Articles:
Osteoporosis
by
Garry F. Gordon MD, DO, MD(H)
President, Gordon Research Institute
www.gordonresearch.com
Osteoporosis is a multifactorial problem and thus I recommend a
broad based therapeutic approach, which does not require or even
tolerate the use of drugs such as Fosamax. Please become informed
about the benefit risk ratio of that drug and the other all to
commonly used pharmacological approaches.
I want to draw your attention to the implication of genetics in this
all too common disease. Suffice it to say that a part of my current
protocol for prevention and treatment of all bone loss, including
Dental, is the RNA NutriSwitch formula called Bone Support. This is
expensive but money is not an object when you face the ramifications
of this disease, i.e. over 20% expire within a year from the date of
their hip fracture. However, I have formulated an all new, all
natural, powerful synergistic group of substances, which I call
Beyond Bone Defense. It not only gives you therapeutic levels of Vit
K2 and D but also Strontium, a well documented approach, as well as
all the natural substances that prevent bone resorption and support
bone growth.
Moreover, the incredible all natural HERB from Thailand is here that
will replace all the Isoflavones (Black Cohosh, Red Clover) and, for
many, even the need for bio identical hormones and it is available
to your patients and your family now. It is called Beyond HRT
(Herbal Remedy from Thailand) and is from a staple in the diet in
Northern Thailand where, as a result of daily consumption of this,
we find the lowest incidence of breast cancer in the world. Also in
well- controlled studies over 90% of women stop the hot flashes,
vaginal dryness, and depression. It is known to be over 3000 times
stronger than Genistein and works on the estrogen receptor, as well
as elsewhere. We find strong bones and low incidence of Alzheimer's,
as a consequence of ingesting this Pueraria Mirifica. Since men also
have osteoporosis, and Estrogen is part of their problem, this is
suitable for both sexes and interestingly it seems to treat prostate
problems too.
For the Bone problem I am not recommending more than 500 mg of
Calcium and that is ONLY if they consume the same level of
Magnesium, as found in the multiple that I formulated called BAM
(Beyond Any Multiple). It is also found in the oral chelation
packets, where you will also be removing slowly the Lead from your
patient's bones permitting even better response to this protocol. So
use the packets, 9 pills twice a day, as part of my total approach
to BONE HEALTH. You may also want to learn more about the safe,
effective, alternative to Growth Hormone injections that I
recommend, Beyond GHS and Maca, for my patients. These will help
support healthier levels of free testosterone but, of course, I
support topical use of Testosterone and Progesterone, and now we
have a safe alternative to the Estrogen part of hormonal
supplementation.
Exercise should include rebounding.
Please try a few tough cases of Osteoporosis on all of the above.
Be aware that gene testing will be in your future. We are doing
this now for all the Autistic Children and significant abnormalities
have been found in every case to date. Without knowing these gene
related problems, all programs will provide suboptimal results.
However, since RNA NutriSwitch products are based on cell: cell
communication and since our food does talk to our genes, just think
of the growing family of over 25 different RNA NutriSwitch Formulas
to deal with everything from anti-aging (ProLongevity) to Heart,
Kidney, Bone, Bowel etc or even neurotransmitter health. These are
available only through Longevity Plus-RNA, as THE FOOD OF THE FUTURE
for your patients. All the benefit with NO RISK. Speak to customer
service at 928-472-2450 to learn more about which of the RNA
products you might want to be taking for yourself.
Garry F. Gordon MD, DO, MD(H)
