Skip to main content

Advertisement

Log in

Comprehensive and Methodical: Diagnostic and Management Approaches to Rapidly Progressive Dementia

  • Dementia (J Pillai, Section Editor)
  • Published:
Current Treatment Options in Neurology Aims and scope Submit manuscript

Abstract

Purpose of review The sudden emergence of a change in cognitive abilities or behavior is an important symptom that warrants medical evaluation and may represent the early stages of a rapidly progressive dementia (RPD). To correctly ascertain the cause of RPD in a given patient, the clinician must be methodical and knowledgeable about the range of potential causes and must move forward with supportive treatment, and in some cases empiric treatment, based on clinical features alone.

Recent findings Significant advances in prion disease biomarkers, the molecular features of rapidly progressive Alzheimer’s disease, and new detection of autoimmune limbic encephalitis disease entities have caused a shift in the diagnostic and treatment framework of RPD. Additionally, in the past decade, emerging retrospective data have led to suggested treatments in autoimmune encephalitis that, if instituted early, can protect patients against residual deficits and disease relapse.

Summary Here, we provide an integrative clinical and diagnostic treatment approach that is applicable to the various forms of RPD. We have highlighted the clinical features of selected types of RPD that have experienced advances in the last 10–15 years.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References and Recommended Reading

Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance

  1. Shrestha R, Wuerz T, Appleby BS. Rapidly progressive young-onset dementias: neuropsychiatric aspects. Psychiatr Clin North Am. 2015;38(2):221–32.

    Article  PubMed  Google Scholar 

  2. Schmidt C, Wolff M, Wietz M, Bartlau T, Korth C, Zerr I. Rapidly progressive Alzheimer disease. Arch Neurol. 2011;68(9):1124–30.

    Article  PubMed  Google Scholar 

  3. • Geschwind MD, Shu H, Haman A, Sejvar JJ, Miller BL. Rapidly progressive dementia. Ann Neurol. 2008;64(1):97–108.Includes an expanded discussion of the clinical features of causes of RPD.

  4. •• Day G, Tang-Wai D. When dementia progresses quickly: a practical approach to the diagnosis and management of rapidly progressive dementia. Neurodegener Dis Manag. 2014;4(1):41–56. The review article features detailed clinical assessment necessities including an expanded discussion of physical exam components. Valuable charts and figures highlight ways of sorting through competing disease etiologies based on a patient's demographic information, speed of decline and testing data

    Article  PubMed  Google Scholar 

  5. Appleby BS, Lyketsos CG. Rapidly progressive dementias and the treatment of human prion diseases. Expert Opin Pharmacother. 2011;12(1):1–12.

    Article  CAS  PubMed  Google Scholar 

  6. Paterson R, Takada L, Geschwind M. Diagnosis and treatment of rapidly progressive dementias. Neurol Clin Pract. 2012;2(3):187–200.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Mead S, Rudge P. CJD mimics and chameleons. Pract Neurol. 2017;17(2):113–21.

    Article  PubMed  PubMed Central  Google Scholar 

  8. •• Geschwind M. Rapidly progressive dementia. Continuum. 2016;22(2 Dementia):510–37. The most updated review of RPD with excellent illustrative cases and demonstrations of relavant brain MRI findings

    PubMed  PubMed Central  Google Scholar 

  9. Armangue T, Leypoldt F, Dalmau J. Autoimmune encephalitis as differential diagnosis of infectious encephalitis. Curr Opin Neurol. 2014;27(3):361–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Aubert L, Pichierri S, Hommet C, Camus V, Berrut G, de Decker L. Association between comorbidity burden and rapid cognitive decline in individuals with mild to moderate Alzheimer’s disease. J Am Geriatr Soc. 2015;63(3):543–7.

    Article  PubMed  Google Scholar 

  11. Schmidt C, Redyk K, Meissner B, Krack L, von Ahsen N, Roeber S, et al. Clinical features of rapidly progressive Alzheimer’s disease. Dement Geriatr Cogn Disord. 2010;29(4):371–8.

    Article  CAS  PubMed  Google Scholar 

  12. Sona A, Zhang P, Ames D, Bush AI, Lautenschlager NT, Martins RN, et al. Predictors of rapid cognitive decline in Alzheimer’s disease: results from the Australian imaging, biomarkers and lifestyle (AIBL) study of ageing. Int Psychogeriatr. 2012;24(2):197–204.

