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Medicine » Critical Care and Emergency Medicine » "Hyperthermia", book edited by Nagraj Huilgol, ISBN 978-953-51-1129-0, Published: May 15, 2013 under CC BY 3.0 license. © The Author(s).

Chapter 7

Effects of Low-Dose Radon Therapy Applied Under Hyperthermic Conditions (RnHT) on Inflammatory and Non- Inflammatory Degenerative Disease Conditions

By Angelika Moder, Heidi Dobias and Markus Ritter
DOI: 10.5772/51401

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Effects of Low-Dose Radon Therapy Applied Under Hyperthermic Conditions (RnHT) on Inflammatory and Non-Inflammatory Degenerative Disease Conditions

Angelika Moder1, Heidi Dobias1 and Markus Ritter1

1. Introduction

Low dose rRadon (222Rn) therapy (RnHT) is a traditional treatment in Central and Eastern Europe typically applied to alleviate chronic pain derived from inflammatory and non-inflammatory disorders of the musculoskeletal system. Additionally it has also been reported to be effective for the treatment of chronic airway inflammation and inflammatory conditions of the skin.

Radon (222Rn) is a radioactiven alpha particle emitting inert gas, present in natural soil and water at several European, Japanese and American health resorts and is administered either transcutaneously byvia balneotherapyeutical or per inhalationem via by balneotherapy or per inhalationem by speleotherapy either at „cold“ ambient temperature of 20° to 23° C (RnT) or at „hot“ ambient temperatures between 37° and 41.5° C (RnHT). Speleotherapy is performed in curative caves and tunnels where radon emanation occurs due to the presence of uranium containing soil. Low d-Dose 222Rn - bBalneotherapy is performed in bath tubs filled with 222Rn radon containing thermal water at a concentration typically found in the respective region but usually between 370 and 1600 Bq/L. WhereasWhereas 222Rn- containing water is typically applied at 37.0° Celsius, speleotherapeutic administration of 222Rn is performed either as RnT [1](Erickson 2007 Dose Response) or RnHT.t „cold“ ambient temperature of 20 to 23 Celsius or at „hot“ ambient temperatures between 38 and 41,5 Celsius. The latter treatment regime is uniquely performed at the Gasteiner Heilstollen in Bad Gastein, Austria, which offers an average 222Rn concentration of 44000 Bq/m³ in a hyperthermic atmosphere between 37.0° and 41.,5° C with high humidity between 70 and 100% that facilitates a mild increase of the body’s core-temperature of 0.5 - 1° Cdue to prevention of heat loss via evaporation confirmed by rectal measurement. A typical low-dose 222Rn-therapy consists of nine9 to ten10 treatment units within a period of three3 weeks and an effective dose of 0.,05 to 2 mSv for balneotherapeutic and speleotherapeutic regimen, respectively [2]. 222Rn has a half-life of 3.8 days and decays via several short-lived daughters into the beta-emitting 210Plumbum with a half-life of 22.3 years. In general, radionuclide-based therapy has a long history in the management of rheumatic diseases and has been proven to alleviate pain and inflammation upon intraarticular or intravenous injection. Apart from conventional corticoid or cytostatikacytostatic based therapy, radiosynoviorthesis is an alternative approach for the management of synovitis in course of chronic inflammatory arthropathies. The intraarticular injection of colloidal betaβ-emitters, e.g. 90Yttrium, 186Rhenium or, 169Erbium, lead to reduction of pain and joint swelling via abrogation of synovia hypertrophy through by radiation- induced inhibition of the proliferative activity of synovial cells. The applied dose depends on the magnitude of the affected joint(s) and the severity of inflammation, whereas factors like intraarticular distribution of the radionuclide and thickness of the synovia dictate the absorbed dose. Therapeutical benefits in terms of pain and reduction of the inflammatory symptoms occur in 40 to 80% of the patients and manifest several months after therapy. However, numerous side effects like headache, fatigue, nausea and sometimes lymph-edema, radiation-induced synovialitis synovitis and periarticular necrosis due to aberrant injections have been reported [3].

