Fortschr Neurol Psychiatr 2000; 68(1): 25-36
DOI: 10.1055/s-2000-11790
ORIGINALARBEIT
Georg Thieme Verlag Stuttgart ·New York

30 Jahre MSA-Konzept:Ein Rück- und Überblick überdie Multisystematrophie

30 Years of MSA-Concept: Review and Survey of Multiple System Atrophy:S. Probst-Cousin, C. Kayser, D. Heuss, B. Neundörfer
  • Neurologische Klinik und Poliklinik der Friedrich-Alexander-Universität Erlangen-Nürnberg (Direktor: Prof. Dr. med.B. Neundörfer)
Further Information

Publication History

Publication Date:
05 November 2004 (online)

Zusammenfassung:

Die Multisystematrophie (MSA) ist eine klinisch-neuropathologisch definierte neurodegenerative Erkrankung unklarer Ätiologie und Pathogenese. Die zuvor benutzten, historisch entstandenen Begriffe olivo-ponto-zerebelläre Atrophie, striato-nigrale Degeneration und Shy-Drager-Syndrom, die schon immer durch eine klinisch-morphologische Überlappung gekennzeichnet waren, sollten den klinischen Sprachgebrauch verlassen und neurodegenerative Erkrankungen mit einem komplexen morphologischen Läsionsmuster, die nicht der Definition der MSA entsprechen, sollten unter die Multisystemdegenerationen eingereiht werden.

Multiple system atrophy represents an enigmatic, clinico-pathologically defined neurodegenerative disease. According to findings of the last three decades, the historically derived, previously used terms olivopontocerebellar atrophy, striatonigral degeneration, and Shy-Drager-syndrome should be avoided in clinical use because of both the clinical and morphological overlap between these syndromes. Complex neurodegenerative syndromes other than multiple system atrophy according to recently developed criteria, should rather be referred to as multiple system degenerations.

