Evidence map›Paper›PMID 37294429›Full record

ReviewInternational orthopaedics2023

The role of apoptosis in the pathogenesis of osteoarthritis.

Si-Qi Xiao, Miao Cheng, Lei Wang, Jing Cao, Liang Fang, Xue-Ping Zhou, Xiao-Jin He, Yu-Feng Hu

Abstract readReview
PubMed Publisher
In one paragraph

Review in International orthopaedics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
13.7field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  16. Echinatin inhibits osteoarthritis through the NF-κB signaling pathway.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

8 authors at 2 institutions in 1 country.

Si-Qi XiaoDepartment of Rheumatology, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.
Miao ChengDepartment of Rheumatology, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.
Lei WangJiangsu Province Hospital of Chinese medicine, Nanjing, 210029, China.
Jing CaoJiangsu Province Hospital of Chinese medicine, Nanjing, 210029, China.
Liang FangDepartment of Rheumatology, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.
Xue-Ping ZhouThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Xiao-Jin HeDepartment of Rheumatology, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China. 260632@njucm.edu.cn.ORCID 0000-0001-6054-9626
Yu-Feng HuThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China. 260569@njucm.edu.cn.
Nanjing University of Chinese Medicine · CNJiangsu Province Hospital · CN

Funding

Government of Jiangsu Province SJCX21_0727Science and Technology Support Program of Jiangsu Province BE2022801
6 · The paper itself

Abstract

purposeApoptosis is an important physiological process, making a great difference to development and tissue homeostasis. Osteoarthritis (OA) is a chronic joint disease characterized by degeneration and destruction of articular cartilage and bone hyperplasia. This purpose of this study is to provide an updated review of the role of apoptosis in the pathogenesis of osteoarthritis.

methodsA comprehensive review of the literature on osteoarthritis and apoptosis was performed, which mainly focused on the regulatory factors and signaling pathways associated with chondrocyte apoptosis in osteoarthritis and other pathogenic mechanisms involved in chondrocyte apoptosis.

resultsInflammatory mediators such as reactive oxygen species (ROS), nitric oxide (NO), IL-1β, tumor necrosis factor-α (TNF-α), and Fas are closely related to chondrocyte apoptosis. NF-κB signaling pathway, Wnt signaling pathway, and Notch signaling pathway activate proteins and gene targets that promote or inhibit the progression of osteoarthritis disease, including chondrocyte apoptosis and ECM degradation. Long non-coding RNAs (LncRNAs) and microRNAs (microRNAs) have gradually replaced single and localized research methods and become the main research approaches. In addition, the relationship between cellular senescence, autophagy, and apoptosis was also briefly explained.

conclusionThis review offers a better molecular delineation of apoptotic processes that may help in designing new therapeutic options for OA treatment.

Indexed as

MicroRNAsOsteoarthritisApoptosisChondrocytesHumansInterleukin-1betaSignal TransductionInterleukin-1betaMicroRNAsApoptosisAutophagyNon-coding RNAsOsteoarthritisSenescenceSignaling pathways

Identifiers

PMID37294429
OpenAlexW4379966357

What Socratic 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 Socratic graph.