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Systematic analysis of the molecular pathophysiology of tenosynovitis: promise for using chondroitin sulfate and glucosamine sulfate

https://doi.org/10.14412/2074-2711-2020-2-64-71

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Abstract

The chondroprotectors glucosamine sulfate (GS) and chondroitin sulfate (CS) show a complex anti-inflammatory effect and therefore may be used in the therapy of many diseases concurrent with osteoarthritis.

Objective: to carry out a systematic analysis of the relationship between the molecular pathophysiology of tenosynovitis and the potential mechanisms of pathogenic action of CS/GS in this disease.

Material and methods. The texts of 15 097 publications were systemized using the current methods for topographic big data analysis, which had been developed as part of topological and metric approaches to recognition/classification problems.

Results and discussion. The investigators created a map showing the molecular pathophysiology of tendosynovitis and including 15 molecular mechanisms and 27 comorbidities and identified mechanisms, through which GS/CS could prevent the development of tenosynovitis, such as inhibition of the effects of proinflammatory cytokines (IL-1, IL-8, γ-interferon, and TNF-α), monocyte chemoattractant protein-1 (MCP-1), macrophage inflammatory protein, NLRP3 inflammasome, NF-κB and JAK/STAT signaling pathways, and O-glucosamination of proteome proteins. To date, no randomized clinical or cohort (non-interventional) studies of the effects of CS/GS have been conducted in patients with tendosynovitis and comorbidities. However, preclinical studies of GS and CS in the treatment of tendinopathies showed that the drugs had analgesic properties, alleviated chronic inflammation and edema, and improved the maturation of collagen bundles and therefore the mechanical properties of connective tissue in the tendons and ligaments.

Conclusion. The experimental and clinical studies indicate that pharmaceutical-grade GS/CS preparations of high standardization are promising in treating tenosynovitis. 

About the Authors

I. Yu. Torshin
Institute of Pharmacoinformatics, Federal Research Center «Informatics and Management», Russian Academy of Sciences; Big Data Storage and Analysis Center, M.V. Lomonosov Moscow State University
Russian Federation

44, Vavilov St., Build. 2, Moscow 119333, Russia

1, Leninskie Gory, Moscow 119234, Russia



O. A. Gromova
Institute of Pharmacoinformatics, Federal Research Center «Informatics and Management», Russian Academy of Sciences; Big Data Storage and Analysis Center, M.V. Lomonosov Moscow State University
Russian Federation

44, Vavilov St., Build. 2, Moscow 119333, Russia

1, Leninskie Gory, Moscow 119234, Russia 



A. M. Lila
V.A. Nasonova Research Institute of Rheumatology; Department of Rheumatology, Russian Medical Academy of Continuing Professional Education, Ministry of Health of Russia
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522, Russia

2/1, Barrikadnaya St., Build. 1, Moscow 125993, Russia



O. A. Limanova
Big Data Storage and Analysis Center, M.V. Lomonosov Moscow State University; Ivanovo State Medical Academy, Ministry of Health of Russia
Russian Federation
1, Leninskie Gory, Moscow 119234, Russia

58, Sheremetevsky Prosp., Ivanovo 153012, Russia



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For citation:


Torshin I.Yu., Gromova O.A., Lila A.M., Limanova O.A. Systematic analysis of the molecular pathophysiology of tenosynovitis: promise for using chondroitin sulfate and glucosamine sulfate. Neurology, Neuropsychiatry, Psychosomatics. 2020;12(2):64-71. (In Russ.) https://doi.org/10.14412/2074-2711-2020-2-64-71

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