Literatur

  • 1 Graham J, Oppenheimer D. Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy.  J Neurol Neurosurg Psychiat. 1969;  32 28-34
  • 2 Papp M I, Kahn J E, Lantos P L. Glial cytoplasmatic inclusions in the CNS of patients with multiple system atrophy (striatonigral dequeneration, olivopontocerebellar atrophy and Shy-Drager syndrome).  J Neurol Sci. 1989;  94 79-100
  • 3 Parkinson J. An assay on the shaking palsy. London; Sherwood, Neely and Jones 1817
  • 4 Oertel W H. Multisystematrophie. In: Conrad, B, Ceballos-Baumann, AO (Hrsg) Bewegungsstörungen in der Neurologie. Richtig erkennen und behandeln. Stuttgart, New York; Thieme 1996: 69-77
  • 5 Déjérine J, Thomas A. L'Atrophie Olivo-Ponto-Cérébelleuse.  Nouv Iconogr Salpêt. 1900;  13 330-370
  • 6 Menzel P. Beitrag zur Kenntnis der hereditären Ataxie und Kleinhirnatrophie.  Arch Psychiat Nervenkrankh. 1891;  22 160-190
  • 7 Loew P. L'atrophie olivo-ponto-cerebelleuse. Thesis. UniversitÅ de Paris 1903 - 1904
  • 8 Berciano J. Olivopontocerebellar atrophy. A review of 117 cases.  J Neurol Sci. 1982;  53 253-272
  • 9 Chokroverty S. Autonomic Dysfunction in Olivopontocerebellar Atrophy. In: Duvoisin, RC, Plaitakis, A (Hrsg) The Olivopontocerebellar Atrophies. New York; Raven Press 1984: 105-141
  • 10 Eadie M J. Olivocerebellar atrophy (Menzel type). In: Vinken, PJ, Bruyn, GW (Hrsg) Handbook of Clinical Neurology. Vol. 21. Amsterdam; North-Holland Publishing Company 1975: 433-449
  • 11 Eadie M J. Olivopontocerebellar atrophy (Déjérine-Thomas type). In: Vinken, PJ, Bruyn, GW (Hrsg) Handbook of Clinical Neurology. Vol. 21. Amsterdam; North-Holland Publishing Company 1975: 415-431
  • 12 Eadie M J. Olivocerebellar atrophy (Variants). In: Vinken, PJ, Bruyn, GW (Hrsg) Handbook of Clinical Neurology. Vol. 21. Amsterdam; North-Holland Publishing Company 1975: 451-457
  • 13 Konigsmark B W, Weiner L P. The olivopontocerebellar atrophies: A Review.  Medicine. 1970;  49 227-241
  • 14 Lutz R, Bodensteiner J, Schaefer B, Gay C. X-linked olivopontocerebellar atrophy.  Clin Genet. 1989;  35 417-422
  • 15 Perry T L. Four Biochemically Different Types of Dominantly Inherited Olivopontocerebellar Atrophy. In: Duvoisin, RC, Plaitakis, A (Hrsg) The Olivopontocerebellar Atrophies. New York; Raven Press 1984: 205-215
  • 16 Probst-Cousin S. Die olivopontozerebelläre Atrophie - ein heterogenes morphologisches Syndrom.  Fortschr Neurol Psychiat. 1997;  65 562-577
  • 17 Bradbury S, Eggleston C. Postural hypotension: a report of three cases.  Am Heart J. 1925;  1 73-86
  • 18 Quinn N. Multiple system atrophy - the nature of the beast.  J Neurol Neurosurg Psychiat Spec Suppl. 1989;  52 78-89
  • 19 Shy G M, Drager G A. A neurological syndrome associated with orthostatic hypotension: a clinical-pathological study.  Arch Neurol. 1960;  2 511-527
  • 20 Adams R D, Van Bogaert L, Vander Eecken H. Striato-nigral Degeneration.  J Neuropathol Exp Neurol. 1964;  23 584-608
  • 21 Adams R D, Salam-Adams M. Striatonigral degeneration. In: Vinken, PJ, Bruyn, GW, Klawans, HL (Hrsg) Handbook of Clinical Neurology. Amsterdam; Elsevier Science Publ. 1986 Vol. 5 (49): 205-259
  • 22 Quinn N. Multiple system atrophy. In: Marsden, CD, Fahn, S (Hrsg) Movement disorders. London; Butterworths 1994: 262-281
  • 23 Lantos P L. The definition of multiple system atrophy: a review of recent developments.  J Neuropathol Exp Neurol. 1998;  57 1099-1111
  • 24 Gilman S, Low P, Quinn N, Albanese A, Ben-Shlomo Y, Fowler C, Kaufmann H, Klockgether T, Lang A, Lantos P, Litvan I, Mathias C, Oliver E, Robertson D, Schatz I, Wenning G. Consensus statement on the diagnosis of multiple system atrophy.  Clin Auton Res. 1998;  8 359-362
  • 25 Bower J H, Maraganore D M, McDonnel S K, Rocca W A. Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990.  Neurology. 1997;  49 1284-1288
  • 26 Trenkwalder C, Schwarz J, Gebhard J, Ruland D, Trenkwalder P, Hense H W, Oertel W H. Starnberg trial on epidemiology of parkinsonism and hypertension in the elderly.  Arch Neurol. 1995;  52 1017-1022