    Article  PubMed  Google Scholar 

  13. • Peters ME, Schwartz S, Han D, Rabins PV, Steinberg M, Tschanz JT, et al. Neuropsychiatric symptoms as predictors of progression to severe Alzheimer’s dementia and death: the Cache County Dementia Progression Study. Am J Psychiatry. 2015;172(5):460–5. This is a high quality longitudinal study that draws attention to the prognostic implications of psychiatric comorbidities in Alzheimer’s dementia

    Article  PubMed  PubMed Central  Google Scholar 

  14. Cohen ML, Kim C, Haldiman T, ElHag M, Mehndiratta P, Pichet T, et al. Rapidly progressive Alzheimer’s disease features distinct structures of amyloid-beta. Brain. 2015;138(Pt 4):1009–22.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Tosto G, Gasparini M, Brickman AM, Letteri F, Renie R, Piscopo P, et al. Neuropsychological predictors of rapidly progressive Alzheimer’s disease. Acta Neurol Scand. 2015;132(6):417–22.

    Article  CAS  PubMed  Google Scholar 

  16. Grau-Rivera O, Gelpi E, Nos C, Gaig C, Ferrer I, Saiz A, et al. Clinicopathological correlations and concomitant pathologies in rapidly progressive dementia: a brain bank series. Neurodegener Dis. 2015;15(6):350–60.

    Article  CAS  PubMed  Google Scholar 

  17. Mann UM, Mohr E, Chase TN. Rapidly progressive Alzheimer’s disease. Lancet. 1989;2(8666):799.

    Article  CAS  PubMed  Google Scholar 

  18. Qiang W, Yau WM, Lu JX, Collinge J, Tycko R. Structural variation in amyloid-beta fibrils from Alzheimer’s disease clinical subtypes. Nature. 2017;541(7636):217–21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Drummond E, Nayak S, Faustin A, Pires G, Hickman RA, Askenazi M, et al. Proteomic differences in amyloid plaques in rapidly progressive and sporadic Alzheimer’s disease. Acta Neuropathol. 2017;133(6):933–54.

    Article  CAS  PubMed  Google Scholar 

  20. • Cohen M, Appleby B, Safar JG. Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer’s disease. Prion. 2016;10(1):9–17. Presents evidence toward prion-like behavior of certain amyloid beta molecular subtypes in different Alzheimer disease phenotypes

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Appleby BS, Appleby KK, Rabins PV. Does the presentation of Creutzfeldt-Jakob disease vary by age or presumed etiology? A meta-analysis of the past 10 years. J Neuropsychiatry Clin Neurosci. 2007;19(4):428–35.

    Article  PubMed  Google Scholar 

  22. Appleby BS, Appleby KK, Crain BJ, Onyike CU, Wallin MT, Rabins PV. Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants. Arch Neurol. 2009;66(2):208–15.

    Article  PubMed  Google Scholar 

  23. Organization WH. Global surveillance, diagnosis and therapy of human transmissible spongiform encephalopathies: report of a WHO consultation. 1998:1–30.

  24. Foutz A, Appleby BS, Hamlin C, Liu X, Yang S, Cohen Y, et al. Diagnostic and prognostic value of human prion detection in cerebrospinal fluid. Ann Neurol. 2017;81(1):79–92.

    Article  CAS  PubMed  Google Scholar 

  25. •• Bongianni M, Orru C, Groveman BR, Sacchetto L, Fiorini M, Tonoli G, et al. Diagnosis of human prion disease using real-time quaking-induced conversion testing of olfactory mucosa and cerebrospinal fluid samples. JAMA Neurol. 2017;74(2):155–62. Demonstrates the sensitivity and specificity of real-time quaking-induced conversion assay for detection of prion disease in comparison with currently recommended disease defining diagnostic criteria

    Article  PubMed  Google Scholar 

  26. Vitali P, Maccagnano E, Caverzasi E, Henry RG, Haman A, Torres-Chae C, et al. Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias. Neurology. 2011;76(20):1711–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P. Sporadic human prion diseases: molecular insights and diagnosis. Lancet Neurol. 2012;11(7):618–28.

    Article  CAS  PubMed  Google Scholar 

  28. Hamaguchi T, Kitamoto T, Sato T, Mizusawa H, Nakamura Y, Noguchi M, et al. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease. Neurology. 2005;64(4):643–8.

    Article  CAS  PubMed  Google Scholar 

  29. Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. Br Med Bull. 2003;66:213–39.

