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Disorders of the Cerebellum: Ataxia, Dysmetria of Thought, and the Cerebellar Cognitive Affective Syndrome

Jeremy Dan Schmahmann·2004·Journal of Neuropsychiatry

Abstract

Many diseases involve the cerebellum and produce ataxia, which is characterized by incoordination of balance, gait, extremity and eye movements, and dysarthria. Cerebellar lesions do not always manifest with ataxic motor syndromes, however. The cerebellar cognitive affective syndrome (CCAS) includes impairments in executive, visual-spatial, and linguistic abilities, with affective disturbance ranging from emotional blunting and depression, to disinhibition and psychotic features. The cognitive and psychiatric components of the CCAS, together with the ataxic motor disability of cerebellar disorders, are conceptualized within the dysmetria of thought hypothesis. This concept holds that a universal cerebellar transform facilitates automatic modulation of behavior around a homeostatic baseline, and the behavior being modulated is determined by the specificity of anatomic subcircuits, or loops, within the cerebrocerebellar system. Damage to the cerebellar component of the distributed neural circuit subserving sensorimotor, cognitive, and emotional processing disrupts the universal cerebellar transform, leading to the universal cerebellar impairment affecting the lesioned domain. The universal cerebellar impairment manifests as ataxia when the sensorimotor cerebellum is involved and as the CCAS when pathology is in the lateral hemisphere of the posterior cerebellum (involved in cognitive processing) or in the vermis (limbic cerebellum). Cognitive and emotional disorders may accompany cerebellar diseases or be their principal clinical presentation, and this has significance for the diagnosis and management of patients with cerebellar dysfunction.

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Research works printed but not linked: 93