President, Gordon Research Institute
www.gordonresearch.com
#1 Medical Hypotheses
Volume 63, Issue 6 , 2004, Pages 1010-1013
Calcium and vitamin D supplementation during bisphosphonate
(Fosamax, Aredia, Didronel, Actonel, Skelid) administration may
increase osteoclastic activity in patients with bone metastasis
Ozden Altundaga, Kadri Altundag, Yavuz Selim Silayb, Mehmet
Gunduzc, Kadir Demircand and Ibrahim Gullua
a Department of Medical Oncology, Hacettepe University Faculty of
Medicine, Sihhiye 06100, Ankara, Turkey
b Department of Neurology, Baylor College of Medicine, Houston, USA
c Department of Oral Pathology and Medicine, Graduate School of
Medicine and Dentistry, Okayama University, Okayama, Japan
d Department of Molecular Biology and Biochemistry, Graduate School
of Medicine and Dentistry, Okayama University, Okayama, Japan
Received 20 April 2004; accepted 20 April 2004. Available online
17 June 2004.
Abstract
Bone metastasis are a frequent complication of cancer, occurring in
up to 70% of patients with advanced breast or prostate cancer. The
consequences of bone metastasis are often devastating. Osteolytic
metastasis can cause different kinds of skeletal related events
including severe pain, pathologic fractures, life-threatening
hypercalcemia, spinal cord compression, and other nerve-compression
syndromes. These skeletal-related events are the result of the
resorption of mineralized bone by osteoclasts. Bisphosphonates are
synthetic analogues of naturally occurring pyrophosphate compounds
that inhibit bone resorption. Potent bisphosphonates, pamidronate
and, more importantly zoledronic acid may cause hypocalcemia, but
mostly asymptomatic, mild, transient in most cases. Sufficient
calcium and vitamin D intake needs to be ensured in patients with
malignancy who have borderline or low levels of calcium when
commencing treatment with bisphosphonates. Vitamin D itself induce
the formation of osteoclasts by increasing the expression of RANKL
on marrow stromal cells. Local calcium also promotes tumor growth
and the production of parathyroid hormone-related peptide which in
turn stimulates bone resorption. Vitamin D and calcium
supplementation during bisphosphonate administration for the purpose
of elimination of the side effects related to hypocalcemia in
patients with bone metastasis may increase the bone resorption and
decrease the efficacy of bisphosphonates. Therefore, vitamin D and
calcium supplementation must not be routinely recommended during
bisphosphonate administration.
#2 Bone Up on Osteoporosis
From The November 2000 Issue of Nutrition Science News
Lifestyle and dietary approaches can prevent this debilitating
condition
by Carmia Borek, Ph.D.
Bones are amazing living structures that are constantly being
remodeled throughout life. Bones continuously mend and rebuild
themselves by the opposing actions of two types of cells: the
osteoblasts that form bone and the osteoclasts that resorb (destroy)
bone. When the activity of the bone-destroying osteoclast cells
outpaces that of bone-forming osteoblasts, the bottom line is bone
loss and increased osteoporosis risk.
Osteoporosis currently affects more than 26 million Americans, of
whom 20 million (77 percent) are women.1 In 1995, the medical costs
of treating osteoporosis were estimated at $13.8 billion and were
predicted to increase to $162 billion by the year 2020. Disease risk
increases with age, as does rate of injury. Therefore, one-third of
women who reach 65 will have a vertebrae fracture, and of those
women who reach 80 years, 32 percent will suffer a hip fracture.1
Osteoporosis develops less often in men because they generally start
with more bone mass, their bone loss begins later in their lives,
and they incur no period of rapid hormonal change that is linked to
bone loss.2 However, men suffer hip fractures at high rates after
the age of 70 (17 percent of 80-year-olds). In addition to hip
fractures, men older than 70 frequently have debilitating spine,
wrist and other bone fractures.
The Nature of the Condition
Osteoporosis silently breaks down the skeleton. Bone substance loss
makes bones more fragile, resulting in spontaneous fractures,
especially of the vertebrae and hip. Bone loss and osteoporosis
occur in otherwise healthy people as result of many factors,
possibly including heredity. One way women lose bone is menopause-
related decreases in estrogen levels. Normally, estrogens bind to
bone-forming osteoblasts, causing a chemical secretion that prevents
osteoclasts from breaking down bone. Estrogens, therefore, help
conserve bone by reducing bone loss and increasing bone density. The
onset of menopause removes this protection. Men, incidentally, also
lose estrogens as well as male hormones (androgens) as they age, but
at a slower rate than women.
A lack of physical activity also increases osteoporosis risk, as
does exposure to various pollutants and toxins, such as those in
cigarette smoke. Insufficient intake of nutrients, particularly
calcium and vitamin D, which play major roles in bone building, is
one of the strongest promoters of bone loss and also one of the most
reversible risk factors.
Nutrients That Help Build Bones
Since they are living tissues, bone cells need the same kinds of
nutrients as do other cells in the body. But bones need extra
nutrients to help osteoblasts form new bone and prevent bone loss.
Following are some of the nutrients, in order of importance, known
to aid in these functions.
Calcium is one of the principal components of bone and is absolutely
essential for bone formation. During the first 20 years of life,
bone minerals accumulate in the skeleton. However, bone mineral loss
begins after age 30. In women, this loss can be slowed with a
combination of calcium and vitamin D supplementation.3 Although
there are few studies of bone loss in men, there is evidence that
dietary intake of more than 1,000 mg a day of calcium may slow this
process in men as well.4
Fortunately, if a lifetime of high calcium intake has not been
possible, women's studies show bone density still can be improved by
increasing calcium and vitamin D intake before a woman enters
menopause. Moreover, high levels of calcium supplementation are
especially important for patients receiving currently approved bone-
maintaining drugs for the prevention of osteoporosis such as
estrogens, Raloxifene and Alendronate.
