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:Calcium:
:Calcium is the most abundant
mineral in the human body. Of 2 or 3 pounds of calcium in the body,
99% forms bones and teeth. Calcium is essential for blood clotting,
transmission of nerve signals, and muscle contraction.
Calcium plays a minor role in lowering blood pressure. 1 The level
of calcium in the blood is regulated by parathyroid hormone (PTH),
and low intake of calcium causes elevations in PTH, which in turn
can cause hypertension. 2 High calcium intake reduces risk of cardiovascular
disease in postmenopausal women. 3
By reducing absorption of oxalate, 4 calcium may reduce risk of kidney
stones. 5 People with a history of kidney stones should talk with
their health practitioner before supplementing calcium as it may increase
risk of stones for a few people who absorb too much calcium.
Calcium partially binds some fats and cholesterol in the gastrointestinal
tract. Some research finds that calcium supplements may lower cholesterol.
6
Animal studies shows calcium helps develop female egg cells (oocytes).
7 8 Some researchers speculate that calcium could help polycystic
ovary syndrome (PCOS). 9
Calcium may have anticancer activity in the colon. Most studies show
high calcium diets reduce colon cancer risk. 10 Most 11 12 13 but
not all 14 studies find calcium supplements reduce risk of colon cancer
or precancer. One study reports that high dietary, but not supplemental,
calcium intake decreases risk of precancerous changes in the colon.
15 In double-blind studies, calcium supplementation protects against
precancerous changes in the colon in some 16 17 but not all studies.
18 19
Sources: Most dietary calcium comes from dairy products
. The myth that calcium from dairy products is not absorbed is not
supported by scientific research. 20 21 Other sources include sardines,
canned salmon, green leafy vegetables and tofu.
Choosing a form of calcium supplement can be confusing. While fewer
pills of the calcium carbonate form are needed, some people may not
absorb this form of calcium as well as some other forms. Most, 22
23 but not all, 24 studies suggest that calcium citrate is better
absorbed than calcium carbonate. Virtually all comparative studies
find that calcium citrate/malate (CCM) is absorbed better than calcium
carbonate. CCM is increasingly the form of calcium recommended by
doctors. Microcrystalline hydroxyapatite (MCHC),
a variation on the bone meal form of calcium, has been shown to improve
bone mass, 25 even though the absorption of MCHC is fairly
low 26 27 perhaps because MCHC doubles absorption of dietary calcium
by stimulating active uptake in the small intestine. Only preliminary
research exists on amino acid chelates of calcium.
Documented uses:
Science supported uses:
Traditional clinical uses:
-
Amenorrhea
(calcium for preventing bone loss)
-
Colon cancer
(reduces risk)
-
Depression
-
Dysmenorrhea
(painful menstruation)
-
Gingivitis
(periodontal disease)
-
Insulin resistance
syndrome (Syndrome X)
-
Kidney stones
-
Migraine headaches
-
Multiple sclerosis
-
Pregnancy and
postpartum support
Warning: Calcium
supplements should be avoided by prostate cancer patients.
Deficiency: Severe deficiency of either calcium or
vitamin D leads to a condition called rickets in children and osteomalacia
in adults. Since vitamin D is required for calcium absorption, people
with conditions causing vitamin D deficiency (e.g., pancreatic insufficiency)
may develop a deficiency of calcium as well. Vegans (pure vegetarians
), people with dark skin, those who live in northern climates, and
people who stay indoors almost all the time are more likely to be
vitamin D deficient, than are other people. Vegans often eat less
calcium and vitamin D than do other people. Most people eat well below
the recommended amount of calcium. This lack of dietary calcium is
thought to contribute to the risk of osteoporosis , particularly in
white and Asian women.
| Calcium or Vitamin D deficiency |
Calcium excess |
| Bone fractures |
Calcification of soft tissues |
| Rickets |
Muscle spasms |
| Osteomalacia |
|
Dosage: The National
Academy of Sciences has established guidelines for calcium that are
25–50% higher than previous recommendations. For ages 19 to
50, calcium intake is recommended to be 1,000 mg daily; for adults
over age 51, the recommendation is 1,200 mg daily. 28 The most common
supplemental amount for adults is 800–1,000 mg per day. 29 General
recommendations for higher daily intakes (1,200–1,500 mg) usually
include the calcium most people consume from their diets. Studies
indicate the average daily amount of calcium consumed by Americans
is about 500–1,000 mg.
