Variant Creutzfeldt-Jakob Disease
(Human Mad Cow Disease; vCJD)
Definition
Variant Creutzfeldt-Jakob disease (vCJD) is a type of prion disease. Bovine spongiform encephalopathy is a prion disease that affects cows; there is evidence that this illness can be transmitted to humans, producing vCJD. This illness is often called “mad cow disease.”
Causes
Prion diseases are a unique form of infectious diseases. The disease is not produced by a bacterial or viral infection; instead, the illness is related to progressive accumulation of prions (infectious protein particles). The central nervous system is progressively damaged as these prions accumulate.
The Nervous System
Risk Factors
Exposure to prion containing tissue is the primary risk factor. Other risk factors include:
- Eating beef from infected cows
- Receiving human growth hormone (HGH) injections prior to the mid-1980s—Changes in the preparation of HGH in the mid-1980s eliminated this risk.
- Working with brain tissue
- Receiving a corneal or dura mater (brain lining) transplantation
Five to ten percent of all cases of the nonvariant form of Creutzfeldt-Jakob are inherited.
Symptoms
The average age of people who get this disease is 29 years old. Rare cases have been reported in children.
Once you are exposed, it can take up to 20 years until symptoms develop. When symptoms develop they usually follow these three phases:
Early Phase (0 to 6 Months)
Psychiatric symptoms predominate:
- Depression
- Anxiety
- Withdrawal
- Memory problems
- Difficulty pronouncing words
Middle Phase
Neurologic symptoms predominate:
- Abnormal gait
- Ataxia (problems with coordination)
- Involuntary movements (muscle jerks and stiffness)
- Cognitive decline (impaired speech)
Late Phase
- Mute
- Immobility
The average length of time from first symptoms to death is 13 months (with a range of 6-39 months).
Diagnosis
The clinical history and physical exam are the primary diagnostic tools. If your physician suspects vCJD, additional tests may be needed, such as:
- Lumbar puncture —a procedure to collect cerebrospinal fluid
- MRI scan —a test that uses magnetic waves to make pictures of structures inside the head
- CT scan —a type of x-ray that uses a computer to make pictures of structures inside the head
- Electroencephalogram (EEG) —a test used to evaluate brain function or disorders
- SPECT or PET scan —tests that produces images showing the amount of functional activity in the tissue; used to differentiate vCJD from other diseases
- Biopsy —removal of a sample of tonsil tissue to test to confirm vCJD
- Blood tests and cerebrospinal fluid analysis—may be used to distinguish this disease from other disease, such as Alzheimer's disease
In many cases, final diagnosis requires autopsy and pathological studies.
Treatment
Currently, there is no cure for vCJD. Treatment is primarily supportive, maximizing function and minimizing discomfort.
Prevention
About 200 worldwide cases of vCJD have occurred to date, most of which were associated with beef consumption in the United Kingdom. There is a great deal of controversy regarding safety of US beef. Two cases of bovine spongiform encephalopathy have been detected in the US. But, no cases of vCJD have been attributed to eating US beef.
To minimize risk, it is generally recommended that you avoid beef products, particularly processed meat (eg, sausage and hotdogs), or beef items containing brain, spinal cord, or bone marrow.
RESOURCES:
Creutzfeldt-Jakob Disease Foundation
http://www.cjdfoundation.org/
The National Creutzfeldt-Jakob Disease Surveillance Unit
http://www.cjd.ed.ac.uk/index.htm
World Health Organization
http://www.who.int/
CANADIAN RESOURCES:
Health Canada
http://www.hc-sc.gc.ca/
Public Health Agency of Canada
http://www.phac-aspc.gc.ca/index-eng.php/
References:
Creutzfeldt-Jakob spongiform encephalopathy. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed/what.php . Updated December 30, 2009. Accessed February 1, 2009.
Roos, RP. Prion diseases. In: Gilman S, ed. MedLink Neurology. San Diego, CA: MedLink Corporation. MedLink website. Available at: http://www.medlink.com . Accessed February 1, 2009.
Churg-Strauss syndrome. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed . Updated December 12, 2007. Accessed February 23, 2008.
Dawidowska K. Where’s the (safe) beef? Prevention . 2004;56:34.
Moo-ve over, beef burgers: EN finds many alternatives. Environmental Nutrition . 2004 Aug;27:5.
NINDS Creutzfeldt-Jakob disease information page. National Institute of Neurological Disorders and Strokes website. Available at: http://www.ninds.nih.gov/disorders/cjd/cjd_pr.htm .
Prusiner SB. Detecting mad cow disease. Scientific American . 2004;291:60-67.
Raloff J. Better protection from mad cow disease. Science News . 2004;165:93.
Smith-Bathgate B. Creutzfeldt-Jakob disease: diagnosis and nursing care issues. Nursing Times . 2005;101:52.
Variant Creutzfeldt-Jakob disease. World Health Organization website. Available at: http://www.who.int/mediacentre/factsheets/fs180/en/ . Updated November 2002. Accessed March 17, 2009.
Zeidler M, Sellar R, Collie DA, et al. The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease. Lancet . 2000;355:1412-1419.
Last reviewed January 2009 by J. Thomas Megerian, MD, PhD, FAAP
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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