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Published in: Journal of Neurology 4/2020

01-04-2020 | Spinocerebellar Degeneration | Neurological Update

The neurological update: therapies for cerebellar ataxias in 2020

Authors: J. Gandini, Mario Manto, T. Bremova-Ertl, K. Feil, M. Strupp

Published in: Journal of Neurology | Issue 4/2020

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Abstract

Cerebellar ataxias (CAs) represent a heterogeneous group of sporadic or inherited disorders. The clinical spectrum of CAs is continuously expanding. Our understanding of the mechanisms leading to the clinical deficits has improved over these last decades, in particular thanks to progress in genetics, neuroimaging and the advent of relevant animal models allowing the identification of the pathophysiological pathways leading to CAs. The rationale behind treatments is now established for most of the CAs encountered during daily practice worldwide. In this update, we will discuss the symptomatic, physical and occupational therapies now being trialled along with individualized exercises, and present key emerging issues on immune-mediated cerebellar ataxias, hereditary cerebellar ataxias. Finally, we will discuss novel therapeutic approaches, including cerebellar non-invasive stimulation and treatments acting on RNA/proteins. So far, no state-of-the art randomized placebo-controlled clinical trial has shown a convincing clinically relevant efficacy of any drug, with the exception of 4-aminopyridine for the symptomatic treatment of episodic ataxia type 2 and downbeat nystagmus (placebo-controlled trials).
Literature
1.
go back to reference Kuo SH (2019) Ataxia. Continuum (Minneap Minn) 25(4):1036–1054 Kuo SH (2019) Ataxia. Continuum (Minneap Minn) 25(4):1036–1054
2.
go back to reference Manto M, Gandini J, Feil K, Strupp M (2020) Cerebellar ataxias: an update. Curr Opin Neurol 33(1):150–160CrossRefPubMed Manto M, Gandini J, Feil K, Strupp M (2020) Cerebellar ataxias: an update. Curr Opin Neurol 33(1):150–160CrossRefPubMed
3.
go back to reference Bürk K, Sival DA (2018) Scales for the clinical evaluation of cerebellar disorders. Handb Clin Neurol 154:329–339CrossRefPubMed Bürk K, Sival DA (2018) Scales for the clinical evaluation of cerebellar disorders. Handb Clin Neurol 154:329–339CrossRefPubMed
5.
go back to reference Schatton C, Synofzik M, Fleszar Z, Giese MA, Schöls L, Ilg W (2017) Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: a rater-blinded, intra-individually controlled trial. Parkinsonism Relat Disord 39:80–84CrossRefPubMed Schatton C, Synofzik M, Fleszar Z, Giese MA, Schöls L, Ilg W (2017) Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: a rater-blinded, intra-individually controlled trial. Parkinsonism Relat Disord 39:80–84CrossRefPubMed
7.
8.
go back to reference Mitoma H, Manto M, Hampe CS (2019) Immune-mediated cerebellar ataxias: practical guidelines and therapeutic challenges. Curr Neuropharmacol 17(1):33–58CrossRefPubMedPubMedCentral Mitoma H, Manto M, Hampe CS (2019) Immune-mediated cerebellar ataxias: practical guidelines and therapeutic challenges. Curr Neuropharmacol 17(1):33–58CrossRefPubMedPubMedCentral
10.
go back to reference Synofzik M, Puccio H, Mochel F, Schöls L (2019) Autosomal recessive cerebellar ataxias: paving the way toward targeted molecular therapies. Neuron 101(4):560–583CrossRefPubMed Synofzik M, Puccio H, Mochel F, Schöls L (2019) Autosomal recessive cerebellar ataxias: paving the way toward targeted molecular therapies. Neuron 101(4):560–583CrossRefPubMed
12.
go back to reference Cook A, Boesch S, Heck S, Brunt E, Klockgether T, Schöls L, Schulz A, Giunti P (2019) Patient-reported outcomes in Friedreich’s ataxia after withdrawal from idebenone. Acta Neurol Scand 139(6):533–539CrossRefPubMed Cook A, Boesch S, Heck S, Brunt E, Klockgether T, Schöls L, Schulz A, Giunti P (2019) Patient-reported outcomes in Friedreich’s ataxia after withdrawal from idebenone. Acta Neurol Scand 139(6):533–539CrossRefPubMed
13.