  • 27 Wenning G K, Ben Shlomo Y, Magalhaes M, Daniel S E, Quinn N P. Clinical features and natural history of multiple system atrophy. An analysis of 100 cases.  Brain. 1994;  117 835-845
  • 28 Wenning G K, Tison F, Ben Shlomo Y, Daniel S E, Quinn N P. Multiple system atrophy: A review of 203 pathologically proven cases.  Mov Disord. 1997;  12 133-147
  • 29 Ben Shlomo Y, Wenning G K, Tison F, Quinn N P. Survival of patients with pathologically proven multiple system atrophy: a metaanalysis.  Neurology. 1997;  48 384-393
  • 30 Klockgether T, Lüdtke R, Kramer B, Abele M, Bürk K, Schols L, Riess O, Laccone F, Boesch S, Lopes-Cendes I, Brice A, Inzelberg R, Zilber N, Dichgans J. The natural history of degenerative ataxia: A retrospective study in 466 patients.  Brain. 1998;  121 589-600
  • 31 Caplan L R. Clinical Features of Sporadic Olivopontocerebellar Atrophy. In: Duvoisin, RC, Plaitakis, A (Hrsg) The Olivopontocerebellar Atrophies. New York; Raven Press 1984: 217-224
  • 32 Hughes R G, Gibbin K P, Lowe J. Vocal fold abductor paralysis as a solitary and fatal manifestation of multiple system atrophy.  J Laryngol Otol. 1998;  112 177-178
  • 33 Litvan I, Goetz C G, Jankovic J, Wenning G K, Booth V, Bartko J J, McKee A, Jellinger K, Lai E C, Brandel J P, Verny M, Chaudhuri K R, Pearce R K, Agid Y. What is the accuracy of the clinical diagnosis of multiple system atrophy? A clinicopathologic study.  Arch Neurol. 1997;  54 937-944
  • 34 Litvan I, Booth V, Wenning G K, Bartko J J, Goetz C G, McKee A, Jankovic J, Jellinger K, Lai E C, Brandel J P, Verny M, Chaudhuri K R, Pearce R K, Agid Y. Retrospective application of a set of clinical diagnostic criteria for the diagnosis of multiple system atrophy.  J Neural Transm. 1998;  105 217-227
  • 35 Parati E A, Fetoni V, Geminiani G C, Soliveri P, Giovannini P, Testa D, Genitrini S, Caraceni T, Girotti F. Response to L-DOPA in multiple system atrophy.  Clin Neuropharmacol. 1993;  16 139-144
  • 36 Klockgether T, Oertel W H. Parkinson-Syndrome. In: Brandt, T, Dichgans, J, Diener, HC (Hrsg) Therapie und Verlauf neurologischer Erkrankungen. Stuttgart, Berlin, Köln; Kohlhammer 1998: 847-880
  • 37 Klockgether T, Dichgans J. Erbliche und nicht-erbliche Ataxien. In: Brandt, T, Dichgans, J, Diener, HC (Hrsg) Therapie und Verlauf neurologischer Erkrankungen. Stuttgart, Berlin, Köln; Kohlhammer 1998: 823-829
  • 38 Timmann D. Vegetative Störungen. In: Brandt, T, Dichgans, J, Diener, HC (Hrsg) Therapie und Verlauf neurologischer Erkrankungen. Stuttgart, Berlin, Köln; Kohlhammer 1998: 1216-1244
  • 39 Jordan J, Shannon J R, Biaggion I, Norman R, Black B K, Robertson D. Contrasting actions of pressor agents in severe autonomic failure.  Am J Med. 1998;  105 116-124
  • 40 Chandiramani V A, Palace J, Fowler C J. How to recognize patients with parkinsonism who should not have urological surgery.  Br J Urol. 1997;  80 100-104
  • 41 Fowler C. Treatment of urogenital symptoms in multiple system atrophy.  Mov Disord. 1997;  12 827
  • 42 Weller M. Neurogene Störungen von Blasen-, Darm- und Sexualfunktion. In: Brandt, T, Dichgans, J, Diener, HC (Hrsg) Therapie und Verlauf neurologischer Erkrankungen. Stuttgart, Berlin, Köln; Kohlhammer 1998: 1245-1261
  • 43 Chou H, Ogawa N, Asanuma M, Hirata H, Mori A. Dopamine deficiency in the weaver mutant mouse: an animal model of olivopontocerebellar atrophy.  Res Com Chem Pathol Pharmacol. 1991;  74 117-120
  • 44 Deutch A, Rosin D, Goldstein M, Roth R. 3-Acetylpyridine-induced degeneration of the nigrostriatal dopamine system: An animal model of olivopontocerebellar atrophy-associated parkinsonism.  Exp Neurol. 1989;  105 1-9
  • 45 Nakao N, Brundin P. Effects of alpha-phenyl-tert-butyl nitrone on neuronal survival and motor function following intrastriatal injections of quinoline or 3-nitropropionic acid.  Neuroscience. 1997;  76 749-761
  • 46 Wenning G K, Granata R, Laboyrie P M, Quinn N P, Jenner P, Marsden C D. Reversal of behavioural abnormalities by fetal allografts in a novel rat model of striatonigral degeneration.  Mov Disord. 1996;  11 522-532
