Frequently
Asked Questions About “Mad Cow Disease” and Human Health
What is Mad Cow Disease?
Mad Cow Disease or bovine spongiform encephalopathy
(BSE) is a brain disease of cattle first identified
in the United Kingdom (UK) in the mid 1980s. BSE is part of a group
of diseases known as transmissible spongiform encephalopathies
(TSEs). All of these diseases are characterized by distinctive changes
in the brain, abnormal behavior and death.
What causes Mad Cow Disease (BSE)?
It is thought that this disease is caused and spread by an abnormal
form of a protein called a "prion". The abnormal protein
triggers a chain-reaction causing other proteins in the brain to
change to the abnormal form. Eventually these abnormal proteins
accumulate in the brain leading to the development of abnormal behavior
and eventually death.
How do cattle get Mad Cow Disease (BSE)?
When cattle are slaughtered, portions of the animal not destined
for human consumption may be used to produce a protein-rich byproduct
that may be mixed with grain and fed back to livestock as feed.
In the UK where the disease was first identified, it is thought
that these byproducts may have contained the prion protein, and
that cattle became infected by consuming feed containing prion-contaminated
animal protein. It is for this reason that the feeding of animal
proteins derived from cattle back to cattle has been banned in the
US.
Are there other animal Transmissible Spongiform Encephalopathies
(TSEs)?
Yes. There are other TSE diseases in animals and humans.
Scrapie, one such prion-related disease, is a TSE
that has been occurring in sheep and goats for at least 400 years.
Despite close contact between people and sheep and goats, and the
importance of lamb and mutton in many diets, there has been no evidence
of human disease due to scrapie.
Chronic wasting disease (CWD) of deer and elk
(cervids) is another TSE disease that has occurred in wild cervids
in the Rocky Mountain states for many years and has recently been
identified in Wisconsin. There are also TSEs in minks, cats and
other animals.
Are there TSEs which occur in humans?
Yes. There are a number of TSE diseases which
occur in humans. One of the human diseases in this group is classic
Creutzfeldt-Jakob disease (CJD). In the classic form of
CJD, a chance (sporadic) mutation of normal brain protein into an
abnormal protein occurs, which then leads to the formation of more
abnormal protein.
CJD-like illness can also be familial, occurring
in families where a genetic mutation favors the initial development
of the abnormal protein. Also, there are cases of CJD that have
followed transplantation of prion-infected cornea
(eye) and other tissues, or the administration of hormones produced
from human glands. More recently variant CJD (vCJD)
has been identified. Variant CJD is a TSE disease in humans linked
to eating meat products from cattle infected with Mad Cow Disease
(BSE).
What are the symptoms of Creutzfeldt-Jacob Disease (CJD)?
Classic CJD is a human disease characterized by progressive dementia,
leading to death. The disease may start with confusion or mental
symptoms. Other symptoms are difficulty moving and muscle jerks.
More and more signs and symptoms of brain damage and movement disorder
follow until the patient goes into a coma and dies. Most of the
cases of classic CJD have been diagnosed in people between the ages
of 55 and 75.
How long does it take to develop classic CJD?
Evidence suggests that it might take between 10 to 40 years to get
sick with classic CJD once abnormal proteins have begun to develop.
Classic CJD almost always occurs in people over 50 years old. Once
someone gets classic CJD, they may live for 6 to 12 months.
How common is classic CJD?
Because classic CJD is caused by the chance, sporadic mutation of
a normal brain protein into the prion, the risk of classic CJD is
the same all over the world, about one per million persons per year.
Studies conducted by the Department of Public Health have identified
that 5-10 cases of classic CJD occurred in Massachusetts’s
residents each year between 1992 and 2000.
What is variant-CJD (vCJD)?
Variant CJD is a disease in humans that has been linked to ingesting
meat infected with the prion that causes mad cow disease (BSE).
Variant CJD tends to occur in younger people (average age 29 rather
than 65 for classic CJD) and has slightly different symptoms than
classic CJD. People with vCJD tend to live slightly longer than
people with classic CJD.
Variant CJD was first recognized in the UK in the mid-1990s, over
ten years after the beginning of the BSE outbreak in cattle. Because
of this and other similarities, vCJD is believed to be the result
of consumption of prion-contaminated meat products. Muscle meat
itself does not contain prions, but in processing of ground beef,
sausage and other meat products, contamination of the product with
nervous tissues containing the infective prion may occur.
How common is vCJD, the human disease related to ingesting
meat products infected with Mad Cow Disease (BSE)?