go back to reference Pandolfo M, Arpa J, Delatycki MB, Le Quan Sang KH, Mariotti C, Munnich A, Sanz-Gallego I, Tai G, Tarnopolsky MA, Taroni F, Spino M, Tricta F (2014) Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial. Ann Neurol 76(4):509–521CrossRefPubMed Pandolfo M, Arpa J, Delatycki MB, Le Quan Sang KH, Mariotti C, Munnich A, Sanz-Gallego I, Tai G, Tarnopolsky MA, Taroni F, Spino M, Tricta F (2014) Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial. Ann Neurol 76(4):509–521CrossRefPubMed
14.
go back to reference Boesch S, Sturm B, Hering S, Scheiber-Mojdehkar B, Steinkellner H, Goldenberg H, Poewe W (2008) Neurological effects of recombinant human erythropoietin in Friedreich’s ataxia: a clinical pilot trial. Mov Disord 23(13):1940–1944CrossRefPubMed Boesch S, Sturm B, Hering S, Scheiber-Mojdehkar B, Steinkellner H, Goldenberg H, Poewe W (2008) Neurological effects of recombinant human erythropoietin in Friedreich’s ataxia: a clinical pilot trial. Mov Disord 23(13):1940–1944CrossRefPubMed
15.
go back to reference Lynch DR, Hauser L, McCormick A et al (2019) Randomized, double-blind, placebo-controlled study of interferon-γ 1b in Friedreich ataxia. Ann Clin Transl Neurol 6(3):546–553CrossRefPubMedPubMedCentral Lynch DR, Hauser L, McCormick A et al (2019) Randomized, double-blind, placebo-controlled study of interferon-γ 1b in Friedreich ataxia. Ann Clin Transl Neurol 6(3):546–553CrossRefPubMedPubMedCentral
16.
go back to reference Lynch DR, Schadt K, Kichula E (2019) Etravirine in Friedreich’s ataxia: lessons from HIV? Mov Disord 34(3):305–306CrossRefPubMed Lynch DR, Schadt K, Kichula E (2019) Etravirine in Friedreich’s ataxia: lessons from HIV? Mov Disord 34(3):305–306CrossRefPubMed
17.
go back to reference Barca E, Emmanuele V, DiMauro S, Toscano A, Quinzii CM (2019) Anti-oxidant drugs: novelties and clinical implications in cerebellar ataxias. Curr Neuropharmacol 17(1):21–32CrossRefPubMedPubMedCentral Barca E, Emmanuele V, DiMauro S, Toscano A, Quinzii CM (2019) Anti-oxidant drugs: novelties and clinical implications in cerebellar ataxias. Curr Neuropharmacol 17(1):21–32CrossRefPubMedPubMedCentral
18.
go back to reference Salviati L, Trevisson E, Doimo M, Navas P (eds) (2017) Primary coenzyme Q10 deficiency. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N (eds) GeneReviews® [Internet]. University of Washington, Seattle, pp 1993–2017 Salviati L, Trevisson E, Doimo M, Navas P (eds) (2017) Primary coenzyme Q10 deficiency. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N (eds) GeneReviews® [Internet]. University of Washington, Seattle, pp 1993–2017
21.
go back to reference Zannolli R, Buoni S, Betti G, Salvucci S, Plebani A, Soresina A, Pietrogrande MC, Martino S, Leuzzi V, Finocchi A, Micheli R, Rossi LN, Brusco A, Misiani F, Fois A, Hayek J, Kelly C, Chessa L (2012) A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia. Mov Disord 27(10):1312–1316CrossRefPubMed Zannolli R, Buoni S, Betti G, Salvucci S, Plebani A, Soresina A, Pietrogrande MC, Martino S, Leuzzi V, Finocchi A, Micheli R, Rossi LN, Brusco A, Misiani F, Fois A, Hayek J, Kelly C, Chessa L (2012) A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia. Mov Disord 27(10):1312–1316CrossRefPubMed
22.
go back to reference Pineda M, Juríčková K, Karimzadeh P, Kolnikova M, Malinova V, Insua JL, Velten C, Kolb SA (2019) Disease characteristics, prognosis and miglustat treatment effects on disease progression in patients with Niemann-Pick disease type C: an international, multicenter, retrospective chart review. Orphanet J Rare Dis 14(1):32CrossRefPubMedPubMedCentral Pineda M, Juríčková K, Karimzadeh P, Kolnikova M, Malinova V, Insua JL, Velten C, Kolb SA (2019) Disease characteristics, prognosis and miglustat treatment effects on disease progression in patients with Niemann-Pick disease type C: an international, multicenter, retrospective chart review. Orphanet J Rare Dis 14(1):32CrossRefPubMedPubMedCentral
23.