Positive therapeutic effects of 224Radiumchloride-injections for patients suffering from ankylosing spondylitis were reported from Koch and Reske in 1952[4], after this therapy had been abolished due to the high incidence of malignant bone tumours and leukaemia in children and young adults previously treated for tuberculosis. Until now several studies have been conducted with a reduced dose regimen of 10 weekly injections with 1 MBq each resulting in an effective dose of 2.,5 Sv [5] and a cumulative bone dose of 0.,6 Gy [6]. The short-lived 224RRadium has a half-life of 3.,6 days and preferentially accumulates in the bone and in recently formed tissue calcifications when introduced into the body. In 2000 it was re-approved in Germany by the Bundesinstitut für Arzneimittel und Medizinprodukte (German Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte) as a pharmaceutical product for patients suffering from ankylosing spondylitis with stage II and III spinal ossification, provided that other therapy options had either failed or been contraindicated. However, recent findings clearly demonstrated an increased incidence of leukaemia and other malignant diseases in patients that were treated between 1948 and 1975 [6]. Despite the analgesic effects elicited by 224RRadiumchloride-injections, the risk for malignant diseases exceeds the benefit and therefore, the committee for quality assurance of the German Ssociety for Rrheumatology no longer recommends this kind of therapy. Compared to a 222Rn-speleotherapy regimen according to dosimetric calculations by Hofmann [7], the average dose to bone achieved by 224Radiumchloride injection regimen is approximately a factor 3x105 higher. In contrast to the bone-seeking 224Radiumchlorid, inhalation of 222Rn and its daughters lead to a dose distribution that predominantly affects the bronchial epithelium in the upper tracheobronchial tree when applied speleotherapeutically. When administered balneotherapeutically, diffusion of 222Rn radon through the skin results in a uniform dose distribution throughout the organism [7]. To the best knowledge of the authors up to date no evidence points to an increased risk for the development of malignant diseases in context with RnHT [1, 2, 8].(Falkenbach Deutsches Ärzteblatt 96, Heft 23, 1999) (Erickson BE., J Altern Complement Med. 2007) und Zitat Nr.1).

Hyperthermia treatment (HT) has been reported to exert analgesic effects in rheumatoid disorders, to reduce systemic levels of the pro-inflammatory cytokines TNF-alpha, IL-1beta, and IL-6 [9, 10] and to accelerate the healing of sport injuries [11]. The postulated mechanisms include increased blood perfusion of the affected tissues and relaxation of muscle tissue. Given the fact, that combined RnHT or hyperthermia alone has been reported to alleviate pain in rheumatic conditions, presently, it cannot clearly be distinguished to which extent each of the active components – 222Rn and/or hyperthermia – are efficient for achieving the clinical-therapeutic benefits. According to empirical observations described below, these two agents may rather act in a synergistic manner.

Apart from clinical observations, evidence from several controlled trials, one meta-analysis and numerous clinical observational studies further substantiate the beneficial effects of intermediate up to long term pain relief and functional improvement in patients suffering from rheumatic disorders of inflammatory or degenerative etiology. From a health economic point of view, cost effective therapies in the prevention or management of rheumatic diseases are of great importance since rheumatic disorders state a relevant cost factor due to the need for long term medication, frequent hospitalizations, joint arthroplasty and loss of productivity. The dramatically increasing proportion of aged individuals further aggravates the health economic issue of rheumatic diseases since at least the prevalence of non-inflammatory, degenerative rheumatic disorders increases with progressing age [12].

