Evidence map›Paper›PMID 41293421›Full record

ReviewFrontiers in cell and developmental biology2025

Efferocytosis: a therapeutic strategy for diabetes and its vascular complications.

Yi Song, Jiayi Yuan, Yifan Li, Yifan Liu, Guijun Qin

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Yi Song *Department of Endocrinology and Metabolism, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jiayi Yuan *The First Clinical Medical College of Zhengzhou University, Zhengzhou, China.
Yifan LiThe First Clinical Medical College of Zhengzhou University, Zhengzhou, China.
Yifan LiuDepartment of Pediatric Transplantation, Tianjin First Central Hospital, Tianjin, China.
Guijun QinDepartment of Endocrinology and Metabolism, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Efferocytosis is a continuous multistep process that efficiently clears dead cells and is essential for maintaining homeostasis in multicellular organisms. Under normal circumstances, apoptotic cells release "find-me" and "eat-me" signals that stimulate their engulfment and clearance. However, in many chronic inflammatory diseases, the clearance of apoptotic cells is significantly impaired. This review explores the relationship between defective efferocytosis and diabetes-related vascular complications, while investigating underlying pathophysiological mechanisms to identify novel therapeutic targets for disease management. Methods: After searching in PubMed and Web of Science databases using 'efferocytosis', 'diabetic vascular complications', and 'efferocytosis-based therapy' as keywords, studies related were compiled and examined. Results: This review summarizes the specific process of phagocytes engulfing and clearing dead cells, and explains the development of diabetes and its vascular complications from the perspective of defects in efferocytosis. Conclusion: The review points out that molecules and pathways associated with efferocytosis are potential targets for treating diabetic vascular complications, providing new ideas for clinical treatment.

Indexed as

diabetesdiabetic vascular complicationsefferocytosisefferocytosis-based therapyimmunologyinflammation

Identifiers

PMID41293421
PMCPMC12640946

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.