Evidence map›Paper›PMID 38325598›Full record

ArticleJournal of thrombosis and haemostasis : JTH2024

Neutrophil peptidylarginine deiminase 4 plays a systemic role in obesity-induced chronic inflammation in mice.

Stijn Van Bruggen, Casey E Sheehy, Sirima Kraisin, Liesbeth Frederix, Denisa D Wagner, Kimberly Martinod

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Stijn Van BruggenCenter for Vascular and Molecular Biology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium; Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA. Electronic address: http://www.twitter.com/Cardio_KULeuven.
Casey E SheehyProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Sirima KraisinCenter for Vascular and Molecular Biology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium. Electronic address: http://www.twitter.com/Cardio_KULeuven.
Liesbeth FrederixCenter for Vascular and Molecular Biology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium. Electronic address: http://www.twitter.com/Cardio_KULeuven.
Denisa D WagnerProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA; Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts, USA. Electronic address: denisa.wagner@childrens.harvard.edu.
Kimberly MartinodCenter for Vascular and Molecular Biology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium. Electronic address: Kim.martinod@kuleuven.be.
Boston Children's Hospital · USKU Leuven · BE

Funding

Inflammation and thrombosis fuel cardiovascular and pulmonary disease: Focus on the interplay of neutrophil inflammasomes with NETsR35HL166556 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI DENISA D WAGNER · 2023 to 2026
$4.9M
NHLBI NIH HHS R35 HL166556
6 · The paper itself

Abstract

backgroundObesity is an increasing problem in our current society and is expected to keep rising in incidence. With its multiorigin, complex pathophysiology, it is difficult to treat and easy to acquire unnoticeably. During obesity, it has been established that the body is in a constant state of low-grade inflammation, thereby causing changes in immune cell physiology.

objectivesHere, we investigated the influence of neutrophils, more specifically as a result of peptidylarginine deiminase 4 (PAD4) activity and the release of neutrophil extracellular traps (NETs), during obesity-induced chronic inflammation.

methodsWild-type mice were placed on a high-fat diet (HFD) and investigated over a period of 10 weeks for NET formation and its impact on the heart. Neutrophil-selective PAD4 knockout (Ne-PAD4

resultsAs a result of high fat intake, we observed clear alteration in the priming status of isolated neutrophils toward NET release, including early stages of speck formation and histone citrullination of apoptosis-associated speck-like protein containing a CARD. Ne-PAD4

conclusionDetrimental physiological effects, the result of obesity progression, can in part be attributed to neutrophil PAD4 and NETs in response to chronic inflammation.

Indexed as

Diet, High-FatExtracellular TrapsInflammationMice, Inbred C57BLMice, KnockoutNeutrophilsObesityProtein-Arginine Deiminase Type 4AnimalsChronic DiseaseCitrullinationDisease Models, AnimalMaleMicepeptidylarginine deiminase 4, mouseProtein-Arginine Deiminase Type 4extracellular trapsneutrophilsobesityvenous thrombosis

Identifiers

PMID38325598
PMCPMC11318106
OpenAlexW4391543326

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.