Evidence map›Paper›PMID 42309513›Full record

ArticleIET systems biology

Metabolic Reprogramming in Recurrent Spontaneous Abortion: Key Biomarkers Identification and Diagnostic Model Development.

Fan Wu, Chuanmei Qin, Xiaowei Wei, Qian Li, Yi Yuan, Weihong Zeng, Yi Lin

Abstract read
In one paragraph

Article in IET systems 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
–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

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

7 authors.

Fan WuInternational Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Chuanmei QinReproductive Medicine Center, Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xiaowei WeiReproductive Medicine Center, Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Qian LiReproductive Medicine Center, Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yi YuanReproductive Medicine Center, Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Weihong ZengInternational Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yi LinReproductive Medicine Center, Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID https://orcid.org/0000-0001-8956-5734

Funding

Funds for Outstanding Newcomers, Shanghai Sixth People's Hospital X-3664National Key Research and Development Program of China 2018YFC1002800National Natural Science Foundation of China 81971403National Natural Science Foundation of China 82171669National Natural Science Foundation of China 82471722National Natural Science Foundation of China 82471726Shanghai Jiao Tong University Trans-Med Awards Research 20210201
6 · The paper itself

Abstract

Recurrent spontaneous abortion (RSA) involves complex and often unexplained pathogenesis. This study investigated metabolic reprogramming in RSA to identify diagnostic biomarkers. We integrated GEO datasets (GSE26787, GSE165004), identified metabolic reprogramming-related differentially expressed genes, and intersected them with WGCNA modules. Module genes were refined using logistic regression, SVM-RFE, and LASSO to construct a diagnostic model validated by ROC, nomogram, calibration, and decision curve analysis. The role of SREBF2 was explored by PCR, western blot, CCK-8, and transwell assays in vitro. Immune infiltration (ssGSEA, CIBERSORT) and single-cell RNA sequencing (GSE214607) explored immune-metabolic crosstalk. Results demonstrate critical involvement of metabolic reprogramming in RSA. Four model genes (SREBF2, PPARG, SQLE, UCP2) were upregulated in RSA and enriched in lipid/cholesterol pathways. Experimental validation confirmed SREBF2 upregulation in RSA decidua. Its overexpression in endometrial stromal cells impaired cell proliferation, decidualization, and trophoblast migration. Immune infiltration revealed correlations between model genes and specific immune subsets. Single-cell analysis identified altered immune cell proportions and cell-type-specific expression patterns, predominantly in macrophage subsets. This study indicates that lipid-centric metabolic remodelling may concurrently affect decidual function, trophoblast behaviour, and immune tolerance in RSA, offering diagnostic and therapeutic insights.

Indexed as

Abortion, HabitualMetabolic ReprogrammingModels, BiologicalBiomarkersFemaleGene Expression ProfilingHumansPregnancyBiomarkersdiagnostic modelimmune microenvironmentmetabolic reprogrammingrecurrent spontaneous abortionsingle‐cell analysis

Identifiers

PMID42309513
PMCPMC13275172

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.