The risk of vCJD is thought to be related to exposure to animal
products contaminated with the prion that causes BSE in cattle.
Nearly all the cases of vCJD in humans have been in the UK or have
been in people with exposure to cattle meat products from the UK.
There have been 153 cases of vCJD reported in the world since the
first case was identified in 1995, with 143 of these in the UK.
Although many millions of people in the UK and around the world
have been exposed to UK beef, and approximately 200,000 cases of
BSE in cattle were reported and removed from the food supply over
the past twenty years, the number of cases of vCJD remains low.
How do people get vCJD?
It is thought that a very small percentage of people who eat meat
products infected with the BSE agent will get vCJD. Experiments
done with cattle and other animals suggest that almost all of the
infectivity is in tissue from the cattle’s brain, spinal cord,
and intestine, and that muscle meat itself is not infectious. Milk
products from cattle are also not associated with any risk of infection
with BSE.
How have BSE and vCJD been controlled in the United Kingdom?
After mad cow disease (BSE) was recognized, millions of cattle were
killed and disposed of. The feeding of animal source protein back
to cattle was banned. Because of these changes, the number of BSE
cases in cattle each year in the UK has been decreasing since 1992.
The number of vCJD cases in humans each year in the UK has been
decreasing since 2000.
Statistics on mad cow disease (BSE) in cattle are available at:
http://www.oie.int/eng/info/en_esb.htm.
Statistics on vCJD in the UK, the human disease thought related
to eating meat contaminated with brain or spinal tissue of cows
infected with BSE, are available at: http://www.cjd.ed.ac.uk/figures.htm.
What is being done in the United States to prevent BSE
and vCJD?
The United States introduced a number of safeguards and surveillance
efforts to lower the chances of BSE getting into the U.S. These
included bans on use of certain animal proteins in animal feed,
bans on UK beef products, and testing programs to quickly identify
BSE in US cattle. The US plan can be obtained at: http://www.aphis.usda.gov/lpa/issues/bse/bsesum.pdf.
Over 57,000 cattle brains have been tested for BSE in the United
States.
The first cow positive for BSE in the United States was found in
December 2003 in Washington State. This animal was imported from
Canada. Because the cow was born in Canada before it was illegal
to feed animal protein back to cattle, the cow may have been exposed
to the prion agent through eating contaminated animal feed.
What has been done in Massachusetts?
State agencies, particularly the Massachusetts Department of Agricultural
Resources (MDAR), work closely with the U.S. Department of Agriculture
and federal health agencies to assure the safety of the food supply.
Bans on imports of beef and cattle from countries with BSE positive
cows have been in place for some time. Bans on imports of deer have
been also in place because of BSE-like disease in deer and elk,
called chronic wasting disease (CWD).
The Massachusetts Department of Public Health has been monitoring
all CJD cases in Massachusetts since 1992. This surveillance includes
intensified follow-up of any cases in people under 50 years old.
Thus far, we have seen cases of CJD as expected (approximately one
per million per year), with no evidence of vCJD. Massachusetts is
one of a few states where CJD is a reportable condition.
Where can I get more information?
The following web sites can provide a great deal of more information
on BSE, CJD, vCJD and related diseases:
- Centers for Diseases Control and Prevention, BSE and CJD Information
and Resources web site at: http://www.cdc.gov/ncidod/diseases/cjd/cjd.htm
- United States Department of Agriculture, Animal Plant Health
Inspection Services, Bovine Spongiform Encephalopathy (BSE) web
site at: http://www.aphis.usda.gov/lpa/issues/bse/bse.html
- United States Department of Agriculture, Animal Plant Health
Inspection Services, Bovine Spongiform Encephalopathy (BSE) Response
Plan Summary located at: http://www.aphis.usda.gov/lpa/issues/bse/bsesum.pdf
- United States Department of Agriculture, Animal Plant Health
Inspection Services, Bovine Spongiform Encephalopathy (BSE), BSE
Risk Assessment located at: http://www.aphis.usda.gov/lpa/issues/bse/bse-riskassmt.html
- World Health Organization, Variant Creutzfeldt-Jakob Disease,
Fact Sheet, located at: http://www.who.int/mediacentre/factsheets/fs180/en/
- World Health Organization, Bovine Spongiform Encephalopathy
Fact Sheet, http://www.who.int/mediacentre/factsheets/fs113/en/
- The UK Creutzfeldt-Jakob Disease Surveillance Unit web site
at: http://www.cjd.ed.ac.uk/index.htm
- The World Organization for Animal Health (OIE), BSE web site
at: http://www.oie.int/eng/info/en_esb.htm
January 2004
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