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Local ice cryotherapy decreases synovial interleukin 6, interleukin 1β, vascular endothelial growth factor, prostaglandin-E2, and nuclear factor kappa B p65 in human knee arthritis: a controlled study

Authors :
Guillot, X.
Tordi, N.
Laheurte, C.
Pazart, L.
Prati, C.
Saas, P.
Wendling, D.
Source :
Arthritis Research & Therapy (formerly Arthritis Research); December 2019, Vol. 21 Issue: 1 p1-11, 11p
Publication Year :
2019

Abstract

The aim of this study was to assess the anti-inflammatory effects of local cryotherapy in human non-septic knee arthritis. In the phase I of the study, patients were randomized to receive either ice (30 min; N= 16) or cold CO2(2 min; N= 16) applied twice during 1 day at an 8-h interval on the arthritic knee. In phase II, 16 other ice-treated arthritic knees according to the same protocol were compared to the contralateral non-treated arthritic knees (N= 16). The synovial fluid was analyzed just before the first cold application, then 24 h later. IL-6, IL-1β, TNF-α, IL-17A, VEGF, NF-kB-p65 protein, and PG-E2 levels were measured in the synovial fluid and compared before/after the two cold applications. Forty-seven patients were included (17 gouts, 11 calcium pyrophosphate deposition diseases, 13 rheumatoid arthritides, 6 spondyloarthritides). Local ice cryotherapy significantly reduced the IL-6, IL-1β, VEGF, NF-kB-p65, and PG-E2 synovial levels, especially in the microcrystal-induced arthritis subgroup, while only phosphorylated NF-kB-p65 significantly decreased in rheumatoid arthritis and spondyloarthritis patients. Cold CO2only reduced the synovial VEGF levels. In the phase II of the study, the synovial PG-E2 was significantly reduced in ice-treated knees, while it significantly increased in the corresponding contralateral non-treated arthritic knees, with a significant inter-class effect size (mean difference − 1329 [− 2232; − 426] pg/mL; N= 12). These results suggest that local ice cryotherapy reduces IL-6, IL-1β, and VEGF synovial protein levels, mainly in microcrystal-induced arthritis, and potentially through NF-kB and PG-E2-dependent mechanisms. Clinicaltrials.gov, NCT03850392—registered February 20, 2019—retrospectively registered

Details

Language :
English
ISSN :
14786354 and 14786362
Volume :
21
Issue :
1
Database :
Supplemental Index
Journal :
Arthritis Research & Therapy (formerly Arthritis Research)
Publication Type :
Periodical
Accession number :
ejs50697710
Full Text :
https://doi.org/10.1186/s13075-019-1965-0