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NEW
MAD COW DISEASE FACTOIDS INDEX
- MAD
COW DISEASE [New
Factoids/Info] [Definitions/History]
[In Humans/Other
Species]
[Feed/Testing/Rendering]
[Politics/Economics]
[Resources/Links
of Note]
IN
HUMANS
Posted
05/24/04]: "Dying
For A Hamburger How Modern Meat-packing Led To An Epidemic
Of Alzheimer's Disease:" "Dr. Murray Waldman,
in collaboration with writer Marjorie Lamb, sets out to show
that Alzheimer's is, indeed, a deadly modern plague. They present
startling evidence that Alzheimer's is one of a family of diseases
caused by a malformed protein - or prion - that also causes
mad cow disease and its human variant, Cruetzfeld-Jakob disease
(CJD). Could Alzheimer's, like CJD, be caused by tainted beef?
In this compelling exposition, the authors come to a frightening
conclusion about our seemingly insatiable hunger for hamburger. " Before
about 1900 Alzheimer's disease did not exist, or if it did,
was so rare as not to be noticed. But just over a hundred years
ago, Alzheimer's disease was unknown, and most people did not
know anyone who exhibited the symptoms of dementia that are
now all too familiar to the families and friends of victims.
Alzheimer's disease (AD) now afflicts 15 million people around
the world, including 250,000 Canadians and 4.5 million Americans.
One in 10 persons over 65 and nearly half of those over 85
have the disease. More significantly, the number of people
with dementia is expected to increase steadily over the next
25 years: in Canada, 10,000 new cases of AD are diagnosed each
year - 27 cases per day."
[Edited from the book summaries and the excerpt below:
http://www.mcclelland.com/catalog/display.pperl?isbn=0771087659
http://www.thebukowskiagency.com/DyingForAHamburger.htm
[Posted
05/23/04]:"Five
CJD Deaths In North N.J. In 15 Months:" (03/24/04): "A
62-year old man in Northern New Jersey has died from a brain
disorder that appears to be Creutzfeldt-Jakob disease, which,
if confirmed, would be the fifth case of the rare disease in
a little over a year in a two-county area, United Press International
has learned. The possible CJD cluster is associated with the
Garden State Race Track in Cherry Hill, where as many as 13
CJD deaths might have occurred among employees and patrons
who ate at the now defunct track. Both variant CJD and the
spontaneously occurring form of the disease -- called sporadic
CJD or simply CJD -- are incurable conditions that degenerate
the brain and ultimately cause death. This would be an unusually
high number for a uncommon disorder that is thought to occur
at the rate of only one case per 1 million population per year.
The combined population of the two counties is approximately
789,000, so they would expect to see no more than one case
of sporadic CJD in that time frame. According to DHSS figures,
which go back to 1979, the two counties have never experienced
two CJD cases in the same year -- let alone five." [Very
edited from:
http://www.upi.com/view.cfm?StoryID=20040323-051052-3359r
[Posted
04/28/04]: "Health
Officials Probing CJD Cases In N.J.: (03/09/04): "Federal
and New Jersey authorities appear to have bowed to pressure
from Congress and are investigating a potential cluster of
cases of a fatal brain disorder called Creutzfeldt-Jakob
disease in the southern part of the state, United Press International
has learned. The investigation was spurred by the persistence
of Janet Skarbek, a private citizen in Cinnaminson, N.J.,
who has been collecting information about local CJD cases
for nearly a year. Skarbek has compiled a [statistically
shocking] list of at least nine -- and as many as 13 -- CJD
cases with ties to the Garden State Race Track in Cherry
Hill.
Skarbek became concerned about the disease after Carol
Olive, a woman with whom her mother had worked at the Race
Track, died last May of CJD. As Skarbek's research
turned up more cases of the rare disease, she began urging the Centers for Disease
Control and Prevention in Atlanta, and the New Jersey Department of Health and
Senior Services, to investigate. But both agencies dismissed her pleas, claiming
there was no evidence of abnormally high occurrences of CJD in the state."