Dairy products are the richest food sources of calcium, followed by
soy and broccoli.5 Calcium supplements such as calcium carbonate and
calcium citrate are also readily available. Which of these two forms
is better-absorbed is unknown because analysis methods have varied.
Regardless of how it is obtained, the recommended daily calcium
intake is 1,200 mg for postmenopausal women and 1,000 mg for
premenopausal women.3 Women in menopause who are not on hormone
replacement therapy (HRT) are often advised by their physicians to
increase their daily dose to 1,500 mg.
Vitamin D is a derivative of cholesterol made in our skin during
exposure to the sun's ultraviolet (UV) rays. Once formed, vitamin D
(called cholecalciferol) is then converted to an active form (1,25-
dihydroxycholecalciferol). This active vitamin D regulates several
biochemical processes including calcium absorption from the
intestines and reabsorption from the kidneys destroying bone by
depositing calcium and bone building phosphate in bone, and by
releasing calcium and phosphate from bone (bone demineralization).
Levels of dietary calcium and vitamin D must be adequate to maintain
the actions of these two nutrients. A deficiency in either or both
will lead to bone loss. Food sources rich in vitamin D are saltwater
fish, fish oil, eggs, milk and other dairy products that are
fortified with vitamin D.
The required intake of vitamin D from both food and supplements is
400800 IU/day. Doses should not exceed 800 IU/day because of
possible side effects including excess calcium in the blood and
kidney stone formation.6 In the elderly who are homebound and have
little sun exposure, vitamin D supplementation is especially
important to prevent deficiency and resulting bone loss.
Vitamin K is a fat-soluble vitamin that exists as K1 in plants and
as K2 when formed by bacteria in the human intestine. Vitamin K is
required for proper blood clotting and for chemical modifications of
a bone protein called osteocalcin, which is important in bone
remodeling. Low serum concentrations of vitamin K have been linked
to increased hip fracture risk.7 Foods rich in vitamin K include
alfalfa, broccoli, cabbage, lettuce, soybeans and turnip greens.
As part of the large, prospective Nurses' Health Study that began in
1976, researchers at Brigham and Women's Hospital and Harvard
Medical School in Boston carried out a collaborative study between
1984 and 1994 on the relationship between high vitamin K intake and
lowered hip fracture risk in women.7 In the study, 72,327 women aged
38 to 63 filled out food frequency questionaires during a 10-year
period. By 1994, 270 of the women had fractures following slight or
moderate injury. The researchers found that, during the 10-year
follow-up period, women who ate less than 109 mcg vitamin K/day (20
percent of women in the study) had a 30 percent higher hip fracture
rate.7 These results suggest that dietary vitamin K intake
requirements should be based on bone health as well as on blood
coagulation, and that the RDA of 65 mcg/day is too low to prevent
bone fractures.
The assessment of vitamin K intake in this study was based on the
amount of broccoli, brussels sprouts, greens and iceberg lettuce
consumed by participants. Researchers found that women who ate
lettuce each day had a significantly lower risk of hip fracture (45
percent) compared to those who ate lettuce once a week.
Magnesium, with an RDA of 280350 mg, is involved with other minerals
in the bone-building process and is necessary for regulating blood-
calcium levels. Sixty percent of the magnesium in the body is
located in bone. Magnesium is present in many foods; rich sources
include cocoa, nuts, seeds and whole grains as well as fruits and
vegetables. Animal studies have shown that magnesium deficiency
leads to impaired bone growth and enhanced osteoclast activity that,
in turn, leads to increased bone loss and skeleton fragility.8
Using data from the Framingham Heart Study that began in 1948,
researchers at the Human Nutrition Research Center on Aging at Tufts
University in Boston examined the relationship between bone density
and intake of dietary magnesium, potassium, and fruits and
vegetables that are high in these minerals. The study reviewed the
dietary records of men and women aged 69 to 97, between 1988 and
1993. The results showed that a greater intake of these nutrients
led to increased hip and forearm bone density in both men and women.9
Other minerals play a role in keeping bones strong. Metabolic
studies have shown that potassium, with a recommended estimated
intake of 2,000 mg/day, promotes calcium retention by the kidneys
and thereby prevents loss through excretion. By improving calcium
balance, potassium influences bone health.