The long term intake of typically employed corticosteroids and non-steroidal anti-inflammatory drugs (NSAID) for the treatment of rheumatic disorders are reported to cause severe side effects that - apart from the primary disease - result in additional medical interventions and dramatically reduce the life quality of the affected individual. Some years ago, the mortality rate caused by gastrointestinal side effects due to NSAID intake was about 2000 per year in Germany [13] and 16.500 per year in the USA [14]. Despite the additional intake of gastro-protective drugstectiva, the ratio of NSAID-consumers suffering from gastrointestinal ulcers was 1 in 400 and the ratio of those who died was 1 in 8000 [15]. The generation of cyclooxygenase-2 inhibitors diminished the risk for gastrointestinal complications, however, the elevated risk for cardio-vascular events remained [16-18]. Taken together, from the patient´s as well as from the socio-economic point of view there is an urgent need for therapeutic strategies that allow either a reduction or discontinuation of medicament intake [19]. Combined RnHT can be regarded as a promising candidate in addressing these issues. Lind-Albrecht et al. demonstrated a long term reduction of analgetics analgesics during a 12-years follow-up in patients suffering from ankylosing spondylitis, who regularly received combined RnHT [20].

A recently published meta-analysis including 338 patients suffering from rheumatic disorders showed a superior effect of combined RnHT compared to hHyperthermia therapy (HT) in terms of pain reduction [21]. Although there was no difference between the treatment groups immediately after the therapeutic regimen, the group receiving the combination of 222Rn radon and hyperthermia showed a significantly lower pain score during the three3 - and six6 - months follow-up. Prospective, randomized studies that comparedcomparing the effect of combined RnTT with either HT or no treatment were included in the meta-analysis and are described along with more recently published findings in detail below.

Franke et. al demonstrated an intermediate to long term pain reduction in patients suffering from rheumatoid arthritis during a nine month follow-up after combined RnHT. This randomized, double-blinded study included 134 patients and compared the efficacy of balneotherapeutic regimen applied at 37° C either with or without 222RnRadon. Although both groups showed a beneficial effect immediately after therapy, the radon group predominated significantly at the three3 and six6 months follow up. Similar results were obtained concerning cut-down in NSAID and cCorticosteroid intake [22]. Consistently with these findings, a previous study including 60 patients with rheumatoid arthritis clearly demonstrated pain reduction and functional improvement of affected joints after a typical regimen of thermal water baths. However, patients receiving 222Rn thermal water showed a significantly pronounced effect on the analyzed parameters [23].

Van Tubergen et al. investigated in course of a randomized, controlled study the efficacy of speleotherapeutically applied RnHT combined with a complex rehabilitation program including gymnastics, hydro – and sport therapy. 120 patients suffering from ankylosing spondylitis were enrolled in the study and randomized in two treatment and one control group. Whereas the control group maintained its regular physiotherapeutic program at home, the intervention groups received the complex rehabilitation program either concomitantly with hyperthermiac treatment in form of sauna regimen or concomitantly with speleotherapeutic combined RnHT. Bath Ankylosing Spondylitis Functional Index (BASFI), quality of life assessment score, pain score on a visual analogue scale and duration of morning stiffness were taken together to a Pooled Index of Change (PIC) as primary endpoint. Immediately after therapy both intervention groups showed a 20 to 30% improvement in contrast to the control group that remained unaffected. In the six6 to nine9 months follow up only the 222Rn radon group significantly prevailed [24, 25].

In line with the se resultsresults of Van Tubergen, Lind-Albrecht demonstrated a significant long-term pain reduction, improved mobility of the spine and reduced medicament drug intake of patients with ankylosing spondylitis receiving a rehabilitation program combined with speleotherapeutic RnHT compared to those, who exclusively received the rehabilitation program [26, 27].

According to two double-blinded, randomized studies by Pratzel et al., an intermediate-term pain reduction could be achieved by serially applied thermal water baths with or without 222Rn in patients with non-inflammatory cervical syndrome and degenerative disorders of spine or joints, respectively. Immediately after therapy both treatment groups benefitted from an elevated threshold of pressure-provoked pain in the paravertebral muscles. A sustainable and significant pain reduction lasting until the 2 two and 4 four months follow-up could be demonstrated only in the 222Rn group [28, 29].

