Evidence map›Paper›PMID 40461719›Full record

ArticleScientific reports2025

Placental whole transcriptome expression profile in patients with early-onset, late-onset preeclampsia and gestational diabetes mellitus.

Zhuo Chen, Li Yang, Li Geng, Xinwen Zhang, Mingyu Du, Yonghu Sun, Lin Zhao, Bing Bai, Xiaohong Li

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

9 authors.

Zhuo Chen *Department of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Li Yang *School of Basic Medicine, Kunming Medical University, Kunming, 650500, Yunnan, China.
Li GengDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Xinwen ZhangDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Mingyu DuDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Yonghu SunDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Lin ZhaoDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Bing BaiDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China.
Xiaohong LiDepartment of Obstetrics, the First Affiliated Hospital of Kunming Medical University, No.295 Xi Chang Rd, Kunming, 650032, Yunnan, China. 422915581@qq.com.

Funding

Financial support from the Yunnan Provincial Science and Technology Department - Kunming Medical University Joint Foundation 202101AY070001-122
6 · The paper itself

Abstract

Preeclampsia (PE) and gestational diabetes mellitus (GDM) are significant pregnancy complications with complex pathogenesis. Therefore, we conducted a comprehensive investigation using whole-transcriptome sequencing of placental samples. The results revealed dysregulation of key pathways in early-onset-PE (OE-PE), including Wnt signaling, PI3K-Akt signaling, MAPK signaling, FoxO signaling, and TNF signaling, along with downregulation of genes related to Ca2 + conduction and hormone pathways. In late-onset-PE (LO-PE) and GDM, abnormalities were observed in immune pathways including chemokine signaling pathway and IL-17 signaling pathway, with differing immune cell infiltration patterns. EO-PE was associated with reduced T cells and B cells, while LO-PE had increased plasmacytoid dendritic and CD56bright natural killer cells. In GDM, a notable increase in the infiltration of various immune cells- including central memory CD8 T cells, monocytes, B cells, T cells, and central memory CD4 T cells - was observed. Additionally, downregulation of HLA-A and HLA-F, particularly in EO-PE, suggests immune dysregulation. CCL26-has-miR-618-has-circ-0001776 could potentially contribute to the progression of EO-PE, while CREB1-has-miR-373-3p-has-circ-0003793/has-circ-0001146 may be implicated in the LO-PE development. Additionally, GZMB-has-miR-199a-5p/has-miR-199b-5p-has-circ-0008959/novel-circ_0008792 may mediate the disease progression of GDM. In summary, genes related to placental cell functions are inhibited in PE, while autoimmune abnormalities may play a role in LO-PE and GDM pathogenesis.

Indexed as

Diabetes, GestationalPlacentaPre-EclampsiaTranscriptomeAdultFemaleGene Expression ProfilingHumansPregnancySignal TransductionCompeting endogenous RNAImmunePreeclampsiaWhole transcriptome analysis

Identifiers

PMID40461719
PMCPMC12134284

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