Beijing Hospital, National Center of Gerontology, Beijing 100730, P. R. China.
Beijing Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFourth Hospital of Hebei Medical University · CNPeking University · CNPeking University First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac-cerebral vascular disease (CCVD), is primarily induced by atherosclerosis, and is a leading cause of mortality. Numerous studies have investigated and attempted to clarify the molecular mechanisms of atherosclerosis; however, its pathogenesis has yet to be completely elucidated. Two expression profiling datasets, GSE43292 and GSE57691, were obtained from the Gene Expression Omnibus (GEO) database. The present study then identified the differentially expressed genes (DEGs), and functional annotation of the DEGs was performed. Finally, an atherosclerosis animal model and neural network prediction model was constructed to verify the relationship between hub gene and atherosclerosis. The results identified a total of 234 DEGs between the normal and atherosclerosis samples. The DEGs were mainly enriched in actin filament, actin binding, smooth muscle cells, and cytokine-cytokine receptor interactions. A total of 13 genes were identified as hub genes. Following verification of animal model, the common DEG, Tropomyosin 2 (TPM2), was found, which were displayed at lower levels in the atherosclerosis models and samples. In summary, DEGs identified in the present study may assist clinicians in understanding the pathogenesis governing the occurrence and development of atherosclerosis, and TPM2 exhibits potential as a promising diagnostic and therapeutic biomarker for atherosclerosis.

Indexed as

AnimalsAorta, AbdominalAtherosclerosisCase-Control StudiesDisease Models, AnimalGene Expression ProfilingHumansMyocytes, Smooth MuscleProtein Interaction MapsRabbitsTropomyosinTunica IntimaTPM2 protein, humanTropomyosinatherosclerosisbioinformatics analysiscardiac-cerebral vascular diseasesdifferentially expressed genesprotein-protein interaction

Identifiers

PMID31487691
PMCPMC6756910
OpenAlexW2971609214

What OpenQuestion holds

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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.