Abstract
Objectives:
Multiple sclerosis (MS) is an autoimmune disease affecting young people and is a major cause of disability. In the course of time, disability progresses and symptoms like spasticity may occur. Spasticity is a major cost factor in MS patients. Various agents are approved for the treatment of spasticity, but each of those agents may have several side effects. Intrathecally administered steroids (triamcinolone-acetonide (TCA)) may be efficient in treating spasticity in patients with lesions in the spinal cord and no response to first-line therapeutics. The aim of this study is to show effects of TCA treatment on clinical parameters in patients with MS.
Methods:
This multicentre open label study included 54 patients with MS. The clinical outcome parameters were spasticity, disability, maximum walking distance, bladder function and quality of life. All patients received physiotherapy in addition to TCA treatment to obtain optimal effects on clinical parameters.
Results:
Spasticity, maximum walking distance as well as disability improved significantly (P⩽0.001) during TCA applications. Bladder function improved in every seventh patient.
Conclusion:
We observed the effects of intrathecally administered TCA on different clinical parameters including bladder function. TCA administration is a safe method to treat different symptoms in MS patients. Longitudinal trials with repeated TCA cycles are needed to show long-term effects. Besides TCA treatment, physiotherapy contributes to the improvement of clinical parameters.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Weinshenker BG . The natural history of multiple sclerosis: update 1998. Semin Neurol 1998; 18: 301–307.
Zwibel HL . Contribution of impaired mobility and general symptoms to the burden of multiple sclerosis. Adv Ther 2009; 26: 1043–1057.
Ginsberg D, Cruz F, Herschorn S, Gousse A, Keppenne V, Aliotta P et al. Onabotulinumtoxin A is effective in patients with urinary incontinence due to neurogenic detrusor activity regardless of concomitant anticholinergic use or neurologic etiology. Adv Ther 2013; 30: 819–833.
Leussink VI, Husseini L, Warnke C, Broussalis E, Hartung HP, Kieseier BC . Symptomatic therapy in multiple sclerosis: the role of cannabinoids in treating spasticity. Ther Adv Neurol Disord 2012; 5: 255–266.
Beard S, Hunn A, Wight J . Treatments for spasticity and pain in multiple sclerosis: a systematic review. Health Technol Assess 2003; 7: 1–111.
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/referrals/Tetrazepam_containing_medicinal_products/human_referral_prac_000015.jsp&mid=WC0b01ac05805c516f Accessed August 15, 2013..
Sheean G . Botulinum toxin treatment of adult spasticity: a benefit-risk assessment. Drug Saf 2006; 29: 31–48.
Svensson J, Borg S, Nilsson P . Costs and quality of life in multiple sclerosis patients with spasticity. Acta Neurol Scand 2014; 129: 13–20.
Boines GJ . Predictable remissions in multiple sclerosis. Del Med J 1963; 35: 200–202.
Müller T . Role of intraspinal steroid application in patients with multiple sclerosis. Expert Rev Neurother 2009; 9: 1279–1287.
Hoffmann V, Schimrigk S, Islamova S, Hellwig K, Lukas C, Brune N et al. Efficacy and safety of repeated intrathecal triamcinolone acetonide application in progressive multiple sclerosis patients. J Neurol Sci 2003; 211: 81–84.
Hoffmann V, Kuhn W, Schimrigk S, Islamova S, Hellwig K, Lukas C et al. Repeat intrathecal triamcinolone acetonide application is beneficial in progressive MS patients. Eur J Neurol 2006; 13: 72–76.
Leussink VI, Jung S, Merschdorf U, Toyka KV, Gold R . High-dose methylprednisolone therapy in multiple sclerosis induces apoptosis in peripheral blood leukocytes. Arch Neurol 2001; 58: 91–97.
Buttgereit F, Wehling M, Burmester GR . A new hypothesis of modular glucocorticoid actions: steroid treatment of rheumatic diseases revisited. Arthritis Rheum 1998; 41: 761–767.
Polman CH, Reingold SC, Banwell B, Clanet M, Cohen JA, Filippi M et al. Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria. Ann Neurol 2011; 69: 292–302.
Berger T . Multiple sclerosis spasticity daily management: retrospective data from Europe. Expert Rev Neurother 2013; 13 (3 Suppl 1): 3–7.
Tullman MJ . A review of current and emerging therapeutic strategies in multiple sclerosis. Am J Manag Care 2013; 19 (2 Suppl): S21–S27.
Patejdl R, Winkelmann A, Benecke R, Zettl UK . Muscle rupture caused by exacerbated spasticity in a patient with multiple sclerosis. J Neurol 2008; 255 (Suppl 6): 115–118.
Burks JS, Bigley GK, Hill HH . Rehabilitation challenges in multiple sclerosis. Ann Indian Acad Neurol 2009; 12: 296–306.
Hauser K, Walsh D . Visual analogue scales and assessment of quality of life in cancer. J Support Oncol 2008; 6: 277–282.
Acknowledgements
We thank Ms Nele Gillwaldt for providing figures.
Author contributions: FK contributed to the design and conceptualisation of the study, analysis and interpretation of the data, conducted the statistical analysis, and revised the manuscript. PSR contributed to the design and conceptualisation of the study, analysis and interpretation of the data, drafted the manuscript, and revised the manuscript. FK and PSR contributed equally to this research paper, and are both listed as first authors. MAM WK, FH, AW and RB contributed to the analysis and interpretation of the data, and revising the manuscript. UKZ contributed to the design and conceptualisation of the study, analysis and interpretation of the data, and revising the manuscript.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
PSR served as consultant to Bayer Pharma AG and received speaker honorary from Shire. He received travel support from Biogen Idec. He has recently entered employment with Novartis. WK received travel support, research grant and speaker fees from Biogen Idec, Bayer Healthcare, Merck-Serono, Novartis and Teva. FH received travel support from Bayer Healthcare and Biogen Idec; received research grants from Allergan, Bayer Healthcare, Biogen Idec, Genzyme, Ipsen, Merz, Novartis, Teva and UCB; received speaker or consultant fees from Allergan, Bayer Healthcare, Biogen Idec, Genzyme, Ipsen, Merz, Novartis and Teva. AW received travel support from Novartis and Genzyme; received speaker and consultant fees from Merck-Serono and Genzyme. UKZ received speaker fees from Almirall,Bayer Healthcare, Biogen Idec, Genzyme, Merck-Serono, Novartis, Sanofi and Teva. The remaining authors declare no conflict of interest.
Rights and permissions
About this article
Cite this article
Kamin, F., Rommer, P., Abu-Mugheisib, M. et al. Effects of intrathecal triamincinolone-acetonide treatment in MS patients with therapy-resistant spasticity. Spinal Cord 53, 109–113 (2015). https://doi.org/10.1038/sc.2014.155
Received:
Revised:
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1038/sc.2014.155
This article is cited by
-
Symptomatische Therapie der Multiplen Sklerose
DGNeurologie (2023)
-
Multiple Sklerose Therapie Konsensus Gruppe (MSTKG): Positionspapier zur verlaufsmodifizierenden Therapie der Multiplen Sklerose 2021 (White Paper)
Der Nervenarzt (2021)
-
Intrathecal triamcinolone acetonide exerts anti-inflammatory effects on Lewis rat experimental autoimmune neuritis and direct anti-oxidative effects on Schwann cells
Journal of Neuroinflammation (2019)


