Creutzfeldt-Jakob disease
From IDWiki
- General term for human prion disease, including sporadic, genetic, and infectiously-acquired forms
Pathophysiology
- A prion protein gene PRNP encodes a protein, PrPC, that is expressed in the brain and reticuloendethelial system
- Mutations of PRNP can create versions of PrP that folds abnormally, called PrPSc
- Misfolded PrPSc catalyzes other PrPC molecules to misfold, thereby converting them into more PrPSc
Syndromes
Sporadic CJD (sCJD)
- Age 45-75
- Myoclonus, cerebellar signs and symptoms, and visual disturbance (includes cortical blindness)
- May have prodromal symptoms including fatigue, insomnia, depression, weight loss, headaches, general malaise and ill-defined pain sensation
- Pyramidal and extrapyramidal signs may also develop, with upper motor neuron signs on exam
- Akinetic mutism commonly develops 2–3 months after the onset of symptoms
- Rapid or subacute decline, with a median survival 7-9 months from symptom onset
- Can detect 14-3-3 protein in CSF
- Can have a variety of subtypes, including visual, cerebellar, thalamic, or striatal-predominant symptoms
Genetic CJD (gCJD)
- Autosomal dominant mutations in PRNP with high penetrance, of which E200K is the most common worldwide
- Median age of onset is 58 years
- There are some specific forms
Gerstmann-Straüssler-Scheinker Syndrome (GSS)
- Prominent early ataxia and corticospinal tract degeneration
- Dementia is a late feature
- Lasts for 3 months to 13 years
Fatal Familial Insomnia (FFI)
- First described in Italian families
- Starts with insomnia, autonomic hyperactivity (increased sweating, teraing, salivation, mild nocturnal hyperthermia, tachycardia, and hypertension)
- Later, motor disturbances including ataxia, myoclonus, spasticity, hyperreflexia, and dysarthria
- Dementia would be a late finding
- Median age of onset is 50 to 56 years, but can occur from 19 to 83 years
Variant CJD (vCJD)
- Younger age (mean 26 years and range 12 to 74 years)
- May be from bovine spongiform encephalopathy in people homozygous 129M polymorphism of PrP
- Large outbreak in UK starting in 1995 related to an outbreak of BSE in 1985
- Can be transmitted via blood transfusion
- Prominent neuropsychiatric features: depression, anxiety, emotional lability, irritability, aggressive behavior, social withdrawal, delusions and hallucination
- Later, cerebellar syndrome with limb and gait ataxia, chorea, myoclonus, and dementia
- Median survival 14 months
- Can be diagnosed with PrPSc on tonsil biopsy
Iatrogenic CJD (iCJD)
- Transmitted by corneal and dura mater grafts, liver transplantation, growth hormone, neurosurgical procedures, and stereotactic EEG
- Incubation period ranges from 16 months to 25 years
- Presentation usually sCJD, but have also been cases of GSS and, rarely, vCJD
Differential Diagnosis
- Alzheimer dementia
- Vascular dementia
- Frontotemporal dementia
- Dementia with Lewy bodies
- Parkinson disease
- Cerebral lymphoma
- Paraneoplastic syndrome
- Psychiatric disorders
- Huntington disease
- Hashimoto encephalitis
Diagnosis
CSF
| Marker | Sn | Sp | LR+ | LR– |
|---|---|---|---|---|
| 14-3-3 | 88% (82-93) | 72% (69-75) | 3.1 (2.8-3.6) | 0.16 (0.1-0.26) |
| Tau >976* | 91% (84-95) | 88% (85-90) | 7.4 (6.9-7.8) | 0.1 (0.06-0.2) |
| Tau >1300** | 84% (76-90) | 92% (90-94) | 10.9 (8.5-13.9) | 0.17 (0.11-0.26) |
| S100B >2.5* | 87% (80-92) | 87% (84-91) | 6.6 (6.1-7.1) | 0.15 (0.09-0.2) |
| S100B >4.2** | 52% (42-61) | 97% (95-98) | 15.3 (10.2-23.1) | 0.5 (0.42-0.6) |
| Tau + S100B* | 18 (12.9-25) | 0.02 (0.01-0.09) | ||
| Tau + S100B + 14-3-3** | 18.6 (13.1-26.3) | 0.03 (0.01-0.1) |
- * Optimal cutoffs based on a Canadian study
- ** Standard threshold
- CSF itself usually bland, non-inflammatory
Imaging
- MRI is the most useful neuroimaging modality, especially with DWI
- Increased T2 FLAIR signals in striatum
- One sign is the "pulvinar sign"
- CT only useful for exclusion of other causes
Other
- EEG can have characteristic abnormalities and should be routinely done
- Bilaterally synchronic periodic sharp wave complexes, but can be transient, and can also be absent at the start and towards the end
- Histopathology of brain tissue biopsy or autopsy is still the gold standard
- Neuronal loss, vacuolation of the neuropil, spongiform changes
Management
- Supportive care
- Pentosan polysulfate may prolong life by weeks
Prevention
- Standard precautions when caring for patients; no need for additional PPE
- No special precautions required for burial
