Evidence map›Paper›PMID 37174948›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Endometrial Staining of CD56 (Uterine Natural Killer), BCL-6, and CD138 (Plasma Cells) Improve Diagnosis and Clinical Pregnancy Outcomes in Unexplained Infertility and Recurrent IVF Failures: Standardization of Diagnosis with Digital Pathology.

Suheyla Ekemen, Cem Comunoglu, Cavit Kerem Kayhan, Ebru Bilir, Ilkay Cavusoglu, Nilay Etiler, Selcuk Bilgi, Umit Ince, Cevayir Coban, Halit Firat Erden

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 7 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

10 authors at 7 institutions in 3 countries.

Suheyla EkemenVocational School of Health Services, Kerem Aydınlar Campus, Acıbadem University, Istanbul 34752, Turkey.ORCID 0000-0001-7135-0233
Cem ComunogluDepartment of Pathology, Dr. Cemil Tascioglu City Hospital, University of Health Sciences, Istanbul 34668, Turkey.ORCID 0000-0003-1083-7042
Cavit Kerem KayhanAcibadem Central Pathology Laboratory, Kerem Aydinlar Campus, Istanbul 34752, Turkey.
Ebru BilirSchool of Medicine, Bahcesehir University, Istanbul 34349, Turkey.ORCID 0000-0002-5997-9861
Ilkay CavusogluWomen's Health and Gynecological Nursing, Institute of Health Sciences, Biruni University, Istanbul 34010, Turkey.
Nilay EtilerDepartment of Public Health, School of Medicine, Istanbul Okan University, Istanbul 34947, Turkey.ORCID 0000-0001-5711-3733
Selcuk BilgiAcibadem Central Pathology Laboratory, Kerem Aydinlar Campus, Istanbul 34752, Turkey.
Umit InceAcibadem Central Pathology Laboratory, Kerem Aydinlar Campus, Istanbul 34752, Turkey.
Cevayir CobanDivision of Malaria Immunology, Department of Microbiology and Immunology, Institute of Medical Science (IMSUT), University of Tokyo, Tokyo 108-8639, Japan.ORCID 0000-0002-4467-7799
Halit Firat ErdenObstetrics and Gynecology Infertility Clinic, Zorlu Center, Istanbul 34340, Turkey.
Acıbadem Adana Hospital · TRAcıbadem University · TRBahçeşehir University · TRBiruni University · TRSağlık Bilimleri Üniversitesi · TRThe University of Tokyo · JPUniversity of Nevada, Reno · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In women with unexplained infertility (UI) and recurrent in vitro fertilization (IVF) failures, the etiology is often unclear. Endometrial immune perturbations and the use of immune markers associated with these dysregulations are of great interest in the diagnosis and treatment of UI. However, reliable biomarkers and standardized quantification methods are lacking. Here, to address endometrial immune dysregulation in UI patients with recurrent IVF failures, we performed endometrial tissue sampling and immunostaining of CD56 (uNK), CD138, and BCL-6. Of these cases, 57.9% had positive CD56 in the endometrial stroma, while 46.1% had positive BCL-6 in the glandular epithelium, and 14.5% of the cases were found to be positive for CD138. Combined staining rates were 60.5%, 68.4%, and 71.05% for (CD56 or BCL-6), (CD56 or CD138), and (CD56, BCL-6, or CD138), respectively. There was a significant correlation between CD56 and BCL-6 positivity, while CD138 positivity was an independent parameter. After the recommended targeted therapy, pregnancy rates were found to increase from 58.5% to 61.6% and 73.8% in CD56-positive, (CD56- or BCL-6-positive), and (CD56-, BCL-6-, or CD138-positive) cases, respectively. Notably, a retrospective evaluation of digital pathology and light microscopy results showed a significant correlation. This study suggests that the examination of CD56, BCL-6, and CD138 in the same endometrial sample may be an effective method in determining the etiology of UI and reaching an early diagnosis and treatment options. Moreover, digital pathology can be used in the evaluation of CD56 and BCL-6 to provide objective, rapid, and reliable results.

Indexed as

BCL-6CD138CD56 (uNK)endometriosisendometritisrecurrent IVF failuresunexplained infertility (UI)

Identifiers

PMID37174948
PMCPMC10177933
OpenAlexW4367183291

What OpenQuestion holds

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LicenceCC BY
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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.