Evidence map›Paper›PMID 36997715›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2023

Identification of three potential novel biomarkers for early diagnosis of acute ischemic stroke via plasma lipidomics.

Yi Yu, Xue Wen, Jin-Guang Lin, Jun Liu, Hong-Feng Liang, Shan-Wen Lin, Qiu-Gui Xu, Ji-Cheng Li

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 3 pooled it
1.7field-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

8 citing papers in PubMed, 3 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
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 3 institutions in 1 country.

Yi Yu *Center for Analyses and Measurements, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310014, Zhejiang, China.ORCID http://orcid.org/0000-0003-2340-5177
Xue Wen *The Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Jin-Guang LinThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Jun LiuThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Hong-Feng LiangThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Shan-Wen LinThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Qiu-Gui XuThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China.
Ji-Cheng LiThe Central Laboratory, Yangjiang People's Hospital, Yangjiang, 529500, Guangdong, China. zjulijicheng@163.com.
Qujiang People's Hospital · CNCentral People's Hospital of Zhanjiang · CNZhejiang University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcute ischemic stroke (AIS) accounts for the majority of all stroke, globally the second leading cause of death. Due to its rapid development after onset, its early diagnosis is crucial.

objectivesWe aim to identify potential highly reliable blood-based biomarkers for early diagnosis of AIS using quantitative plasma lipid profiling via a machine learning approach.

methodsLipidomics was used for quantitative plasma lipid profiling, based on ultra-performance liquid chromatography tandem mass spectrometry. Our samples were divided into a discovery and a validation set, each containing 30 AIS patients and 30 health controls (HC). Differentially expressed lipid metabolites were screened based on the criteria VIP > 1, p < 0.05, and fold change > 1.5 or < 0.67. The least absolute shrinkage and selection operator (LASSO) and random forest algorithms in machine learning were used to select differential lipid metabolites as potential biomarkers.

resultsThree key differential lipid metabolites, CarnitineC10:1, CarnitineC10:1-OH and Cer(d18:0/16:0), were identified as potential biomarkers for early diagnosis of AIS. The former two, associated with thermogenesis, were down-regulated, whereas the latter, associated with necroptosis and sphingolipd metabolism, was upregulated. Univariate and multivariate logistic regressions showed that these three lipid metabolites and the resulting diagnostic model exhibited a strong ability in discriminating between AIS patients and HCs in both the discovery and validation sets, with an area under the curve above 0.9.

conclusionsOur work provides valuable information on the pathophysiology of AIS and constitutes an important step toward clinical application of blood-based biomarkers for diagnosing AIS.

Indexed as

Ischemic StrokeLipidomicsBiomarkersEarly DiagnosisHumansLipidsMetabolomicsBiomarkersLipidsAcute ischemic strokeBiomarkerLipid metabolitesLipidomicsMetabolomicsQuantitative lipid profiling

Identifiers

PMID36997715
OpenAlexW4362506968

What OpenQuestion holds

Textmetadata
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.