Are there any side effects or interactions? Constipation , bloating,
and gas are sometimes reported with the use of calcium supplements.
30 A very high intake of calcium from dairy products plus supplemental
calcium carbonate was reported in the past to cause a condition called
“milk alkali syndrome.” This toxicity is rarely reported
today because most medical doctors no longer tell people with ulcers
to use this approach as treatment for their condition.
People with hyperparathyroidism, chronic kidney disease, or kidney
stones should not supplement with calcium without consulting a physician.
For other adults, the highest amount typically suggested by doctors
(1,200 mg per day) is considered quite safe.
In the past, calcium supplements in the forms of bone meal (including
MCHC), dolomite, and oyster shell have sometimes had higher lead levels
than permitted by stringent California regulations, though generally
less than the levels set by the federal government. 31 “Refined”
forms (which would include CCM, calcium citrate, and most calcium
carbonate) have low levels. 32 More recently, a survey of over-the-counter
calcium supplements found low or undetectable levels of lead in most
products, 33 representing a sharp decline in lead content of calcium
supplements since 1993. People who decide to take bone meal, dolomite,
or oyster shell calcium for long periods of time can contact the supplying
supplement company to request independent laboratory analysis showing
minimal lead levels.
Calcium competes for absorption with a number of other minerals. Therefore,
people taking calcium for more than a few weeks should also take a
multimineral supplement.
Vitamin D’s most important role is maintaining blood levels
of calcium. Therefore, many doctors recommend that those supplementing
with calcium also supplement with 400 IU of vitamin D per day.
Animal studies have shown that essential fatty acids (EFAs) increase
calcium absorption from the gut, in part by enhancing the effects
of vitamin D and reducing loss of calcium in the urine. 34
Lysine supplementation increases the absorption of calcium and may
reduce its excretion. 35 As a result, some researchers believe that
lysine may eventually be shown to have a role in the prevention and
treatment of osteoporosis. 36
Medication interactions:
Albuterol (Depletion or interference)
Alendronate: Calcium supplements may interfere with absorption, but
one researcher suggests that large doses of calcium in bone metastases
(with evidence of osteomalacia) related to prostate cancer may improve
clinical outcome. Calcium and alendronate are commonly used simultaneously
for osteoporosis. Take alendronate two hours before or after calcium.
Aluminum Hydroxide (Depletion or interference)
Anticonvulsants (Depletion or interference)
Bile Acid Sequestrants (Depletion or interference)
Caffeine (Depletion or interference)
Calcitonin (Supportive interaction)
Calcium Acetate (Adverse interaction)
Ciprofloxacin (Reduced drug absorption/bioavailability)
Cisplatin (Depletion or interference)
Colestipol (Depletion or interference)
Inhaled Corticosteroids (Depletion or interference)
Oral Corticosteroids (Depletion or interference)
Cycloserine (Depletion or interference)
Diclofenac (Depletion or interference)
Doxycycline (Reduced drug absorption/bioavailability)
Erythromycin may interfere with absorption and/or activity of calcium.
If taking erythromycin longer than two weeks, supplement with a multivitamin-mineral.
Estrogens (Combined) (Supportive interaction)
Felodipine (Depletion or interference)
Flurbiprofen (Depletion or interference)
Gabapentin (Depletion or interference)
Gentamicin (Depletion or interference)
Hydroxychloroquine (Depletion or interference)
Indapamide (Depletion or interference)
Indomethacin (Depletion or interference)
Isoniazid (Depletion or interference)
Lactase: Lactase-deficient people may not consume dairy products as
a source of calcium. Lactase allows lactase-deficient people to digest
milk sugar. The calcium requirement is reduced by about half where
dairy is not eaten.