  • 47 Klein C, Brown R, Wenning G, Quinn N. The “cold hands sign” in multiple system atrophy.  Mov Disord. 1997;  12 514-518
  • 48 Kimber J A, Watson L, Mathias C J. Distinction of idiopathic Parkinson's disease from multiple-system atrophy by stimulation of growth-hormone release with clonidine.  Lancet. 1997;  349 1877-1881
  • 49 Ravits J, Hallett M, Nilsson J, Polinsky R, Dambrosia J. Electrophysiological tests of autonomic function in patients with idiopathic autonomic failure syndromes.  Muscle Nerve. 1996;  19 758-763
  • 50 Stocchi F, Carbone A, Inghilleri M, Monge A, Ruggieri S, Beradelli A, Manfredi M. Urodynamic and neurophysiological evaluation in Parkinson's disease and multiple system atrophy.  J Neurol Neurosurg Psychiatry. 1997;  62 507-511
  • 51 Palace J, Chaniramani V A, Fowler C J. Value of sphincter electromyography in the diagnosis of multiple system atrophy.  Muscle Nerve. 1997;  20 1396-1403
  • 52 Pramstaller P P, Wenning G K, Smith S JM, Beck R O, Quinn N P, Fowler C J. Nerve conduction studies, skeletal muscle EMG, and sphincter EMG in multiple system atrophy.  J Neurol Neurosurg Psychiat. 1995;  458 618-621
  • 53 Abbruzzese G, Marchese R, Trompetto C. Sensory and motor evoked potentials in multiple system atrophy: a comparative study with Parkinson's disease.  Mov Disord. 1997;  12 315-321
  • 54 Delalande I, Hache J C, Forzy G, Bughin M, Benhadjali J, Destee A. Do visual-evoked potentials and spatiotemporal contrast sensitivity help to distinguish idiopathic Parkinson's disease and multiple system atrophy.  Mov Disord. 1998;  13 446-452
  • 55 Klockgether T, Schulz J B, Bürk K, Abele M, Wedekind K, Welte D, Luft A R, Skalej M. Magnetic resonance imaging volumetry in multiple system atrophy.  Mov Disord. 1997;  12 825
  • 56 Savoiardo M, Strada L, Girotti F, Zimmermann R, Grisoli M, Testa D, Petrillo R. Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy.  Radiology. 1990;  174 693-696
  • 57 Schulz J B, Klockgether T, Petersen D, Jauch M, Müller-Schauenburg W, Spieker S, Voigt K, Dichgans J. Multiple system atrophy: Natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT.  J Neurol Neurosurg Psychiatry. 1994;  57 1047-1056
  • 58 Lang A E, Curran T, Provias J, Bergeron C. Striatonigral degeneration: iron deposition in putamen correlates with the slit-like void signal of magnetic resonance imaging.  Can J Neurol Sci. 1994;  21 311-318
  • 59 Lu X, Chen J, Wang L, Liang Y, Gui Q. Correlative studies of MR findings with neuropathology in Shy-Drager syndrome and striatonigral degeneration.  Chin Med J Engl. 1997;  110 628-631
  • 60 Martin W R, Roberts T E, Ye F Q, Allen P S. Increased basal ganglia iron in striatonigral degeneration: in vivo estimation with magnetic resonance.  Can J Neurol Sci. 1998;  25 44-47
  • 61 Schwarz J, Weis S, Kraft E, Tatsch K, Bandmann O, Mehraein P, Vogl T, Oertel W H. Signal changes on MRI and increases in reactive microgliosis, astrogliosis, and iron in the putamen of two patients with multiple system atrophy.  J Neurol Neurosurg Psychiatry. 1996;  60 98-101
  • 62 Schrag A, Kingsley D, Phatouros C, Mathias C J, Lees A J, Daniel S E, Quinn N P. Clinical usefullness of magnetic resonance imaging in multiple system atrophy.  J Neurol Neurosurg Psychiatry. 1998;  65 65-71
  • 63 Federico F, Simone I L, Lucivero V, Iliceto G, De Mari M, Giannini P, Mezzapesa D M, Tarantino A, Lamberti P. Proton magnetic resonance spectroscopy in Parkinson's disease and atypical parkinson disorders.  Mov Disord. 1997;  12 903-909
  • 64 Kuwert T, Bartenstein P, Grünwald F, Herholz K, Larisch R, Sabri O, Biersack H J, Moser E, Müller-Gärtner H W, Schober O, Schwaiger M, Büll U, Heiss W D. Klinische Wertigkeit der Positronen-Emissions-Tomographie in der Neuromedizin.  Nervenarzt. 1998;  69 1045-1060
  • 65 Antonini A, Leenders K L, Vontobel P, Maguire R P, Missimer J, Psylla M, Gunther I. Complementary PET studies of striatal neuronal function in the differential diagnosis between multiple system atrophy and Parkinson's disease.  Brain. 1997;  120 2187-2195
