Evidence map›Paper›PMID 41357060›Full record

ArticleJournal of the ASEAN Federation of Endocrine Societies2025

Evaluating Serum Endosialin (CD248) Levels as a Diagnostic Marker in Gestational Diabetes: A Case-Control Study.

Tevfik Berk Bildaci, Can Ata, Ufuk Atlihan, Huseyin Aytug Avsar, Secuk Erkilinc

Abstract read
In one paragraph

Article in Journal of the ASEAN Federation of Endocrine Societies, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

5 authors.

Tevfik Berk BildaciObygynecology Department, Izmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital, Faculty of Medicine, Izmir, Turkey.
Can AtaObygynecology Department, Izmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital, Faculty of Medicine, Izmir, Turkey.
Ufuk AtlihanObgynecology Department, Private Izmir Karataş Hospital, Izmir, Turkey.
Huseyin Aytug AvsarObgynecology Department, Tinaztepe University Galen Hospital, Faculty of Medicine, Izmir, Turkey.
Secuk ErkilincObygynecology Department, Izmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital, Faculty of Medicine, Izmir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Gestational diabetes mellitus (GDM), a pregnancy-induced hyperglycemia, affects approximately 17% of pregnancies globally. Its pathophysiology remains unclear, with inflammation and vascular remodeling playing key roles. CD248, a glycoprotein linked to inflammation and vascular remodeling, has been implicated in various conditions, but its role in GDM is uncertain. Methodology: A prospective case-control study was conducted with 169 pregnant women aged 18 to 49 at a tertiary hospital. Serum CD248 levels were assessed at 24 to 28 weeks of gestation prior to the oral glucose tolerance test (OGTT). Statistical analyses evaluated the association between CD248 levels, BMI and GDM status. Results: Of the participants, 32 (18.9%) were diagnosed with GDM. CD248 levels were lower in GDM patients (8.15 ± 10.16 ng/mL) than in controls (11.42 ± 15.44 ng/mL), but the difference was not statistically significant ( Conclusion: Unlike earlier findings associating elevated CD248 levels with early pregnancy GDM risk, this study found no significant relationship during later gestational stages. These results highlight a potentially complex and context-dependent role for CD248 in GDM pathophysiology.

Indexed as

Antigens, CDDiabetes, GestationalAdolescentAdultApyraseBiomarkersBody Mass IndexCase-Control StudiesFemaleGlucose Tolerance TestHumansMiddle AgedPregnancyProspective StudiesYoung AdultAntigens, CDApyraseBiomarkersENTPD1 protein, humanCD248EndosialinGestational Diabetes MellitusInflammationOGTT

Identifiers

PMID41357060
PMCPMC12680864

What Socratic holds

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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.