Evidence map›Paper›PMID 38549083›Full record

ArticleThrombosis journal2024

Insight into antiphospholipid syndrome: the role and clinical utility of neutrophils extracellular traps formation.

Shams ElDoha Galal ElDin Zaiema, Menna Allah Zakaria Mohammad Ali Abou Elwafa, Shaymaa Gamal Arafa Hassan, Radwa Hassan Abou El Fotoh El Adwey, Raghda Mohammed Mostafa Ghorab, Raghda El Sayed Abdel Monem Galal

Open access · goldAbstract read
In one paragraph

Article in Thrombosis journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Regulation of histones in thromboinflammation.Frontiers in immunology · 2026
    Review
  3. Article
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 1 country.

Shams ElDoha Galal ElDin ZaiemaDepartment of Clinical and Chemical Pathology, Ain shams University, Faculty of medicine, Cairo, Egypt. ShamsZaeima@med.asu.edu.eg.ORCID https://orcid.org/0009-0000-7046-6146
Menna Allah Zakaria Mohammad Ali Abou ElwafaDepartment of Clinical and Chemical Pathology, Ain shams University, Faculty of medicine, Cairo, Egypt.
Shaymaa Gamal Arafa HassanDepartment of Rheumatology-Internal Medicine, Ain shams University, Faculty of medicine, Cairo, Egypt.
Radwa Hassan Abou El Fotoh El AdweyDepartment of Immunology-Internal Medicine, Ain shams University, Faculty of medicine, Cairo, Egypt.
Raghda Mohammed Mostafa GhorabImmunogenetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Raghda El Sayed Abdel Monem GalalDepartment of Clinical and Chemical Pathology, Ain shams University, Faculty of medicine, Cairo, Egypt.
Ain Shams University · EGNational Research Centre · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiphospholipid syndrome (APLS) is a systemic immune dysregulation distinguished by repetitive complications and pregnancy loss in the absence of definite etiology. Most research focuses on the laboratory detection and clinical features of APLS, but its precise etiology remains to be deeply explored. NETosis is a newly developed theory in the pathophysiology of APLS which may serve as the missing bridge between coagulation and inflammation reaching the disease progression and severity. We aimed in this study to navigate the prognostic role of NETosis in thrombotic APLS. Our study included 49 newly diagnosed APLS patients (both 1ry and 2ry) who met clinical and laboratory criteria as per the international consensus statement on the update of the classification criteria for definite APLS and were sub-classified according to the occurrence of thrombotic events in thrombotic and non-thrombotic types. In addition, 20 sex and age-matched reactive subjects and 20 sex and age-matched healthy volunteer controls were enrolled. NETosis formation was assessed by measuring serum Myeloperoxidase (MPO) and Histones level using the enzyme-linked immunosorbent assay (ELISA) technique. Both MPO and Histones levels were able to discriminate among APLS cases from normal controls, showing significant cutoffs of > 2.09 ng/ml for MPO and > 1.45 ng/ml for Histones (AUC values were 0.987and 1.000, respectively). These values can be used as predictors for NETosis pathophysiology in APLS patients. Additionally, these markers demonstrated a significant association with several prognostic indicators, including thrombosis, higher PT and INR, and lower hemoglobin (Hb) levels which are supposed to be ameliorated by using NETs inhibitors. In conclusion, we suggest that measuring NETosis markers, MPO, and Histones, in the early course of APLS using proposed cutoff values will facilitate the timely initiation of anti-NETosis therapy and improve the overall prognosis, particularly for patients with thrombotic APLS.

Indexed as

Anti-NETosis therapy/NETs inhibitorsAntiphospholipid antibodiesAntiphospholipid syndromeCutoff for NETs activationHistonesMyeloperoxidaseNETosisThrombosis

Identifiers

PMID38549083
PMCPMC10979549
OpenAlexW4393259625

What OpenQuestion holds

Textmetadata
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.