  • 66 DeVolder A G, Francart J, Laterre C, Dooms G, Bol A, Michel C, Goffinet A M. Decreased glucose utilization in the striatum and frontal lobe in probable striatonigral degeneration.  Ann Neurol. 1989;  26 239-247
  • 67 Gilman S, Markel D, Koeppe R, Junck L, Kluin K, Gebarski S, Hichwa R. Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography.  Ann Neurol. 1988;  23 223-230
  • 68 Otsuka M, Kuwabara Y, Ichiya Y, Hosokawa S, Sasaki M, Yoshida T, Fukumura T, Kato M, Masuda K. Differentiating between multiple system atrophy and Parkinson's disease by positron emission tomography with 18F-dopa and 18F-FDG.  Ann Nucl Med. 1997;  11 251-257
  • 69 Perani D, Bressi S, Testa D, Grassi F, Cortelli P, Gentrini S, Savoiardo M, Caraceni T, Fazio F. Clinical/metabolic correlations in multiple system atrophy. A fludeoxyglucose F 18 positron emission tomographic study.  Arch Neurol. 1995;  52 179-185
  • 70 Gray F, Vincent D, Hauw J J. Quantitative study of lateral horn cells in 15 cases of multiple system atrophy.  Acta Neuropathol. 1988;  75 513-518
  • 71 Schwarz J, Tatsch K, Gasser T, Arnold G, Pogarell O, Kunig G, Oertel W H. 123I-IBZM binding compared with long-term clinical follow up in patients with de novo parkinsonism.  Mov Disord. 1998;  13 16-19
  • 72 Schwarz J, Tatsch K, Arnold G, Gasser T, Trenkwalder C, Kirsch C M, Oertel W H. 123I-Iodobenzamide-SPECT predicts dopaminergic responsiveness in patients with de novo parkinsonism.  Neurology. 1992;  42 556-561
  • 73 Yoshita M. Differentiation of idiopathic Parkinson's disease from striatonigral degeneration and progressive supranuclear palsy using iodine-123-meta-iodobenzylguanidine myocardial scintigraphy.  J Neurol Sci. 1998;  155 60-67
  • 74 Lowe J, Lennox F, Leigh P N. Disorders of movement and system degenerations. In: Graham, DI, Lantos, PL (Hrsg) Greenfield's Neuropathology. 6th ed. London; Arnold 1997: 281-366
  • 75 Kume A, Takahashi A, Hashizume Y. Neuronal cell loss of the striatonigral system in multiple system atrophy.  J Neurol Sci. 1993;  117 33-40
  • 76 Wenning G K, Ben-Shlomo Y, Magalhaes M, Daniel S E, Quinn N P. Clinicopathological study of 35 cases of multiple system atrophy.  J Neurol Neurosurg Psychiatry. 1995;  58 160-166
  • 77 Spargo E, Papp M I, Lantos P L. Decrease in neuronal density in the cerebral cortex in multiple system atrophy.  Eur J Neurol. 1996;  3 450-456
  • 78 Benarroch E E, Smithson I L, Low P A, Parisi J E. Depletion of catecholaminergic neurons of the rostral ventrolateral medulla in multiple system atrophy with autonomic failure.  Ann Neurol. 1998;  43 156-163
  • 79 Kato S, Oda M, Hayashi H, Shimizu T, Hayashi M, Kanata A, Tanabe H. Decrease of medullary catecholaminergic neurons in multiple system atrophy and Parkinson's disease and their preservation in amyotrophic lateral sclerosis.  J Neurol Sci. 1995;  132 216-221
  • 80 Nakamura S, Ohnishi K, Nishimura M, Suenaga T, Akiguchi I, Kimura J, Kimura T. Large neurons in the tuberomammillary nucleus in patients with Parkinson's disease and multiple system atrophy.  Neurology. 1996;  46 1693-1696
  • 81 Noda K, Katayama S, Watanabe C, Yamamura Y, Nakamura S. Decrease of neurons in the medullary arcuate nucleus of multiple system atrophy: Quantitative comparison with Parkinson's disease and amyotrophic lateral sclerosis.  J Neurol Sci. 1997;  151 89-91
  • 82 Ozawa T, Oyanagi K, Tanaka H, Horikawa Y, Takahashi H, Morita T, Tsuji S. Suprachiasmatic nucleus in a patient with multiple system atrophy with abnormal circadian rhythm of arginine-vasopressin secretion into plasma.  J Neurol Sci. 1998;  154 116-121
  • 83 Terao S, Sobue G, Hashizume Y, Mitsuma T, Takahashi A. Disease specific pattern of neuronal cell loss in the ventral horn in amyotrophic lateral sclerosis, multiple system atrophy and X-linked bulbospinal neuronopathy, with special reference to loss of small neurons in the intermediate zone.  J Neurol. 1994;  241 196-203
  • 84 Kume A, Takahashi A, Hashizume Y, Asai J. A histometrical and comparative study on Purkinje cell loss and olivary nucleus cell loss in multiple system atrophy.  J Neurol Sci. 1991;  101 178-186