- Use disposable instruments whenever possible, especially when it will contact high-infectivity tissue
High-risk patients
- High-risk patients: confirmed, probable, or possible CJD, familial CJD, GSS, or FFI, undiagnosed rapidly-progressive dementia, or asymptomatic carrier of a genetic transmissible spongiform encephalopathy
At-risk patients
- At-risk patients: recipients of human-derived pituitary hormones, dura mater grafts (until 1992 for Lyodura or 1997 for Tutoplast Dura grafts), or corneal graft from jurisdiction that does not screen for neurological diseases; or patients who have been exposed to high-infectivity tissue/instruments of a confirmed case of CJD
Tissue infectivity
- Risk of transmission
- High (>50%): brain, CSF, dura mater, pituitary gland, posterior eye (optic nerve and retina), spinal cord, spinal ganglia, trigeminal ganglia
- Low (10-20%, though no reported human cases): cornea, kidney, liver, lung, lymph nodes, placenta, spleen
- None (0%): adipose tissue, adrenal gland, appendix, blood, cord blood, blood vessels, bone marrow, breast milk, dental pulp, epididymis, esophagus, feces, gingival tissue, heart, ileum, jejunum, large intestine, nasal mucosa, nasal mucous, ovaries, pancreas, pericardium, peripheral nerves, placental fluid, prostate, saliva, semen, seminal vesicl, skeletal muscle, skin, sweat, tears, testis, thymus, thyroid gland, tongue, tonsil, trachea, urine, uterus
CJD reprocessing
- Instruments should be kept moist until they are processed
- Stainless steel instruments can tolerate this procedure, while plastics, electronics, and steel alloys cannot
- Items, including endoscopes, that cannot undergo this procedure should be discarded
- The recommended process is:
- Clean thoroughly
- Soak in 1N sodium hydroxide for 1 hour
- Rinse thoroughly
- Sterilize in a prevacuum autoclave at 134ºC for 60 minutes
- Alternatively, can use 2% NaOCl rather than the NaOH, and autoclave for 18 minutes rather than 60 minutes
High-risk patients managed prospectively
| High-infectivity tissue | Low-infectivity tissue | No infectivity tissue | |
|---|---|---|---|
| Confirmed CJD | Discard | CJD decontamination if possible, or discard |
Routine reprocessing |
| Suspected CJD | Quarantine and discard if CJD confirmed | CJD decontamination if possible, or quarantine and discard if CJD confirmed |
Routine reprocessing |
| Asymptomatic carrier | Discard | Routine reprocessing | Routine reprocessing |
High-risk patients managed retrospectively
| High-infectivity tissue | Low-infectivity tissue | No infectivity tissue | |
|---|---|---|---|
| High-risk patient | Follow above algorithm, if instruments are identifiable or have been reprocessed 9 or fewer times; otherwise, there is the option of continuing to reuse without specific reprocessing | Continue to reuse | |
At-risk patients
- Following routine reprocessing
Case Definitions
Sporadic CJD
Possible
- Progressive dementia, and
- EEG atypical or not known, and
- Duration <2 years, and
- At least two of the following four clinical features:
- Myoclonus
- Visual or cerebellar disturbance
- Pyramidal/extrapyramidal dysfunction
- Akinetic mutism
Probable
- Progressive dementia, and
- At least two of the following four clinical features:
- Myoclonus
- A typical EEG, whatever the clinical duration of the disease, and/or
- A positive 14-3-3 assay for CSF, and
- A clinical duration to death < years
Definite
- Neuropathologic confirmation, and/or
- Confirmation of protease-resistant prion protein (immunocytochemistry or Western blot) and/or
- The presence of scrapie-associated fibrils
Variant CJD
- I: Presentation
- A. Progressive neuropsychiatric disorder
- B. Duration of illness >6 months
- C. Routine investigations do not suggest an alternative diagnosis
- D. No history of potential iatrogenic exposure
- E. No evidence of a familial form of transmissible spongiform encephalopathy
- II: Symptoms
- A. Early psychiatric symptoms
- B. Persistent painful sensory symptoms
- C. Ataxia
- D. Myoclonus or chorea or dystonia
- E. Dementia
- III: Investigations
- A. EEG does not chow the typical appearance of sCJD, or no EEG performed
- B. MRI brain scan shows bilateral symmetrical pulvinar high signal
- IV: Pathology
- A. Positive tonsil biopsy
- Definite: I.A and neuropathologic confirmation of vCJD
- Probable: I and 4/5 of II and III.A and III.B, or I and IV.A
- Possible: I and 4/5 of II and III.A
Further Reading
- Classic Creutzfeldt-Jakob Disease in Canada: Quick Reference Guide 2007. Public Health Agency of Canada. 2007.
