Evidence map›Paper›PMID 38453635›Full record

ArticleJournal of Zhejiang University. Science. B2024

Advances in the study of mitophagy in osteoarthritis.

Hong Cao, Xuchang Zhou, Bowen Xu, Han Hu, Jianming Guo, Miao Wang, Nan Li, Zou Jun

Open access · greenAbstract read
In one paragraph

Article in Journal of Zhejiang University. Science. B, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Emerging roles of the metabolite succinate in bone-related diseases.Journal of Zhejiang University. Science. B · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Identification of mitophagy-related biomarkers in osteoarthritis.Animal models and experimental medicine · 2024
    Article
  15. Review
  16. Article
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

8 authors at 3 institutions in 2 countries.

Hong CaoDepartment of Sport Rehabilitation, Shanghai University of Sport, Shanghai 200438, China.
Xuchang ZhouDepartment of Sport Rehabilitation, Shanghai University of Sport, Shanghai 200438, China.
Bowen XuNational Key Laboratory of Immunity and Inflammation, Naval Medical University, Shanghai 200433, China.
Han HuNational Key Laboratory of Immunity and Inflammation, Naval Medical University, Shanghai 200433, China.
Jianming GuoDepartment of Sport Rehabilitation, Shanghai University of Sport, Shanghai 200438, China.
Miao WangDepartment of Sport Rehabilitation, Shanghai University of Sport, Shanghai 200438, China.
Nan LiNational Key Laboratory of Immunity and Inflammation, Naval Medical University, Shanghai 200433, China. linan@immunol.org.
Zou JunDepartment of Sport Rehabilitation, Shanghai University of Sport, Shanghai 200438, China. junzou@sus.edu.cn.
Shanghai University of Sport · CNNaval University of Engineering · CNInstitute of Infection and Immunity · CA

Funding

the 2021 Capacity Building of Shanghai Universities 21010503600the National Natural Science Foundation of China 82071762the Shanghai Key Lab of Human Performance (Shanghai University of Sport) 11DZ2261100
6 · The paper itself

Abstract

Osteoarthritis (OA), characterized by cartilage degeneration, synovial inflammation, and subchondral bone remodeling, is among the most common musculoskeletal disorders globally in people over 60 years of age. The initiation and progression of OA involves the abnormal metabolism of chondrocytes as an important pathogenic process. Cartilage degeneration features mitochondrial dysfunction as one of the important causative factors of abnormal chondrocyte metabolism. Therefore, maintaining mitochondrial homeostasis is an important strategy to mitigate OA. Mitophagy is a vital process for autophagosomes to target, engulf, and remove damaged and dysfunctional mitochondria, thereby maintaining mitochondrial homeostasis. Cumulative studies have revealed a strong association between mitophagy and OA, suggesting that the regulation of mitophagy may be a novel therapeutic direction for OA. By reviewing the literature on mitophagy and OA published in recent years, this paper elaborates the potential mechanism of mitophagy regulating OA, thus providing a theoretical basis for studies related to mitophagy to develop new treatment options for OA.

Indexed as

Cartilage, ArticularOsteoarthritisAgedChondrocytesHumansInflammationMiddle AgedMitophagyApoptosisChondrocyteMitochondriaMitophagyOsteoarthritis

Identifiers

PMID38453635
PMCPMC10918408
OpenAlexW4392866751

What OpenQuestion holds

Textmetadata
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.