  • 85 Tsuchiya K, Watabiki S, Sano M, Iobe H, Shiotsu H, Taki K, Hashimoto K. Distribution of cortical lesions in multiple system atrophy: a topographic neuropathological study of three autopsy cases in Japan.  J Neurol Sci. 1998;  155 80-85
  • 86 Holmberg B, Rosengren L, Karlsson J J, Johnels B. Increased cerebrospinal fluid levels of neurofilament protein in progressive supranuclear palsy and multiple system atrophy compared with Parkinson's disease.  Mov Disord. 1998;  13 70-77
  • 87 Matsuo A, Akiguchi I, Lee G C, McGeer E G, McGeer P L, Kimura J. Myelin degeneration in multiple system atrophy detected by unique antibodies.  Am J Pathol. 1998;  153 735-744
  • 88 Castellani R. Multiple system atrophy. Clues from inclusions.  Am J Pathol. 1998;  153 671-676
  • 89 Kanda T, Tsukagoshi H, Oda M, Miyamoto K, Tanabe H. Changes of unmyelinated nerve fibers in sural nerve in amyotrophic lateral sclerosis, Parkinson's disease and multiple system atrophy.  Acta Neuropathol. 1996;  91 145-154
  • 90 Blin O, Desnuelle C, Rascol O, Borg M, Peyro Saint Paul H, Azulay J P, Bille F, Figarella D, Coulom F, Pellissier J F, Montastruc J L, Chatel M, Serratrice G. Mitochondrial respiratory failure in skeletal muscle from patients with Parkinson's disease and multiple system atrophy.  J Neurol Sci. 1994;  125 95-101
  • 91 Costa C, Duyckaerts C, Cervera P, Hauw J. Les inclusions oligodendrogliales, un marqueur des atrophies multisystematisees.  Rev Neurol Paris. 1992;  148 274-280
  • 92 Horoupian D S, Dickson D. Striatonigral Degeneration, olivopontocerebellar atrophy and “atypical” Pick disease.  Acta Neuropathol. 1991;  81 287-295
  • 93 Horoupian D S. Oligodendroglial and neuronal cytoplasmic inclusions in multisystem atrophy.  Progr Brain Res. 1992;  94 423-428
  • 94 Kato S, Nakamura H, Hirano A, Ito H, Llena J, Yen S. Argyrophilic ubiquitinated cytoplasmic inclusions of Leu-7-positive glial cells in olivopontocerebellar atrophy.  Acta Neuropathol. 1991;  82 488-493
  • 95 Kobayashi K, Miyazu K, Katsukawa K, Fukutani Y, Mukai M, Nakamura I, Yamaguchi N, Matsubara R, Isaki K. Cytoskeletal protein abnormalities in patients with olivopontocerebellar atrophy - an immunocytochemical and Gallyas silver impregnation study.  Neuropathol Appl Neurobiol. 1992;  18 237-249
  • 96 Mochizuki A, Mizusawa H, Ohkoshi N, Yoshizawa K, Komatzuzaki Y, Inoue K, Kanazawa I. Argentophilic intracytoplasmic inclusions in multiple system atrophy.  J Neurol. 1992;  239 311-316
  • 97 Nakazato Y, Yamazaki H, Hirato J, Ishida Y, Yamaguchi H. Oligodendroglial microtubular tangles in olivopontocerebellar atrophy.  J Neuropathol Exp Neurol. 1990;  49 521-530
  • 98 Papp M I, Lantos P L. Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy.  J Neurol Sci. 1992;  107 172-182
  • 99 Probst-Cousin S, Bergmann M, Kuchelmeister K, Schröder R, Schmid K W. Ubiquitin-positive inclusions in different types of multiple system atrophy: Distribution and specificity.  Pathol Res Pract. 1996;  192 453-461
  • 100 Wenning G, Wagner S, Daniel S, Quinn N. Multiple system atrophy: sporadic or familial.  Lancet. 1993;  342 681
  • 101 Costa C, Duyckaerts C. Oligodendroglial and neuronal inclusions in multiple system atrophy.  Curr Opin Neurol. 1993;  6 865-871
  • 102 Lantos P L, Papp M I. Cellular pathology of multiple system atrophy: a review.  J Neurol Neurosurg Psychiatry. 1994;  57 129-133
  • 103 Wenning G, Quinn N, Magalhaes M, Mathias C, Daniel S. “Minimal change” multiple system atrophy.  Mov Dis. 1994;  9 161-166
  • 104 Arai N, Nishimura M, Oda M, Morimatsu Y, Ohe R, Nagatomo H. Immunohistochemical expression of microtubule-associated protein 5 (MAP5) in glial cells in multiple system atrophy.  J Neurol Sci. 1992;  109 102-106
  • 105 Papp M I, Lantos P L. The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology.  Brain. 1994;  117 235-243
  • 106 Inoue M, Yagishita S, Ryo M, Hasegawa K, Amano N, Matsushita M. The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems.  Acta Neuropathol. 1997;  93 585-591