Phosphorus is another mineral that is as important for bone
formation as calcium. In the form of phosphate, it makes up nearly
half of bone minerals. It is found in all foods and many soft
drinks. The RDA for phosphorus is 1,200 mg/day, reduced to 800
mg/day for women and men older than 51.10 There has been concern
that drinking soft drinks results in excessive amounts of
phosphates, which actually promotes bone loss. High intake of these
products can suppress the hormone calcitriol, which is needed for
calcium absorption. Reduced calcium absorption leads to other
hormonal changes that promote bone loss and increase the risk for
osteoporosis.
In addition to the right amounts of phosphates, several minerals
notably zinc, manganese, boron, copper and fluoride are needed in
trace amounts as cofactors for building bone. These trace minerals
are found in a balanced diet containing fruit, vegetables, grains,
nuts, seafood, meats and dairy. These minerals accumulate in minute
amounts in bone, keeping them healthy.
Zinc, with an RDA of 1215 mg/day, is needed for the activity of more
than 200 enzymes, one of which is responsible for incorporating
minerals into bone matrix. Manganese, with no RDA but an Estimated
Safe and Adequate Daily Dietary Intake (ESADDI) of 2.02.5 mg for
adults, is important for forming collagen in bone. Boron has no RDA
but no more than 1 mg/day is required. It affects bone strength and
is needed for calcium and magnesium metabolism. Copper, a cofactor
for many enzymes involved in bone formation, has no RDA but an
ESADDI of 1.53.0 mg. Copper deficiency in animals results in
osteoporosis. Fluoride, with no RDA but an ESADDI of 1.54.0 mg, is
required for hardening bones and teeth. Taken in great excess,
fluoride begins to accumulate in soft tissue and leads to deformed
bones.11
Soy foods contain calcium and potassium, two minerals, as explained
above, that are important for bone health. Soy also contains
isoflavones, which are capable of binding to estrogen receptors on
cells but that have other nonhormone benefits as well. When
isoflavones bind to estrogen receptors, they prevent estrogen from
binding to these same sites and exerting its effects. Since it is
believed that many cancers are estrogen-dependent, blocking the
actions of estrogen can at times be important in health maintenance.
Most research demonstrates that soy foods also increase mineral
density in menopausal women and reduce bone loss; however, many of
the studies have been short-term and have involved only small
numbers of women.12 Furthermore, the appropriate dose of soy needed
to protect against bone loss is still unknown.
In addition to isoflavones' direct effect on bone, soy protein may
increase bone strength indirectly. Animal studies show that soy
protein decreases calcium excretion from the kidneys, which suggests
that people who eat soy foods may reap a similar benefit.12 Animal
studies also demonstrate that soy isoflavones prevent bone loss in
female animals that are made estrogen-deficient by removal of their
ovariesoffering hope to both menopausal women and those who have
had hysterectomies.
Ipriflavone is a synthetic form of naturally occurring isoflavones.
Synthesized from the soy isoflavone daidzein, ipriflavone has shown
promising results in a number of studies for its ability to increase
bone density. In one such study conducted by researchers in Siena,
Italy, 56 postmenopausal women with low vertebral bone density were
randomly assigned to receive either 200 mg ipriflavone three times a
day or placebo. All subjects also received 1,000 mg/day of calcium.
After two years of treatment, women taking only calcium showed close
to 5 percent decline in vertebral bone density. However, no change
was seen in women taking ipriflavone, indicating that the isoflavone
prevented rapid bone loss following menopause.14
In a separate study conducted at Keio University in Tokyo, 60 women
with postmenopausal bone loss or osteoporosis received either 600
mg/day ipriflavone or 800 mg/day calcium lactate. Bone density of
the second and fourth vertebrae was evaluated as was bone
metabolism. After one year of treatment, the ipriflavone-treated
group's bone density remained the same as before treatment. In
contrast, subjects treated with only calcium showed a marked
decrease in both rate and amount of bone mineral density, suggesting
that the isoflavone suppressed bone resorption.15
While ipriflavone seems to increase estrogenic effects by preventing
bone loss and increasing bone formation, it does not appear to
increase risk of breast cancer in the way estrogen therapy can.
Therefore, based on available data, ipriflavone may be an attractive
adjunct or alternative to conventional HRT for postmenopausal women.
Some early studies show that ipriflavone prevents the bone loss
associated with therapeutic steroid use, immobility, ovariectomy and
other conditions associated with bone loss.16
The data on naturally occurring isoflavonesfound in the greatest
amounts in soy but also present in clover, cabbage and other legumes
and plantsare limited but suggest that their inclusion in the diet
could result in a reduction in bone resorption caused by estrogen
deficiency. The data are more extensive on ipriflavone, and studies
suggest that it is a useful and safe alternative to estrogen therapy
for treating osteoporosis in postmenopausal women. Additional
studies are needed to examine ipriflavone's role as a preventive
agent as well as to assess the clinical effects of the naturally
occurring isoflavones in maintaining bone health.
