Evidence map›Paper›PMID 35736428›Full record

ArticleMetabolites2022

Identification of Serum Oxylipins Associated with the Development of Coronary Artery Disease: A Nested Case-Control Study.

Kuang-Mao Chiang, Jia-Fu Chen, Chin-An Yang, Lili Xiu, Hsin-Chou Yang, Lie-Fen Shyur, Wen-Harn Pan

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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 6 institutions in 1 country.

Kuang-Mao ChiangInstitute of Biomedical Sciences, Academia Sinica, Taipei 11529, Taiwan.ORCID 0000-0002-8745-2004
Jia-Fu ChenInstitute of Public Health, School of Medicine, National Yang-Ming Chiao Tung University, Taipei 11221, Taiwan.
Chin-An YangDepartment of Biochemical Science and Technology, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0003-0232-794X
Lili XiuInstitute of Population Health Sciences, National Health Research Institutes, Miaoli 35053, Taiwan.
Hsin-Chou YangInstitute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Lie-Fen ShyurAgricultural Biotechnology Research Center, Academia Sinica, Taipei 11529, Taiwan.ORCID 0000-0003-3043-3707
Wen-Harn PanInstitute of Biomedical Sciences, Academia Sinica, Taipei 11529, Taiwan.
National Yang Ming Chiao Tung University · TWAgricultural Biotechnology Research Center, Academia Sinica · TWInstitute of Biomedical Sciences, Academia Sinica · TWInstitute of Statistical Science, Academia Sinica · TWNational Health Research Institutes · TWNational Taiwan University · TW

Funding

Ministry of Science and Technology of Taiwan MOST-107-2320-B-001-001-MY3
6 · The paper itself

Abstract

Coronary artery disease (CAD) is among the leading causes of death globally. The American Heart Association recommends that people should consume more PUFA-rich plant foods to replace SFA-rich ones to lower serum cholesterol and prevent CAD. However, PUFA may be susceptible to oxidation and generate oxidized products such as oxylipins. In this study, we investigated whether the blood oxylipin profile is associated with the risk of developing CAD and whether including identified oxylipins may improve the predictability of CAD risk. We designed a nested case-control study with 77 cases and 148 matched controls from a 10-year follow-up of the Nutrition and Health Survey in a Taiwanese cohort of 720 people aged 50 to 70. A panel of 46 oxylipins was measured for baseline serum samples. We discovered four oxylipins associated with CAD risk. 13-oxo-ODE, which has been previously found in formed plagues, was positively associated with CAD (OR = 5.02, 95%CI = 0.85 to 15.6). PGE2/PGD2, previously shown to increase cardiac output, was inversely associated (OR = 0.16, 95%CI = 0.06 to 0.42). 15-deoxy-PGJ2, with anti-inflammatory and anti-apoptosis effects on cardiomyocytes (OR = 0.26, 95%CI = 0.09 to 0.76), and 5-HETE, which was associated with inflammation (OR = 0.28, 95%CI = 0.10 to 0.78), were also negatively associated as protective factors. Adding these four oxylipins to the traditional risk prediction model significantly improved CAD prediction.

Indexed as

coronary artery diseasefried oillinoleic acidmetabolomicsNAHSIToxylipin

Identifiers

PMID35736428
PMCPMC9231201
OpenAlexW4281611186

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.