go back to reference Bremova T, Malinová V, Amraoui Y, Mengel E, Reinke J, Kolníková M, Strupp M (2015) Acetyl-dl-leucine in Niemann-Pick type C: a case series. Neurology 85(16):1368–1375CrossRefPubMed Bremova T, Malinová V, Amraoui Y, Mengel E, Reinke J, Kolníková M, Strupp M (2015) Acetyl-dl-leucine in Niemann-Pick type C: a case series. Neurology 85(16):1368–1375CrossRefPubMed
24.
go back to reference Vibert N, Vidal PP (2001) In vitro effects of acetyl-DL-leucine (tanganil) on central vestibular neurons and vestibulo-ocular networks of the guinea-pig. Eur J Neurosci 13:735–748CrossRefPubMed Vibert N, Vidal PP (2001) In vitro effects of acetyl-DL-leucine (tanganil) on central vestibular neurons and vestibulo-ocular networks of the guinea-pig. Eur J Neurosci 13:735–748CrossRefPubMed
25.
go back to reference Narita A, Shirai K, Itamura S, Matsuda A, Ishihara A, Matsushita K, Fukuda C, Kubota N, Takayama R, Shigematsu H, Hayashi A, Kumada T, Yuge K, Watanabe Y, Kosugi S, Nishida H, Kimura Y, Endo Y, Higaki K, Nanba E, Nishimura Y, Tamasaki A, Togawa M, Saito Y, Maegaki Y, Ohno K, Suzuki Y (2016) Ambroxol chaperone therapy for neuronopathic gaucher disease: a pilot study. Ann Clin Transl Neurol 3(3):200–215CrossRefPubMedPubMedCentral Narita A, Shirai K, Itamura S, Matsuda A, Ishihara A, Matsushita K, Fukuda C, Kubota N, Takayama R, Shigematsu H, Hayashi A, Kumada T, Yuge K, Watanabe Y, Kosugi S, Nishida H, Kimura Y, Endo Y, Higaki K, Nanba E, Nishimura Y, Tamasaki A, Togawa M, Saito Y, Maegaki Y, Ohno K, Suzuki Y (2016) Ambroxol chaperone therapy for neuronopathic gaucher disease: a pilot study. Ann Clin Transl Neurol 3(3):200–215CrossRefPubMedPubMedCentral
26.
go back to reference Wolf B (2017) Successful outcomes of older adolescents and adults with profound biotinidase deficiency identified by newborn screening. Genet Med 19(4):396–402CrossRefPubMed Wolf B (2017) Successful outcomes of older adolescents and adults with profound biotinidase deficiency identified by newborn screening. Genet Med 19(4):396–402CrossRefPubMed
27.
go back to reference Szmulewicz DJ, McLean CA, Rodriguez ML, Chancellor AM, Mossman S, Lamont D, Roberts L, Storey E, Halmagyi GM (2014) Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS. Neurology 82(16):1410–1415CrossRefPubMedPubMedCentral Szmulewicz DJ, McLean CA, Rodriguez ML, Chancellor AM, Mossman S, Lamont D, Roberts L, Storey E, Halmagyi GM (2014) Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS. Neurology 82(16):1410–1415CrossRefPubMedPubMedCentral
28.
go back to reference Szmulewicz DJ, Roberts L, McLean CA, MacDougall HG, Halmagyi GM, Storey E (2016) Proposed diagnostic criteria for cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS). Neurol Clin Pract 6(1):61–68CrossRefPubMedPubMedCentral Szmulewicz DJ, Roberts L, McLean CA, MacDougall HG, Halmagyi GM, Storey E (2016) Proposed diagnostic criteria for cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS). Neurol Clin Pract 6(1):61–68CrossRefPubMedPubMedCentral
30.
go back to reference Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, Humphrey J, Jaunmuktane Z, Sivakumar P, Polke J, Ilyas M, Tribollet E, Tomaselli PJ, Devigili G, Callegari I, Versino M, Salpietro V, Efthymiou S, Kaski D, Wood NW, Andrade NS, Buglo E, Rebelo A, Rossor AM, Bronstein A, Fratta P, Marques WJ, Züchner S, Reilly MM, Houlden H (2019) Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Nat Genet 51(4):649–658CrossRefPubMedPubMedCentral Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, Humphrey J, Jaunmuktane Z, Sivakumar P, Polke J, Ilyas M, Tribollet E, Tomaselli PJ, Devigili G, Callegari I, Versino M, Salpietro V, Efthymiou S, Kaski D, Wood NW, Andrade NS, Buglo E, Rebelo A, Rossor AM, Bronstein A, Fratta P, Marques WJ, Züchner S, Reilly MM, Houlden H (2019) Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Nat Genet 51(4):649–658CrossRefPubMedPubMedCentral
31.
