Evidence map›Paper›PMID 41590612›Full record

ArticleMetabolites2025

Comprehensive Analysis of Different Subtypes of Oxylipins to Determine a LC-MS/MS Approach in Clinical Research.

Yurou Zhao, Zhengyu Fang, Zeyu Li, Yizhe Liu, Yang Bai, Xiaoqing Wang, Hongjun Yang, Na Guo

Abstract read
In one paragraph

Article in Metabolites, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yurou ZhaoExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Zhengyu FangExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Zeyu LiExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Yizhe LiuExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Yang BaiExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Xiaoqing WangExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Hongjun YangExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Na GuoExperimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.ORCID 0000-0002-3350-3507

Funding

National Natural Science Foundation of China 82474204Scientific and Technological Innovation Project of China Academy of Chinese Medical Sciences CI2021B017Scientific and Technological Innovation Project of China Academy of Chinese Medical Sciences NLTS2025005the Fundamental Research Funds for the Central Public Welfare Research Institutes JBGS2023001
6 · The paper itself

Abstract

BACKGROUND/

objectivesDifferent oxylipin subtypes have unique biological properties, requiring effective analytical protocols. However, establishing a complete pathway detection protocol for comprehensive oxylipin analysis is challenging. This study aimed to evaluate the adaptability and specificity of oxylipin subtypes under different extraction schemes and to develop a robust analytical platform for clinical biomarker investigation.

methodsWe revealed the adaptability and specificity of oxylipin subtypes based on different single-step extraction schemes. A high-throughput quantitative automated solid-phase extraction coupled with a liquid chromatography-tandem mass spectrometry (aSPE-LC-MS/MS) analytical platform was established for a broad panel of complex oxylipins. The method was applied to serum samples of patients with coronary heart disease (CHD).

resultsOur results verified that oxo-oxylipins, resolvin, and eicosanoids showed the best extraction efficiency under SPE protocol. Most hydroxy-oxylipins, dihydroxy-oxylipins, and HOTrEs are suitable for methanol protocol, HDHA for acetonitrile protocol, and epoxy-oxylipins for the methyl tert-butyl ether protocol, while medium-chain HETE is suitable for ethyl acetate protocol. Importantly, a novel sensitive fast method with wide coverage by the aSPE-LC-MS/MS analytical platform with satisfying sensitivity, accuracy and precision, extraction efficiency, low matrix effect, and linear calibration curves was obtained. Furthermore, we have successfully applied this method and found that 5-HETE, 11-HETE, and 15-HETE can serve as integrated biomarkers for patients with CHD, with high diagnostic performance.

conclusionsThe study provides the best protocol for the clinically targeted detection of oxylipins and provides an important means for studying biomarkers of diseases.

Indexed as

clinical protocolsextraction protocolextraction recovery ratematrix effectoxylipin

Identifiers

PMID41590612
PMCPMC12843908

What Socratic 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 Socratic graph.