A recent prospective study including 222 patients suffering from non-inflammatory, degenerative rheumatoid disorders investigated the sustainability of beneficial effects achieved by serially applied 222Rn containing thermal water baths. Compared to baseline levels, pain score and functional restriction of affected joints were significantly reduced up to twelve12 or six6 months, respectively. The fraction of patients with sickness absence was significantly reduced within one year after versus one year prior to therapy [30].

Although the clinical benefit of combined RnHT has been investigated, to date little is known about the underlying cellular and molecular mechanisms of action. According to findings of Reinisch et al., suppression of the oxidative burst in neutrophileneutrophil granulocytes of patients suffering of ankylosing spondylitis may be at least one key element explaining the therapeutic efficacy of speleotherapeutically applied combined RnHT. Reactive oxygen species (ROS) are released from activated phagocytes in course of inflammation and play a major role in tissue destruction in rheumatoid disorders. Neutrophile granulocytes isolated from peripheral blood of patients produced significantly less superoxide anions when restimulated ex vivo after a regimen of 10 ten to 12 twelve units of combined RnHT [31].

According to a previous study by Shehata et al., pain alleviation in ankylosing spondylitis correlates to an elevation in post-treatment serum levels of the anti-inflammatory cytokine TGF-betaβ [32].

Apart from its role as an immune-modulator, TGF-betaβ1 also plays a crucial role in bone homoeostasis, particularly by acting as differentiation factor for osteoclasts and via stimulation of osteoblast and downregulation of osteoclast activity [33]. TGF-betaβ1 exerts its effects in concert with other cytokines and hormones by influencing the OPG/RANKL/RANK system, which is crucial in the control of osteoblast and osteoclast interplay. Receptor activator of nuclear factor κB-ligand (RANKL) is a potent stimulator of osteoclast-mediated bone resorption and promotes osteolysis. It acts via binding to receptor activator of nuclear factor-κB (RANK) on osteoclasts. Osteoprotegerin (OPG) is the functional antagonist of RANKL as it acts as a soluble RANKL decoy receptor that, upon engagement with RANKL, abrogates the interaction with RANK and consequently inhibits maturation and activation of osteoclasts and their precursors. The relative concentrations of OPG and RANKL determine the status of bone metabolism and thus, the OPG/RANKL ratio has become an important marker to assess the prevailing metabolic bone turnover situation. An increased OPG/RANKL ratio indicates an anabolic and a decreased ratio a katabolic bone metabolism state. Chronic inflammatory processes give rise to increased bone resorption, which frequently results in secondary osteoporosis, a typical complication in rheumatic diseases. Moreover, osteoporosis is further aggravated by functional and pain-related disuse bone atrophy and frequently employed glucocorticoid medication hence, predisposing the patient to a high risk of bone fracture [34]. In line with the results of Shehata et al. and the osteoimmunologic context explained above, a recently published pilot study confirmed the elevation of TGF-betaβ1 and demonstrated an increase of the OPG/RANKL ratio, thus indicating a shift of bone metabolism towards anabolic processes after combined speleotherapeutically applied RnHT [35, 36]. (HIER ZITAT Abstract von Uwe Lange,.. B. Kürten --- siehe unten)

2. Conclusions

Numerous studies have demonstrated a sustaining beneficial effect of combined low-dose RnHT when serially applied either by speleo therapy- or balneotherapyeutical to patients suffering from inflammatory or non-inflammatory degenerative disorders of the musculo-skeletal-system. Of note, the most dominant effect is recognized several months rather than immediately after therapy. Combined RnHT represents a cost effective method that alleviates pain and, thus, allows reducing medicament drug intake which, in turn, may contribute to the prevention of adverse events caused by NSAIDs and gGlucocorticoids. As mentioned above, radionuclide-based therapy has been employed in the management of rheumatic disorders for decades. However, the poor benefit-risk ratio led to severe limitations or complete discontinuation in clinical use. RnHT poses doses to the patients that which are in magnitude 10-5 lower in respect to the bone dose compared to 224Radiumchloride-injection regimens. However, further studies are necessary to evaluate potential risks of low-dose RnHT. Although some studies implicate a beneficial effect of hyperthermia therapy for rheumatic diseases, combined RnHT turned out to be more effective than sauna or balneotherapy at an ambient temperature of 37° C lacking 222Rn. As combined RnHT may also exert beneficial effects in other disease entities, further studies are necessary to prove its place among the current treatment options.


