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EDTA chelation therapy does not selectively increase chromium losses

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Abstract

Chelation therapy and supplemental Cr have both been shown to lead to improved blood glucose, lipids, and insulin activity. Chelation therapy leads to the removal of toxic as well as essential metals. To determine if chelation therapy leads to increased urinary Cr losses and altered Cr homeostasis, 2 groups of subjects (1 group that had undergone only 1 or no chelation therapy and 1 group in which all subjects had undergone at least 19 chelation sessions) were evaluated for differences in possible Cr homeostasis based on urinary Cr losses. There were no significant differences in urinary Cr losses between the two groups of subjects and there were no significant increases in urinary Cr losses resulting from chelation therapy. Increases in urinary Cr losses were strongly influenced by supplementation but not chelation therapy.

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References

  1. E. M. Cranton and J. P. Frackelton, Free radical pathology in age-associated diseases: treatment with EDTA chelation, nutrition, and antioxidants,J. Adv. Med. 2, 17–54 (1989).

    Google Scholar 

  2. R. A. Anderson, Recent advances in the clinical and biochemical manifestation of chromium deficiency in human and animal nutrition,J. Trace Element Exp. Med. 11, 241–250 (1998).

    Article  CAS  Google Scholar 

  3. L. T. Chappell and M. Janson, EDTA chelation therapy in the treatment of vascular disease,J. Cardiovasc. Nutr. 10, 78–86 (1996).

    CAS  Google Scholar 

  4. E. M. Cranton, Z. X. Liu, and I. M. Smith, Urinary trace and toxic elements and min- erals in untimed urine specimens relative to urine creatinine, Part I: concentrations of elements in fasting urine,J. Adv. Med. 2, 331–348 (1989).

    Google Scholar 

  5. R. A. Anderson, Stress effects on chromium nutrition of humans and farm animals, inProc. Alltech’s Tenth Symposium Biotechnology in the Feed Industry, Nottingham Uni- versity Press, Loughbrough, England, pp. 267–274 (1994).

    Google Scholar 

  6. R. A. Anderson and A. S. Kozlovsky, Chromium intake, absorption and excretion of subjects consuming self-selected diets,Am. J. Clin. Nutr. 41, 1177–1183 (1985).

    PubMed  CAS  Google Scholar 

  7. R. A. Anderson, N. A. Bryden, and M. M. Polansky, Dietary chromium intake-freely chosen diets, institutional diets and individual foods,Biol. Trace Element Res. 32, 117–121 (1992).

    Article  CAS  Google Scholar 

  8. D. W. Cockcroft and M. H. Gault, Prediction of creatinine clearance from serum cre- atinine,Nephron 16, 31–41 (1976).

    Article  PubMed  CAS  Google Scholar 

  9. A. Anderson, M. M. Polansky, N. A. Bryden, K. Y. Patterson, C. Veillon, and W. Glinsmann, Effects of chromium supplementation on urinary Cr excretion of human subjects and correlation of Cr excretion with selected clinical parameters,J. Nutr. 113, 276–281 (1983).

    PubMed  CAS  Google Scholar 

  10. C. Veillon, W. R. Wolf, and B. E. Guthrie, Determination of chromium in biological materials by stable isotope dilution,Anal. Chem. 51, 1022–1024 (1979).

    Article  PubMed  CAS  Google Scholar 

  11. A. Popovici, C. F. Geschichter, A. Reinovsky, and M. Rubin, Experimental control of serum calcium levels in vivo,Proc. Soc. Exp. Biol. Med. 74, 415–422 (1950).

    PubMed  CAS  Google Scholar 

  12. N. E. Clarke, C. N. Clarke, and R. E. Moscher, Treatment of angina pectoris with dis- odium ethylene diamine tetraacetic acid,Am. J. Med. Sci. 4, 654–666 (1956).

    Google Scholar 

  13. S. K. Tandon and J. S. Gaur, Chelation in metal intoxication. IV. Removal of chromium from organs of experimentally poisoned animals,Clin. Toxicol. 11, 257–264 (1977).

    PubMed  CAS  Google Scholar 

  14. W. Banner, Jr., M. Koch, D. M. Capin, S. B. Hopf, S. Chang, and T. G. Tong, Experi- mental chelation therapy in chromium, lead and boron intoxication with N-acetyl- cysteine and other compounds,Toxicol. Appl. Pharmacol. 83, 142–147 (1986).

    Article  PubMed  CAS  Google Scholar 

  15. F. Sata, S. Araki, K. Murata, and H. Aono, Behavior of heavy metals in human urine and blood following calcium disodium ethylenediamine tetraacetate injection: obser- vations in metal workers,J. Toxicol. Environ. Health 54, 167–178 (1988).

    Article  Google Scholar 

  16. R. A. Anderson, N. A. Bryden, M. M. Polansky, and J. W. Thorp, Effect of carbohy- drate loading and underwater exercise on circulating cortisol, insulin and urinary losses of chromium and zinc,Eur. J. Appl. Physiol. 63, 146–150 (1991).

    Article  CAS  Google Scholar 

  17. L. S. Goodman and A. Gilman,The Pharmacological Basis of Therapeutics, 3rd ed., MacMillian Co., New York, p. 950 (1985).

    Google Scholar 

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Anderson, R.A., Bryden, N.A. & Waters, R. EDTA chelation therapy does not selectively increase chromium losses. Biol Trace Elem Res 70, 265–272 (1999). https://doi.org/10.1007/BF02783835

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  • DOI: https://doi.org/10.1007/BF02783835

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