Zinc, Plasma or Serum
Zinc, Plasma or Serum
    
Number
001800
CPT
84630
Related Information
  • Zinc, Urine
  • Synonyms
    Zn, Serum
    Specimen
    Plasma (preferred) or serum
    Volume
    2 mL
    Minimum Volume
    0.6 mL
    ContainerContainer - Updated June 20 2008
    Royal blue-top (EDTA or heparin) tube or red-top tube.
    CollectionCollection - Updated February 8 2007
    Separate serum from cells within 45 minutes of collection and transfer to a plastic transport tube. Plasma may be separated immediately and transfer to a plastic transport tube for shipment to the laboratory.
    Storage Instructions
    Maintain specimen at room temperature.
    Causes for RejectionCauses for Rejection - Updated February 8 2007
    Gel-barrier tube; unspun red-top tube
    Reference Interval
    Environmental exposure: 70-150 μg/dL
    Use
    Monitor exposure to zinc; evaluate suspected nutritional inadequacy, especially in enteral or parental nutrition, critically ill or burn patients; cases of diabetes or delayed wound healing; growth retardation; follow therapy, for example when higher intravenous zinc doses are used to balance excessive ongoing GI losses in long-term total parenteral nutrition; follow oral zinc therapy in Wilson disease; confirm acrodermatitis enteropathica and follow therapy
    Limitations
    Levels may be low in fever, sepsis, estrogen therapy, stress, or myocardial infarction, reflecting mobilization from serum to the liver by interleukin. Levels are usually low in uremia with normal tissue levels. Levels may be high in familial hyperzincemia without toxicity or high zinc stores.
    Methodology
    Atomic absorption spectrometry (AAS); inductively-coupled plasma-mass spectrometry (ICP-MS)
    Additional Information
    Chronic oral zinc supplementation interferes with copper absorption and may precipitate copper deficiency. Albumin is the primary zinc binding protein: zinc levels should be interpreted with awareness of serum albumin level.
    References

    Alfrey AC, “Essential Trace Elements,” The Kidney: Physiology and Pathophysiology, 2nd ed, Seldin DW and Giebisch G, eds, New York, NY: Raven Press, Ltd, 1992, 2993-3003.

    Ruz M, Cavan KR, Bettger WJ, et al, “Development of a Dietary Model for the Study of Mild Zinc Deficiency in Humans and Evaluation of Some Biochemical and Functional Indices of Zinc Status,” Am J Clin Nutr, 1991, 53(5):1295-303.


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