1 - B. E. Erickson, pain. Radioactive, health. relief, strategies. care, assessment. risk, elderly. among, with. persons, at. arthritis, health. radon, mines, J Altern Complement Med, 2007375379
2 - A. Kaul, Risiko. Strahlenbedingtes, Radon. in, Heilmittel. als, P. Deetjen, et al. Editors, 2005Verlag Dr. Kovac: Hamburg. 5771
3 - Bahous I., Radiosynoviorthesis: local treatment of rheumatoid arthritis, in Biological Effects of 224-Ra, Müller W.A.and Ebert H.G., Editors. 1978Martinus Nijhoff Medical Division the Hague / Boston for The Commission of the European Communities: Boston. 7178
4 - W. Koch, W. Reske, Ergebnisse. Die, Thorium. X. der intravenösen-Behandlung, Spondylarthritis. bei der, . M. ankylopoetica, Bechterew). Strahlenther, 1952439457
5 - Lassmann M., Nosske D., and Reiners C., Therapy of ankylosing spondylitis with 224Ra-radium chloride: dosimetry and risk considerations.Radiat Environ Biophys, 2002173178
6 - Wick R., Atkinson M.J., and Nekolla E.A., Incidence of leukaemia and other malignant diseases following injections of the short-lived α-emitter 224Ra into man.Radiat Environ Biophys, 2009287294
7 - Hofmann W., Radon doses compared to X-ray doses, in Radon in der Kurortmedizin, Pratzel H.G.and Deetjen P., Editors. 1997ISMH Verlag: Geretsried. 5767
8 - Falkenbach A., Radon und Gesundheit. Dt Ärztebl,1999A1576A1577
9 - I. H. Tarner, et al.effect. The, mild. of, hyperthermia. whole-body, systemic. on, of. T. N. levels, I. F-alpha, L-1beta, I. L. , patients. in, ankylosing. with, spondylitis, Clin Rheumatol, 2009397402
10 - F. G. Oosterveld, et al.sauna. Infrared, patients. in, rheumatoid. with, arthritis, spondylitis. ankylosing, A pilot study showing good tolerance, short-term improvement of pain and stiffness, and a trend towards long-term beneficial effects. Clin Rheumatol, 20092934
11 - Giombini A., et al., Hyperthermia induced by microwave diathermy in the management of muscle and tendon injuries.Br Med Bull, 2007379396
12 - Nowossadeck E., Population aging and hospitalization for chronic disease in Germany.Dtsch Arztebl Int, 2012151157
13 - Singh G., Gastrointestinal complications of prescription and over-the-counter nonsteroidal anti-inflammatory drugs: a view from the ARAMIS database.Arthritis, Rheumatism, and Aging Medical Information System. Am J Ther, 2000115121
14 - Koelz H.R. and Michel B., Nichtsteroidale Antirhematika: Magenschutztherapie oder COX-2-Hemmer? Dt Arztebl,2004A3041A3046
15 - Laine L., et al., Stratifying the risk of NSAID-related upper gastrointestinal clinical events: results of a double-blind outcomes study in patients with rheumatoid arthritis.Gastroenterology, 200210061012
16 - E. J. Topol, the. Failing, health--rofecoxib. public, Merck, F. D. A. the, N Engl J Med, 200417071709
17 - E. J. Topol, G. W. Falk, A. coxib, a. day, keep. won’t, doctor. the, away, Lancet, 2004639640
18 - G. A. Fitzgerald, Coxibs, disease. cardiovascular, N Engl J Med, 200417091711
19 - Bolten W.W., et al., Konsequenzen und Kosten der NSA-Gastropathie in Deutschland.Aktuelle Rheumatol, 1999127134