  • 107 Cairns N J, Atkinson P F, Hanger D P, Anderton B H, Daniel S E, Lantos P L. Tau protein in the glial cytoplasmic inclusions of multiple system atrophy can be distinguished from abnormal tau in Alzheimer's disease.  Neurosci Lett. 1997;  230 49-52
  • 108 Cairns N J, Mackay D, Daniel S E, Lantos P L. Tau-pathology of oligodendroglial inclusions in multiple system atrophy, progressive supranuclear palsy and corticobasal degeneration.  Neuropathol Appl Neurobiol. 1998;  24 131
  • 109 Takeda A, Mallory M, Sundsmo M, Honer W, Hansen L, Masliah E. Abnormal accumulation of NACP/a-synuclein in neurodegenerative disorders.  Am J Pathol. 1998;  152 367-372
  • 110 Takeda A, Arai N, Komori T, Iseki E, Kato S, Oda M. Tau immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy.  Neurosci Lett. 1997;  134 63-66
  • 111 Furiya Y, Sahara N, Mori H. Okadaic acid enhances abnormal phosphorylation on tau proteins.  Neurosci Lett. 1993;  156 67-69
  • 112 Kosik K. The molecular and cellular biology of tau.  Brain Pathol. 1993;  3 39-43
  • 113 Brandt R, Lee G. The balance between tau protein's microtubule growth and nucleation activities: implications for the formation of axonal microtubules.  J Neurochem. 1993;  61 997-1005
  • 114 Mattson M, Lovell M, Ehmann W, Markesbery W. Comparison of the effects of elevated intracellular aluminium and calcium levels on neuronal survival and tau immunoreactivity.  Brain Res. 1993;  602 21-31
  • 115 Kunze D, Röstow B. Pathobiochemical aspects of cytoskeleton components.  Eur J Clin Chem Clin Biochem. 1993;  31 477-489
  • 116 Nakamura S, Kawamoto Y, Nakano S, Akiguchi I, Kimura J. Cyclin-dependent kinase 5 and mitogen-activated protein kinase in glial cytoplasmic inclusions in multiple system atrophy.  J Neuropathol Exp Neurol. 1998;  57 690-698
  • 117 Gai W P, Power J HT, Blumbergs P C, Blessing W W. Multiple system atrophy: A new α-synuclein disease.  Lancet. 1998;  352 547-548
  • 118 Mezey E, Dehejia A, Harta G, Papp M I, Polymeropoulos M, Brownstein M J. Alpha synuclein in neurodegenerative disorders: Murderer of accomplice.  Nature Medicine. 1998;  4 755-757
  • 119 Spillantini M G, Crowther R A, Jakes R, Cairns N J, Lantos P L, Goedert M. Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies.  Neurosci Lett. 1998;  251 205-208
  • 120 Wakabayashi K, Yoshimoto M, Tsuji S, Takahashi H. α-Synuclein immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy.  Neurosci Lett. 1998;  249 180-182
  • 121 Spillantini M G, Schmidt M L, Lee V MY, Trojanowski J Q, Jakes R, Goedert M. Alpha-synuclein in Lewy bodies.  Nature. 1997;  388 839-840
  • 122 Wakabayashi K, Hayashi S, Kakita A, Yamada M, Toyoshima Y, Yoshimoto M, Takahashi H. Accumulation of alpha-synuclein/NACP is a cytopathological feature common to Lewy body disease and multiple system atrophy.  Acta Neuropathol. 1998;  96 445-452
  • 123 Tamaoka A, Mizusawa H, Mori H, Shoji S. Ubiquitinated α B-crystallin in glial cytoplasmic inclusions from the brain of a patient with multiple system atrophy.  J Neurol Sci. 1995;  129 192-198
  • 124 Ciechanover A. The Ubiquitin-mediated proteolytic pathway.  Brain Pathol. 1993;  3 67-75
  • 125 Lowe J, Mayer R J, Landon M. Ubiquitin in neurodegenerative diseases.  Brain Pathol. 1993;  3 55-65
  • 126 Mayer R J, Lowe J, McDermott H, Laszlo L. The role of protein ubiquitination in neurodegenerative disease.  Acta Biol Hung. 1991;  41 21-26
  • 127 Mayer R J, Doherty F J. Ubiquitin.  Ess Biochem. 1992;  27 37-48
  • 128 Mayer R J, Laszlo L, Middleton A, Landon M, Hope J, Lowe J. Ubiquitin, lysosomes and neurodegenerative diseases.  Biochem Soc Trans. 1992;  20 645-648
  • 129 Manetto V, Perry G, Tabaton M, Mulvihill P, Fried V, Smith H, Gambetti P, Autilio-Gambetti L. Ubiquitin is associated with abnormal cytoplasmic filaments characteristic of neurodegenerative diseases.  Proc Nat Acad Sci USA. 1988;  85 4501-4505
  • 130 Abe H, Yagishita S, Amano N, Iwabuchi K, Hasegawa K, Kowa K. Argyrophilic glial intracytoplasmic inclusions in multiple system atrophy: an immunocytochemical and ultrastructural study.  Acta Neuropathol. 1992;  84 273-277
