You
are visiting
www.rawfoodinfo.com
10/14/05
Author: Shane Ellison, M.Sc.
Source: www.HealthMyths.net
Cholesterol-Lowering
Drugs and Cancer
By Shane Ellison, M.Sc.
Copyright © 2005
The use of cholesterol-lowering drugs for the prevention of heart
disease may increase your chances of suffering from the pandemic killer known
as cancer. Few doctors are aware of this real and present danger.
Well-designed studies have shown the link between cholesterol-lowering drug
use and cancer. In a study published in the Journal of the American Medical
Association (JAMA), Thomas B. Newman MD, MPH and co-workers show that all cholesterol-lowering
drugs, both the early drugs known as fibrates (glofibrate, gemfibrozil) and
the newer drugs known as statins (Lipitor, Pravachol, Zocor), cause cancer in
rodents at the equivalent doses used by man. [1]
The extrapolation of evidence of cancer from rodent to human is very uncertain.
This is the argument of those in favor of using cholesterol-lowering drugs.
The argument would only be plausible if human studies also showed an increase
in cancer rates. And in fact, that is what scientists are finding.
Evidence from the cholesterol-lowering drug trial known as CARE (Cholesterol
And Recurrent Events) showed that Pravachol (a cholesterol-lowering drug
made by Bristol-Myer Squib) reduced the chance of suffering from a heart attack
by an absolute reduction rate of 1.1%. This miniscule benefit was accompanied
by a 1500% increase in breast cancer among women taking Pravachol. An increase
in cancer rates among Pravachol users was also shown in the drug trial known
as PROSPER.
It is rare that cancer would show up in most other cholesterol-lowering drug
trials. Drug company-funded studies for these drugs are conveniently short in
nature, typically 5 years or less. It can take decades for cancer to develop.
Consequently, cancer is rarely seen among test subjects. In fact, even heavy
smoking will not cause lung cancer within 5 years. [2] Yet it is a well-known
fact that smoking leads to lung cancer. Therefore, as long as statin drug trials
last only 5 years, this side effect will continue to fly below the radar.
If cancer were to show up as a negative side effect, there is concern whether
or not it would be reported. The British Medical Journal (BMJ) has reported
that of 164 statin drug trials reviewed, only 48 reported the number of participants
with one or more negative side effects caused by the drug. [3]
As if in recognition of this, attempts have been made to warn the public. Dr.
Gloria Troendle, deputy director for the Division of Metabolism and Endocrine
Drug Products for the FDA, noted that the cholesterol-lowering drug, gemfibrozil,
belonged to a class of drugs that has repeatedly been shown to increase death
rates among users. Moreover, Dr. Troendle stated that she does not believe the
FDA has ever approved a drug for long-term use that was as cancer causing at
human doses as gemfibrozil. Elizabeth Barbehenn, PhD, concluded to the FDA,
fibrates must be considered as potential human carcinogens and their carcinogenic
potential should be part of the risk benefit equation for evaluating gemfibrozil.
Historically, FDA advisors were reluctant to approve the cholesterol-lowering
drugs. When asked to vote whether or not gemfibrozil should be approved for
the prevention of heart disease, only 3 out of 9 members of the FDA advisory
committee voted in favor of approval. Unfortunately, these votes are only advisory
and the FDA decided to approve gemfibrozil for human consumption against the
better judgment of the committee.
One mechanism by which cholesterol-lowering drugs may cause cancer has been
identified. Published in Nature Medicine, Dr. Michael Simons of Beth Israel
Deaconess Medical Center in Boston shows that statin drugs mimic a substance
known as vascular endothelial growth factors (VEGF). The biochemical VEGF promotes
the growth of new blood vessels, a process known as angiogenesis. While angiogenesis
may help the growth of arteries, the benefit is quickly negated by the potential
for growth of cancer. The British Journal of Cancer reports that VEGF plays
an important role in the spread of colorectal cancer. Further, for those who
already have tumors, VEGF and compounds that mimic VEGF significantly diminishes
that persons survival time. [4]
Benefits associated with cholesterol-lowering drugs do not exceed risk. Looking
at the statin-drug trials, only two of the many cholesterol-lowering
trials prevented all-cause death rates when compared to a placebo. The Long
Term Intervention with Pravastatin (Pravachol) in Ischemic Heart Disease
(LIPID) trial showed a contemptible 3.1% reduction in absolute total mortality
rates. Similarly, the 4S trial showed a minimal 3.3% reduction in absolute total
mortality rates among those taking 20-40mg/day of Zocor. These numbers
may be statistically significant, yet the low percentages conclude
that the statins have little clinical benefit to users.
USA Today reported that, Statins have killed and injured more people than
the government has acknowledged. [5] Oblivious to their dangers, medical
doctors are calling cholesterol-lowering drugs the new aspirin and
are even recommending that children be prescribed cholesterol-lowering drugs.
This is a great example of how marketing hype supersedes medical science.
Health and longevity was not meant to be risky, complicated or expensive. To
attenuate the risk of using cholesterol-lowering drugs while preventing heart
disease, the general public must utilize healthy lifestyle habits. Most notably,
that would be the act of removing highly processed food, especially sugar, from
the diet. This will prove to be simple, effective and most affordable.
About
the Author
Shane
holds a Masters degree in organic chemistry and has first-hand industry
experience with drug research, design and synthesis. He understands that Americans
want and deserve education rather than prescriptions. His shocking ebook surrounding
cholesterol-lowering drugs can be downloaded for FREE as a pdf file at www.health-fx.net/eBook.pdf.
His book Health Myths Exposed is available at www.healthmyths.net or Amazon.
References:
[1] Newman, Thomas B. et al. Carcinogenicity of Lipid-Lowering Drugs. Journal
of the American Medical Association. January 3, 1996-Vol 275, No. 1.
[2] Ravnskov, Uffe. Statins as the new aspirin. Letters. British Medical Journal.
2002; 324:789 (30 March).
[3] Law, M.R. et al. Quantifying effect of statins on low-density lipoprotein
cholesterol, ischaemic heart disease, and stroke: systematic review and meta-analysis.
BMJ. 2003 June 28; 326 (7404): 1423.
[4] Wentao Yang, Kristine Klos, Ying Yang, Terry L. Smith, Daren Shi, Dihua
Yu. ErbB2 overexpression correlates with increased expression of vascular endothelial
growth factors A, C, and D in human breast carcinoma. Cancer. Volume 94, Issue
11, 2002. Pages 2855-2861.
[5] Sternberg, Steve. USA Today. 08/20/2001.
Home |
New to Raw?
|
Hotline |
Action Forum |
|
Multi/Media |
Events |
Press/Media
|