  1. Ferrier D, Turner WA: A record of experiments illustrative of the symptomatology and degenerations following lesions of the cerebellum and its peduncles and related structures in monkeys. Phil Trans R Soc Lond B 1893; 185:719–778 · DOI
  2. Russell JSR: Experimental researches into the functions of the cerebellum. Phil Trans R Soc Lond B 1894; 185:819–861 · DOI
  3. Brown S: On hereditary ataxia, with a series of twenty-one cases. Brain 1892; 15:250–282 · DOI
  4. Marie P: Sur l'hérédo-ataxie cérébelleuse. Semaine méd 1893; 13:444–447
  5. Babinski JFF: De l'asynergie cerebelleuse. Rev Neurol 1899; 7:806–816
  6. Holmes G: The symptoms of acute cerebellar injuries due to gunshot wounds. Brain 1917; 40:461–535 · DOI · Paper page
  7. Zervas NT, Horner FG, Gordy PD: Cerebellar dentatectomy in primates and humans. Trans Am Neurol Assoc 1967; 92:27–30
  8. Margolis RL: The spinocerebellar ataxias: order emerges from chaos. Curr Neurol Neurosci Rep 2002; 2:447–456 · DOI
  9. Dow RS: Some novel concepts of cerebellar physiology. Mt Sinai J Med 1974; 41:103–119
  10. Heath RG: Modulation of emotion with a brain pacemaker: treatment for intractable psychiatric illness. J Nerv Ment Dis 1977; 165:300–317 · DOI · Paper page
  11. Watson PJ: Nonmotor functions of the cerebellum. Psychol Bull 1978; 85:944–967 · DOI · Paper page
  12. Frick RB: The ego and the vestibulocerebellar system. Psychoanal Q 1982; 51:93–122 · DOI
  13. Leiner HC, Leiner AL, Dow RS: Does the cerebellum contribute to mental skills? Behav Neurosci 1986; 100:443–454 · DOI · Paper page
  14. Schmahmann JD, Pandya DN: Anatomical investigation of projections to the basis pontis from posterior parietal association cortices in rhesus monkey. J Comp Neurol 1989; 289:53–73 · DOI · Paper page
  15. Schmahmann JD: An emerging concept: the cerebellar contribution to higher function. Archiv Neurol 1991; 48:1178–1187 · DOI · Paper page
  16. Combettes: Absence complete du cervelet, des pedoncles posterieurs et la protuberance cerebrale chez une jeune fille morte dans sa onzieme année. Bull Soc Anat de Paris 1831; 5:148–157
  17. Heath RG, Franklin DE, Shraberg D: Gross pathology of the cerebellum in patients diagnosed and treated as functional psychiatric disorders. J Nerv Ment Dis 1979; 167:585–592 · DOI · Paper page
  18. Moriguchi I: A study of schizophrenic brains by computerized tomography scans. Folia Psychiatr Neurol Jpn 1981; 35:55–72 · DOI
  19. Lippmann S, Manshadi M, Baldwin H, et al: Cerebellar vermis dimensions on computerized tomographic scans of schizophrenic and bipolar patients. Am J Psychiatry 1982; 139:667–668 · DOI
  20. Dickson DW, Lin W, Liu WK, et al: Multiple system atrophy: a sporadic synucleinopathy. Brain Pathol 1999; 9:721–732 · DOI · Paper page
  21. Landis DMD, Rosenberg RN, Landis SC, et al: Olivopontocerebellar degeneration. Arch Neurol 1974; 31:295–307 · DOI
  22. Kish SJ, El-Awar M, Schut L, et al: Cognitive deficits in olivopontocerebellar atrophy: implications for the cholinergic hypothesis of Alzheimer's dementia. Ann Neurol 1988; 24:200–206 · DOI
  23. Bracke-Tolkmitt R, Linden A, Canavan AGM, et al: The cerebellum contributes to mental skills. Behav Neurosci 1989; 103:442–446 · DOI · Paper page
  24. Botez-Marquard T, Botez MI: Cognitive behavior in heredodegenerative ataxias. Eur Neurol 1993; 33:351–357 · DOI
  25. Grafman J, Litvan I, Massaquoi S, et al: Cognitive planning deficit in patients with cerebellar atrophy. Neurology 1992; 42:1493–1496 · DOI · Paper page
  26. Pascual-Leone A, Grafman J, Clark K, et al: Procedural learning in Parkinson's disease and cerebellar degeneration. Ann Neurol 1993; 34:594–602 · DOI · Paper page
  27. Geschwind DH: Focusing attention on cognitive impairment in spinocerebellar ataxia. Arch Neurol 1999; 56:20–22 · DOI
