Voluntary Society - Action - Health
Hidden Cardiac Risk Factors
By William Faloon
Despite significant advances in heart attack prevention over the past
35 years, cardiac disease remains the leading cause of death in the
Western world.1
Conventional medical doctors routinely prescribe drugs that reduce
potentially dangerous cholesterol and low-density lipoprotein (LDL)
while sometimes boosting beneficial high-density lipoprotein (HDL).
Although more people take cardiac drugs than ever before, hundreds of
thousands of Americans still perish each year from heart failure while
under a doctor’s care.
New members often ask us why their coronary arteries continue to narrow
even when they have followed all the steps their cardiologist has
prescribed. The answer is that atherosclerosis has multiple underlying
causes. Unless every one of these risk factors is corrected, aging
adults will continue to suffer epidemic levels of vascular diseases,
including heart attack and stroke.
We at Life Extension long ago uncovered cardiac risks that mainstream
doctors ignore. Recent scientific studies have validated that
atherosclerosis is indeed a multifactorial process,2-5 and that taking
aggressive preventive actions can dramatically reduce one’s chances of
dying from cardiovascular disease.
Why Excess Fibrinogen Is So Dangerous
Fibrinogen, a protein produced by the liver, plays a role in the
development of atherosclerotic plaque. Fibrinogen can also cause acute
blood clot formation that may block a coronary artery (causing a heart
attack) or a cerebral artery (causing an ischemic stroke).
Back in 1996, Life Extension published data indicating that high blood
levels of fibrinogen predisposed people to heart attacks. In 2001, we
reported on studies indicating that high levels of fibrinogen are also
a significant risk factor for suffering a stroke.6-9
Numerous reports now link elevated fibrinogen to increased heart attack
and stroke risk.10 One compelling study measured fibrinogen blood
levels at baseline and then carefully tracked a large group of
physicians over a period of several years.11 In physicians with
fibrinogen levels higher than 343 (milligrams per deciliter of blood),
heart attack risk doubled compared to physicians with a fibrinogen
reading below this number.
Even after adjusting for other risk factors such as body mass index,
diabetes, hypertension, alcohol consumption, and HDL there was an
approximately twofold increase in heart attack risk among physicians
with the higher fibrinogen levels. In the physician study subjects who
were given 325 mg of aspirin every other day, heart attack rates were
still twice as high in those with elevated fibrinogen (though aspirin
did reduce heart attack incidence across all fibrinogen ranges). Study
subjects who did not take aspirin and had higher fibrinogen levels had
a startling 3.6-fold increase in heart attack incidence.11
The scientists who conducted this study stated that fibrinogen “appears
to be an independent risk factor for cardiovascular disease.”11 This
means that even if you control all other cardiac risk factors, if your
fibrinogen level is over 343 mg/dL, this by itself could cause you to
suffer a heart attack.
Elevated fibrinogen is not only a powerful predictor of who will
develop coronary artery disease. A brand-new study shows that high
fibrinogen foretells who is likely to die within 42 months of suffering
a heart attack. According to the scientists who conducted this 2006
study, “fibrinogen levels were the only independent predictor of
mortality...”12
Despite all of this scientific evidence, few doctors today bother to
check their patients’ blood levels of fibrinogen. This may start to
change.
Fibrinogen Finally Gets Mainstream Respect
The October 28, 2005, issue of the Journal of the American Medical
Association contains an evaluation of pooled human data on fibrinogen
and various diseases. A total of 154,211 study subjects were analyzed.
Based on age and sex alone, the findings show that for each 100-mg/dL
increase in fibrinogen over the initial baseline level, there was a
2.4-fold greater likelihood of contracting coronary heart disease.13
After adjusting for other risk factors such as diabetes, blood
pressure, body mass index, and LDL, the coronary heart disease risk was
1.8-fold greater for each 100-mg/dL increase in fibrinogen levels.13
These findings corroborate previous studies suggesting that fibrinogen
is a significant risk factor for heart attack and stroke!14-21
In those with fibrinogen in-creases of 100-mg/dL over baseline, deaths
from cancers of the digestive tract, smoking-related cancers, and
hormone-related cancers were also greater.13
What These Studies Tell Us
In the United States, fibrinogen is typically measured in milligrams
per deciliter (mg/dL) of blood. Today’s standard laboratory reference
range for fibrinogen is 193-423 mg/dL. Thus, according to conventional
standards, fibrinogen levels as high as 423 mg/dL are acceptable.
Previous studies have indicated higher risks of heart attack, stroke,
and other vascular diseases as fibrinogen levels rise above 300
mg/dL.22-26
The doctors who authored this study published in the American Medical
Association’s own journal found that regardless of one’s fibrinogen
level at baseline (levels evaluated at baseline were between 250 and
562 mg/dL), any increase of 100 mg/dL over baseline is associated with
a significantly increased risk of heart attack, stroke, other vascular
diseases, and cancer.13
Based on data from dozens of published studies, it would appear that
aging adults should strive for a fibrinogen level of 200-300 mg/dL.
