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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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CUU<br />

8590<br />

Reference Values:<br />

ANTINUCLEAR ANTIBODIES (ANA)<br />

< or =1.0 U (negative)<br />

1.1-2.9 U (weakly positive)<br />

3.0-5.9 U (positive)<br />

> or =6.0 U (strongly positive)<br />

Reference values apply to all ages.<br />

CYCLIC CITRULLINATED PEPTIDE ANTIBODIES, IgG<br />

or =60.0 U (strong positive)<br />

Reference values apply to all ages.<br />

Clinical References: 1. Kavanaugh A, Tomar R, Reveille J, et al: Guidelines for clinical use of the<br />

antinuclear antibody test and tests for specific autoantibodies to nuclear antigens. Arch Pathol Lab Med<br />

2000;124:71-81 2. Homburger HA: Cascade testing for autoantibodies in connective tissue diseases.<br />

<strong>Mayo</strong> Clin Proc 1995;70:183-184 3. van Boekel MA, Vossenaar ER, van den Hoogen FH, van Venrooij<br />

WJ: Autoantibody systems in rheumatoid arthritis: specificity, sensitivity and diagnostic value. Arthritis<br />

Res 2002;4:87-93 4. Tomar R, Homburger H: Assessment of immunoglobulins and antibodies. In Clinical<br />

Immunology Principles and Practice, 2nd edition. Edited by R Rich, T Fleisher, W Shearer, et al, St.<br />

Louis, Mosby-Year Book, 2001, pp 120.1-120.14<br />

Copper, 24 Hour, Urine<br />

Clinical Information: The biliary system is the major pathway of copper excretion. Biliary excretion<br />

of copper requires an ATP-dependent transporter protein. Mutations in the gene for the transporter protein<br />

cause hepatolenticular degeneration (Wilson disease). Ceruloplasmin, the primary copper-carrying protein<br />

in the blood, is also reduced in Wilson disease. Urine copper excretion is increased in Wilson disease due<br />

to a decreased serum binding of copper to ceruloplasmin, or due to allelic variances in cellular metal ion<br />

transporters. Hypercupriuria is also found in Menkes disease (kinky hair disease), hemochromatosis,<br />

biliary cirrhosis, thyrotoxicosis, various infections, and a variety of other acute, chronic, and malignant<br />

diseases (including leukemia). Urine copper concentrations are also elevated in patients taking<br />

contraceptives or estrogens and during pregnancy. Low urine copper levels are seen in malnutrition,<br />

hypoproteinemias, malabsorption, and nephrotic syndrome. Increased zinc consumption interferes with<br />

normal copper absorption from the gastrointestinal tract causing hypocupremia.<br />

Useful For: Investigation of Wilson disease and obstructive liver disease<br />

Interpretation: Humans normally excrete 60 mcg/day may be seen in: -Wilson disease -Menkes disease -Obstructive biliary disease (eg,<br />

primary biliary cirrhosis, primary sclerosing cholangitis) -Nephrotic syndrome (due to leakage through the<br />

kidney) -Chelation therapy -Estrogen therapy -Mega-dosing of zinc-containing vitamins Because<br />

ceruloplasmin is an acute phase reactant, urine copper is elevated during acute inflammation. During the<br />

recovery phase, urine copper is usually below normal, reflecting the expected physiologic response to<br />

replace the copper that was depleted during inflammation.<br />

Reference Values:<br />

0-15 years: not established<br />

> or =16 years: 15-60 mcg/specimen<br />

Clinical References: 1. Zorbas YG, Kakuris KK, Deogenov VA et al: Copper homeostasis during<br />

hypokinesia in healthy subjects with higher and lower copper consumption. Trace Elements and<br />

Electrolytes 2008;25:169-178 2. Lech T, Sadlik JK: Contribution to the data on copper concentration in<br />

blood and urine in patients with Wilson's disease and in normal subjects. Biol Trace Elem Res 2007<br />

July;118(1):16-20<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 518

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