Metformin (Side effect reduction/prevention)
Mineral Oil (Depletion or interference)
Minocycline (Depletion or interference)
Nadolol (Reduced drug absorption/bioavailability)
Neomycin (Depletion or interference)
Ofloxacin (Reduced drug absorption/bioavailability)
Oral Contraceptives may increase absorption of calcium
Phenobarbital (Depletion or interference)
Risedronate (Depletion or interference)
Rofecoxib (Reduced drug absorption/bioavailability)
Sodium Fluoride: calcium from leg bones may transfer to the spine
causing stress fractures when fluoride is taken. Supplementing with
1,500 mg of calcium each day together with slow-release forms of fluoride
increases the bone density of the lumbar spine without causing fractures.
People taking sodium fluoride to treat osteoporosis should supplement
with calcium. Taking fluoride and calcium at the same time reduces
absorption of fluoride, so they should be taken at least an hour apart.
Sotalol (Reduced drug absorption/bioavailability)
Sucralfate (Depletion or interference)
Sulfamethoxazole (Depletion or interference)
Tetracycline (Reduced drug absorption/bioavailability)
Tetracyclines (Reduced drug absorption/bioavailability)
Thiazide Diuretics decrease calcium loss in the urine.
Thyroid Hormones (Depletion or interference)
Tobramycin (Depletion or interference)
Triamterene (Depletion or interference)
Trimethoprim (Depletion or interference)
Valproic Acid (Depletion or interference)
Verapamil (Adverse interaction)
References:
1. Osborne CG, McTyre
RB, Dudek J, et al. Evidence for the relationship of calcium to
blood pressure. Nutr Rev 1996;54:365–81.
2. Jorde R, Sundsfjord J, Haug E, Bønaa KH. Relation between
low calcium intake, parathyroid hormone, and blood pressure. Hypertension
2000;35:1154–9.
3. Bostick RM, Kushi LH, Wu Y, et al. Relation of calcium, vitamin
D, and dairy food intake to ischemic heart disease mortality among
postmenopausal women. Am J Epidemiol 1999;149:151–61.
4. Barilla DE, Notz C, Kennedy D, Pak CYC. Renal oxalate excretion
following oral oxalate loads in patients with ileal disease and
with renal and absorptive hypercalciurias: effect of calcium and
magnesium. Am J Med 1978;64:579–85.
5. Curhan GC, Willett WC, Rimm EB, Stampfer MJ. A prospective study
of dietary calcium and other nutrients and the risk of symptomatic
kidney stones. N Engl J Med 1993;328:833–83.
6. Bell L, Halstenson CE, Halstenson CJ, et al. Cholesterol-lowering
effects of calcium carbonate in patients with mild to moderate hypercholesterolemia.
Arch Intern Med 1992;152:2441–4.
7. Homa ST, Carroll J, Swann K. The role of calcium in mammalian
oocyte maturation and egg activation. Hum Reprod 1993;8:1274–81.
8. Kaufman M, Homa ST. Defining a role for calcium in the resumption
and progression of meiosis in the pig oocyte. J Exp Zool 1993;265:69–76.
9. Thys-Jacobs S, Donovan D, Papadopoulos A, et al. Vitamin D and
calcium dysregulation in the polycystic ovarian syndrome. Steroids
1999;64:430–5.
10. Lipkin M, Newmark H. Calcium and the prevention of colon cancer.
J Cell Biochem Suppl 1995;22:65–73 [review].
11. Whelan RL, Horvath KD, Gleason NR, et al. Vitamin and calcium
supplement use is associated with decreased adenoma recurrence in
patients with a previous history of neoplasia. Dis Colon Rectum
1999;42:212–7.
12. White E, Shannon JS, Patterson RE. Relationship between vitamin
and calcium supplement use and colon cancer. Cancer Epidemiol Biomarkers
Prev 1997;6:769–74.
13. Kampman E, Slattery ML, Caan B, Potter JD. Calcium, vitamin
D, sunshine exposure, dairy products and colon cancer risk (United
States). Cancer Causes Control 2000;11:459–66.
14. Neugut AI, Horvath K, Whelan RL, et al. The effect of calcium
and vitamin supplements on the incidence and recurrence of colorectal
adenomatous polyps. Cancer 1996;78:723–8.