go back to reference Rafehi H, Szmulewicz DJ, Bennett MF, Sobreira NLM, Pope K, Smith KR, Gillies G, Diakumis P, Dolzhenko E, Eberle MA, Barcina MG, Breen DP, Chancellor AM, Cremer PD, Delatycki MB, Fogel BL, Hackett A, Halmagyi GM, Kapetanovic S, Lang A, Mossman S, Mu W, Patrikios P, Perlman SL, Rosemergy I, Storey E, Watson SRD, Wilson MA, Zee DS, Valle D, Amor DJ, Bahlo M, Lockhart PJ (2019) Bioinformatics-based identification of expanded repeats: a non-reference intronic pentamer expansion in RFC1 causes CANVAS. Am J Hum Genet 105(1):151–165CrossRefPubMedPubMedCentral Rafehi H, Szmulewicz DJ, Bennett MF, Sobreira NLM, Pope K, Smith KR, Gillies G, Diakumis P, Dolzhenko E, Eberle MA, Barcina MG, Breen DP, Chancellor AM, Cremer PD, Delatycki MB, Fogel BL, Hackett A, Halmagyi GM, Kapetanovic S, Lang A, Mossman S, Mu W, Patrikios P, Perlman SL, Rosemergy I, Storey E, Watson SRD, Wilson MA, Zee DS, Valle D, Amor DJ, Bahlo M, Lockhart PJ (2019) Bioinformatics-based identification of expanded repeats: a non-reference intronic pentamer expansion in RFC1 causes CANVAS. Am J Hum Genet 105(1):151–165CrossRefPubMedPubMedCentral
32.
go back to reference Zesiewicz TA, Wilmot G, Kuo SH, Perlman S, Greenstein PE, Ying SH, Ashizawa T, Subramony SH, Schmahmann JD, Figueroa KP et al (2018) Comprehensive systematic review summary: treatment of cerebellar motor dysfunction and ataxia: report of the guideline development, dissemination, and implementation subcommittee of the American academy of neurology. Neurology 90(10):464–471CrossRefPubMedPubMedCentral Zesiewicz TA, Wilmot G, Kuo SH, Perlman S, Greenstein PE, Ying SH, Ashizawa T, Subramony SH, Schmahmann JD, Figueroa KP et al (2018) Comprehensive systematic review summary: treatment of cerebellar motor dysfunction and ataxia: report of the guideline development, dissemination, and implementation subcommittee of the American academy of neurology. Neurology 90(10):464–471CrossRefPubMedPubMedCentral
33.
go back to reference Manes M, Alberici A, Di Gregorio E et al (2017) Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38. Ann Neurol 82(4):615–621CrossRefPubMedPubMedCentral Manes M, Alberici A, Di Gregorio E et al (2017) Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38. Ann Neurol 82(4):615–621CrossRefPubMedPubMedCentral
34.
go back to reference Gómez-Ruiz M, Rodríguez-Cueto C, Luna-Piñel E, Hernández-Gálvez M, Fernández-Ruiz J (2019) Endocannabinoid system in spinocerebellar ataxia type-3 and other autosomal-dominant cerebellar ataxias: potential role in pathogenesis and expected relevance as neuroprotective targets. Front Mol Neurosci 12:94CrossRefPubMedPubMedCentral Gómez-Ruiz M, Rodríguez-Cueto C, Luna-Piñel E, Hernández-Gálvez M, Fernández-Ruiz J (2019) Endocannabinoid system in spinocerebellar ataxia type-3 and other autosomal-dominant cerebellar ataxias: potential role in pathogenesis and expected relevance as neuroprotective targets. Front Mol Neurosci 12:94CrossRefPubMedPubMedCentral
35.
go back to reference Griggs RC, Moxley RT 3rd, Lafrance RA, McQuillen J (1978) Hereditary paroxysmal ataxia: response to acetazolamide. Neurology 28(12):1259–1264CrossRefPubMed Griggs RC, Moxley RT 3rd, Lafrance RA, McQuillen J (1978) Hereditary paroxysmal ataxia: response to acetazolamide. Neurology 28(12):1259–1264CrossRefPubMed
36.
go back to reference Strupp M, Kalla R, Dichgans M, Freilinger T, Glasauer S, Brandt T (2004) Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine. Neurology 62(9):1623–1625CrossRefPubMed Strupp M, Kalla R, Dichgans M, Freilinger T, Glasauer S, Brandt T (2004) Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine. Neurology 62(9):1623–1625CrossRefPubMed
37.
