Evidence map›Paper›PMID 36144851›Full record

ArticleMolecules (Basel, Switzerland)2022

NMR-Based Metabolomic Analysis of Cardiac Tissues Clarifies Molecular Mechanisms of CVB3-Induced Viral Myocarditis and Dilated Cardiomyopathy.

Qing Kong, Jinping Gu, Ruohan Lu, Caihua Huang, Lili Chen, Weifeng Wu, Donghai Lin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 8 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

7 authors at 4 institutions in 1 country.

Qing KongDepartment of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Jinping GuKey Laboratory for Chemical Biology of Fujian Province, MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Ruohan LuKey Laboratory for Chemical Biology of Fujian Province, MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Caihua HuangResearch and Communication Center of Exercise and Health, Xiamen University of Technology, Xiamen 361024, China.
Lili ChenDepartment of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Weifeng WuDepartment of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Donghai LinKey Laboratory for Chemical Biology of Fujian Province, MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Xiamen University · CNGuangxi Medical University · CNFirst Affiliated Hospital of GuangXi Medical University · CNXiamen University of Technology · CN

Funding

Joint Funds for the Innovation of Science Technology of Fujian Province 2018Y9100National Natural Science Foundation of China 31971357, 81160032, 21906147Natural Science Foundation of Guangxi Province 2018JJB140169
6 · The paper itself

Abstract

Viral myocarditis (VMC), which is defined as inflammation of the myocardium with consequent myocardial injury, may develop chronic disease eventually leading to dilated cardiomyopathy (DCM). Molecular mechanisms underlying the progression from acute VMC (aVMC), to chronic VMC (cVMC) and finally to DCM, are still unclear. Here, we established mouse models of VMC and DCM with Coxsackievirus B3 infection and conducted NMR-based metabolomic analysis of aqueous metabolites extracted from cardiac tissues of three histologically classified groups including aVMC, cVMC and DCM. We showed that these three pathological groups were metabolically distinct from their normal counterparts and identified three impaired metabolic pathways shared by these pathological groups relative to normal controls, including nicotinate and nicotinamide metabolism; alanine, aspartate and glutamate metabolism; and D-glutamine and D-glutamate metabolism. We also identified two extra impaired metabolic pathways in the aVMC group, including glycine, serine and threonine metabolism; and taurine and hypotaurine metabolism Furthermore, we identified potential cardiac biomarkers for metabolically distinguishing these three pathological stages from normal controls. Our results indicate that the metabolomic analysis of cardiac tissues can provide valuable insights into the molecular mechanisms underlying the progression from acute VMC to DCM.

Indexed as

Cardiomyopathy, DilatedCoxsackievirus InfectionsMyocarditisNiacinAlanineAnimalsAspartic AcidBiomarkersEnterovirus B, HumanGlutamic AcidGlutamineGlycineMiceMice, Inbred BALB CNiacinamideSerineAlanineAspartic AcidBiomarkersGlutamic AcidGlutamineGlycineNiacinNiacinamideSerineTaurineThreoninecardiac tissuedilated cardiomyopathymetabolomicsNMRviral myocarditis

Identifiers

PMID36144851
PMCPMC9500976
OpenAlexW4296794598

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.