15. Hyman J, Baron JA, Dain BJ, et al. Dietary and supplemental
calcium and the recurrence of colorectal adenomas. Cancer Epidemiol
Biomarkers Prev 1998;7:291–5.
16. Baron JA, Beach M, Mandel JS, et al. Calcium supplements for
the prevention of colorectal adenomas. N Engl J Med 1999;340:101–7.
17. Bostick RM, Fosdick L, Wood JR, et al. Calcium and colorectal
epithelial cell proliferation in sporadic adenoma patients: a randomized,
double-blinded, placebo-controlled clinical trial. J Natl Cancer
Inst 1995;87:1307–15.
18. Cats A, Kleibeuker JH, van der Meer R, et al. Randomized, double-blinded,
placebo-controlled intervention study with supplemental calcium
in families with hereditary nonpolyposis colorectal cancer. J Natl
Cancer Inst 1995;87:598–603.
19. Baron JA, Tosteson TD, Wargovich MJ, et al. Calcium supplementation
and rectal mucosal proliferation: a randomized controlled trial.
J Natl Cancer Inst 1995;87:1303–7.
20. Sheikh MS, Santa Ana CA, Nicar MJ, et al. Gastrointestinal absorption
of calcium from milk and calcium salts. N Engl J Med 1987;317:532–6.
21. Levenson DI, Bockman RS. A review of calcium preparations. Nutr
Rev 1994;52:221–32 [review].
22. Nicar MJ, Pak CYC. Calcium bioavailability from calcium carbonate
and calcium citrate. J Clin Endocrinol Metabol 1985;61:391–3.
23. Harvey JA, Kenny P, Poindexter J, Pak CYC. Superior calcium
absorption from calcium citrate than calcium carbonate using external
forearm counting. J Am Coll Nutr 1990;9:583–7.
24. Sheikh MS, Santa Ana CA, Nicar MJ, et al. Gastrointestinal absorption
of calcium from milk and calcium salts. N Engl J Med 1987;317:532–6.
25. Epstein O, Kato Y, Dick R, Sherlock S. Vitamin D, hydroxyapatite,
and calcium gluconate in treatment of cortical bone thinning in
postmenopausal women with primary biliary cirrhosis. Am J Clin Nutr
1982;36:426–30.
26. Heaney RP, Recker RR, Weaver CM. Absorbability of calcium sources:
the limited role of solubility. Calcif Tissue Int 1990;46:300–4.
27. Deroisy R, Zartarian M, Meurmans L, et al. Acute changes in
serum calcium and parathyroid hormone circulating levels induced
by the oral intake of five currently available calcium salts in
healthy male volunteers. Clin Rheumatol 1997;16:249–53.
28. Standing Committee on the Scientific Evaluation of Dietary Reference
Intakes, Food and Nutrition Board, Institute of Medicine. Dietary
reference intakes for calcium, phosphorus, magnesium, vitamin D
and fluoride. Washington DC: National Academy Press, 1997, 108–17
[review].
29. Heaney RP, Recker RR, Weaver CM. Absorbability of calcium sources:
the limited role of solubility. Calcif Tissue Int 1990;46:300–4.
30. Levenson DI, Bockman RS. A review of calcium preparations. Nutr
Rev 1994;52:221–32 [review].
31. Burros M. Testing calcium supplements for lead. New York Times
June 4, 1997, B7.
32. Bourgoin BP, Evans DR, Cornett JR, et al. Lead content in 70
brands of dietary calcium supplements. Am J Public Health 1993;83:1155–60.
33. Ross EA, Szabo NJ, Tebbett IR. Lead content of calcium supplements.
JAMA 2000;284:1425–9.
34. Kruger MC, Horrobin DF. Calcium metabolism, osteoporosis and
essential fatty acids: a review. Prog Lipid Res 1997;36:131–51
[review].
35. Civitelli R, Villareal DT, Agnusdei D, et al. Dietary L-lysine
and calcium metabolism in humans. Nutrition 1992;8:400–5.
36. Flodin NW. The metabolic roles; pharmacology, and toxicology
of lysine. J Am Coll Nutr 1997;16:7–21 [review].
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