  28. Burk K, Bosch S, Globas C, et al: Executive dysfunction in spinocerebellar ataxia type 1. Eur Neurol 2001; 46:43–48 · DOI
  29. Gambardella A, Annesi G, Bono F, et al: CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity. J Neurol 1998; 245:647–652 · DOI
  30. Storey E, Forrest SM, Shaw JH, et al: Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunction. Arch Neurol 1999; 56:43–50 · DOI
  31. Zawacki TM, Grace J, Friedman JH, et al: Executive and emotional dysfunction in Machado-Joseph disease. Mov Disord 2002; 17:1004–1010 · DOI
  32. Herman-Bert A, Stevanin G, Netter JC, et al: Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. Am J Hum Genet 2000; 67:229–235 · doi:10.1086/302958
  33. Koide R, Kobayashi S, Shimohata T, et al: A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? Hum Molec Genet 1999; 8:2047–2053 · DOI · Paper page
  34. Nakamura K, Jeong S-Y, Uchihara T, et al: SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum Molec Genet 2001; 10:1441–1448 · DOI · Paper page
  35. Devos D, Schraen-Maschke S, Vuillaume I, et al: Clinical features and genetic analysis of a new form of spinocerebellar ataxia. Neurology 2001; 56:234–238 · DOI
  36. Wollmann T, Barroso J, Monton F, et al: Neuropsychological test performance of patients with Friedreich's ataxia. J Clin Exp Neuropsychol 2002; 24:677–686 · doi:10.1076/jcen.24.5.677.1014
  37. White M, Lalonde R, Botez-Marquard T: Neuropsychologic and neuropsychiatric characteristics of patients with Friedreich's ataxia. Acta Neurol Scand 2000; 102:222–226 · doi:10.1034/j.1600-0404.2000.102004222.x
  38. Silveri MC, Leggio MG, Molinari M: The cerebellum contributes to linguistic production: a case of agrammatic speech following a right cerebellar lesion. Neurology 1994; 44:2047–2050 · DOI · Paper page
  39. Molinari M, Leggio MG, Silveri MC: Verbal fluency and agrammatism. Int Rev Neurobiol 1997; 41:325–339 · DOI
  40. Fiez JA, Petersen SE, Cheney MK, et al: Impaired non-motor learning and error detection associated with cerebellar damage. Brain 1992; 115:155–178 · DOI · Paper page
  41. Courchesne E, Townsend J, Akshoomoff NA, et al: Impairment in shifting attention in autistic and cerebellar patients. Behav Neurosci 1994; 108:848–865 · DOI · Paper page
  42. Sanes JN, Dimitrov B, Hallett M: Motor learning in patients with cerebellar dysfunction. Brain 1990; 113:103–120 · DOI · Paper page
  43. Thach WT, Goodkin HP, Keating JG: The cerebellum and the adaptive coordination of movement. Annu Rev Neurosci 1992; 15:403–442 · DOI · Paper page
  44. Doyon J, Song AW, Karni A, et al: Experience-dependent changes in cerebellar contributions to motor sequence learning. Proc Natl Acad Sci USA 2002; 99:1017–1022 · DOI · Paper page
  45. Solomon PR, Stowe GT, Pendlebury WW: Disrupted eyelid conditioning in a patient with damage to cerebellar afferents. Behav Neurosci 1989; 103:898–902 · DOI
  46. Snider RS: Recent contributions to the anatomy and physiology of the cerebellum. AMA Arch Neurol Psychiatry 1950; 64:196–219 · DOI · Paper page
  47. Zanchetti A, Zoccolini A: Autonomic hypothalamic outbursts elicited by cerebellar stimulation: J Neurophysiol 1954; 17:473–483 · DOI
  48. Martner J: Cerebellar influences on autonomic mechanisms. Acta Physiol Scand Suppl 1975; 425:1–42
  49. Reis DJ, Doba N, Nathan MA: Predatory attack, grooming and consummatory behaviors evoked by electrical stimulation of cat cerebellar nuclei. Science 1973; 182:845–847 · DOI · Paper page
  50. Thompson RF, Bao S, Chen L, et al: Associative learning. Int Rev Neurobiol 1997; 41:151–189 · DOI
  51. Schmahmann JD, Sherman JC: The cerebellar cognitive affective syndrome. Brain 1998; 121:561–579 · DOI · Paper page
  52. Neau JP, Arroyo-Anllo E, Bonnaud V, et al: Neuropsychological disturbances in cerebellar infarcts. Acta Neurol Scand 2000; 102:363–370 · DOI
