Evidence map›Paper›PMID 36513052›Full record

ArticleJournal of Korean medical science2022

Increased Pro-Inflammatory T Cells, Senescent T Cells, and Immune-Check Point Molecules in the Placentas of Patients With Gestational Diabetes Mellitus.

Yea Eun Kang, Hyon-Seung Yi, Min-Kyung Yeo, Jung Tae Kim, Danbit Park, Yewon Jung, Ok Soon Kim, Seong Eun Lee, Ji Min Kim, Kyong Hye Joung and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Hofbauer Cells in Pregnancies Complicated by Gestational Diabetes Mellitus and Pathological Fetal Growth.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Role of Arg1Scientific reports · 2025
    Article
  11. Review
  12. T-Cell Senescence in Human Metabolic Diseases.Diabetes & metabolism journal · 2024
    Review
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

14 authors at 3 institutions in 1 country.

Yea Eun Kang *Division of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-2012-3716
Hyon-Seung Yi *Division of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-3767-1954
Min-Kyung Yeo *Department of Pathology, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0001-8873-0021
Jung Tae KimDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-3920-0064
Danbit ParkDepartment of Obstetrics and Gynecology, Chungnam National University Hospital, Daejeon, Korea.ORCID https://orcid.org/0000-0002-3053-5204
Yewon JungDepartment of Obstetrics and Gynecology, Chungnam National University Sejong Hospital, Sejong, Korea.ORCID https://orcid.org/0000-0002-2257-2638
Ok Soon KimDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-6493-3745
Seong Eun LeeDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0001-5793-3774
Ji Min KimDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-0177-1849
Kyong Hye JoungDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0001-6674-9506
Ju Hee LeeDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0001-5976-7175
Bon Jeong KuDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0002-3414-8949
Mina LeeDepartment of Obstetrics and Gynecology, Chungnam National University College of Medicine, Daejeon, Korea. minari73@cnuh.co.kr.ORCID https://orcid.org/0000-0002-2285-2381
Hyun Jin KimDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea. kimhj43@cnuh.co.kr.ORCID https://orcid.org/0000-0002-6760-4963
Chungnam National University · KRChungnam National University Hospital · KRSejong University · KR

Funding

Chungnam National University HospitalKorea Health Industry Development Institute HR20C0025National Research Foundation Korea NRF-2021R1A2C4001829National Research Foundation Korea NRF-2022R1F1A1074608
6 · The paper itself

Abstract

backgroundGestational diabetes mellitus (GDM) is the most common metabolic complication of pregnancy. To define the altered pathway in GDM placenta, we investigated the transcriptomic profiles from human placenta between GDM and controls.

methodsClinical parameters and postpartum complications were reviewed in all participants. Differentially expressed canonical pathways were analyzed between the GDM and control groups based on transcriptomic analysis. CD4

resultsGene ontology analysis revealed that the placenta of GDM revealed upregulation of diverse mitochondria or DNA replication related pathways and downregulation of T-cell immunity related pathways. The maternal placenta of the GDM group had a higher proportion of CD4

conclusionThis study demonstrated increased proinflammatory T cells, senescent T cells and immune-check point molecules in GDM placentas, suggesting that changes in senescent T cells and immune-escape signaling might be related to the pathophysiology of GDM.

Indexed as

Diabetes, GestationalCD8-Positive T-LymphocytesFemaleFlow CytometryHumansPlacentaPregnancyT-Lymphocyte SubsetsGestational DiabetesImmune-Check Point MoleculesPlacentaRNA-SequencingSenescent T CellsT Cell Immunity

Identifiers

PMID36513052
PMCPMC9745681
OpenAlexW4312066520

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.