[Quite edited from:
http://www.upi.com/view.cfm?StoryID=20040309-011038-7707rUSDA
[Posted
02/15/04]: (02/05/04): "Experts
Predict More U.S. Cases Of Mad Cow: More American
cattle probably are infected with mad-cow disease, and the
federal government needs to expand its testing program and
tighten feed rules to prevent the infection from spreading,
a panel of international experts said yesterday. It's unlikely
the single Holstein discovered in Washington state is the
only sick animal ever imported into the country from Canada,
and possibly Europe, panel members said at a U.S. Department
of Agriculture (USDA) meeting.
Since none of the other animals was detected, their infected
tissues were almost certainly processed into cattle feed
years ago, spreading and amplifying the
disease "so that cattle in the U.S.A. have also been indigenously infected," says
a report presented to Agriculture Secretary Ann Veneman.
Panel chairman Ulrich Kihm, former chief veterinary officer of Switzerland, estimated
that one new U.S. mad-cow case a month might appear, based on the experience
of other European countries. Though the rate of infection is low, the government
should consider several steps, including a ban on the use in human and animal
food of brains, spinal cords and other high-risk tissue from animals older than
one year, Kihm said. The panel also recommended a ban on the use of all mammal
and bird protein in cattle feed.
Consumer advocates praised the report, which they said
validated many of their criticisms of the U.S. mad-cow
safety net. Industry reacted strongly against
the report, and predicted the proposals, if adopted, would have substantial
impacts on everyone involved in the beef business - from
cattle growers earning less
per animal to consumers paying more for less variety at the meat counter."
[Very edited from - more recommendations and issues at:
http://seattletimes.nwsource.com/html/localnews/2001851143_madrecommend05m.html
[Posted
02/15/04]: (01/18/04): "How
Safe Is Beef? U.S. Kept In Dark: Since the discovery
of a mad-cow infected Holstein in Washington state, our
public officials have been busy telling consumers that
there is
nothing to worry about. President Bush and Agriculture
Secretary Ann Veneman even made a point of serving beef
at their holiday
tables. But given how little we know about the scope of
the contamination and the nature of the disease, such gestures
are little more than acts of faith, not demonstrations
of
safety. The evidence that could demonstrate the safety
-- or absence thereof -- of U.S. beef is in large part
not being
revealed by U.S. officials, and in some cases isn't even
being collected. For starters, the Department of Agriculture
-- a conflicted agency charged with simultaneously promoting
the consumption of, and protecting consumers from, U.S.
beef -- has yet to give us a transparent definition of
what "safe" means
when it comes to transmission of this brain-wasting disease,
also known as bovine spongiform encephalopathy (BSE), to
humans.
Does "safe" mean there's no risk of contracting
the disease, or merely a relatively small risk? What information
is being used to determine the difference?
Answers to these questions would first require an estimate of the number of
cattle infected. This is not a number the USDA has released.
..... consumers -- and
researchers -- would benefit from better information about exactly how BSE
is transmitted from cow to human.
U.S. officials have consistently discounted and downplayed
these indirect [non-beef consumption] avenues. In the Washington
Post article on Dec. 23 that first reported
the U.S. BSE-infection, Veneman was quoted as saying that BSE is "not known
to be transmitted" through the consumption of these non-beef products.
The secretary's statement is extremely misleading and gives consumers the mistaken
impression that there is no risk associated with eating these foods. BSE is
neither
known nor not known to be transmitted through non-beef products. The truth
is we have no idea.
Secretary Veneman and the beef industry have been quick
to act on a handful of long-overdue, common-sense reforms.
However, it's an outrage that there's no
such urgency when it comes to collecting and releasing vital information that
will allow the American public to make informed choices about the foods we
eat. The American people deserve hard evidence and policy
changes made in their best
interests."
[Very very edited from the excellent
essay at: http://www.sacbee.com/content/opinion/story/8123078p-9055134c.html
[Posted
02/15/04]: (01/18/04): "New
Research Indicates Human Form Of Mad Cow More Complex Than
First Thought: New research suggests that the human
form of mad cow disease is a lot more complicated than originally
thought, and, potentially, much scarier. Scientists have
long agreed that eating cattle tissue infected with bovine
spongiform encephalopathy - mad cow disease - can cause the
human form of the disease, known as variant Creutzfeld-Jacob
disease. But recent animal tests indicate that eating infected
beef may also cause another form of the disease, classical
CJD, forcing scientists to re-examine assumptions about the
nature of the deadly disease and raising fears that it may
be more widespread than previously thought.