FOUR WAYS FIBRINOGEN CAUSES HEART DISEASE
Fibrinogen has been shown to be a significant risk factor for
cardiovascular disease. While scientists have yet to confirm all of
fibrinogen’s pathological mechanisms, they have discovered the
following:
1. As a
key factor in blood viscosity (thickness), elevated fibrinogen may
decrease blood flow, especially through partially blocked arteries.27-29
2. Through
its conversion to fibrin, fibrinogen may promote the formation of
abnormal blood clots inside coronary arteries.30-32
3.
Fibrinogen appears to directly contribute to the
atherosclerosis process by binding to LDL and stimulating the
proliferation of vascular smooth muscle, thereby disrupting the
endothelium.33,34
4. By
binding to certain platelet membrane receptor sites, fibrinogen may
facilitate platelet aggregation inside blood vessels, thus initiating
occlusive arterial blood clots.35
How Fibrinogen Facilitates Cancer
The doctors who conducted this huge study published by the American
Medical Association were surprised to see increased rates of cancer in
those with higher fibrinogen levels. However, in light of what Life
Extension has published since 1997, this was not a revelation.
Fibrinogen is the precursor to fibrin in the body. Researchers believe
that cancer cells use fibrin to coat themselves in order to hinder
their recognition by the immune system. In addition, fibrin relays a
signal to cancer cells to initiate angiogenesis, which is the growth of
new blood vessels into the tumor. Fibrin-associated angiogenesis sets
the stage for tumor growth and metastasis.
Cancer patients often demonstrate a hyper-coagulation state, with
elevated fibrinogen playing a significant role in the process. The
administration of anti-coagulant drugs like low-molecular-weight
heparin has been shown to improve survival in those stricken with
cancer.36,37 Anti-coagulant drugs break down fibrin in the body. Those
with higher fibrinogen levels produce more fibrin. Cancer cells use
this fibrin to protect themselves against the body’s immune system and
facilitate growth. Based on these understandings, taking steps to lower
fibrinogen not only reduces heart attack and stroke risk, but also may
reduce one’s odds of developing cancer.
With the confirmatory findings about the lethal dangers of excess
fibrinogen, it is more important than ever to have one’s blood checked,
to initiate fibrinogen-reducing strategies, and to have follow-up
fibrinogen blood tests to assess how your fibrinogen-lowering
intervention is working!
Glucose: The Sweet, Silent Killer
Scientists have known for decades that diabetics have far greater
incidences of heart attack and stroke. Those with uncontrolled diabetes
exhibit chronic and dangerously high levels of blood glucose.
In a startling study released by Johns Hopkins University scientists,
even healthy people with higher normal blood glucose levels were shown
to have more cardiac events.87
The researchers used a blood test (hemoglobin A1C) that evaluates
glucose control over the previous three to four months. This test
measures the percentage of sugar reactions (glycation) that have
occurred in red blood cells. The “standard reference range” states that
hemoglobin A1C up to 5.7% is “normal.” However, the Johns Hopkins
researchers found that hemoglobin A1C levels above 4.5% (even in
non-diabetics) predicted greater heart attack risk.
Those with higher-than-desired blood glucose levels display no
symptoms. In too many instances, however, excess glucose silently
contributes to atherosclerosis and ensuing heart disease. This is why
annual blood testing and proper evaluation of test results are so
crucial.
PROTECTING AGAINST FIBRINOGEN’S LETHAL EFFECTS
Many dietary supplements and drugs used today exert some
fibrinogen-lowering effect. For example:
Fish oil taken in daily doses of 3000 mg or greater has been shown to
lower fibrinogen levels.38-41 It may be no coincidence that fish oil
has also been shown to reduce heart attack risk.42-44 In addition to
reducing triglycerides,45-48 suppressing inflammation,49-51 decreasing
platelet stickiness,52,53 and protecting against arrhythmia,54-56 fish
oil’s ability to lower fibrinogen may be another mechanism responsible
for its cardioprotective effects.
Olive oil has also been shown to lower fibrinogen in humans with
elevated fibrinogen levels.57,58
For those able to tolerate its usually harmless but unpleasant side
effects, niacin can help lower fibrinogen.59-61
High serum vitamin A and beta-carotene levels have been associated with
reduced fibrinogen levels in humans.62 Animals fed a vitamin
A-deficient diet have an impaired ability to break down fibrinogen.
When animals are injected with vitamin A, they produce tissue
plasminogen activator (tPA), which breaks down fibrinogen.63-65
Excessive homocysteine blocks the natural breakdown of fibrinogen by
inhibiting the production of tissue plasminogen activator (tPA).66
Folic acid,67-69 trimethylglycine (TMG),70 vitamin B12,67,71-74 and
vitamin B675 reduce elevated homocysteine levels.