    Article  CAS  PubMed  Google Scholar 

  30. Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Ann Neurol. 2010;68(2):162–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE, Sathirapongsasuti JF, et al. Quantifying prion disease penetrance using large population control cohorts. Sci Transl Med. 2016;8(322):322ra9.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Krasnianski A, Sanchez Juan P, Ponto C, Bartl M, Heinemann U, Varges D, et al. A proposal of new diagnostic pathway for fatal familial insomnia. J Neurol Neurosurg Psychiatry. 2014;85(6):654–9.

    Article  CAS  PubMed  Google Scholar 

  33. Cortelli P, Perani D, Montagna P, Gallassi R, Tinuper P, Provini F, et al. Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. Brain. 2006;129(Pt 3):668–75.

    Article  PubMed  Google Scholar 

  34. Sano K, Satoh K, Atarashi R, Takashima H, Iwasaki Y, Yoshida M, et al. Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay. PLoS One. 2013;8(1):e54915.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Brown P, Brandel JP, Sato T, Nakamura Y, MacKenzie J, Will RG, et al. Iatrogenic Creutzfeldt-Jakob disease, final assessment. Emerg Infect Dis. 2012;18(6):901–7.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet. 1996;347(9006):921–5.

    Article  CAS  PubMed  Google Scholar 

  37. Zeidler M, Sellar RJ, Collie DA, Knight R, Stewart G, Macleod MA, et al. The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease. Lancet. 2000;355(9213):1412–8.

    Article  CAS  PubMed  Google Scholar 

  38. Dalmau J, Tuzun E, Wu HY, Masjuan J, Rossi JE, Voloschin A, et al. Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma. Ann Neurol. 2007;61(1):25–36.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Vincent A, Buckley C, Schott JM, Baker I, Dewar BK, Detert N, et al. Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis. Brain. 2004;127(Pt 3):701–12.

    Article  PubMed  Google Scholar 

  40. Irani SR, Alexander S, Waters P, Kleopa KA, Pettingill P, Zuliani L, et al. Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia. Brain. 2010;133(9):2734–48.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Lai M, Huijbers MG, Lancaster E, Graus F, Bataller L, Balice-Gordon R, et al. Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series. Lancet Neurol. 2010;9(8):776–85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Lee S, Lee S. Laboratory diagnosis of autoimmune encephalitis. J Epilepsy Res. 2016;6(2):45–52.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Titulaer MJ, McCracken L, Gabilondo I, Armangue T, Glaser C, Iizuka T, et al. Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study. Lancet Neurol. 2013;12(2):157–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. van Sonderen A, Arino H, Petit-Pedrol M, Leypoldt F, Kortvelyessy P, Wandinger K, et al. The clinical spectrum of Caspr2 antibody-associated disease. Neurology. 2016;87(5):521–8.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Chitravas N, Jung RS, Kofskey DM, Blevins JE, Gambetti P, Leigh RJ, et al. Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease. Ann Neurol. 2011;70(3):437–44.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Celicanin M, Blaabjerg M, Maersk-Moller C, Beniczky S, Marner L, Thomsen C, et al. Autoimmune encephalitis associated with voltage-gated potassium channels-complex and leucine-rich glioma-inactivated 1 antibodies - a national cohort study. Eur J Neurol. 2017;

  47. van Sonderen A, Thijs RD, Coenders EC, Jiskoot LC, Sanchez E, de Bruijn MA, et al. Anti-LGI1 encephalitis: clinical syndrome and long-term follow-up. Neurology. 2016;87(14):1449–56.

    Article  PubMed  Google Scholar 

  48. Graus F, Titulaer MJ, Balu R, Benseler S, Bien CG, Cellucci T, et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol. 2016;15(4):391–404.

    Article  PubMed  PubMed Central  Google Scholar 

  49. •• Titulaer MJ, Soffietti R, Dalmau J, Gilhus NE, Giometto B, Graus F, et al. Screening for tumours in paraneoplastic syndromes: report of an EFNS task force. Eur J Neurol. 2011;18(1):19-e3. Clearly delineates clinical diagnostic criteria for autoimmune encephalitis

    Article  PubMed  Google Scholar 

  50. Rosenfeld M, Dalmau J. Paraneoplastic disorders of the CNS and autoimmune synaptic encephalitis. Continuum. 2012;18(2):366–83.

    PubMed  Google Scholar 

  51. •• Titulaer MJ, Dalmau J. Seizures as first symptom of anti-NMDA receptor encephalitis are more common in men. Neurology. 2014;82(7):550–1. This review gives a thorough and pragmatic discussion of paraneoplastic disorders of the central nervous system

    Article  PubMed  Google Scholar 

  52. Dalmau J, Gleichman AJ, Hughes EG, Rossi JE, Peng X, Lai M, et al. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies. Lancet Neurol. 2008;7(12):1091–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Irani SR, Bera K, Waters P, Zuliani L, Maxwell S, Zandi MS, et al. N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes. Brain. 2010;133(Pt 6):1655–67.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Gaspard N. Autoimmune epilepsy. Continuum. 2016;22(1):227–45.

