Evidence map›Paper›PMID 34552562›Full record

ArticleFrontiers in endocrinology2021

Association of Pericardiac Adipose Tissue With Coronary Artery Disease.

Mingxuan Li, Lin Qi, Yanglei Li, Shuyi Zhang, Lei Lin, Lijin Zhou, Wanlin Han, Xinkai Qu, Junfeng Cai, Maoqing Ye and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 18 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

11 authors at 2 institutions in 1 country.

Mingxuan LiDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Lin QiDepartment of Computed Tomography, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Yanglei LiDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Shuyi ZhangDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Lei LinDepartment of Cardiovascular Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Lijin ZhouDepartment of Cardiovascular Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Wanlin HanDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Xinkai QuDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Junfeng CaiDepartment of Cardiovascular Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Maoqing YeDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Kailei ShiDepartment of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Fudan University · CNHuadong Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Coronary artery disease (CAD) poses a worldwide health threat. Compelling evidence shows that pericardial adipose tissue (PAT), a brown-like adipose adjacent to the external surface of the pericardium, is associated with CAD. However, the specific molecular mechanisms of PAT in CAD are elusive. This study aims to characterize human PAT and explore its association with CAD. Methods: We acquired samples of PAT from 31 elective cardiac surgery patients (17 CAD patients and 14 controls). The transcriptome characteristics were assessed in 5 CAD patients and 4 controls Results: A total of 147 different genes (104 up-regulated genes and 43 down-regulated genes) were identified in CAD patients. These different genes were associated with immunity and inflammatory dysfunction. Cibersort analysis showed monocytes and macrophages were the most common subsets in immune cells, whereas immunohistochemical results revealed there were more macrophages and higher proportion of M1 subtype cells in PAT of CAD patients. The PPI network and module analysis uncovered several crucial genes, defined as candidate genes, including Jun, ATF3, CXCR4, FOSB, CCl4, which were validated through RT-qPCR. The miRNA-mRNA network implicated hsa-miR-185-5p as diagnostic targets and drug-gene network showed colchicine, fenofibrate as potential therapeutic drugs, respectively. Conclusion: This study demonstrates that PAT is mainly associated with the occurrence of CAD following the dysfunction of immune and inflammatory processes. The identified hubgenes, predicted drugs and miRNAs are promising biomarkers and therapeutic targets for CAD.

Indexed as

Adipose TissueAgedCase-Control StudiesCoronary Artery DiseaseFemaleGene Expression ProfilingHumansMaleMicroRNAsMiddle AgedPericardiumRisk FactorsRNA, MessengerRNA-SeqTranscriptomeMicroRNAsRNA, MessengerbioinformationCAD (Coronary artery disease)inflammationmacrophage cellPAT (pericardial adipose tissue)

Identifiers

PMID34552562
PMCPMC8451419
OpenAlexW3198727289

What Socratic holds

Textmetadata
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 Socratic graph.