Criteria for the diagnosis of corticobasal degeneration
- PMID: 23359374
- PMCID: PMC3590050
- DOI: 10.1212/WNL.0b013e31827f0fd1
Criteria for the diagnosis of corticobasal degeneration
Abstract
Current criteria for the clinical diagnosis of pathologically confirmed corticobasal degeneration (CBD) no longer reflect the expanding understanding of this disease and its clinicopathologic correlations. An international consortium of behavioral neurology, neuropsychology, and movement disorders specialists developed new criteria based on consensus and a systematic literature review. Clinical diagnoses (early or late) were identified for 267 nonoverlapping pathologically confirmed CBD cases from published reports and brain banks. Combined with consensus, 4 CBD phenotypes emerged: corticobasal syndrome (CBS), frontal behavioral-spatial syndrome (FBS), nonfluent/agrammatic variant of primary progressive aphasia (naPPA), and progressive supranuclear palsy syndrome (PSPS). Clinical features of CBD cases were extracted from descriptions of 209 brain bank and published patients, providing a comprehensive description of CBD and correcting common misconceptions. Clinical CBD phenotypes and features were combined to create 2 sets of criteria: more specific clinical research criteria for probable CBD and broader criteria for possible CBD that are more inclusive but have a higher chance to detect other tau-based pathologies. Probable CBD criteria require insidious onset and gradual progression for at least 1 year, age at onset ≥ 50 years, no similar family history or known tau mutations, and a clinical phenotype of probable CBS or either FBS or naPPA with at least 1 CBS feature. The possible CBD category uses similar criteria but has no restrictions on age or family history, allows tau mutations, permits less rigorous phenotype fulfillment, and includes a PSPS phenotype. Future validation and refinement of the proposed criteria are needed.
Similar articles
-
[Criteria for the diagnosis of corticobasal degeneration].Brain Nerve. 2015 Apr;67(4):513-23. doi: 10.11477/mf.1416200168. Brain Nerve. 2015. PMID: 25846600 Review. Japanese.
-
[Diagnoses of corticobasal syndrome and corticobasal degeneration].Rinsho Shinkeigaku. 2016;56(3):149-57. doi: 10.5692/clinicalneurol.cn-000841. Epub 2016 Mar 13. Rinsho Shinkeigaku. 2016. PMID: 26876110 Review. Japanese.
-
Features of Patients With Nonfluent/Agrammatic Primary Progressive Aphasia With Underlying Progressive Supranuclear Palsy Pathology or Corticobasal Degeneration.JAMA Neurol. 2016 Jun 1;73(6):733-42. doi: 10.1001/jamaneurol.2016.0412. JAMA Neurol. 2016. PMID: 27111692 Free PMC article.
-
Validation of the new consensus criteria for the diagnosis of corticobasal degeneration.J Neurol Neurosurg Psychiatry. 2014 Aug;85(8):925-9. doi: 10.1136/jnnp-2013-307035. Epub 2014 Feb 12. J Neurol Neurosurg Psychiatry. 2014. PMID: 24521567 Free PMC article.
-
Clinicopathological correlations in corticobasal degeneration.Ann Neurol. 2011 Aug;70(2):327-40. doi: 10.1002/ana.22424. Ann Neurol. 2011. PMID: 21823158 Free PMC article.
Cited by
-
Current Perspectives on Olfactory Loss in Atypical Parkinsonisms-A Review Article.Biomedicines. 2024 Oct 4;12(10):2257. doi: 10.3390/biomedicines12102257. Biomedicines. 2024. PMID: 39457570 Free PMC article. Review.
-
APP-Related Corticobasal Syndrome: Expanding the List of Corticobasal Degeneration Look Alikes.Mov Disord Clin Pract. 2020 Aug 29;7(7):849-851. doi: 10.1002/mdc3.13037. eCollection 2020 Oct. Mov Disord Clin Pract. 2020. PMID: 33043082 Free PMC article. No abstract available.
-
Digital Histological Study of Neocortical Grey and White Matter Tau Burden Across Tauopathies.J Neuropathol Exp Neurol. 2022 Nov 16;81(12):953-964. doi: 10.1093/jnen/nlac094. J Neuropathol Exp Neurol. 2022. PMID: 36269086 Free PMC article.
-
Dynamic aphasia as an early sign of corticobasal degeneration: Clinico-radio-pathological correlation.eNeurologicalSci. 2024 Sep 4;37:100526. doi: 10.1016/j.ensci.2024.100526. eCollection 2024 Dec. eNeurologicalSci. 2024. PMID: 39309449 Free PMC article.
-
The clinical diagnosis of Parkinson's disease.Arq Neuropsiquiatr. 2024 Jun;82(6):1-10. doi: 10.1055/s-0043-1777775. Epub 2024 Feb 7. Arq Neuropsiquiatr. 2024. PMID: 38325391 Free PMC article. Review.
References
-
- Rebeiz JJ, Kolodny EH, Richardson EP., Jr Corticodentatonigral degeneration with neuronal achromasia: a progressive disorder in late adult life. Trans Am Neurol Assoc 1967;92:23–26 - PubMed
-
- Gibb WR, Luthert PJ, Marsden CD. Corticobasal degeneration. Brain 1989;112:1171–1192 - PubMed
-
- Dickson DW, Bergeron C, Chin SS, et al. Office of Rare Diseases neuropathologic criteria for corticobasal degeneration. J Neuropathol Exp Neurol 2002;61:935–946 - PubMed
-
- Kumar R, Bergeron C, Pollanen M, Lang AE. Cortical-basal ganglionic degeneration. In: Jankovic J, Tolosa E, eds. Parkinson's Disease & Movement Disorders. Baltimore: Williams & Wilkins; 1998:297–316
-
- Lang AE, Riley DE, Bergeron C. Cortical-basal ganglionic degeneration. In: Calne DB, ed. Neurodegenerative Diseases. Philadelphia: W.B. Saunders; 1994:877–894
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical