Evidence map›Paper›PMID 42756641›Full record

ArticleReproductive medicine and biology

Plasma Cell Counting Methodology Determines Chronic Endometritis Prevalence.

Jan Gruszczyński, Kacper Trębacz, Beata Kubiaczyk-Paluch, Grzegorz Dworacki, Michał J Dopierała, Agata Kolecka-Bednarczyk, Andrzej Frankowski, Miłosz Kadziński, Tomasz Żak

Abstract read
In one paragraph

Article in Reproductive medicine and biology. 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
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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

9 authors.

Jan GruszczyńskiCenter for Diagnosis and Treatment of Infertility MedART Poznan Poland.ORCID https://orcid.org/0009-0004-9405-6415
Kacper TrębaczCenter for Diagnosis and Treatment of Infertility MedART Poznan Poland.ORCID https://orcid.org/0009-0006-5615-5935
Beata Kubiaczyk-PaluchCenter for Diagnosis and Treatment of Infertility MedART Poznan Poland.ORCID https://orcid.org/0009-0008-4588-5398
Grzegorz DworackiCenter for Diagnosis and Treatment of Infertility MedART Poznan Poland.ORCID https://orcid.org/0000-0002-5740-6736
Michał J DopierałaDepartment of Oncological Pathology University Clinical Hospital, Poznań University of Medical Sciences Poznan Poland.ORCID https://orcid.org/0009-0004-9753-5948
Agata Kolecka-BednarczykDepartment of Immunology Poznań University of Medical Sciences Poznan Poland.ORCID https://orcid.org/0000-0002-0182-076X
Andrzej FrankowskiDepartment of Pathology, Obstetrics and Gynecology University Clinical Hospital, Poznań University of Medical Sciences Poznan Poland.
Miłosz KadzińskiInstitute of Computing Science Poznan University of Technology Poznan Poland.ORCID https://orcid.org/0000-0003-1806-3715
Tomasz ŻakCenter for Diagnosis and Treatment of Infertility MedART Poznan Poland.ORCID https://orcid.org/0009-0007-0962-3860

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Histopathological assessment of plasma cells (PCs) via CD138 immunohistochemistry, the diagnostic gold standard for chronic endometritis (CE), is methodologically heterogeneous. Does reported variation in CE prevalence reflect underlying pathobiology, or is it primarily an artifact of counting methodology? We quantified how HPF selection strategy, field count, and magnification influence observed prevalence. Methods: We retrospectively studied 886 treatment-naïve patients suspected of CE. CD138-stained biopsies were digitized; a three-pathologist consensus reference validated an AI pipeline for PC detection. Four counting methods were applied across two magnifications (200× vs. 400×) and multiple thresholds. Results: Inter-observer reliability was higher for digital (ICC = 0.99) than microscopy-based assessment (ICC = 0.73). The AI pipeline (F1: 0.89-0.97) outperformed manual microscopy (F1: 0.67-0.89) and matched digital assessment (F1: 0.81-1.00). At a fixed threshold and field count (≥ 5 PCs, ×400, 10 HPFs), field-selection strategy alone shifted prevalence from 3.1% (Random Sampling) to 69.5% (Independent Hotspot), Conclusions: Diagnostic threshold alone does not fully specify a CE criterion; field-selection strategy, field count, and magnification must also be reported for prevalence estimates to be comparable. Hotspot-based and AI-assisted counting are recommended over random field selection for reproducibility and sensitivity.

Indexed as

CD138 immunohistochemistrychronic endometritisdeep learningdiagnostic reproducibilitydigital pathologyplasma cell counting

Identifiers

PMID42756641
PMCPMC13583455

What OpenQuestion 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 OpenQuestion graph.