go back to reference Strupp M, Kalla R, Claassen J, Adrion C, Mansmann U, Klopstock T, Freilinger T, Neugebauer H, Spiegel R, Dichgans M, Lehmann-Horn F, Jurkat-Rott K, Brandt T, Jen JC, Jahn K (2011) A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias. Neurology 77(3):269–275CrossRefPubMedPubMedCentral Strupp M, Kalla R, Claassen J, Adrion C, Mansmann U, Klopstock T, Freilinger T, Neugebauer H, Spiegel R, Dichgans M, Lehmann-Horn F, Jurkat-Rott K, Brandt T, Jen JC, Jahn K (2011) A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias. Neurology 77(3):269–275CrossRefPubMedPubMedCentral
38.
go back to reference Strupp M, Teufel J, Zwergal A, Schniepp R, Khodakhah K, Feil K (2017) Aminopyridines for the treatment of neurologic disorders. Neurol Clin Pract 7(1):65–76CrossRefPubMedPubMedCentral Strupp M, Teufel J, Zwergal A, Schniepp R, Khodakhah K, Feil K (2017) Aminopyridines for the treatment of neurologic disorders. Neurol Clin Pract 7(1):65–76CrossRefPubMedPubMedCentral
39.
go back to reference Etzion Y, Grossman Y (2001) Highly 4-aminopyridine sensitive delayed rectifier current modulates the excitability of guinea pig cerebellar Purkinje cells. Exp Brain Res 139:419–425CrossRefPubMed Etzion Y, Grossman Y (2001) Highly 4-aminopyridine sensitive delayed rectifier current modulates the excitability of guinea pig cerebellar Purkinje cells. Exp Brain Res 139:419–425CrossRefPubMed
41.
go back to reference Hourez R, Servais L, Orduz D et al (2011) Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1. J Neurosci 31:11795–11807CrossRefPubMedPubMedCentral Hourez R, Servais L, Orduz D et al (2011) Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1. J Neurosci 31:11795–11807CrossRefPubMedPubMedCentral
42.
43.
go back to reference Wagner JN, Glaser M, Brandt T, Strupp M (2008) Downbeat nystagmus: aetiology and comorbidity in 117 patients. J Neurol Neurosurg Psychiatry 79:672–677CrossRefPubMed Wagner JN, Glaser M, Brandt T, Strupp M (2008) Downbeat nystagmus: aetiology and comorbidity in 117 patients. J Neurol Neurosurg Psychiatry 79:672–677CrossRefPubMed
44.
go back to reference Kalla R, Deutschlander A, Hufner K et al (2006) Detection of floccular hypometabolism in downbeat nystagmus by fMRI. Neurology 66:281–283CrossRefPubMed Kalla R, Deutschlander A, Hufner K et al (2006) Detection of floccular hypometabolism in downbeat nystagmus by fMRI. Neurology 66:281–283CrossRefPubMed
45.
go back to reference Strupp M, Schüler O, Krafczyk S, Jahn K, Schautzer F, Büttner U, Brandt T (2003) Treatment of downbeat nystagmus with 3,4-diaminopyridine: a placebo-controlled study. Neurology 61(2):165–170CrossRefPubMed Strupp M, Schüler O, Krafczyk S, Jahn K, Schautzer F, Büttner U, Brandt T (2003) Treatment of downbeat nystagmus with 3,4-diaminopyridine: a placebo-controlled study. Neurology 61(2):165–170CrossRefPubMed
46.
go back to reference Claassen J, Spiegel R, Kalla R et al (2013) A randomised double-blind, cross-over trial of 4-aminopyridine for downbeat nystagmus–effects on slowphase eye velocity, postural stability, locomotion and symptoms. J Neurol Neurosurg Psychiatry 84:1392–1399CrossRefPubMed Claassen J, Spiegel R, Kalla R et al (2013) A randomised double-blind, cross-over trial of 4-aminopyridine for downbeat nystagmus–effects on slowphase eye velocity, postural stability, locomotion and symptoms. J Neurol Neurosurg Psychiatry 84:1392–1399CrossRefPubMed
48.
go back to reference Claassen J, Feil K, Bardins S et al (2013) Dalfampridine in patients with downbeat nystagmus: an observational study. J Neurol 260:1992–1996CrossRefPubMed Claassen J, Feil K, Bardins S et al (2013) Dalfampridine in patients with downbeat nystagmus: an observational study. J Neurol 260:1992–1996CrossRefPubMed
49.
