Evidence map›Paper›PMID 35268388›Full record

ArticleJournal of clinical medicine2022

Is Oxidative Stress an Emerging Player in the Thrombosis of Patients with Anti-Phosphatidylethanolamine Autoantibodies?

Xavier Heim, Daniel Bertin, Noémie Resseguier, Abdelouahab Beziane, Audrey Metral, Alexandre Brodovitch, Régis Guieu, Jean-Guillaume Steinberg, Marcel Blot-Chabaud, Pierre-Emmanuel Morange and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

12 authors at 3 institutions in 1 country.

Xavier HeimService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.ORCID 0000-0002-9459-4318
Daniel BertinService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Noémie ResseguierService de Santé Publique, Unité de Recherche EA 3279, Aix-Marseille Université, 13005 Marseille, France.ORCID 0000-0003-0816-4053
Abdelouahab BezianeService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Audrey MetralService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Alexandre BrodovitchService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Régis GuieuCenter for CardioVascular and Nutrition Research C2VN, INSERM, INRAE Faculty of Pharmacy, Timone Campus, Aix-Marseille University, 13005 Marseille, France.
Jean-Guillaume SteinbergCenter for CardioVascular and Nutrition Research C2VN, INSERM, INRAE Faculty of Pharmacy, Timone Campus, Aix-Marseille University, 13005 Marseille, France.
Marcel Blot-ChabaudCenter for CardioVascular and Nutrition Research C2VN, INSERM, INRAE Faculty of Pharmacy, Timone Campus, Aix-Marseille University, 13005 Marseille, France.
Pierre-Emmanuel MorangeCenter for CardioVascular and Nutrition Research C2VN, INSERM, INRAE Faculty of Pharmacy, Timone Campus, Aix-Marseille University, 13005 Marseille, France.
Jean-Louis MegeService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Nathalie BardinService d'Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille (AP-HM), 13005 Marseille, France.
Inserm · FRAssistance Publique Hôpitaux de Marseille · FRAix-Marseille Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The detection of anti-phosphatidylethanolamine autoantibodies (aPEs) has been proposed to improve the diagnosis and management of patients presenting clinical manifestations of antiphospholipid syndrome (APS), such as thrombosis, and who are persistently negative for conventional markers. After selecting the most specific ELISA for their detection, we evidenced the interest of aPEs in the exploration of thrombosis when APS conventional markers were negative through a 1-year retrospective study including 1131 consecutive patients routinely tested for aPEs. To validate this result, we assessed aPEs in a newly selected population of 77 patients with unexplained deep vein thrombosis (DVT). With a total prevalence of 19.5%, we confirmed the interest of aPE detection in patients with unexplained DVT who were devoid of other aPLs markers. Since endosomal compartment, a source of ROS production, has been recently identified as the cellular target of aPEs in vitro, we then investigated an association between aPE positivity and reactive oxygen species (ROS) production by measuring the production of thiobarbituric acid-reactive substances. We showed, for the first time, a significant association between aPE positivity and systemic ROS production in patients which led us to hypothesize a new mechanism of action of aPEs in thrombosis through a signaling related to oxidative stress.

Indexed as

anti-phosphatidylethanolamine autoantibodiesantiphospholipid syndromeELISAreactive oxygen species (ROS)thiobarbituric acid-reactive substances (TBARs)thrombosis

Identifiers

PMID35268388
PMCPMC8911245
OpenAlexW4214548746

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.