Evidence mapPaperPMID 40641978Full record

ReviewFrontiers in medicine2025

Energy metabolism dysfunction and therapeutic strategies for treating temporomandibular disorders.

Wenjie Gao, Zhiheng Gao, Heting Xiao, Yuchen Qian, Rongkang Fan, Yonggang Li, Shaofeng Yang, Yanjun Yang, Yusen Qiao

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Wenjie Gao *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Zhiheng Gao *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Heting Xiao *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Yuchen Qian *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Rongkang FanDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Yonggang LiDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Shaofeng YangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Yanjun YangDepartment of Orthopedics, Suzhou Ninth People's Hospital Afffliated to Soochow University, Suzhou, China.
Yusen QiaoDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Temporomandibular disorders (TMD) are prevalent and multifactorial conditions affecting the temporomandibular joint (TMJ). Recent studies have highlighted the central role of energy metabolism in their pathogenesis. This review focuses on how disturbances in glucose, lipid, and mitochondrial energy pathways contribute to TMJ dysfunction and degeneration. The TMJ's complex structure relies heavily on a balanced energy supply to maintain its physiological functions. Disruptions in glucose metabolism lead to oxidative stress, inflammatory cytokine release, and chondrocyte damage. Similarly, altered lipid metabolism-particularly imbalances in ω-3 and ω-6 fatty acids-modifies inflammatory responses. Hormonal influences, including cholesterol and estrogen, further exacerbate joint degeneration via signaling pathways such as Notch and NF-κB. These metabolic disturbances trigger cellular senescence, impaired matrix synthesis, and structural breakdown of cartilage and bone. The review also evaluates current and emerging therapeutic strategies. Standard treatments such as NSAIDs and corticosteroids relieve symptoms but fail to address underlying metabolic dysfunctions. Promising alternatives include intra-articular growth factors, metabolic modulators targeting oxidative stress, and autophagy inducers that restore mitochondrial balance. These approaches aim to correct cellular energy imbalances and support tissue regeneration. TMD involve significant metabolic dysregulation in the TMJ. Understanding the role of energy metabolism offers new insights into disease mechanisms and potential therapies. Future research should prioritize metabolic regulation as a target for long-term and disease-modifying treatments in TMD management.

Indexed as

energy metabolismmetabolic dysregulationtemporomandibular disorderstemporomandibular jointtherapeutic strategies

Identifiers

PMID40641978
PMCPMC12240951

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.