  53. Levisohn L, Cronin-Golomb A, Schmahmann JD: Neuropsychological consequences of cerebellar tumor resection in children: cerebellar cognitive affective syndrome in a pediatric population. Brain 2000; 123:1041–1050 · DOI · Paper page
  54. Riva D, Giorgi C: The cerebellum contributes to higher function during development: evidence from a series of children surgically treated for posterior fossa tumors. Brain 2000; 123:1051–1061 · DOI · Paper page
  55. Wisoff JH, Epstein FJ: Pseudobulbar palsy after posterior fossa operation in children. Neurosurgery 1984; 15:707–709 · DOI
  56. Kingma A, Mooij JJA, Metemaekers JDM, et al: Transient mutism and speech disorders after posterior fossa surgery in children with brain tumors. Acta Neurochir 1994; 131:74–79 · DOI
  57. Pollack IF, Polinko P, Albright AL, et al: Mutism and pseudobulbar symptoms after resection of posterior fossa tumors in children: Incidence and pathophysiology. Neurosurgery 1995; 37:885–893 · doi:10.1097/00006123-199511000-00006
  58. Glickstein M: Cerebellar agenesis. Brain 1994; 117:1209–1212 · DOI
  59. Gardner RJ, Coleman LT, Mitchell LA, et al: Near-total absence of the cerebellum. Neuropediatrics 2001; 32:62–68 · DOI
  60. Mostofsky SH, Reiss AL, Lockhart P, et al: Decreased cerebellar posterior vermis size in fragile X syndrome: correlation with neurocognitive performance. Neurology 1998; 50:121–130 · DOI · Paper page
  61. Castellanos FX, Giedd JN, Berquin PC, et al: Quantitative brain magnetic resonance imaging in girls with attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 2001; 58:289–295 · DOI · Paper page
  62. Allin M, Matsumoto H, Santhouse AM, et al: Cognitive and motor function and the size of the cerebellum in adolescents born very pre-term. Brain 2001; 124:60–66 · DOI · Paper page
  63. Nicolson RI, Fawcett AJ, Berry EL, et al: Association of abnormal cerebellar activation with motor learning difficulties in dyslexic adults. Lancet 1999; 353:1662–1667 · DOI · Paper page
  64. Nopoulos PC, Ceilley JW, Gailis EA, et al: An MRI study of cerebellar vermis morphology in patients with schizophrenia: evidence in support of the cognitive dysmetria concept. Biol Psychiatry 1999; 46:703–711 · DOI · Paper page
  65. Wassink TH, Andreasen NC, Nopoulos P, et al: Cerebellar morphology as a predictor of symptom and psychosocial outcome in schizophrenia. Biol Psychiatry 1999; 45:41–48 · DOI
  66. Loeber RT, Sherwood AR, Renshaw PF, et al: Differences in cerebellar blood volume in schizophrenia and bipolar disorder. Schizophr Res 1999; 37:81–89 · DOI
  67. Loeber RT, Cintron CMB, Yurgelun-Todd DA: Morphometry of individual cerebellar lobules in schizophrenia. Am J Psychiatry 2001; 158:952–954 · DOI
  68. Ichimiya T, Okubo Y, Suhara T, et al: Reduced volume of the cerebellar vermis in neuroleptic-naive schizophrenia. Biol Psychiatry 2001; 49:20–27 · DOI · Paper page
  69. Volz H, Gaser C, Sauer H: Supporting evidence for the model of cognitive dysmetria in schizophrenia—a structural magnetic resonance imaging study using deformation-based morphometry. Schizophr Res 2000; 46:45–56 · DOI
  70. Staal WG, Hulshoff Pol HE, Schnack HG, et al: Structural brain abnormalities in chronic schizophrenia at the extremes of the outcome spectrum. Am J Psychiatry 2001; 158:1140–1142 · doi:10.1176/appi.ajp.158.7.1140
  71. Levitt JJ, McCarley RW, Nestor PG, et al: Quantitative volumetric MRI study of the cerebellum and vermis in schizophrenia: clinical and cognitive correlates. Am J Psychiatry 1999; 156:1105–1107 · DOI
  72. Deicken RF, Feiwell R, Schuff N, et al: Evidence for altered cerebellar vermis neuronal integrity in schizophrenia. Psychiatry Res 2001; 107:125–134 · DOI
  73. Andreasen NC, O'Leary DS, Flaum M, et al: Hypofrontality in schizophrenia: distributed dysfunctional circuits in neuroleptic-naive patients. Lancet 1997; 349:1730–1734 · DOI · Paper page
