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Nutrient & Toxic Elements 24 Hr - Urine
Nutrient and Toxic Elements in Urine*

Some elements can accumulate in tissues causing toxic effects. Metal toxicity is a significant environmental health concern. A toxic load of lead, cadmium, mercury or arsenic is capable of rendering considerable damage to the brain and nervous system, particularly in children. Toxic elements produce their many negative effects through various mechanisms. One mechanism, irreversible enzyme inhibition, is illustrated by the anemia caused when lead binds to enzymes in the hemoglobin synthesis pathway. The cancer-inducing effect of arsenic seems to be due to an inhibition of DNA repair. Genotoxicity, in which chromosomes are damaged, is linked to the free radical generation abilities of cadmium, lead and nickel. Mercury causes enzyme poisoning.

Which Test Should I use?

Urine element testing is primarily useful to monitor levels of toxic metals such as aluminum, arsenic, cadmium, lead, and mercury and for special mineral uptake testing. The 6-8 hour collection profiles are primarily for patients who are receiving oral or IV metal chelating agents to mobilize toxic elements from body pools. The 24-hour collection profiles may be used with or without administration of chelating agents to assess the rate of excretion of the elements reported. The total output of urine over 24 hours is collected and the daily output of nutrient and/or toxic elements is determined.

Metametrix offers flexibility in urine element testing. Clinicians can select from challenged and unchallenged protocols. They can select both nutrient and toxic elements or toxic elements only. Although many clinicians do both pre- and post-challenge testing, some now elect to only test following the oral or IV administration of a chelating agent.

*Some analytes may not be reported in New York profiles. Please see Clinician Info and CPT codes for details

In order to allow comparison between different test protocols, Metametrix results are reported using standardized units. 24-hour urine collections are reported as units per day. 6-8 hour collections are reported as units per mg creatinine to allow for variations in urine dilution.

Metametrix urine element analysis features:

  • Testing with the latest advances in technology (ICP/MS), which can guide therapy by pinpointing imbalances of these important substances.
  • Flexible test configurations to fit your protocols.
  • A cost-effective approach for monitoring nutrient and toxic elements.

 

Clinician Info
Test name: 0058 - Nutrient & Toxic Elements 24 Hr
0059 - Nutrient & Toxic Elements 24 Hr NY
Description: In the Metametrix Nutrient & Toxic Elements Profile, the total output of urine over 24 hours is collected and the daily output of elements is determined. The test may be used with or without administration of chelating agents to assess the rate of excretion of the elements reported.
Method: ICP/MS
Turnaround time: 7-14 days, 11 days average
Analytes: HIGHLY TOXIC HEAVY METALS
Arsenic
Cadmium
Lead*
Mercury


POTENTIALLY TOXIC METALS
Aluminum
Boron


ESSENTIAL ELEMENTS
Calcium
Cobalt
Copper
Chromium
Manganese
Magnesium
Molybdenum
Nickel
Selenium
Vanadium
Zinc


*Lead is not included in NY profile.
CPT codes:

82108 - Aluminum
82175 - Arsenic
82300 - Cadmium
82340 - Calcium
82495 - Chromium
82525 - Copper
82570 - Creatinine
83655 - Lead*
83735 - Magnesium
83785 - Manganese
83825 - Mercury
83885 - Nickel
84255 - Selenium
84630 - Zinc
84311 x4 - Spectrophotometry, NES:
84311 x4 - Boron
84311 x4 - Cobalt
84311 x4 - Vanadium
84311 x4 - Molybdenum
 
* - Not reported in NY profile
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references nutrient elements urine
 

Association between urinary potassium, urinary sodium, current diet, and bone density in prepubertal children.
Jones G, Riley MD, Whiting S. Am J Clin Nutr. 2001;73(4):839-844.

Tissue zinc levels and zinc excretion during experimental zinc depletion in young men.
Baer MT, King JC. Am J Clin Nutr. 1984;39(4):556-570.

Occupational Mn parkinsonism: magnetic resonance imaging and clinical patterns following CaNa2-EDTA chelation.[In Process Citation].
Discalzi G, Pira E, Hernandez EH, et al. Neurotoxicology. 2000;21(5):863-866.

Provocative chelation with DMSA and EDTA: evidence for differential access to lead storage sites.
Lee BK, Schwartz BS, Stewart W, et al. Occup Environ Med. 1995;52(1):13-19.

Chemical forms of selenium for cancer prevention.
Abdulah R, Miyazaki K, Nakazawa M, et al. J Trace Elem Med Biol. 2005;19(2-3):141-150.

Recent advances in the nutritional biochemistry of trivalent chromium.
Vincent JB. Proc Nutr Soc. 2004;63(1):41-47.

Levels of Calcium, Magnesium and Zinc in Urine among Adult Women in Relation to Age with Special Reference to Menopause.
Ikeda M, Ezaki T, Moriguchi J. J Nutr Health Aging. 2007 Sep-Oct;11(5):394-401.

Moderate magnesium deprivation results in calcium retention and altered potassium and phosphorus excretion by postmenopausal women.
Nielsen FH, Milne DB, Gallagher S, Johnson L, Hoverson B. Magnes Res. 2007 Mar;20(1):19-31.

Microbial synthesis of p-hydroxybenzoic acid from glucose.
Barker JL, Frost JW. Biotechnol Bioeng. 2001;76(4):376-390.