Vitamin C may help reduce fibrinogen. In one study, heart disease
patients were given either 1000 or 2000 mg a day of vitamin C to
measure the fibrinogen breakdown effect. At 1000 mg a day, there was no
detectable change in fibrinolytic activity or cholesterol. At 2000 mg a
day of vitamin C, there was a 27% decrease in the platelet aggregation
index, a 12% reduction in total cholesterol, and a 45% increase in
fibrinolysis (fibrinogen breakdown) activity.76
The fibric acid class of drugs (especially fenofibrate) can lower
fibrinogen by 15-40%. This drug’s primary side effect is increases in
indicators of liver damage in 7.5% of users (compared to only 1.4% in
the placebo group). High doses of niacin may also induce increases in
indices of liver damage.77
Agents that inhibit platelet aggregation may reduce the risk that
fibrinogen will cause an abnormal arterial blood clot. Platelet
aggregation inhibitors include aspirin,78 green tea,79 ginkgo,80
garlic,81 and vitamin E.82 Drugs such as pentoxifylline and Plavix®
also inhibit abnormal platelet aggregation and improve blood flow
through the capillaries.83-86
For optimal protection against heart attack, it makes sense to try to
reduce fibrinogen levels to around 200-300 mg/dL. Some people will find
this impossible, but from what we now know, any reduction in fibrinogen
may correlate with a reduced risk of heart attack, stroke, and cancer.
A common misconception among supplement users is that if they take
nutrients that have been shown to favorably influence a risk factor
(such as reducing fibrinogen), then they do not have to worry about
that risk factor. Since 30-50% of plasma fibrinogen level is
genetically determined, it makes sense to have your blood tested to
make sure that you do not have to take additional steps to reduce your
fibrinogen.
Deadly Consequences of Flawed Reference Ranges
A blood chemistry test can reveal your glucose level. Regrettably, the
medical establishment has misjudged the safe upper limit for fasting
glucose. The result is that doctors are failing to warn patients when
their glucose levels are too high.
Initially, back in 1979, doctors diagnosed diabetes when fasting
glucose levels reached 140 mg/dL on two separate occasions. In 1997,
the guidelines were changed, and fasting glucose levels of 126 mg/dL or
greater became the new standard for diagnosing diabetes, with concern
about impaired glucose metabolism being raised when blood sugar levels
were between 110 and 125 mg/dL. The slow-to-respond conventional
medical establishment finally advised in 2003 that doctors should be
concerned about impaired glucose metabolism when blood sugar levels
reach 100 mg/dL.
Conventional medicine’s flawed understanding of glucose metabolism has
caused tens of millions of needless deaths. As you will soon read, even
today’s accepted normal glucose ranges can predispose aging adults to
startlingly high mortality rates.
Life Extension has always advised members that optimal glucose levels
are below 100 mg/dL.
We based our position on published studies showing increased longevity
for those in lower glucose ranges.88-91 We also had the advantage of
inside information about calorie-restriction experiments that indicated
ideal glucose levels to be around 74 mg/dL.
Keep Glucose in Lower Reference Ranges
Several years ago, Life Extension alerted members that those with
higher “normal” blood glucose readings were at increased risk of
premature death.92
Our warning was based on a study showing greater cardiovascular disease
incidence as blood glucose levels rise past 85 mg/dL.93 Back in those
days, doctors did not worry about glucose until it reached far higher
levels. Contrary to conventional wisdom, we advised members to try to
keep their glucose levels at 85 mg/dL or lower.
Newly published studies have documented the fact that higher glucose
readings elevate vascular disease risk.94-99 In heart attack victims
admitted to the hospital, those with the highest glucose levels have
been shown to be much more likely to suffer severe cardiac outcomes
(and death).95,97,98 One study looked at emergency room cardiac
patients in 2002 and found that 65% were either diabetic or had
impaired glucose control.96 The cumulative findings from these studies
mandate that aging humans take aggressive steps to maintain optimal
blood glucose levels.
An annual blood chemistry test is the best way to make sure your
glucose level is in an optimal range. The hemoglobin A1C test is an
even better indicator of your glucose levels, as it measures that
amount of glycation that glucose has inflicted on your red blood cells
during the previous three to four months.
HEMOGLOBIN A1C AND CARDIAC RISK
The hemoglobin A1C blood test measures the percentage of hemoglobin
that has become glycated as a result of glucose-protein reactions.
Hemoglobin A1C has long been used to monitor long-term control of
diabetes.
The level of hemoglobin A1C is increased in the red blood cells of
people with poorly controlled glucose. Since the test evaluates
hemoglobin in red blood cells (which normally live about 120 days), the
level of hemoglobin A1C reflects the average blood glucose level over
the previous three to four months.
Based on recent findings, an ideal reading of hemoglobin A1C is 4.5% or
lower.87 Standard laboratory reference ranges, however, erroneously
indicate that non-diabetics can have a hemoglobin A1C reading as high
as 5.7%. We now know that the greater the level of hemoglobin A1C above
4.5%, the more likely one is to suffer a heart attack.