The accepted wisdom has been that classical CJD has nothing
to do with mad cows. It affects older people, those over
55, and generally occurs spontaneously
at the rate of about one person per million per year. It has been confused
with Alzheimer's disease and there is some concern that because of misdiagnosis,
it may be more widespread than the confirmed numbers indicate. The question
is, could an epidemic of classical CJD be lying dormant in the brains of
people who have eaten infected cattle products - specifically
products containing
brain or spinal cord matter?"
[Edited from:
http://www.canoe.com/CNEWS/Canada/2004/01/18/317283-cp.html
http://bmj.bmjjournals.com/cgi/content/full/328/7432/118
[Posted
02/15/04]: (01/16/04): "Action
Urged To Stop Human 'Mad Cow' In UK Blood: In a
letter published in the British Medical Journal, a senior
member of
the UK's Medical Research Council calls for urgent action
to prevent the spread of variant Creutzfeldt-Jakob disease
(vCJD)
-- the human form of mad cow disease -- through blood transfusions.
Last month, UK health secretary John Reid announced the first
case of vCJD that is believed to have to have occurred through
blood donation. In light of this event, Dr. Sheila M. Bird,
a statistician with the MRC, emphasizes that "we now need
to take steps" to spell out the rights and responsibilities
of people who have received blood and blood products that
were possibly contaminated with vCJD, as well as those of
the rest
of the population.
In her letter, Dr. Bird outlines several steps that can
be taken to prevent further human-to-human spread of
vCJD.... Until more is known about bloodborne transmission,
she concludes, "we must hope for the best and protect against the worst."
[Edited from:
http://www.reuters.com/newsArticle.jhtml?type=healthNews&storyID=4150456
[Their source: BMJ
2004;328:118-119 (17 January)
[Posted
02/15/04]: (01/17/04): "Mad
Cow In Milk?: The one dairy cow infected with Mad
Cow Disease from a Washington herd, whose milk was pooled with
3,000
others from that same herd, had the potential to infect every
American thousands of times over. Her "pooled" milk
was distributed on the West Coast. Her infected milk was made
into cheese and butter
and ice cream, and shipped from the West Coast to the East
Coast, and to all points."
[From the Robert Cohen essay building
on the above BMJ Editorial:
http://health.groups.yahoo.com/group/notmilk/message/1530
[Posted
01/27/04]: (01/12/04): "Studies
Quietly Raise Questions About Threat To Humans:
Below the drumbeat of reassurances from government and
the cattle industry that mad cow disease poses no threat
to public health, a small universe of scientists working
on a family of related illnesses are finding disturbing
evidence to the contrary.... Just last week, for example,
the National Cattlemen's Beef Association described mad
cow disease solely as an animal and economic problem -
not a human health problem. The U.S. Department of Agriculture
and Colorado's own commissioner of agriculture have made
similar pronouncements. Such statements, offered frequently
since the December discovery of a Holstein with mad cow
in Washington state, spark criticism from scientists and
consumer advocates who say that the government and industry
are injecting certainty into a field where uncertainty
remains the dominant theme."
[Very edited from the comprehensive/informative article
[Posted
12/28/03]: 07/22/03: Steve
Mitchell, UPI Medical Correspondent: "CJD
Screening May Miss Thousands Of Cases: The federal
government's monitoring system for cases of Creutzfeldt-Jakob
disease, a fatal human brain illness, could
be missing tens of thousands of victims, scientists and consumer advocates
have told United Press International. Creutzfeldt-Jakob
disease or CJD can be caused by eating beef contaminated
with mad cow disease, but the critics assert without a
better tracking system it might be impossible to determine
whether any CJD cases are due to mad cow or obtain an accurate
picture of the prevalence of the disorder in the United
States. Diagnosing CJD or Alzheimer's
is difficult because no test exists that can identify either
disease in a living
patient with certainty. So physicians must rely on the
patient's symptoms to determine which illness might be
present. Sometimes, however, the symptoms of one disease
can appear similar to the other disorder. The only way
to determine the disease conclusively is to perform an
autopsy on the brain after death. Unfortunately, although
autopsies once were performed on approximately half of
all corpses, the frequency has dropped to 15 percent or
less in the United States. The National Center for Health
Statistics -- a branch of the CDC -- stopped collecting
autopsy data in 1995. [Edited from:
http://www.upi.com/print.cfm?StoryID=20030721-102924-4786r
[Posted
12/25/03]: "Prions NOT Found
in Just Central Nervous System Tissue:" (Nov.
