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Chromium
Browse Sections:
 Summary
 Other Names
 Traditional Internal Uses
 Pharmacological Summary
 Precautions / Contraindications
 Interaction with Medications
 Possible Side Effects
 Dosage
 References

Common Name
Chromium
 
Other Names
Chromium (III), Chromium Aspartate, Chromium Chloride, Chromium Citrate, Chromium Nicotinate, Chromium Picolinate, Trivalent Chromium, Cr, Element 24, GTF, Glucose Tolerance Factor

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Traditional Internal Uses
Chromium is used primarily to assist in the control of blood sugar in cases of impaired glucose tolerance and diabetes.(1,2)

Chromium may be useful to reduce obesity, enhance lean body mass, and to lower triglycerides and total cholesterol, since chromium mediated insulin function is related to these concerns.(1,2)

Chromium may be useful in treating and managing reactive hypoglycemia.(3)

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Pharmacological Summary
In 1957 Walter Mertz and Kenneth Schwartz isolated a substance from pork kidney that was able to overcome impaired glucose tolerance in rats, hypothesizing the existence of a glucose tolerance factor. In 1959 chromium was found to be the active constituent in the glucose tolerance factor. The hypothesized structure of the glucose tolerance factor envisions chromium bound to nicotinic acid, and the amino acids glycine, cysteine, and glutamic acid. It has not been possible to purify the glucose tolerance factor to date, but low molecular weight chromium compounds isolated from biological fluids do show an ultraviolet absorption peak corresponding to nicotinic acid.(2)

Following the identification of chromium as a key player in the performance of the glucose tolerance factor substance, other researchers and clinicians found that giving simple chromium chloride in the order of 250 mcg per day markedly improved glycemic control and reduced exogenous insulin requirements in diabetic patients.(2) These observations were particularly important to patients on long-term total parenteral nutrition who had drifted into diabetes and dyslipidemia because chromium was not supplied.(2) Chromium has now become thoroughly established as an important nutrient in the management of blood sugar and lipids. Clinical studies have shown that chromium can decrease fasting blood sugar, improve glucose tolerance, lower insulin levels, decrease total cholesterol and triglycerides, and raise HDL cholesterol.(1,2) Even in non-diabetics, chromium may have something to offer, however, its effects are not remarkable in those who are not chromium deficient.(1,2) Other factors contribute to insulin resistance and the many spin-off effects associated with it. Chromium has also been used for weight loss, and is often used in conjunction with hydroxycitric acid (Citrimax).

Chromium has a theoretical basis for being able to assist in weight loss, since inappropriate weight gain is one of the features associated with insulin resistance. However, chromium is not expected to do well if it is not depleted from body stores. It should be encouraged for weight loss because its usefulness can only be determined empirically. However, used with Citrimax, the effect of chromium may not be evident. Chromium then becomes more important after the Citrimax is discontinued. The older a person is, the greater is the risk of being chromium depleted, and so chromium supplementation in an older person may provide more noticeable help in weight loss over time.

People who eat whole grains and whole grain flours and plant foods well, may actually have sufficient chromium in their bodies. Too many calories, too much carbohydrate high up on the glycemic index, and too much saturated fat with too little omega-3 fat, are three common conditions that will drive in the direction of insulin resistance, which will in turn drive body fat mass up.

Chromium works at the insulin receptor site, but it is not the principal agent in controlling how many receptors will be maintained and how efficiently they work. The number and functionality of insulin receptors is significantly influenced by cell membrane fluidity, which is related to the degree that long chain omega-3 fatty acids comprise the phospholipid tails, and by the degree that saturated fatty acid concentrations are optimal. So even with good chromium stores, insulin receptors may under perform due to membrane fluidity issues.(7,8)

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Precautions / Contraindications
Protracted high stress conditions contributes to chromium excretion and may be a factor in the emergence of high blood sugar and dyslipidemia.(2)

Initiation of chromium supplementation in diabetic patients on sulfonylurea medication or insulin may potentiate sugar clearance quickly enough to effect some degree of hypoglycemia.