Diabetics often have hemoglobin A1C levels higher than 7%, which helps
explain the multitude of sugar-related complications suffered by those
unable to maintain healthy blood glucose levels.
It is commonly recommended that hemoglobin A1C be measured every three
to six months in diabetics. The new data show that higher hemoglobin
A1C levels in non-diabetics predict heart attack risk. This indicates
that the hemoglobin A1C blood test may have a role in alerting those
with less-than-optimal glucose control that they should make lifestyle
changes. Lowering the level of hemoglobin A1C by any amount improves
one’s chances of staying healthy.
Best Value in Comprehensive Blood Testing
Since the early 1980s, Life Extension has advised its members to have
annual blood tests to identify disease risk factors that can be
reversed before serious illness develops. The impact of these blood
tests in preventing future disease and premature death is incalculable.
The problem members previously encountered was that their doctors
refused to prescribe blood tests for important health markers such as
prostate-specific antigen (PSA), homocysteine, and C-reactive protein.
The price of these tests was also prohibitive. Ten years ago, Life
Extension resolved this problem by offering blood tests at discounted
prices directly to its members.
Once a year, we reduce our everyday low prices. Until May 31, 2006, we
are discounting all blood tests so that members can obtain
comprehensive blood evaluations at a fraction of the price charged by
commercial laboratories.
To provide members with an even greater assessment of their disease
risks, we are virtually giving away the fibrinogen and hemoglobin A1C
tests when members order the popular Male or Female Life Extension
Panels.
In this month’s issue, we describe the most important blood tests you
should have at least once a year. We also introduce a new test panel
that separates different fractions of LDL, HDL, and other lipoproteins
involved in the atherosclerosis process. This new test panel is
especially critical to those at high risk for vascular disease.
Whether you use your own doctor, a commercial laboratory, or our blood
testing service, I encourage every member to have his or her blood
tested at least once a year.
For longer life,
William Faloon
References
1. Available at: http://www.cdc.gov/nchs/fastats/lcod.htm. Accessed
January 31, 2006.
2. Li JJ, Chen JL. Inflammation may be a bridge connecting hypertension
and atherosclerosis. Med Hypotheses. 2005;64(5):925-9.
3. Liao JK. Clinical implications for statin pleiotropy. Curr Opin
Lipidol. 2005 Dec;16(6):624-9.
4. Li JJ, Fang CH. Atheroscleritis is a more rational term for the
pathological entity currently known as atherosclerosis. Med Hypotheses.
2004;63(1):100-2.
5. Muhlestein JB. Infectious agents, antibiotics, and coronary artery
disease. Curr Interv Cardiol Rep. 2000 Nov;2(4):342-8.
6. Chyi-Huey Bai, et al. Relations between coagulation profiles, lipid
profiles, and other risk factors with risk of first-ever ischemic
stroke: a novel case-control study. Abstracts of the International
Stroke Conference 2000 32: 367-b Poster Presentation. P 156.
7. Chen Jiunn-Rong. Dilatation of common carotid artery is strongly
associated with cerebral ischemic stroke with or without the presence
of carotid atherosclerosis Abstracts of the International Stroke
Conference 2000 32: 365-d.
8. Audebert Heinrich J. Predictors of Progression in Lacunar Stroke.
Abstracts of the International Stroke Conference 2000 32: 347-c.
9. Trouillas P. The “making” of a parenchymal hematoma. An early
coagulopathy and specific risk factors contribute to grave
intracerebral bleeding after intravenous rtPA thrombolysis. Abstracts
of the International Stroke Conference 2000 32: 345-a.
10. Pearson TA, Mensah GA, Alexander RW, et al. Markers of inflammation
and cardiovascular disease: application to clinical and public health
practice: A statement for healthcare professionals from the Centers for
Disease Control and Prevention and the American Heart Association.
Circulation. 2003 Jan 28;107(3):499-511.
11. Ma J, Hennekens CH, Ridker PM, Stampfer MJ. A prospective study of
fibrinogen and risk of myocardial infarction in the Physicians’ Health
Study. J Am Coll Cardiol. 1999 Apr;33(5):1347-52.
12. Coppola G, Rizzo M, Abrignani MG, et al. Fibrinogen as a predictor
of mortality after acute myocardial infarction: a forty-two-month
follow-up study. Ital Heart J. 2005 Apr;6(4):315-22.
13. Danesh J, Lewington S, Thompson SG, et al. Plasma fibrinogen level
and the risk of major cardiovascular diseases and nonvascular
mortality: an individual participant meta-analysis. JAMA. 2005 Oct
12;294(14):1799-809.
14. Acevedo M, Foody JM, Pearce GL, Sprecher DL. Fibrinogen:
associations with cardiovascular events in an outpatient clinic. Am
Heart J. 2002 Feb;143(2):277-82.