    PubMed  Google Scholar 

  55. Schmitt SE, Pargeon K, Frechette ES, Hirsch LJ, Dalmau J, Friedman D. Extreme delta brush: a unique EEG pattern in adults with anti-NMDA receptor encephalitis. Neurology. 2012;79(11):1094–100.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Finke C, Pruss H, Heine J, Reuter S, Kopp UA, Wegner F, et al. Evaluation of cognitive deficits and structural hippocampal damage in encephalitis with leucine-rich, glioma-inactivated 1 antibodies. JAMA Neurol. 2017;74(1):50–9.

    PubMed  Google Scholar 

  57. Bakpa OD, Reuber M, Irani SR. Antibody-associated epilepsies: clinical features, evidence for immunotherapies and future research questions. Seizure. 2016;41:26–41.

    Article  PubMed  PubMed Central  Google Scholar 

  58. Irani SR, Michell AW, Lang B, Pettingill P, Waters P, Johnson MR, et al. Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis. Ann Neurol. 2011;69(5):892–900.

    Article  PubMed  Google Scholar 

  59. Arino H, Armangue T, Petit-Pedrol M, Sabater L, Martinez-Hernandez E, Hara M, et al. Anti-LGI1-associated cognitive impairment: presentation and long-term outcome. Neurology. 2016;87(8):759–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Iwasaki Y, Kinoshita M, Ikeda K, Takamiya K, Shiojima T. Concurrence of myasthenia gravis and choree fibrillaire de Morvan. Eur Arch Psychiatry Neurol Sci. 1990;239(5):335–6.

    Article  CAS  PubMed  Google Scholar 

  61. Lancaster E. The diagnosis and treatment of autoimmune encephalitis. J Clin Neurol. 2016;12(1):1–13.

    Article  PubMed  Google Scholar 

  62. McKeon A. Autoimmune encephalopathies and dementias. Continuum (Minneap Minn). 2016;22(2 Dementia):538–58.

    Google Scholar 

  63. Haik S, Marcon G, Mallet A, Tettamanti M, Welaratne A, Giaccone G, et al. Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial. Lancet Neurol. 2014;13(2):150–8.

    Article  CAS  PubMed  Google Scholar 

  64. Bone I, Belton L, Walker AS, Darbyshire J. Intraventricular pentosan polysulphate in human prion diseases: an observational study in the UK. Eur J Neurol. 2008;15(5):458–64.

    Article  CAS  PubMed  Google Scholar 

  65. Collinge J, Gorham M, Hudson F, Kennedy A, Keogh G, Pal S, et al. Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial. Lancet Neurol. 2009;8(4):334–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Forloni G, Tettamanti M, Lucca U, Albanese Y, Quaglio E, Chiesa R, et al. Preventive study in subjects at risk of fatal familial insomnia: innovative approach to rare diseases. Prion. 2015;9(2):75–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Bueler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M, et al. Mice devoid of PrP are resistant to scrapie. Cell. 1993;73(7):1339–47.

    Article  CAS  PubMed  Google Scholar 

  68. Nazor Friberg K, Hung G, Wancewicz E, Giles K, Black C, Freier S, et al. Intracerebral infusion of antisense oligonucleotides into prion-infected mice. Mol Ther Nucleic Acids. 2012;1:e9.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Nicoll AJ, Collinge J. Preventing prion pathogenicity by targeting the cellular prion protein. Infect Disord Drug Targets. 2009;9(1):48–57.

    Article  CAS  PubMed  Google Scholar 

  70. White MD, Mallucci GR. RNAi for the treatment of prion disease: a window for intervention in neurodegeneration? CNS Neurol Disord Drug Targets. 2009;8(5):342–52.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Brian S. Appleby MD.

Ethics declarations

Conflict of Interest

The authors declare that there is no conflict of interest.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

Additional information

This article is part of the Topical Collection on Dementia

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mahajan, S., Appleby, B.S. Comprehensive and Methodical: Diagnostic and Management Approaches to Rapidly Progressive Dementia. Curr Treat Options Neurol 19, 40 (2017). https://doi.org/10.1007/s11940-017-0474-1

Download citation

  • Published:

  • DOI: https://doi.org/10.1007/s11940-017-0474-1

Keywords

Navigation