Evidence map›Paper›PMID 42328561›Full record

ArticleFrontiers in medicine2026

PBMC-derived FGF, PDGF, VEGF and GM-CSF secretion in endometriosis: a case-control

Marcin Sadlocha, Aleksandra Krzywon, Jakub Marcin Staniczek, Jakub Toczek, Zenon Czuba, Rafal Stojko

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Marcin SadlochaChair and Clinical Department of Gynaecology, Obstetrics and Gynaecologic Oncology, Faculty of Health Sciences, Medical University of Silesia in Katowice, Katowice, Poland.
Aleksandra KrzywonDepartment of Applied Informatics, Silesian University of Technology, Gliwice, Poland.
Jakub Marcin StaniczekChair and Clinical Department of Gynaecology, Obstetrics and Gynaecologic Oncology, Faculty of Health Sciences, Medical University of Silesia in Katowice, Katowice, Poland.
Jakub ToczekChair and Clinical Department of Gynaecology, Obstetrics and Gynaecologic Oncology, Faculty of Health Sciences, Medical University of Silesia in Katowice, Katowice, Poland.
Zenon CzubaDepartment of Microbiology and Immunology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Katowice, Poland.
Rafal StojkoChair and Clinical Department of Gynaecology, Obstetrics and Gynaecologic Oncology, Faculty of Health Sciences, Medical University of Silesia in Katowice, Katowice, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Endometriosis is a chronic inflammatory disease with immune dysregulation in which angiogenic, and hematopoietic mediators are thought to contribute to ectopic lesion establishment and persistence. Whether circulating immune cells are intrinsically primed to secrete higher levels of pro-angiogenic growth factors remains unclear. This study evaluated Methods: In a case-control design, women with laparoscopically and histopathologically confirmed endometriosis ( Results: Baseline secretion of FGF, PDGF, VEGF and GM-CSF by PBMCs did not differ significantly between women with endometriosis and controls after correction for multiple comparisons. PHA stimulation induced marked shifts in secretion profiles across participants- characterized by increases in FGF, PDGF and VEGF and a decrease in GM-CSF-but neither stimulated concentrations nor percent changes differed significantly between groups following false discovery rate adjustment. In univariate logistic regression analyses, none of the baseline growth-factor measures significantly predicted the presence of endometriosis. Conclusion: Under standardized

Indexed as

angiogenesiscytokinesendometriosisgrowth factorsin vitro cultureperipheral blood mononuclear cells

Identifiers

PMID42328561
PMCPMC13275388

What Socratic 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 Socratic graph.