With great fanfare, the establishment medical journal The New England Journal of Medicine (NEJM) published a paper "Rosuvastatin to Prevent Vascular Events in Men and Women with Elevated C-Reactive Protein." Rosuvastatin (Crestor) is a drug marketed by the pharmaceutical company AstraZeneca as a HMG-CoA reductase inhibitor (they called it a 'super-statin'). AstraZeneca funded this study, and the lead author is one of the patent holders for the high sensitivity C-Reactive Protein test (hs-CRP), a sensitive blood marker of inflammation. Of course there are no real vested interests apart from the health of the nation, and as such, the American Heart Association meeting wondered whether it should be "put in the water". This harks back to the PolyPill hypothesis, where it was suggested everyone should take pharmaceutical medication before they inevitably get ill. Shares in AstraZeneca rose since the NEJM publication, as it would cost $116 USD per month for an individual (over $1,300 USD per year) to take it daily, according to USA Today. This means that each life saved would cost approximately $557,000 (if you believe the studies). AND that does not include the cost of the patented hs-CRP test (more expensive than a cholesterol test). And according to The Blog of Michael R Eades MD, the drug might only give a little protection to a very few people:
If you believe the data from this study..., it indicates that men over 50 and women over 60 with normal LDL-cholesterol levels AND elevated C-reactive protein levels who took the very expensive ($3.50 per day) statin drug rosuvastatin (Crestor) minimally reduced their risk of developing heart disease or dying of any cause as compared to those who took placebo.
So what else should we put in the water - the toxic chemical fluoride? But that's another story ...
What is counted by medics as 'high' cholesterol has been gradually dropping over the years as drug companies push the 'benefits' of statins as a simple magic bullet to the ubiquitous deaths from heart disease. Yet simple epigenetic cardiovascular disease risks such as low birth weight in males who regain a normal or above average Body Mass Index in childhood, or men with shorter legs or shorter index fingers than ring fingers (high 2D:4D ratio) are ignored until the individual becomes a patient with heart disease later in life.
Back to the paper, which was dubbed the JUPITER trial: "The primary objective of the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) was to investigate whether treatment with rosuvastatin, 20 mg daily, as compared with placebo, would decrease the rate of first major cardiovascular events." Eades translates this as "by God we’re going to prove that statins prevent something. "
And what it did prove is that more people taking Crestor got diabetes than the people not taking Crestor:
We did detect a small but significant increase in the rate of physician-reported diabetes with rosuvastatin, as well as a small, though significant, increase in the median value of glycated hemoglobin. Increases in glucose and glycated hemoglobin levels, the incidence of newly diagnosed diabetes, and worsening glycemic control have been reported in previous trials of pravastatin, simvastatin, and atorvastatin.
Even though physician-reported diabetes was been significantly increased in this and previous Crestor studies, and statins are given to people who have diabetes because they have diabetes, the authors say that "further study is needed before any causative effect can be established or refuted." Eades suggests that this is why the study was stopped when it was by outside observers. Ok, let's further poison our water supply with an expensive drug that gives people diabetes (not to mention muscle pain) all in the name of health.
1. Ridker PM, Danielson E, Fonseca FA, et. al. Rosuvastatin to Prevent Vascular Events in Men and Women with Elevated C-Reactive Protein. N Engl J Med. 2008 Nov 9.
2. US Patent 6040147 - Systemic inflammatory markers as diagnostic tools in the prevention of atherosclerotic diseases and as tools to aid in the selection of agents to be used for the prevention and treatment of atherosclerotic disease. Paul M Ridker.
3. "Cholesterol Pills in the Water? Crestor Market Widens (Update3)". Bloomberg.com news, Nov 10 2008.
4. Wald NJ, Law MR. "A strategy to reduce cardiovascular disease by more than 80%". BMJ 2003;326:1419 (28 June), doi:10.1136/bmj.326.7404.1419
5. "Crestor would save lives at $500,000 each" Steve Sternberg, USA Today, Nov 10 2008.
6. Eades, M. Weblog: "Truth versus hype in the Jupiter study" 10. November 2008.
7. Eriksson JG, Forsén T, Tuomilehto J, Winter PD, Osmond C, Barker DJP "Catchup growth in childhood and death from coronary heart disease: longitudinal study." BMJ 1999;318;427-431
8. Davey Smith G, Greenwood R, Gunnell D, Sweetnam P, Yarnell J, Elwood P. "Leg length, insulin resistance, and coronary heart disease risk: The Caerphilly Study." J. Epidemiol. Community Health 2001;55;867-872 doi:10.1136/jech.55.12.867
9. Manning JT, Bundred PE, Flanagan BF. "The ratio of 2nd to 4th digit length: a proxy for transactivation activity of the androgen receptor gene?" Med Hypotheses. 2002 Sep;59(3):334-6. Pubmed 12208164
Dear Dr. Greenfield,
I own the English original of "Eat right for your type". I recently bought a German translation for a friend. The lists of food stuff are not the same. E.g. in the type O beneficial fruit list it has cherries, blueberries and mangoes in addition to figs and plums. Did Dr. D'Adamo change the lists or were the German translators inventive?
Thanks in advance,
The German edition of Eat Right 4 Your Type, published as 4 Blutgruppen - Vier Strategien für ein gesundes Leben was published in hardback in 1998, and then in paperback in January 2001. The later German edition appears to have been updated with the new food lists that were available after new research for the American publication of Live Right 4 Your Type (and English The Eat Right Diet), the Complete Blood Type Encyclopedia, and online in Typebase 4. The American and English editions of Eat Right 4 Your Type have not been updated since they were published. Also read this clarification about differences between the books.