go back to reference Schniepp R, Wuehr M, Neuhaeusser M, Benecke AK, Adrion C, Brandt T, Strupp M, Jahn K (2012) 4-aminopyridine and cerebellar gait: a retrospective case series. J Neurol 259:2491–2493CrossRefPubMed Schniepp R, Wuehr M, Neuhaeusser M, Benecke AK, Adrion C, Brandt T, Strupp M, Jahn K (2012) 4-aminopyridine and cerebellar gait: a retrospective case series. J Neurol 259:2491–2493CrossRefPubMed
50.
go back to reference Giordano I, Bogdanow M, Jacobi H, Jahn K, Minnerop M, Schoels L et al (2013) Experience in a short-term trial with 4-aminopyridine in cerebellar ataxia. J Neurol 260:2175–2176CrossRefPubMed Giordano I, Bogdanow M, Jacobi H, Jahn K, Minnerop M, Schoels L et al (2013) Experience in a short-term trial with 4-aminopyridine in cerebellar ataxia. J Neurol 260:2175–2176CrossRefPubMed
51.
go back to reference van Dun K, Bodranghien F, Manto M, Mariën P (2014) Targeting the cerebellum by noninvasive neurostimulation: a review. Cerebellum 16(3):695–741CrossRef van Dun K, Bodranghien F, Manto M, Mariën P (2014) Targeting the cerebellum by noninvasive neurostimulation: a review. Cerebellum 16(3):695–741CrossRef
52.
go back to reference Oldrati V, Schutter D (2018) Targeting the human cerebellum with transcranial direct current stimulation to modulate behavior: a meta-analysis. Cerebellum 17(2):228–236CrossRefPubMed Oldrati V, Schutter D (2018) Targeting the human cerebellum with transcranial direct current stimulation to modulate behavior: a meta-analysis. Cerebellum 17(2):228–236CrossRefPubMed
53.
go back to reference Bodranghien F, Oulad Ben Taib N, Van Maldergem L, Manto M (2017) A postural tremor highly responsive to transcranial cerebello-cerebral DCS in ARCA3. Front Neurol 8:71CrossRefPubMedPubMedCentral Bodranghien F, Oulad Ben Taib N, Van Maldergem L, Manto M (2017) A postural tremor highly responsive to transcranial cerebello-cerebral DCS in ARCA3. Front Neurol 8:71CrossRefPubMedPubMedCentral
54.
go back to reference Benussi A, Koch G, Cotelli M, Padovani A, Borroni B (2015) Cerebellar transcranial direct current stimulation in patients with ataxia: a double-blind, randomized, sham-controlled study. Mov Disord 30(12):1701–1705CrossRefPubMed Benussi A, Koch G, Cotelli M, Padovani A, Borroni B (2015) Cerebellar transcranial direct current stimulation in patients with ataxia: a double-blind, randomized, sham-controlled study. Mov Disord 30(12):1701–1705CrossRefPubMed
55.
go back to reference Benussi A, Dell'Era V, Cotelli MS, Turla M, Casali C, Padovani A, Borroni B (2017) Long term clinical and neurophysiological effects of cerebellar transcranial direct current stimulation in patients with neurodegenerative ataxia. Brain Stimul 10(2):242–250CrossRefPubMed Benussi A, Dell'Era V, Cotelli MS, Turla M, Casali C, Padovani A, Borroni B (2017) Long term clinical and neurophysiological effects of cerebellar transcranial direct current stimulation in patients with neurodegenerative ataxia. Brain Stimul 10(2):242–250CrossRefPubMed
56.
go back to reference Benussi A, Dell'Era V, Cantoni V, Bonetta E, Grasso R, Manenti R, Cotelli M, Padovani A, Borroni B (2018) Cerebello-spinal tDCS in ataxia: a randomized, double-blind, sham-controlled, crossover trial. Neurology 91(12):e1090–e1101CrossRefPubMed Benussi A, Dell'Era V, Cantoni V, Bonetta E, Grasso R, Manenti R, Cotelli M, Padovani A, Borroni B (2018) Cerebello-spinal tDCS in ataxia: a randomized, double-blind, sham-controlled, crossover trial. Neurology 91(12):e1090–e1101CrossRefPubMed
57.