20 - Lind-Albrecht G., Ergebnisse der Langzeitbeobachtung von Morbus-Bechterew-Patienten nach wiederholter Radonstollenbehandlung, in Tagungsband: Herbsttagung der Arbeitsgemeinschaften Europäischer Radonheilbäder2004Bad Kreuznach.
21 - Falkenbach, A., et al., Radon therapy for the treatment of rheumatic diseases--review and meta-analysis of controlled clinical trials.Rheumatol Int, 2005205210
22 - A. Franke, L. Reiner, K. L. Resch, benefit. Long-term, radon. of, therapy. spa, the. in, of. rehabilitation, arthritis. a. rheumatoid, double-blinded. randomised, trial, Rheumatol Int, 2007703713
23 - Franke, A., et al., Long-term efficacy of radon spa therapy in rheumatoid arthritis--a randomized, sham-controlled study and follow-up.Rheumatology, 2000894902
24 - Van Tubergen A., et al., Cost effectiveness of combined spa-exercise therapy in ankylosing spondylitis: a randomized controlled trial.Arthritis Rheum, 2002459467
25 - Van Tubergen A., et al., Combined spa-exercise therapy is effective in patients with ankylosing spondylitis: a randomized controlled trial.Arthritis Rheum, 2001430438
26 - Lind-Albrecht G., Einfluss der Radonstollentherapie auf Schmerzen und Verlauf bi Spondylitis ankylosans., in Dissertation1994Johannes Gutenberg-University: Mainz.
27 - Lind-Albrecht G., Radoninhalation bei Morbus Bechterew, in Radon und Gesundheit, Deetjen P., Editor1999Verlag Peter Lang: Frankfurt am Main. 131137
28 - Pratzel H., Wirksamkeitsnachweis von Radonbädern im Rahmen einer kurortmedizinischen Behandlung des zervikalen Schmerzsyndroms.Phys Rehab Kurmed, 19937682
29 - Pratzel H., Schmerzstillender Langzeiteffekt durch Radonbäder bei nicht-entzündlichen rheumatischen Erkrankungen, in Radon und Gesundheit, Deetjen P., Editor1999Verlag Peter Lang: Frankfurt/Main.
30 - Moder A., et al., Schmerz, Krankenstände, Befindlichkeit, Medikamentenverbrauch und Funktionsverbesserung im Jahr vor und nach einer kombinierten Radonthermalkur.Phys Med Rehab Kuror, 2011215219
31 - Reinisch N., et al., Decrease of respiratory burst in neutrophils of patients with ankylosing spondylitis by combined radon-hyperthermia treatment.Clin Exp Rheumatol, 1999335338
32 - Shehata M., et al., Effect of combined spa-exercise therapy on circulating TGF-beta1 levels in patients with ankylosing spondylitis.Wien Klin Wochenschr, 2006266272
33 - S. W. Fox, A. C. Lovibond, insights. Current, the. into, of. role, growth. transforming, in. factor-beta, resorption. bone, Mol Cell Endocrinol, 20051926
34 - P. Sambrook, N. E. Lane, osteoporosis. Corticosteroid, Best Pract Res Clin Rheumatol, 2001401413
35 - Moder A., et al., Effect of combined Low-Dose Radon- and Hyperthermia Treatment (LDRnHT) of patients with ankylosing spondylitis on serum levels of cytokines and bone metabolism markers: a pilot study.Int J Low Radiation, 2010423435
36 - Lange U., Müller-Ladner U., and Kürten B., Einfluss einer seriellen niedrig dosierten Radonstollen-Hyperthermie auf zentrale Zytokine des Knochenmetabolismus bei ankylosierender Spondylitis, in Osteologie2011Schattauer: Fürth. 54