2003): In patients with sporadic Creutzfeldt-Jakob disease,
pathologic disease-associated prion protein (PrP(Sc)) has
been identified only in the central nervous system and
olfactory-nerve tissue. We search[ed] for PrP(Sc)) in extraneural
organs
of 36 patients with sporadic CJD who died between 1996
and 2002. Results: PrP(Sc)) was present in the brain tissue
of
all patients. In addition, we found PrP(Sc)) in 10 of 28
spleen specimens and in 8 of 32 skeletal-muscle samples.
Three patients had PrP(Sc)) in both spleen and muscle specimens.
...we identified extraneural deposition of PrP(Sc)) in
spleen and muscle samples from approximately one third
of patients
who died with sporadic CJD. Extraneural PrP(Sc)) appears
to correlate with a long duration of disease." [From abstract:
N Engl J Med 2003;349: 1812-20]
"Compelling
scientific evidence suggests so-called prion disease can
and has infected humans...
at present, there is no reliable antemortem
diagnosis,
specific treatment,
or
vaccine to prevent the disease. The
agent
thought to be responsible for this
unusual class of
disease is a rogue
protein (called a prion) that, unlike
all other agents known to cause infectious
disease, contains
neither
DNA nor RNA. The "bad" prion forms holes or a spongy
appearance in the brain in all disease variants, hence
the generic designation of spongiform encephalopathy." [Quintessence
International, 1998 May, 29:5]
"A
24-year-old vegetarian has been diagnosed with
Cruetzfeld-Jacob disease. Scientists fear that milk
and cheese may be the source of infection." [Michael
Hornsby, London Times, August 23, 1997]
"The
destruction of milk from suspected cows was recommended
in England to insure the public's safety... Experiments
also indicate that temperatures reached during pasteurization
of milk and household cooking does not kill the agent.
In the United Kingdom on December 1, 1988 the government
announced a ban on the sale of milk from infected cattle..." [Virgil
Hulse, M.D., Mad Cows and Milkgate]
"Transmission
of prions from infected cattle to humans by oral intake seems
no only possible but also very probable." [Annals
of Italian Medicine, 1998 Oct, 13:4]
"How
many people will come down with the disease from having eaten
British
beef is literally incalculable, because people typically are infected
with nvCJD for 10 to 30 years before symptoms appear." Cited
in "Deaths From
CJD..." John von Radowitz, Medical Correpondent, PA News, Jan 20,
2000 [02.06.27:10]
"...the
expected rate of occurrence of CJD (the human variation of mad
cow disease) has been 1 in 1,000,000 people. Up until the
advent of mad cow disease, CJD was, literally, a "one-in-a-million" disease.
Yet in one U.S. study, when people diagnosed with Alzheimer's
disease (whose symptoms can be difficult to distinguish from
CJD)
were examined after death, 5.5% of the presumed Alzheimer's victims
were found actually to have CJD." Boller, Francois, et al,
"Diagnosis of Dementia: Clinicopathologic correlations," Neurology,
Jan 1989, pg 76-79 [02.06.27:12]
"And
in another study, at Yale University, when people diagnosed with
Alzheimer's disease were examined after death it was found that
13% of the presumed Alzheimer's victims actually had CJD."
Manuelidis, E.E., et al. "Suggested links between different types
of dementias: Creutzfeld-Jakob disease, Alzheimer disease, and
retroviral CNS infections," Alzheimer Disease and Associated Disorders,
Vol 3, Nos. 1-2, 1989, pgs 100-09 [02.06.27:13]
"Four
million Americans are currently diagnosed with Alzheimer's."
