Evidence map›Paper›PMID 33026085›Full record

Observational studyRheumatology (Oxford, England)2021

Neutrophil subpopulations and their activation potential in patients with antiphospholipid syndrome and healthy individuals.

Lisa-Marie Mauracher, Moritz Krall, Johanna Roiß, Lena Hell, Silvia Koder, Thomas M Hofbauer, Johanna Gebhart, Hubert Hayden, Christine Brostjan, Cihan Ay and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Neutrophil Subset Immunophenotyping.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. Review
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  10. Neutrophil extracellular traps in homeostasis and disease.Signal transduction and targeted therapy · 2024
    Review
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  12. Article
  13. Article
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  15. Article
  16. Review
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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

11 authors.

Lisa-Marie MauracherClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Moritz KrallClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Johanna RoißClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Lena HellClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Silvia KoderClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Thomas M HofbauerDivision of Cardiology, Department of Internal Medicine II, Vienna, Austria.
Johanna GebhartClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Hubert HaydenDepartment of Surgery, Surgical Research Laboratories, Medical University of Vienna, Vienna, Austria.
Christine BrostjanDepartment of Surgery, Surgical Research Laboratories, Medical University of Vienna, Vienna, Austria.
Cihan AyClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.
Ingrid PabingerClinical Division of Haematology and Haemostaseology, Department of Medicine I, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatients with APS are at increased risk of thromboembolism. Neutrophils have been shown to play a role in inducing thrombosis. We aimed to investigate differences in neutrophil subpopulations, their potential of activation and neutrophil extracellular trap (NET) formation comparing high and low-density neutrophils (HDNs/LDNs) as well as subpopulations in patients with APS and controls to gain deeper insight into their potential role in thrombotic manifestations in patients with APS.

methodsHDNs and LDNs of 20 patients with APS and 20 healthy donors were isolated by density gradient centrifugation and stimulated. Neutrophil subpopulations, their activation and NET release were assessed by flow cytometry.

resultsLDNs of both groups showed higher baseline activation, lower response to stimulation (regulation of activation markers CD11b/CD66b), but higher NET formation compared with HDNs. In patients with APS, the absolute number of LDNs was higher compared with controls. HDNs of APS patients showed higher spontaneous activation [%CD11b high: median (interquartile range): 2.78% (0.58-10.24) vs 0.56% (0.19-1.37)] and response to stimulation with ionomycin compared with HDNs of healthy donors [%CD11b high: 98.20 (61.08-99.13) vs 35.50% (13.50-93.85)], whereas no difference was found in LDNs. NET formation was increased in patients' HDNs upon stimulation.

conclusionHDNs and LDNs act differently, unstimulated and upon various stimulations in both healthy controls and APS patients. Differences in HDNs and LDNs between patients with APS and healthy controls indicate that neutrophils may enhance the risk of thrombosis in these patients and could thus be a target for prevention of thrombosis in APS.

Indexed as

Neutrophil ActivationAdultAntibodiesAntigens, CDAntiphospholipid Syndromebeta 2-Glycoprotein ICase-Control StudiesCD11b AntigenCell Adhesion MoleculesCohort StudiesExtracellular TrapsFemaleGPI-Linked ProteinsHumansIonomycinLupus Coagulation InhibitorAntibodiesAntigens, CDbeta 2-Glycoprotein ICD11b AntigenCEACAM8 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsIonomycinLupus Coagulation Inhibitorantiphospholipid syndromelow density neutrophilslupus anticoagulantneutrophil extracellular traps

Identifiers

PMID33026085
PMCPMC8024003

What OpenQuestion holds

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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 OpenQuestion graph.