58.
go back to reference Scoles DR, Meera P, Schneider MD, Paul S, Dansithong W, Figueroa KP, Hung G, Rigo F, Bennett CF, Otis TS, Pulst SM (2017) Antisense oligonucleotide therapy for spinocerebellar ataxia type 2. Nature 544(7650):362–366CrossRefPubMedPubMedCentral Scoles DR, Meera P, Schneider MD, Paul S, Dansithong W, Figueroa KP, Hung G, Rigo F, Bennett CF, Otis TS, Pulst SM (2017) Antisense oligonucleotide therapy for spinocerebellar ataxia type 2. Nature 544(7650):362–366CrossRefPubMedPubMedCentral
59.
go back to reference Moore LR, Rajpal G, Dillingham IT, Qutob M, Blumenstein KG, Gattis D, Hung G, Kordasiewicz HB, Paulson HL, McLoughlin HS (2017) Evaluation of antisense oligonucleotides targeting ATXN3 in SCA3 mouse models. Mol Ther Nucleic Acids 7:200–210CrossRefPubMedPubMedCentral Moore LR, Rajpal G, Dillingham IT, Qutob M, Blumenstein KG, Gattis D, Hung G, Kordasiewicz HB, Paulson HL, McLoughlin HS (2017) Evaluation of antisense oligonucleotides targeting ATXN3 in SCA3 mouse models. Mol Ther Nucleic Acids 7:200–210CrossRefPubMedPubMedCentral
60.
go back to reference McLoughlin HS, Moore LR, Chopra R, Komlo R, McKenzie M, Blumenstein KG, Zhao H, Kordasiewicz HB, Shakkottai VG, Paulson HL (2018) Oligonucleotide therapy mitigates disease in spinocerebellar ataxia type 3 mice. Ann Neurol 84(1):64–77CrossRefPubMedPubMedCentral McLoughlin HS, Moore LR, Chopra R, Komlo R, McKenzie M, Blumenstein KG, Zhao H, Kordasiewicz HB, Shakkottai VG, Paulson HL (2018) Oligonucleotide therapy mitigates disease in spinocerebellar ataxia type 3 mice. Ann Neurol 84(1):64–77CrossRefPubMedPubMedCentral
61.
go back to reference Pérez Ortiz JM, Orr HT (2018) Spinocerebellar ataxia type 1: molecular mechanisms of neurodegeneration and preclinical studies. Adv Exp Med Biol 1049:135–145CrossRefPubMed Pérez Ortiz JM, Orr HT (2018) Spinocerebellar ataxia type 1: molecular mechanisms of neurodegeneration and preclinical studies. Adv Exp Med Biol 1049:135–145CrossRefPubMed
62.
go back to reference Cendelin J, Buffo A, Hirai H, Magrassi L, Mitoma H, Sherrard R, Vozeh F, Manto M (2019) Task force paper on cerebellar transplantation: are we ready to treat cerebellar disorders with cell therapy? Cerebellum 18(3):575–592CrossRefPubMed Cendelin J, Buffo A, Hirai H, Magrassi L, Mitoma H, Sherrard R, Vozeh F, Manto M (2019) Task force paper on cerebellar transplantation: are we ready to treat cerebellar disorders with cell therapy? Cerebellum 18(3):575–592CrossRefPubMed
63.
go back to reference Piguet F, de Montigny C, Vaucamps N, Reutenauer L, Eisenmann A, Puccio H (2018) Rapid and complete reversal of sensory ataxia by gene therapy in a novel model of Friedreich ataxia. Mol Ther 26(8):1940–1952CrossRefPubMedPubMedCentral Piguet F, de Montigny C, Vaucamps N, Reutenauer L, Eisenmann A, Puccio H (2018) Rapid and complete reversal of sensory ataxia by gene therapy in a novel model of Friedreich ataxia. Mol Ther 26(8):1940–1952CrossRefPubMedPubMedCentral
64.
go back to reference Gérard C, Xiao X, Filali M, Coulombe Z, Arsenault M, Couet J, Li J, Drolet MC, Chapdelaine P, Chikh A, Tremblay JP (2014) An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse models. Mol Ther Methods Clin Dev 1:14044CrossRefPubMedPubMedCentral Gérard C, Xiao X, Filali M, Coulombe Z, Arsenault M, Couet J, Li J, Drolet MC, Chapdelaine P, Chikh A, Tremblay JP (2014) An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse models. Mol Ther Methods Clin Dev 1:14044CrossRefPubMedPubMedCentral
65.
go back to reference Nayler S, Kozlov SV, Lavin MF, Wolvetang E (2017) Lentiviral reprogramming of A-T patient fibroblasts to induced pluripotent stem cells. Methods Mol Biol 1599:401–418CrossRefPubMed Nayler S, Kozlov SV, Lavin MF, Wolvetang E (2017) Lentiviral reprogramming of A-T patient fibroblasts to induced pluripotent stem cells. Methods Mol Biol 1599:401–418CrossRefPubMed
66.