Estimate from Alzheimer's Association, Chicago, IL [02.06.27:14]
[up
to index]
[Posted
05/23/04] "Mad
Cow Disease May Have Spread Into Sheep:" (04/08/04): "Scientists
have detected the first signs that bovine spongiform encephalopathy
(BSE) may have crossed into sheep in a study that is likely to
rekindle anxieties over the safety of lamb and mutton. One of three
tests used to determine whether sheep that had seemingly died from
scrapie were in fact infected with BSE (also known as "mad
cow" disease) has produced positive results. The four-year-old
animal was thought to have developed scrapie, a brain disorder
that affects sheep and is believed to be harmless to humans. It
was always theoretically possible for sheep to be infected with
BSE because they were once fed the same infected material that
had spread the brain disease in cattle during the 1980s and early
1990s. But there is no simple test to distinguish BSE from sheep
scrapie, and sheep experimentally infected with BSE show the same
symptoms as scrapie, which means that scrapie in the field could
be masking a hidden BSE epidemic in sheep. Experiments suggest
that BSE could be easily transmitted to sheep, and it could, like
scrapie, be passed down the generations. This would mean that BSE
could still be infecting the national flock today, more than a
decade after meat and bonemeal was banned."
[Edited from:
http://www.organicconsumers.org/madcow/sheep040804.cfm
[Posted
12/28/03]: "BSE
Killing Europe's Pets:" "Contaminated
material from cattle infected with BSE has been rendered
and used in commercial pet foods in Europe. Most scientists
determined the practice would be safe; that BSE would not
cross the species barrier. They
were wrong. As of January
2000, more than 100 cats in the UK had died from illnesses
attributed to eating diseased meat contained in commercial
pet foods made in Europe. Some veterinarians believe the
actual number of cats who died from feline spongiform encephalopathy
(the feline variant of mad cow disease) is far greater. In
1996... not only were household cats contracting the disease
but it had also spread to animals in zoos where it killed
a lion, five cheetahs, three ocelots, two tigers, three pumas,
six eland, six kudu and one bison. For years, government
officials claimed that dogs were not susceptible to a canine
form of BSE. But were we getting the truth? In 1997, Reuters
European Business unearthed a 1991 study on the brains of
444 dead hunting hounds that suggested some of the animals
had developed the first signs of "spongiform disease." Despite
the concerns of medical doctors and veterinarians, no further
tests on the tissue samples from these animals were ever
done." [Edited from: Autumn,
2001 Earth Island Journal Vol. 16, No. 3 by Ann N. Martin]
[Posted
12/28/03]: "Fish
Too Can Suffer Version Of Mad Cow Disease:" 02/02/03:
London, Feb 2 (ANI)[excerpted]: "Now fish like sheep,
elk and humans could suffer a version of mad cow disease,
or BSE, according to preliminary evidence. The results might
help reveal how the disease jumps from species to species.
Infectious prions are thought to cause BSE and human variant
Creutzfeldt-Jakob disease (vCJD). They probably crossed from
sheep to cows and then to humans in infected meat. Now a
team at the University of Konstanz in Germany has identified
a cousin of the prion protein in pufferfish. The discovery
of a prion in fish - which are evolutionarily distant from
humans - suggest that the protein is "probably doing
something fairly important and basic", says Jonathan
Weissman, who studies protein folding at the University of
California in San Francisco." [Full
article: http://in.news.yahoo.com/030202/139/20qaf.html]
[Posted
12/28/03]: "...the
form of the disease that afflicts elk and deer (called
Chronic Wasting Disease, or CWD) is not only present but
spreading
among elk in Montana, and among wild deer and elk in
northern Colorado and southern Wyoming. Between four and
eight percent
of the 62,000 deer in the area between Fort Collins, Colorado,
and Cheyenne, Wyoming have the disease." "Mad Cow Disease
in Humans," Rachel's Environment and Health Weekly. Jan
20, 2000 [02.06.27:11]
[up
to index]
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