15. Bots ML, Elwood PC, Salonen JT, et al. Level of fibrinogen and risk
of fatal and non-fatal stroke. EUROSTROKE: a collaborative study among
research centres in Europe. J Epidemiol Community Health. 2002 Feb;56
Suppl 1i14-8.
16. de Maat MP. Effects of diet, drugs, and genes on plasma fibrinogen
levels. Ann NY Acad Sci. 2001;936:509-21.
17. Lindahl B, Toss H, Siegbahn A, Venge P, Wallentin L. Markers of
myocardial damage and inflammation in relation to long-term mortality
in unstable coronary artery disease. FRISC Study Group. Fragmin during
Instability in Coronary Artery Disease. N Engl J Med. 2000 Oct
19;343(16):1139-47.
18. Packard CJ, O’Reilly DS, Caslake MJ, et al. Lipoprotein-associated
phospholipase A2 as an independent predictor of coronary heart disease.
West of Scotland Coronary Prevention Study Group. N Engl J Med. 2000
Oct 19;343(16):1148-55.
19. Maresca G, Di BA, Marchioli R, Di MG. Measuring plasma fibrinogen
to predict stroke and myocardial infarction: an update. Arterioscler
Thromb Vasc Biol. 1999 Jun;19(6):1368-77.
20. Behar S. Lowering fibrinogen levels: clinical update. BIP Study
Group. Bezafibrate Infarction Prevention. Blood Coagul Fibrinolysis.
1999 Feb;10 Suppl 1S41-3.
21. Thompson SG, Kienast J, Pyke SD, Haverkate F, van de Loo JC.
Hemostatic factors and the risk of myocardial infarction or sudden
death in patients with angina pectoris. European Concerted Action on
Thrombosis and Disabilities Angina Pectoris Study Group. N Engl J Med.
1995 Mar 9;332(10):635-41.
22. ez-Ewald M, Campos G, Rivero F, et al. Hemostatic coronary risk
factors in a healthy population of Maracaibo, Venezuela. Invest Clin.
2003 Mar;44(1):21-30.
23. Salobir B, Sabovic M, Peternel P, Stegnar M. Fibrinolytic
parameters and lipoprotein(a) in young women with myocardial
infarction. Angiology. 2002 Mar;53(2):157-63.
24. Cantin B, Despres JP, Lamarche B, et al. Association of fibrinogen
and lipoprotein(a) as a coronary heart disease risk factor in men (The
Quebec Cardiovascular Study). Am J Cardiol. 2002 Mar 15;89(6):662-6.
25. Sato S, Nakamura M, Iida M, et al. Plasma fibrinogen and coronary
heart disease in urban Japanese. Am J Epidemiol. 2000 Sep
1;152(5):420-3.
26. Baller D, Gleichmann U, Miche E, Mannebach H, Seggewiss H. Clinical
significance of the cardiovascular risk factor fibrinogen in secondary
prevention. Versicherungsmedizin. 1995 Apr 1;47(2):55-60.
27. Ulrich MM, Alink GM, Kumarathasan P, et al. Health effects and time
course of particulate matter on the cardiopulmonary system in rats with
lung inflammation. J Toxicol Environ Health A. 2002 Oct
25;65(20):1571-95.
28. Allen JD, Wilson JB, Tulley RT, Lefevre M, Welsch MA. Influence of
age and normal plasma fibrinogen levels on flow-mediated dilation in
healthy adults. Am J Cardiol. 2000 Sep 15;86(6):703-5.
29. Leschke M, Strauer BE. The significance of rheologic mechanisms in
atherogenesis. Arzneimittelforschung. 1990 Mar;40(3A):356-62.
30. Drouet L, Bal dit SC. Is fibrinogen a predictor or a marker of the
risk of cardiovascular events? Therapie. 2005 Mar;60(2):125-36.
31. Spuentrup E, Buecker A, Katoh M, et al. Molecular magnetic
resonance imaging of coronary thrombosis and pulmonary emboli with a
novel fibrin-targeted contrast agent. Circulation. 2005 Mar
22;111(11):1377-82.
32. Reganon E, Vila V, Aznar J, et al. Studies on the functionality of
newly synthesized fibrinogen after treatment of acute myocardial
infarction with streptokinase, increase in the rate of fibrinopeptide
release. Thromb Haemost. 1993 Dec 20;70(6):978-83.
33. Smith EB. Lipids and plasma fibrinogen: early and late composition
of the atherosclerotic plaque. Cardiologia. 1994 Dec;39(12 Suppl
1):169-72.
34. Brown NJ, Staton CA, Rodgers GR, et al. Fibrinogen E fragment
selectively disrupts the vasculature and inhibits the growth of tumours
in a syngeneic murine model. Br J Cancer. 2002 Jun 5;86(11):1813-6.
35. Bennett JS. Platelet-fibrinogen interactions. Ann N Y Acad Sci.
2001;936:340-54.
36. Lebeau B, Chastang C, Brechot JM, et al. Subcutaneous heparin
treatment increases survival in small cell lung cancer. “Petites
Cellules” Group. Cancer. 1994 Jul 1;74(1):38-45.