Better Bone Care
Osteoporosis develops in older adults when bones are broken down
quicker than they are formed. Bones become thin and fragile and
fracture easily. Estrogen loss due to menopause and aging helps
trigger the condition. Poor dietary habits, smoking, high alcohol
intake and lack of exercise also promote osteoporosis.
Osteoporosis can be effectively and easily prevented with dietary
modifications. Although the primary goal is to achieve peak bone
mass in early adulthood, with adequate calcium intake, good
nutrition and exercise, it is never too late to stay a step ahead of
osteoporosis.
Sidebars:
Exercise And Osteoporosis
Homeopathy Addresses Osteoporosis
Carmia Borek, Ph.D., a research professor at Tufts University School
of Medicine in Boston, is author of Maximize Your Health-Span With
Antioxidants: The Baby-Boomer's Guide (Keats Publishing, 1995).
References
1. Cooper C, et al. Hip fracture in the elderly, a worldwide
projection. Osteoporosis Int 1992;2(b):285-9.
2. Anderson FH. Osteoporosis in men. Int J Clin Prac 1998;52:176-80.
3. Institute of Medicine. Dietary Reference Intakes, 2000.
Washington, DC: National Academy Press; 2000. p 484.
4. Holbrook TL, et al. Dietary calcium intake and risk of hip
fracture. 14-year prospective population study. Lancet 1988;2:1046-
9.
5. Heaney R. Calcium, dairy products and osteoporosis. J Am Coll
Nutr 2000;19:83S-99S.
6. NIH Consensus Conference on Osteoporosis, JAMA 1984;252:799-802.
7. Feskanish D, et al. Vitamin K intake and hip fractures in women.
Am J Clin Nut 1999;69:74-9.
8. Rude RK, et al. Magnesium deficiency induced osteoporosis in the
rat: uncoupling of bone formation and bone resorption. Magnes Res
1999;12:257-67.
9. Tucker KL, et al. Potassium, magnesium and fruit and vegetable
intake are associated with greater bone density in elderly men. Am J
Clin Nut 1999;69:727-36.
10. Recommended Dietary Allowances, 10th. Washington DC: National
Academy Press; 1989. p 175-257.
11. Mertz W, et al. Trace elements in human and animal nutrition,
volume 1. San Diego: Academic Press; 1987. p 301-64.
12. Messina M, Messina V. Soyfood, soybean isoflavones and bone
health: a brief overview. J Ren Nutr 2000;10:63-8.
13. Anderson JJ, Garner SC. Phytoestrogens and bone. Baillieres Clin
Endocrinol Metabo 1998;12:543-57.
14. Gennari C, et al. Effect of ipriflavonea synthetic derivative
of natural isoflavoneon bone mass loss in early years after
menopause. Menopause 1998;5:9-15.
15. Ohta H, et al. Effect of 1 year ipriflavone treatment on lumbar
one mineral density and bone metabolism markers in postmenopausal
women with low bone mass. Hormone Res 1999;51:178-83.
16. Head KA. Ipriflavone: an important bone-building isoflavone. Alt
Med Rev 1999;4:10-22.
#3 Vitamin D levels low in almost all hip fracture patients
03/08/2005 - Nearly all hip fracture patients are deficient,
sometimes severely, in vitamin D, researchers in Scotland reported
this week.
Reviewing the cases of 548 patients over the age of 60 who were
admitted at South Glasgow University Hospital during a four-year
period, the researchers found that 97.8 per cent had vitamin D
levels below normal.
In around a quarter of the group studied, levels were so low that
they were "effectively unrecordable", said the authors in the online
issue of Current Medical Research and Opinion (DOI:
10.1185/030079905X59148).
Vitamin D currently only makes up 4 per cent of all vitamin sales
and lags well behind calcium in terms of bone health supplements.
But increasing evidence underlines its importance in protecting
against fractures.
In a second prospective study phase, the researchers looked at
vitamin D levels among the first 50 patients admitted to the
hospital with an osteoporosis fracture after November 2004.
More than 80 per cent had vitamin D levels below 70 nmol/L and 72
per cent had vitamin D levels below 50 nmol/L.
"Although numbers were too small to justify extensive subgroup
analyses, the mean vitamin D level in the 13 patients with hip
fracture was lower than in the 37 with non-hip fractures," said the
researchers.
They conclude: "It may be that vitamin D represents a correctable
risk factor for fragility fracture in the elderly, possibly
specifically for the hip."
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