Anti-inflammatory effect as a mechanism of effectiveness underlying the clinical benefits of pelotherapy in osteoarthritis patients: regulation of the altered inflammatory and stress feedback response

Authors: Ortega E (1) , Gálvez I (1) , Hinchado MD (1) , Guerrero J (2) , Martín-Cordero L (3) , Torres-Piles S (4)
Affiliations:
(1) Research Group in Immunophysiology, Department of Physiology, Faculty of Sciences, University of Extremadura (2) Department of Nursing, Faculty of Medicine, University of Extremadura (3) Research Group in Immunophysiology, Department of Nursing, University Center of Plasencia, University of Extremadura (4) Research Group in Immunophysiology, Department of Medical-Surgical Therapy, Faculty of Medicine, University of Extremadura
Source: Int J Biometeorol. 2017 Apr 29
DOI: 10.1007/s00484-017-1361-x Publication date: Not specified E-Publication date: April 29, 2017 Availability: abstract Copyright: © ISB 2017
Language: English Countries: Spain Location: El Raposo Correspondence address: igalvez@unex.es

Keywords

Article abstract

The purpose of the present investigation was to evaluate whether an anti-inflammatory effect together with an improvement of the regulation of the interaction between the inflammatory and stress responses underlies the clinical benefits of pelotherapy in osteoarthritis (OA) patients. This study evaluated the effects of a 10-day cycle of pelotherapy at the spa centre 'El Raposo' (Spain) in a group of 21 OA patients diagnosed with primary knee OA. Clinical assessments included pain intensity using a visual analog scale; pain, stiffness and physical function using the Western Ontario and McMaster Universities Arthritis Index; and health-related quality of life using the EuroQol-5D questionnaire. Serum inflammatory cytokine levels (IL-1β, TNF-α, IL-8, IL-6, IL-10 and TGF-β) were evaluated using the Bio-Plex® Luminex® system. Circulating neuroendocrine-stress biomarkers, such as cortisol and extracellular 72 kDa heat shock protein (eHsp72), were measured by ELISA. After the cycle of mud therapy, OA patients improved the knee flexion angle and OA-related pain, stiffness and physical function, and they reported a better health-related quality of life. Serum concentrations of IL-1β, TNF-α, IL-8, IL-6 and TGF-β, as well as eHsp72, were markedly decreased. Besides, systemic levels of cortisol increased significantly. These results confirm that the clinical benefits of mud therapy may well be mediated, at least in part, by its systemic anti-inflammatory effects and neuroendocrine-immune regulation in OA patients. Thus, mud therapy could be an effective alternative treatment in the management of OA.

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