Evidence map›Paper›PMID 39028624›Full record

ReviewAsian journal of andrology2025

Autophagy in erectile dysfunction: focusing on apoptosis and fibrosis.

Pei-Yue Luo, Jun-Rong Zou, Tao Chen, Jun Zou, Wei Li, Qi Chen, Le Cheng, Li-Ying Zheng, Biao Qian

Abstract readReview
In one paragraph

Review in Asian journal of andrology, 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.

  1. Review
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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.

Pei-Yue LuoThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Jun-Rong ZouDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
Tao ChenThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Jun ZouThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Wei LiThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Qi ChenThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Le ChengThe First Clinical College, Gannan Medical University, Ganzhou 341000, China.
Li-Ying ZhengDepartment of Graduate, The First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
Biao QianDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIn most types of erectile dysfunction, particularly in advanced stages, typical pathological features observed are reduced parenchymal cells coupled with increased tissue fibrosis. However, the current treatment methods have shown limited success in reversing these pathologic changes. Recent research has revealed that changes in autophagy levels, along with alterations in apoptosis and fibrosis-related proteins, are linked to the progression of erectile dysfunction, suggesting a significant association. Autophagy, known to significantly affect cell fate and tissue fibrosis, is currently being explored as a potential treatment modality for erectile dysfunction. However, these present studies are still in their nascent stage, and there are limited experimental data available. This review analyzes erectile dysfunction from a pathological perspective. It provides an in-depth overview of how autophagy is involved in the apoptotic processes of smooth muscle and endothelial cells and its role in the fibrotic processes occurring in the cavernosum. This study aimed to develop a theoretical framework for the potential effectiveness of autophagy in preventing and treating erectile dysfunction, thus encouraging further investigation among researchers in this area.

Indexed as

ApoptosisAutophagyErectile DysfunctionPenisAnimalsEndothelial CellsFibrosisHumansMaleMyocytes, Smooth Muscle

Identifiers

PMID39028624
PMCPMC11949458

What OpenQuestion holds

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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.