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Interaction with Medications
Increasing gastric pH as in chronic use of antacids, H2-blockers, or proton pump inhibitors may reduce the absorption of chromium.(2,5)

ASA and NSAID medications may increase chromium absorption and retention by blocking a prostaglandin inhibition to absorption, and 16,16-dimethyl-protaglandin E2 decreased chromium absorption.(2,5)

Corticosteroids can increase blood sugar by increasing urinary excretion of chromium, and may precipitate diabetes or make diabetic control more difficult.(6)

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Possible Side Effects
Chromium HVP is well tolerated at 200 mcg or less. There have been many supplementation trials in humans with chromium chloride and chelated chromium compounds without reports of toxicity.(2)

Reported adverse side effects are associated with amounts in excess of 200 mcg. Chronic use of high amounts of chromium picolinate, an American form of chromium not legally sold in Canada, has been associated with significant adverse effects. Amounts as high as 1200 to 2400 mcg per day have been related to inappropriate weight loss, anemia, thrombocytopenia, hemolysis, liver dysfunction, and renal failure.(4) Such use might be possible in those who are irrationally concerned about losing weight or achieving an athletic muscular body.

A concern that chromium may accumulate to toxic levels when excessive amounts are used over a long time, have been expressed. Trivalent chromium has been shown in animal models to cause DNA damage at high enough concentrations.(9) What constitutes an amount that will lead to human toxicity is not known, but there is no reason for consumers to use more than 200 mcg per day, which is the amount that is most commonly found in stores, and which is expected.

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Dosage
The traditionally recommended amount for adults is 50 to 200 mcg per day.(1) Research done in the mid to late 80s to establish an adequate daily intake of chromium demonstrated that 25 mcg per day from dietary sources was able to keep tested subjects in chromium equilibrium. This observation most likely precludes any need to encourage use of more than the commonly accepted 200 mcg per day, unless called for by a clinician.

Among other factors, absorption of chromium is a function of dose, and the status of chromium depletion. Higher does lead to reduced absorption by an intrinsic homeostatic mechanism, and depleted subjects and animals absorb incrementally more up to equilibrium and over time.(2) In one carefully conducted study, supplemented chromium was excreted in the feces, and not via a bile route, with a mean of 981 percent recoverable in the feces.(2)

However, adequate intake in diabetic patients may be better stated as 200 mcg per day.(2) Higher amounts may be useful in diabetes. Chromium deficiency is common in type 2 diabetics.(1)

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References
1. Murray, Michael T., Encyclopedia of Nutritional Supplements, Prima Publishing, Rocklin, CA, 1996
2. Stoecker, Barbara J., Chromium, in Maurice E Shils, James A. Olson, Moshe Shike, A Catharine Ross, editors, Modern Nutrition In Health and Disease, ninth edition, Lippincott Williams & Wilkins New York, 1999
3. Anderson, R.A., et al, Effects of supplemental chromium on patients with symptoms of reactive hypoglycemia, Metabolism, 36(4): 351-355, 1987
4. Cerulli, J., et al, Chromium picolinate toxicity, Ann Pharmacotherapy, 32: 428-431, 1998
5. www.nap.edu/books/0309072794/html/
6. Ravina, A., et al, Reversal of corticosteroid-induced diabetes mellitus with supplemental chromium, Diabet Med, 16(2): 164- 167, 1999
7. Simopoulos, Artemis P., Jo Robinson, The Omega Plan, HarperCollins, New York, 1998
8. Slater, Simon J., et al, Polyunsaturation in cell membranes and lipid bilayers and its effects on membrane proteins, Lipids, Vol 31, Supplement, S189-S192, 1996
9. Sterns, D.M., et al, A prediction of chromium (III) accumulation in humans from chromium dietary supplements, FASEB J, 9(15): 1650-1657, 1995

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These statements have not been evaluated by the Food and Drug Administration (FDA). Products are intended to support general well being and are not intended to treat, diagnose, mitigate, prevent, or cure any condition or disease. If conditions persist, please seek advice from your medical doctor.



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