37. Green D, Hull RD, Brant R, Pineo GF. Lower mortality in cancer
patients treated with low-molecular-weight versus standard heparin.
Lancet. 1992 Jun 13;339(8807):1476.
38. Vanschoonbeek K, Feijge MA, Paquay M, et al. Variable hypocoagulant
effect of fish oil intake in humans: modulation of fibrinogen level and
thrombin generation. Arterioscler Thromb Vasc Biol. 2004
Sep;24(9):1734-40.
39. de BA, Mennen LI, Hercberg S, Galan P. Evidence for a protective
(synergistic?) effect of B-vitamins and omega-3 fatty acids on
cardiovascular diseases. Eur J Clin Nutr. 2004 May;58(5):732-44.
40. Uauy R, Valenzuela A. Marine oils: the health benefits of n-3 fatty
acids. Nutrition. 2000 Jul;16(7-8):680-4.
41. Conquer JA, Cheryk LA, Chan E, Gentry PA, Holub BJ. Effect of
supplementation with dietary seal oil on selected cardiovascular risk
factors and hemostatic variables in healthy male subjects. Thromb Res.
1999 Nov 1;96(3):239-50.
42. Mori TA, Vandongen R, Beilin LJ, et al. Effects of varying dietary
fat, fish, and fish oils on blood lipids in a randomized controlled
trial in men at risk of heart disease. Am J Clin Nutr. 1994
May;59(5):1060-8.
43. Ghafoorunissa, Vani A, Laxmi R, Sesikeran B. Effects of dietary
alpha-linolenic acid from blended oils on biochemical indices of
coronary heart disease in Indians. Lipids. 2002 Nov;37(11):1077-86.
44. Andriamampandry MD, Leray C, Freund M, Cazenave JP, Gachet C.
Antithrombotic effects of (n-3) polyunsaturated fatty acids in rat
models of arterial and venous thrombosis. Thromb Res. 1999 Jan
1;93(1):9-16.
45. Available at: http://www.ahrq.gov/news/press/pr2004/omega3pr.htm.
Accessed January 31, 2006.
46. Marckmann P, Bladbjerg EM, Jespersen J. Dietary fish oil (4 g
daily) and cardiovascular risk markers in healthy men. Arterioscler
Thromb Vasc Biol. 1997 Dec;17(12):3384-91.
47. Bruckner G. Microcirculation, vitamin E and omega 3 fatty acids: an
overview. Adv Exp Med Biol. 1997;415:195-208.
48. Mori TA, Vandongen R, Beilin LJ, Burke V, Morris J, Ritchie J.
Effects of varying dietary fat, fish, and fish oils on blood lipids in
a randomized controlled trial in men at risk of heart disease. Am J
Clin Nutr. 1994 May;59(5):1060-8.
49. Calder PC. N-3 polyunsaturated fatty acids and inflammation: from
molecular biology to the clinic. Lipids. 2003 Apr;38(4):343-52.
50. Jolly CA, Muthukumar A, Avula CP, Troyer D, Fernandes G. Life span
is prolonged in food-restricted autoimmune-prone (NZB x NZW)F(1) mice
fed a diet enriched with (n-3) fatty acids. J Nutr. 2001
Oct;131(10):2753-60.
51. Grimble RF. Nutritional modulation of immune function. Proc Nutr
Soc. 2001 Aug;60(3):389-97.
52. Eschen O, Christensen JH, De CR, Schmidt EB. Soluble adhesion
molecules in healthy subjects: a dose-response study using n-3 fatty
acids. Nutr Metab Cardiovasc Dis. 2004 Aug;14(4):180-5.
53. Andrioli G, Carletto A, Guarini P, et al. Differential effects of
dietary supplementation with fish oil or soy lecithin on human platelet
adhesion. Thromb Haemost. 1999 Nov;82(5):1522-7.
54. Anon. Dietary supplementation with n-3 polyunsaturated fatty acids
and vitamin E after myocardial infarction: results of the
GISSI-Prevenzione trial. Gruppo Italiano per lo Studio della
Sopravvivenza nell’Infarto miocardico. Lancet. 1999 Aug
7;354(9177):447-455.
55. Singh RB, Niaz MA, Sharma JP, et al. Randomized, double-blind,
placebo-controlled trial of fish oil and mustard oil in patients with
suspected acute myocardial infarction: the Indian experiment of infarct
survival—4. Cardiovasc Drugs Ther. 1997 Jul;11(3):485-91.
56. Nair SS, Leitch JW, Falconer J, Garg ML. Prevention of cardiac
arrhythmia by dietary (n-3) polyunsaturated fatty acids and their
mechanism of action. J Nutr. 1997 Mar;127(3):383-93.
57. Flaten H, Hostmark AT, Kierulf P, et al. Fish-oil concentrate:
effects on variables related to cardiovascular disease. Am J Clin Nutr.
