Evidence map›Paper›PMID 32485807›Full record

ArticleMetabolites2020

Oxylipin Profiles in Plasma of Patients with Wilson's Disease.

Nadezhda V Azbukina, Alexander V Lopachev, Dmitry V Chistyakov, Sergei V Goriainov, Alina A Astakhova, Vsevolod V Poleshuk, Rogneda B Kazanskaya, Tatiana N Fedorova, Marina G Sergeeva

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Hepatic oxylipin profiles in mouse models of Wilson disease: New insights into early hepatic manifestations.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2024
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Wilson Disease: Update on Pathophysiology and Treatment.Frontiers in cell and developmental biology · 2022
    Review
  11. 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

9 authors at 4 institutions in 1 country.

Nadezhda V AzbukinaFaculty of Bioengineering and Bioinformatics, Moscow Lomonosov State University, Moscow 119234, Russia.ORCID 0000-0002-2546-2418
Alexander V LopachevLaboratory of Clinical and Experimental neurochemistry, Research Center of Neurology, Moscow 125367, Russia.
Dmitry V ChistyakovBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.ORCID 0000-0003-0137-8585
Sergei V GoriainovSREC PFUR Peoples' Friendship University of Russia (RUDN University), Moscow 117198, Russia.
Alina A AstakhovaBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.
Vsevolod V PoleshukResearch Center of Neurology, Moscow 125367, Russia.
Rogneda B KazanskayaBiological Department, Saint Petersburg State University, Universitetskaya Emb. 7/9, St Petersburg 199034, Russia.
Tatiana N FedorovaLaboratory of Clinical and Experimental neurochemistry, Research Center of Neurology, Moscow 125367, Russia.
Marina G SergeevaBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.
Lomonosov Moscow State University · RUResearch Center of Neurology · RUPeoples' Friendship University of Russia · RUSt Petersburg University · RU

Funding

Russian Foundation for Basic Research 19-29-01243
6 · The paper itself

Abstract

Wilson's disease (WD) is a rare autosomal recessive metabolic disorder resulting from mutations in the copper-transporting, P-type ATPase gene ATP7B gene, but influences of epigenetics, environment, age, and sex-related factors on the WD phenotype complicate diagnosis and clinical manifestations. Oxylipins, derivatives of omega-3, and omega-6 polyunsaturated fatty acids (PUFAs) are signaling mediators that are deeply involved in innate immunity responses; the regulation of inflammatory responses, including acute and chronic inflammation; and other disturbances related to any system diseases. Therefore, oxylipin profile tests are attractive for the diagnosis of WD. With UPLC-MS/MS lipidomics analysis, we detected 43 oxylipins in the plasma profiles of 39 patients with various clinical manifestations of WD compared with 16 healthy controls (HCs). Analyzing the similarity matrix of oxylipin profiles allowed us to cluster patients into three groups. Analysis of the data by VolcanoPlot and partial least square discriminant analysis (PLS-DA) showed that eight oxylipins and lipids stand for the variance between WD and HCs: eicosapentaenoic acid EPA, oleoylethanolamide OEA, octadecadienoic acids 9-HODE, 9-KODE, 12-hydroxyheptadecatrenoic acid 12-HHT, prostaglandins PGD2, PGE2, and 14,15-dihydroxyeicosatrienoic acids 14,15-DHET. The compounds indicate the involvement of oxidative stress damage, inflammatory processes, and peroxisome proliferator-activated receptor (PPAR) signaling pathways in this disease. The data reveal novel possible therapeutic targets and intervention strategies for treating WD.

Indexed as

copperCOXCYP450lipidomicsLOXoxylipinsPUFAsUPLC-MS/MSWilson’s disease

Identifiers

PMID32485807
PMCPMC7345781
OpenAlexW3032141359

What OpenQuestion holds

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Registered trials

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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.