A new study to be published in Schizophrenia Research has found that markings on the hand may be a sensitive marker for genetic and environmental factors in schizophrenia.
Anthropologists in Barcelona, Spain studied the hand patterns of patients with schizophrenia, their relatives and healthy 'control' subjects. They looked at A-B ridge count, which is the number of ridges between two points on the palm called A and B (defined by specific areas where patterns converge under the second and third digits). There was no overall difference in A-B ridge count, but A-B ridge count was lower (fewer ridges) in schizophrenic patients with a low birth weight, and also in patients who did not have a family history of schizophrenia.
According to the study, the frequency of ectodermic derivates abnormalities (that is, Ridge Dissociation [RD] and/or Abnormal Palmar Flexion Creases [APFC] - abnormalities originating from the embryonic ectodermal layer of tissue, including the epidermis) appeared to be higher in patients and relatives than in controls. Ridge dissociation refers to short broken segments of lines that cover the patterns of dermatoglyphic areas in a disorganized way. Examples of abnormal palmar flexion creases are the Simian line, the Sydney line, clear broken proximal and distal palmar creases, and very rudimentary creases. Associations of this kind studying RD and APFC have been found in previous studies, one of them concluding that factors affecting early foetal development may increase the risk for psychotic disorder. In this new study males had more of these abnormalities than females, which also shows the potential influence of male hormones in response to stress. Males also had more fluctuating asymmetry of their A-B ridge count (difference between left and right hands).
Overall these studies show the importance of maintaining a peaceful and stress-free environment for the unborn child, as well as highlighting a potentially observable risk factor for schizophrenia.
1: Fatjó-Vilas M, Gourion D, Campanera S, et. al.
"New evidences of gene and environment interactions affecting prenatal neurodevelopment in schizophrenia-spectrum disorders: A family dermatoglyphic study."
Schizophr Res. 2008 Jun 24.
2: Rosa A, Fañanas L, Bracha HS, Torrey EF, van Os J.
Am J Psychiatry. 2000 Sep;157(9):1511-3.
Congenital dermatoglyphic malformations and psychosis: a twin study.
hello- I have been using the blood type diet for approx 4 yrs with great success. My blood type is A, and in Jan. I switched to the geno diet. I must say that the experience has not been good. I would hve considered myself to been in good shape, I eat great healthy and excercise almost 4-5 times a week. Since Jan I have had an eruption in the corner of my mouth that tingles. It is now after 5 months looking better, but the area remains sensitve. Now for the 3rd time since the end of April I have a itchy red rash on my face. It seems to last for 10 days, go away for a couple of days and then its back. Nothing I do seems to help, any suggestions?
The eruption on your mouth sounds like symptoms of the herpes virus. You can get this confirmed by your naturopathic or conventional doctor. As a short term measure the amino acid lysine can often help with the symptoms of active herpes infection. Long-term you should get your naturopath to address the focus of infection, which can be anywhere in the body.
You told us your blood group but did not say whether you are a secretor or non-secretor, and what your GenoType is - Teacher, Explorer or Warrior - all these make a difference to the detoxification process. When starting the GenoType Diet if you avoid the black dot foods for some time this will enhance the body's detoxification process. Sometimes detoxifying can bring on a healing crisis, which can take many forms depending on individual circumstances.
hi tom! i'm writing an article for teenagers, and am giving a very introductory picture of the blood type diet. can you give me a brief description of how, if at all, your rh factor affects your metabolism or food choices? it would really help me (and the readers)!
thanks so much,
In the Rhesus blood group the main antigens are C, D, E, c and e (capital letters and lower case letters are different antigens). The Rhesus antigens come from two adjacent gene loci, the RHD gene which encodes the D antigen and the RHCE gene which encodes both the C and E antigens. There is no d antigen: Rhesus "d" signifies the absence of the D antigen (the RHD gene is usually non-functional or null), and that person is described as Rhesus (D) negative. Similar to non-secretor status, Rhesus negative is traditionally a "recessive" phenotype, which means in practice that if an individual has no functional Rhesus (D) genes, they are classed as Rhesus negative, but inheriting at least one Rhesus (D) gene will give that person the Rhesus (D) positive phenotype. The Rhesus negative phenotype is generally less common than Rhesus positive. Unlike the ABO blood group antigens, the resulting Rhesus blood group antigen is limited to the red blood cells.
Rhesus D incompatibility is best known as the main cause of newborn fatal blood reactions in the children of Rhesus negative women. Lesser known associations with the Rhesus blood group system are Natural Killer Cell (immune system) activity, transport of ammonia in the kidney and susceptibility to urinary tract tumours, myasthenia gravis, ovarian cysts and tumours, and spinal osteochondrosis. Offspring of a Rhesus positive mother may be more prone to hearing loss.
The question of Rhesus blood group significance is often asked in relation to the Blood Group Diet, but the Rhesus factor takes on a new and greater significance with The GenoType Diet: Rhesus negative phenotype can make a difference to individuals in both systems.
In Live Right 4 Your Type, individuals with Rhesus negative phenotype will find that there are specific recommendations for frequency of eating certain food groups: fewer portions of grain (blood groups A, B and O), fruit (blood group A), and more protein (blood groups B and O).
For an individual's GenoType, being Rhesus negative can mean the difference between being one GenoType or another. The GT4 Explorer is often Rhesus negative, which can change the entire diet and lifestyle advice for that individual.