1990 Aug;52(2):300-6.
58. Oosthuizen W, Vorster HH, Jerling JC, et al. Both fish oil and
olive oil lowered plasma fibrinogen in women with high baseline
fibrinogen levels. Thromb Haemost. 1994 Oct;72(4):557-62.
59. Chesney CM, Elam MB, Herd JA, et al. Effect of niacin, warfarin,
and antioxidant therapy on coagulation parameters in patients with
peripheral arterial disease in the Arterial Disease Multiple
Intervention Trial (ADMIT). Am Heart J. 2000 Oct;140(4):631-6.
60. Philipp CS, Cisar LA, Saidi P, Kostis JB. Effect of niacin
supplementation on fibrinogen levels in patients with peripheral
vascular disease. Am J Cardiol. 1998 Sep 1;82(5):697-9, A9.
61. Johansson JO, Egberg N, splund-Carlson A, Carlson LA. Nicotinic
acid treatment shifts the fibrinolytic balance favourably and decreases
plasma fibrinogen in hypertriglyceridaemic men. J Cardiovasc Risk. 1997
Jun;4(3):165-71.
62. van Herpen-Broekmans WM, Klopping-Ketelaars IA, Bots ML, et al.
Serum carotenoids and vitamins in relation to markers of endothelial
function and inflammation. Eur J Epidemiol. 2004;19(10):915-21.
63. Ceriello A, Bortolotti N, Pirisi M, et al. Total plasma antioxidant
capacity predicts thrombosis-prone status in NIDDM patients. Diabetes
Care. 1997 Oct;20(10):1589-93.
64. Back O, Nilsson TK. Retinoids and fibrinolysis. Acta Derm Venereol.
1995 Jul;75(4):290-2.
65. Lagente V, Boichot E, Carre C, et al. Effects of the platelet
activating factor antagonists BN 52021 and BN 50730 on antigen-induced
bronchial hyperresponsiveness and eosinophil infiltration in lung from
sensitized guinea-pigs. Clin Exp Allergy. 1993 Dec;23(12):1002-10.
66. Midorikawa S, Sanada H, Hashimoto S, Watanabe T. Enhancement by
homocysteine of plasminogen activator inhibitor-1 gene expression and
secretion from vascular endothelial and smooth muscle cells. Biochem
Biophys Res Commun. 2000 May 27;272(1):182-5.
67. Nurk E, Tell GS, Vollset SE, et al. Changes in lifestyle and plasma
total homocysteine: the Hordaland Homocysteine Study. Am J Clin Nutr.
2004 May;79(5):812-9.
68. Malinow MR, Duell PB, Hess DL, et al. Reduction of plasma
homocyst(e)ine levels by breakfast cereal fortified with folic acid in
patients with coronary heart disease. N Engl J Med. 1998 Apr
9;338(15):1009-15.
69. Tucker KL, Mahnken B, Wilson PW, Jacques P, Selhub J. Folic acid
fortification of the food supply. Potential benefits and risks for the
elderly population. JAMA. 1996 Dec 18;276(23):1879-85.
70. Dudman NP, Guo XW, Gordon RB, Dawson PA, Wilcken DE. Human
homocysteine catabolism: three major pathways and their relevance to
development of arterial occlusive disease. J Nutr. 1996 Apr;126(4
Suppl):1295S-300S.
71. Stott DJ, MacIntosh G, Lowe GD, et al. Randomized controlled trial
of homocysteine-lowering vitamin treatment in elderly patients with
vascular disease. Am J Clin Nutr. 2005 Dec;82(6):1320-6.
72. Elian KM, Hoffer LJ. Hydroxocobalamin reduces hyperhomocysteinemia
in end-stage renal disease. Metabolism. 2002 Jul;51(7):881-6.
73. Aleman G, Tovar AR, Torres N. Homocysteine metabolism and risk of
cardiovascular diseases: importance of the nutritional status on folic
acid, vitamins B6 and B12. Rev Invest Clin. 2001 Mar;53(2):141-51.
74. Bostom AG, Shemin D, Lapane KL, et al. High dose-B-vitamin
treatment of hyperhomocysteinemia in dialysis patients. Kidney Int.
1996 Jan;49(1):147-52.
75. Schnyder G, Roffi M, Flammer Y, Pin R, Hess OM. Effect of
homocysteine-lowering therapy with folic acid, vitamin B12, and vitamin
B6 on clinical outcome after percutaneous coronary intervention: the
Swiss Heart study: a randomized controlled trial. JAMA. 2002 Aug
28;288(8):973-9.
76. Bordia AK. The effect of vitamin C on blood lipids, fibrinolytic
activity and platelet adhesiveness in patients with coronary artery
disease. Atherosclerosis. 1980 Feb;35(2):181-7.
77. McCarty MF. Co-administration of equimolar doses of betaine may
alleviate the hepatotoxic risk associated with niacin therapy. Med
Hypotheses. 2000 Sep;55(3):189-94.
