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Sympathosensory interactions - Possible relevance in osteoarthritis
Zsuzsa Jenei-Lanzl1, Susanne Grässel2, Hans-Georg Schaible3
1Dr. Rolf M. Schwiete Research Unit for Osteoarthritis, Department of Trauma Surgery and Orthopedics, Goethe University Frankfurt, University Hospital, Frankfurt 60528, Germany; Division for Biochemistry of Joint and Connective Tissue Diseases, Department of Orthopedics, University of Ulm, Ulm 89081, Germany.
Sympathosensory interactions influence osteoarthritis (OA) progression. Understanding these connections, from peripheral to central levels, is key to managing OA and its comorbidities through a new biopsychosocial model.
Area of Science:
- Neuroscience
- Rheumatology
- Physiology
Background:
- The sympathetic and sensory nervous systems play recognized roles in osteoarthritis (OA) development and progression.
- Interactions between these systems are known, but their specific nature during OA progression is unclear.
Purpose of the Study:
- To review scientifically proven or putative sympathosensory interactions at peripheral, spinal, and central levels in OA.
- To describe the mechanisms of interaction and factors influencing coupling.
- To discuss the clinical relevance of these interactions within a new biopsychosocial OA model.
Main Methods:
- Narrative review of existing scientific literature.
- Analysis of direct and indirect sympathosensory coupling.
- Examination of signaling and cross-signaling mechanisms.
- Introduction of a novel biopsychosocial OA model.
Main Results:
- Sympathosensory interactions occur at peripheral, spinal, and central levels.
- Specific factors and mechanisms govern the coupling between these systems.
- These interactions are linked to chronic inflammation, pain, sleep deprivation, and stress in OA.
Conclusions:
- Sympathosensory interactions are integral to OA progression and its associated comorbidities.
- A new biopsychosocial model highlights the cycle of inflammation, pain, and autonomic imbalance in OA.
- Understanding these interactions offers potential therapeutic targets for OA management.
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