Evidence map›Paper›PMID 41040587›Full record

ReviewJournal of dental sciences2025

Accelerated senescence animal models and application in dentistry: A scoping review.

Si-Wei Wang, Jia-Yu Mou, Jia-Rui Jiang, Qi He, Mu-Lan Qahar, Daniele De- Santis, Fang Qi, Guang-Chao Xu, Jian-Guo Liu

Abstract readReview
In one paragraph

Review in Journal of dental sciences, 2025. 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

9 authors.

Si-Wei WangKey Laboratory of Oral Disease Research, School of Stomatology, Zunyi Medical University, Zunyi, China.
Jia-Yu MouKey Laboratory of Oral Disease Research, School of Stomatology, Zunyi Medical University, Zunyi, China.
Jia-Rui JiangKey Laboratory of Oral Disease Research, School of Stomatology, Zunyi Medical University, Zunyi, China.
Qi HeThe Collaborative Innovation Center of Tissue Damage Repair and Regeneration Medicine, Zunyi Medical University, Zunyi, China.
Mu-Lan QaharThe Collaborative Innovation Center of Tissue Damage Repair and Regeneration Medicine, Zunyi Medical University, Zunyi, China.
Daniele De- SantisHead and Neck Department, Department of Surgery, Dentistry, Pediatrics and Gynecology, University of Verona, Verona, Italy.
Fang QiThe Collaborative Innovation Center of Tissue Damage Repair and Regeneration Medicine, Zunyi Medical University, Zunyi, China.
Guang-Chao XuThe Collaborative Innovation Center of Tissue Damage Repair and Regeneration Medicine, Zunyi Medical University, Zunyi, China.
Jian-Guo LiuKey Laboratory of Oral Disease Research, School of Stomatology, Zunyi Medical University, Zunyi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accelerated senescence models are increasingly utilized in aging research; however, their application in dental studies remains relatively limited. This scoping review investigates the use of these models within oral research. A systematic search of PubMed and Web of Science was conducted, following PRISMA-ScR guidelines and registered with the Open Science Framework, to identify relevant in vivo studies published between January 2020 and March 2025. Eligible studies involved accelerated senescence animal models in oral health contexts. Data were extracted on animal types, induction methods, aging biomarkers (e.g., P53, P21, P16, SA-β-gal), and outcomes for narrative synthesis. From 377 screened articles, 29 met the inclusion criteria. Three primary types of models were identified: chemically induced, physically stress-induced, and genetically based. The majority of studies focused on periodontitis (41.4 %), followed by salivary gland dysfunction. Key aging features examined included cell cycle arrest (79.3 %), senescence-associated secretory phenotypes, oxidative stress, and lysosomal alterations. Diabetes-induced aging was employed in 37.9 % of studies, and mice were the predominant animal model used (75.9 %). The findings suggest that accelerated senescence models show promise in oral aging research, especially in periodontitis and diabetes-related conditions. Incorporating multiple biomarkers may enhance model relevance and support targeted strategies in geriatric oral care.

Indexed as

Accelerated senescence modelBiomarkersDiabetes-related conditionsOral agingOral diseasesPeriodontitis

Identifiers

PMID41040587
PMCPMC12485460

What OpenQuestion holds

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Registered trials

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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.