78. Bossavy JP, Thalamas C, Sagnard L, et al. A double-blind randomized
comparison of combined aspirin and ticlopidine therapy versus aspirin
or ticlopidine alone on experimental arterial thrombogenesis in humans.
Blood. 1998 Sep 1;92(5):1518-25.
79. Kang WS, Lim IH, Yuk DY, et al. Antithrombotic activities of green
tea catechins and (-)-epigallocatechin gallate. Thromb Res. 1999 Nov
1;96(3):229-37.
80. Logani S, Chen MC, Tran T, Le T, Raffa RB. Actions of ginkgo biloba
related to potential utility for the treatment of conditions involving
cerebral hypoxia. Life Sci. 2000 Aug 11;67(12):1389-96.
81. Rahman K, Billington D. Dietary supplementation with aged garlic
extract inhibits ADP-induced platelet aggregation in humans. J Nutr.
2000 Nov;130(11):2662-5.
82. Azzi A, Breyer I, Feher M, et al. Specific cellular responses to
alpha-tocopherol. J Nutr. 2000 Jul;130(7):1649-52.
83. Evangelista V, Manarini S, Dell’Elba G, et al. Clopidogrel inhibits
platelet-leukocyte adhesion and platelet-dependent leukocyte
activation. Thromb Haemost. 2005 Sep;94(3):568-77.
84. Jagroop IA, Matsagas MI, Geroulakos G, Mikhailidis DP. The effect
of clopidogrel, aspirin and both antiplatelet drugs on platelet
function in patients with peripheral arterial disease. Platelets. 2004
Mar;15(2):117-25.
85. de la Cruz JP, Romero MM, Sanchez P, et al. Antiplatelet effect of
pentoxifylline in human whole blood. Gen Pharmacol. 1993
May;24(3):605-9.
86. Gaur SP, Garg RK, Kar AM, Srimal RC. Effect of anti-platelet
therapy (aspirin + pentoxiphylline) on plasma lipids in patients of
ischaemic stroke. Indian J Physiol Pharmacol. 1993 Apr;37(2):158-60.
87. Selvin E, Coresh J, Golden SH, et al. Glycemic control and coronary
heart disease risk in persons with and without diabetes: the
atherosclerosis risk in communities study. Arch Intern Med. 2005 Sep
12;165(16):1910-6.
88. Miller RA, Buehner G, Chang Y, et al. Methionine-deficient diet
extends mouse lifespan, slows immune and lens aging, alters glucose,
T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and
stress resistance. Aging Cell. 2005 Jun;4(3):119-25.
89. Jiang JC, Jaruga E, Repnevskaya MV, Jazwinski SM. An intervention
resembling caloric restriction prolongs life span and retards aging in
yeast. FASEB J. 2000 Nov;14(14):2135-7.
90. Lane MA, Ingram DK, Roth GS. Calorie restriction in nonhuman
primates: effects on diabetes and cardiovascular disease risk. Toxicol
Sci. 1999 Dec;52(2 Suppl):41-8.
91. Wanagat J, Allison DB, Weindruch R. Caloric intake and aging:
mechanisms in rodents and a study in nonhuman primates. Toxicol Sci.
1999 Dec;52(2 Suppl):35-40.
92. Available at:
http://www.lef.org/magazine/mag2004/jan2004_awsi_01.htm. Accessed
January 31, 2006.
93. Bjornholt JV, Erikssen G, Aaser E, et al. Fasting blood glucose: an
underestimated risk factor for cardiovascular death. Results from a
22-year follow-up of healthy nondiabetic men. Diabetes Care. 1999
Jan;22(1):45-9.
94. Zeller M, Steg PG, Ravisy J, et al. Prevalence and impact of
metabolic syndrome on hospital outcomes in acute myocardial infarction.
Arch Intern Med. 2005 May 23;165(10):1192-8.
95. Ainla T, Baburin A, Teesalu R, Rahu M. The association between
hyperglycaemia on admission and 180-day mortality in acute myocardial
infarction patients with and without diabetes. Diabet Med. 2005
Oct;22(10):1321-5.
96. Sasaki M, Saito T, Kubo N, et al. Alteration in risk factor
accumulations of acute myocardial infarction during the last one
decade: Analysis of patients admitted in Coronary Care Unit. Diabetes
Res Clin Pract. 2005 Sep 20.
97. Stranders I, Diamant M, van Gelder RE, et al. Admission blood
glucose level as risk indicator of death after myocardial infarction in
patients with and without diabetes mellitus. Arch Intern Med. 2004 May
10;164(9):982-8.
98. Timmer JR, van dH, I, Ottervanger JP, et al. Prognostic value of
admission glucose in non-diabetic patients with myocardial infarction.
Am Heart J. 2004 Sep;148(3):399-404.
99. Wong VW, Ross DL, Park K, Boyages SC, Cheung NW. Hyperglycemia:
still an important predictor of adverse
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