ReviewPain research & management2026
Pathological Mechanisms of Tendinopathy Pain: From Mechanical Overload to Neuroimmune-Vascular Crosstalk.
Review in Pain research & management, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed.
- Pathological Mechanisms of Tendinopathy Pain: From Mechanical Overload to Neuroimmune-Vascular Crosstalk.Pain research & management · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Characterized by localized pain and functional impairment, tendinopathy remains a significant challenge in sports medicine. Traditional models of structural degeneration and inflammation inadequately explain the clinical discordance between tissue damage and pain severity. This review explores the paradigm shift in understanding tendinopathic pain, elucidating the transition from a simple mechanical stress model to a complex neuroplastic disorder. We narratively review the multilayered pathophysiological mechanisms underlying chronic tendinopathic pain. Specifically, we outline abnormal mechanical load transduction, peripheral neuroimmune-vascular coupling, and central nervous system (CNS) remodeling. Abnormal mechanical overload initially activates mechanosensitive ion channels, transducing physical stress into biochemical nociceptive signals. Subsequently, chronic immune responses and neurovascular coupling drive peripheral sensitization, which is further amplified by aberrant sensory neoinnervation and neuroimmune crosstalk. Furthermore, CNS involvement manifests as spinal-level central sensitization and maladaptive remodeling of the motor cortex. Managing chronic tendinopathic pain requires transcending the traditional focus on localized structural lesions. Future strategies should prioritize precise clinical phenotyping, targeted pharmacotherapy, and neuroplasticity-informed rehabilitation to optimize patient outcomes.
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Registered trials
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