go back to reference Carranza D, Torres-Rusillo S, Ceballos-Pérez G, Blanco-Jimenez E, Muñoz-López M, García-Pérez JL, Molina IJ (2018) Reconstitution of the ataxia-telangiectasia cellular phenotype with lentiviral vectors. Front Immunol 9:2703CrossRefPubMedPubMedCentral Carranza D, Torres-Rusillo S, Ceballos-Pérez G, Blanco-Jimenez E, Muñoz-López M, García-Pérez JL, Molina IJ (2018) Reconstitution of the ataxia-telangiectasia cellular phenotype with lentiviral vectors. Front Immunol 9:2703CrossRefPubMedPubMedCentral
67.
go back to reference Dezawa M, Ishikawa H, Hoshino M, Itokazu Y, Nabeshima Y (2005) Potential of bone marrow stromal cells in applications for neuro-degenerative, neuro-traumatic and muscle degenerative diseases. Curr Neuropharmacol 3(4):257–266CrossRefPubMedPubMedCentral Dezawa M, Ishikawa H, Hoshino M, Itokazu Y, Nabeshima Y (2005) Potential of bone marrow stromal cells in applications for neuro-degenerative, neuro-traumatic and muscle degenerative diseases. Curr Neuropharmacol 3(4):257–266CrossRefPubMedPubMedCentral
68.
go back to reference Hayashi T, Onoe H (2013) Neuroimaging for optimization of stem cell therapy in Parkinson’s disease. Expert Opin Biol Ther 13(12):1631–1638CrossRefPubMed Hayashi T, Onoe H (2013) Neuroimaging for optimization of stem cell therapy in Parkinson’s disease. Expert Opin Biol Ther 13(12):1631–1638CrossRefPubMed
69.
go back to reference Choumerianou DM, Dimitriou H, Kalmanti M (2008) Stem cells: promises versus limitations. Tissue Eng Part B Rev 14(1):53–60CrossRefPubMed Choumerianou DM, Dimitriou H, Kalmanti M (2008) Stem cells: promises versus limitations. Tissue Eng Part B Rev 14(1):53–60CrossRefPubMed
70.
go back to reference Lee PH, Lee JE, Kim HS, Song SK, Lee HS, Nam HS, Cheong JW, Jeong Y, Park HJ, Kim DJ, Nam CM, Lee JD, Kim HO, Sohn YH (2012) A randomized trial of mesenchymal stem cells in multiple system atrophy. Ann Neurol 72(1):32–40CrossRefPubMed Lee PH, Lee JE, Kim HS, Song SK, Lee HS, Nam HS, Cheong JW, Jeong Y, Park HJ, Kim DJ, Nam CM, Lee JD, Kim HO, Sohn YH (2012) A randomized trial of mesenchymal stem cells in multiple system atrophy. Ann Neurol 72(1):32–40CrossRefPubMed
71.
go back to reference Matsuura S, Shuvaev AN, Iizuka A, Nakamura K, Hirai H (2014) Mesenchymal stem cells ameliorate cerebellar pathology in a mouse model of spinocerebellar ataxia type 1. Cerebellum 13(3):323–330CrossRefPubMed Matsuura S, Shuvaev AN, Iizuka A, Nakamura K, Hirai H (2014) Mesenchymal stem cells ameliorate cerebellar pathology in a mouse model of spinocerebellar ataxia type 1. Cerebellum 13(3):323–330CrossRefPubMed
72.
go back to reference Oliveira Miranda C, Marcelo A, Silva TP, Barata J, Vasconcelos-Ferreira A, Pereira D, Nóbrega C, Duarte S, Barros I, Alves J, Sereno J, Petrella LI, Castelhano J, Paiva VH, Rodrigues-Santos P, Alves V, Nunes-Correia I, Nobre RJ, Gomes C, Castelo-Branco M, Pereira de Almeida L (2018) Repeated mesenchymal stromal cell treatment sustainably alleviates machado-joseph disease. Mol Ther 26(9):2131–2151CrossRefPubMedPubMedCentral Oliveira Miranda C, Marcelo A, Silva TP, Barata J, Vasconcelos-Ferreira A, Pereira D, Nóbrega C, Duarte S, Barros I, Alves J, Sereno J, Petrella LI, Castelhano J, Paiva VH, Rodrigues-Santos P, Alves V, Nunes-Correia I, Nobre RJ, Gomes C, Castelo-Branco M, Pereira de Almeida L (2018) Repeated mesenchymal stromal cell treatment sustainably alleviates machado-joseph disease. Mol Ther 26(9):2131–2151CrossRefPubMedPubMedCentral
Metadata
Title
The neurological update: therapies for cerebellar ataxias in 2020
Authors
J. Gandini
Mario Manto
T. Bremova-Ertl
K. Feil
M. Strupp
Publication date
01-04-2020
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 4/2020
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-020-09717-3

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