  74. Williams RS, Hauser SL, Purpura DP, et al: Autism and mental retardation. Arch Neurol 1980; 37:749–753 · DOI · Paper page
  75. Ritvo ER, Freeman BJ, Scheibel AB, et al: Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC autopsy research report. Am J Psychiatry 1986; 143:862–866 · DOI · Paper page
  76. Kemper TL, Bauman M: Neuropathology of infantile autism. J Neuropathol Exp Neurol 1998; 57:645–652 · DOI · Paper page
  77. Murakami JW, Courchesne E, Press GA, et al: Reduced cerebellar hemisphere size and its relationship to vermal hypoplasia in autism. Arch Neurol 1989; 46:689–694 · DOI · Paper page
  78. Rapin I: Autism in search of a home in the brain. Neurology 1999; 52:902–904 · DOI
  79. Leroi I, O'Hearn E, Marsh L, et al: Psychopathology in patients with degenerative cerebellar diseases: a comparison to Huntington's disease. Am J Psychiatry 2002; 159:1306–1314 · DOI
  80. DelBello MP, Strakowski SM, Zimmerman ME, et al: MRI analysis of the cerebellum in bipolar disorder: a pilot study. Neuropsychopharmacology 1999; 21:63–68 · DOI · Paper page
  81. Parvizi J, Anderson SW, Martin CO, et al: Pathological laughter and crying: a link to the cerebellum. Brain 2001; 124:1708–1719 · DOI · Paper page
  82. Annoni JM, Ptak R, Caldara-Schnetzer AS, et al: Decoupling of autonomic and cognitive emotional reactions after cerebellar stroke. Ann Neurol 2003; 53:654–658 · DOI
  83. Desmond JE, Fiez JA: Neuroimaging studies of the cerebellum: language, learning and memory. Trends Cogn Sci 1998; 2:355–362 · DOI · Paper page
  84. Voogd J, Glickstein M: The anatomy of the cerebellum. Trends Neurosci 1998; 21:370–375 · DOI · Paper page
  85. Haines DE, Dietrichs E: An HRP study of hypothalamo-cerebellar and cerebello-hypothalamic connections in squirrel monkey (Saimiri sciureus). J Comp Neurol 1984; 229:559–575 · DOI
  86. Andrezik JA, Dormer KJ, Foreman RD, et al: Fastigial nucleus projections to the brain stem in beagles: pathways for autonomic regulation. Neuroscience 1984; 11:497–507 · DOI
  87. Heath RG: Fastigial nucleus connections to the septal region in monkey and cat: a demonstration with evoked potentials of a bilateral pathway. Biol Psychiatry 1973; 6:193–196
  88. Schmahmann JD, Pandya DN: The cerebrocerebellar system. Int Rev Neurobiol 1997; 41:31–60 · DOI · Paper page
  89. Schmahmann JD, Pandya DN: Projections to the basis pontis from the superior temporal sulcus and superior temporal region in the rhesus monkey. J Comp Neurol 1991; 308:224–248 · DOI · Paper page
  90. Schmahmann JD, Pandya DN: Course of the fiber pathways to pons from parasensory association areas in the Rhesus monkey. J Comp Neurol 1992; 326:159–179 · DOI
  91. Schmahmann JD, Pandya DN: Prelunate, occipitotemporal, and parahippocampal projections to the basis pontis in rhesus monkey. J Comp Neurol 1993; 337:94–112 · DOI · Paper page
  92. Schmahmann JD: From movement to thought: anatomic substrates of the cerebellar contribution to cognitive processing. Hum Brain Mapp 1996; 4:174–198 · doi:10.1002/(sici)1097-0193(1996)4:3<174::aid-hbm3>3.0.co;2-0
  93. Schmahmann JD: The role of the cerebellum in affect and psychosis. J Neurolinguistics 2000; 13:189–214 · DOI · Paper page

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Metadata

Authors
Schmahmann, J. D.
Venue
Journal of Neuropsychiatry
Published
2004-08
Volume
16
Issue
3
Pages
367-378
ISSN
  • 0895-0172 (ISSN-L)
  • 1545-7222
OpenAlex
W2171876105
Cited by
1,447
References
7
FWCI
22.95
Type
journal article
Language
en
Open access
closed

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Schmahmann, J. D. (2004). Disorders of the Cerebellum: Ataxia, Dysmetria of Thought, and the Cerebellar Cognitive Affective Syndrome. Journal of Neuropsychiatry. https://doi.org/10.1176/appi.neuropsych.16.3.367

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