  • 131 Murayama S, Arima K, Nakazato Y, Satoh J, Oda M, Inose T. Immunocytochemical and ultrastructural studies of neuronal and oligodendroglial cytoplasmic inclusions in multiple system atrophy. 2 Oligodendroglial cytoplasmic inclusions.  Acta Neuropathol. 1992;  84 32-38
  • 132 Kato S, Nakamura H. Cytoplasmic argyrophilic inclusions in neurons of pontine nuclei in patients with olivopontocerebellar atrophy: immunohistochemical and ultrastructural studies.  Acta Neuropathol. 1990;  79 584-594
  • 133 Kato S, Ohama E. Immunohistochemical and ultrastructural comparison between neuronal and oligodendroglial inclusions in olivopontocerebellar atrophy.  Neuropathology. 1993;  13 1-6
  • 134 Sugiura K, Hashizume Y, Kume A, Takahashi A. Distribution of neuronal cytoplasmic inclusions in multiple system atrophy.  Nagoya J Med Sci. 1995;  58 117-126
  • 135 Arima K, Ueda K, Sunohara N, Arakawa K, Hirai S, Nakamura M, Tonozuka-Uehara H, Kawai M. NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy.  Acta Neuropathol. 1998;  96 439-444
  • 136 Bandmann O, Sweeney M G, Daniel S E, Wenning G K, Quinn N P, Marsden C D, Wood N W. Multiple system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.  Neurology. 1997;  49 1598-1604
  • 137 Cairns N J, Atkinson P F, Kovacs T, Lees A J, Daniel S E, Lantos P L. Apolipoprotein E e4 allele frequency in patients with multiple system atrophy.  Neurosci Lett. 1997;  221 161-164
  • 138 Hashida H, Goto J, Zhao N, Takahashi N, Hirai M, Kanazawa I, Sakahi Y. Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA).  Genomics. 1998;  54 50-58
  • 139 Nee L E, Gomez M R, Dambrosia J, Bale S, Eldridge R, Polinsky R J. Environmental-occupational risk factors and familial associations in multiple system atrophy: a preliminary investigation.  Clin Auton Res. 1991;  1 9-13
  • 140 Dexter D T, Jenner P, Schapira A HV, Marsden C D. Alterations in level of iron, ferritin, and other trace metals in neurodegenerative diseases affecting the basal ganglia.  Ann Neurol. 1992;  32 S94-S100
  • 141 Kato S, Meshitsuka S, Ohama E, Tanaka J, Llena J F, Hirano A. Increased iron content in the putamen of patients with striatonigral degeneration.  Acta Neuropathol. 1992;  84 328-330
  • 142 Kageyama Y. An autopsy case of mitochondrial encephalomyopathy with prominent degeneration in olivopontocerebellar system.  Acta Neuropathol. 1991;  83 99-103
  • 143 van Bogaert L, Bertrand I. Une Variété D'Atrophie Olivo-Pontine a Èvolution subaigue avec Troubles démentiels.  Rev Neurol. 1929;  2 165-178
  • 144 Scherer H J. Beiträge zur pathologischen Anatomie des Kleinhirns: III. Die Marksklerosen.  Zeitschr ges Neurol Psychiat. 1933;  145 375-396
  • 145 Oppenheimer D R, Esiri M M. Diseases of the basal ganglia, cerebellum and motor neurons. In: Adams, JH, Duchen, LW (Hrsg) Greenfield's Neuropathology 5. ed. London; Edward Arnold 1992: 988-1045
  • 146 Lantos P L. Multiple system atrophy.  Brain Pathol. 1997;  7 1293-1297
  • 147 Kaplan M R, Meyer-Franke A, Lambert S, Bennett V, Duncan I D, Levinson S R, Barres B A. Induction of sodium channel clustering by oligodendrocytes.  Nature. 1997;  386 724-728
  • 148 Trapp B D, Peterson J, Ransohoff R M, Rudick R, Mork S, Bo L. Axonal transection in the lesions of multiple sclerosis.  N Engl J Med. 1998;  338 278-285
  • 149 Bleichenki P V, Celio M R. Relationship between oligodendrocytes and axons.  Neuroreport. 1997;  8 3965-3967
  • 150 Ludwin S K. The pathobiology of oligodendrocytes.  J Neuropathol Exp Neurol. 1997;  56 111-124
  • 151 Probst-Cousin S, Rickert C H, Schmid K W, Gullotta F. Cell death mechanisms in multiple system atrophy.  J Neuropathol Exp Neurol. 1998;  57 814-821
  • 152 de la Monte S M, Sohn Y K, Ganju N, Wands J R. p53- and CD95-associated apoptosis in neurodegenerative diseases.  Lab Invest. 1998;  78 401-411

Dr. Stefan Probst-Cousin

Zentrum für Neuromuskuläre Erkrankungen

Neurologische Klinik und Poliklinik

der Friedrich-Alexander-Universität Erlangen-Nürnberg

Schwabachanlage 6

91054 Erlangen

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