Creutzfeldt-Jakob disease classification: Difference between revisions
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==Classification== | ==Classification== | ||
The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable conformations. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates. | The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable conformations. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates. | ||
There are two | There are two types of CJD, classic and variant form. Classic CJD characteristics, as compared to variant CJD, are presented in the table below. | ||
The classic types of CJD are: | The classic types of CJD are: | ||
{|Class="wikitable" | |||
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|Sporadic CJD|| Most prevalent, idiopathic, average age of onset is 65 years | |||
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|Familial CJD|| Results when a person inherited the abnormal prion (rare) | |||
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Transmissible spongiform encephalopathy diseases are caused by prions. The diseases are thus sometimes called prion diseases. | Transmissible spongiform encephalopathy diseases are caused by prions. The diseases are thus sometimes called prion diseases. | ||
Other prion diseases include [[Gerstmann-Sträussler-Scheinker syndrome]] ([[GSS]]) | Other prion diseases include: | ||
* [[Gerstmann-Sträussler-Scheinker syndrome]] ([[GSS]]) | |||
* [[Fatal familial insomnia]] (FFI) | |||
* [[Kuru]] in humans | |||
* [[Bovine spongiform encephalopathy]] ([[BSE]]) commonly known as [[mad cow disease]] | |||
* [[Chronic wasting disease]] ([[CWD]]) | |||
* Scrapie in sheep | |||
*Clinical and Pathologic Characteristics:<ref>{{cite journal |author=Belay ED, Schonberger LB |title=Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy |journal=Clin. Lab. Med. |volume=22 |issue=4 |pages=849-62, v-vi |year=2002 |pmid=12489284 |doi=}}</ref> | *Clinical and Pathologic Characteristics:<ref>{{cite journal |author=Belay ED, Schonberger LB |title=Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy |journal=Clin. Lab. Med. |volume=22 |issue=4 |pages=849-62, v-vi |year=2002 |pmid=12489284 |doi=}}</ref> | ||
Revision as of 19:02, 14 February 2014
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Creutzfeldt-Jakob disease Microchapters |
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Differentiating Creutzfeldt-Jakob disease from other Diseases |
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Creutzfeldt-Jakob disease classification On the Web |
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Risk calculators and risk factors for Creutzfeldt-Jakob disease classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Classification
The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable conformations. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates.
There are two types of CJD, classic and variant form. Classic CJD characteristics, as compared to variant CJD, are presented in the table below. The classic types of CJD are:
| Sporadic CJD | Most prevalent, idiopathic, average age of onset is 65 years |
| Familial CJD | Results when a person inherited the abnormal prion (rare) |
Transmissible spongiform encephalopathy diseases are caused by prions. The diseases are thus sometimes called prion diseases. Other prion diseases include:
- Gerstmann-Sträussler-Scheinker syndrome (GSS)
- Fatal familial insomnia (FFI)
- Kuru in humans
- Bovine spongiform encephalopathy (BSE) commonly known as mad cow disease
- Chronic wasting disease (CWD)
- Scrapie in sheep
- Clinical and Pathologic Characteristics:[1]
| Characteristic | Classic CJD | Variant CJD |
| Median age at death | 68 years | 28 years |
| Median duration of illness | 4-5 months | 13-14 months |
| Clinical signs and symptoms | Dementia; early neurologic signs | Prominent psychiatric/behavioral symptoms; painful dysesthesias; delayed neurologic signs |
| Periodic sharp waves on electroencephalogram | Often present | Often absent |
| Signal hyperintensity in the caudate nucleus and putamen on diffusion-weighted and FLAIR MRI | Often present | Often absent |
| Pulvinar sign on MRI | Not reported | Present in >75% of cases |
| Immunohistochemical analysis of brain tissue | Variable accumulation. | Marked accumulation of protease-resistant prion protein |
| Presence of agent in lymphoid tissue | Not readily detected | Readily detected |
| Increased glycoform ratio on immunoblot analysis of protease-resistant prion protein | Not reported | Marked accumulation of protease-resistant prion protein |
| Presence of amyloid plaques in brain tissue | May be present | May be present |