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

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MGCRU<br />

60244<br />

FMASC<br />

90054<br />

Magnesium/Creatinine Ratio, Random, Urine<br />

Clinical Information: Magnesium, along with potassium, is a major intracellular cation. Magnesium<br />

is a cofactor of many enzyme systems. All adenosine triphosphate (ATP)-dependent enzymatic reactions<br />

require magnesium as a cofactor. Approximately 70% of magnesium ions are stored in bone. The<br />

remainder is involved in intermediary metabolic processes; about 70% is present in free form, while the<br />

other 30% is bound to proteins (especially albumin), citrates, phosphate, and other complex formers. The<br />

serum magnesium level is kept constant within very narrow limits. Regulation takes place mainly via the<br />

kidneys, primarily in the ascending loop of Henle. Conditions that interfere with glomerular filtration<br />

result in retention of magnesium and, hence, elevation of serum concentrations. Hypermagnesemia is<br />

found in acute and chronic renal failure, magnesium overload, and magnesium release from the<br />

intracellular space. Mild-to-moderate hypermagnesemia may prolong atrioventricular conduction time.<br />

Magnesium toxicity may result in central nervous system (CNS) depression, cardiac arrest, and<br />

respiratory arrest. Numerous studies have shown a correlation between magnesium deficiency and<br />

changes in calcium-, potassium-, and phosphate-homeostasis, which are associated with cardiac disorders<br />

such as ventricular arrhythmias that cannot be treated by conventional therapy, increased sensitivity to<br />

digoxin, coronary artery spasms, and sudden death. Additional concurrent symptoms include<br />

neuromuscular and neuropsychiatric disorders. Conditions associated with hypomagnesemia include<br />

chronic alcoholism, childhood malnutrition, lactation, malabsorption, acute pancreatitis, hypothyroidism,<br />

chronic glomerulonephritis, aldosteronism, and prolonged intravenous feeding.<br />

Useful For: Assessing the cause of abnormal serum magnesium concentrations Determining whether<br />

the body is receiving adequate nutrition<br />

Interpretation: With normal dietary intake of 200 to 500 mg of magnesium per day, urine excretion is<br />

typically 30 to 210 mg/gm creatinine in children and adults. The remainder of the dietary intake passes<br />

through the gastrointestinal tract and is excreted in the feces. Decreased renal function, such as in<br />

dehydration, diabetic acidosis, or Addison's disease, results in reduced output of magnesium. Poor diet<br />

(alcoholism), malabsorption, and hypoparathyroidism result in low urine magnesium due to low uptake<br />

from the diet. Chronic glomerulonephritis, aldosteronism, and drug therapy (cyclosporine, thiazide<br />

diuretics) enhance excretion, resulting in high output of magnesium.<br />

Reference Values:<br />

0-15 years: 110-210 mg/g creatinine<br />

> or =16 years: 30-100 mg/g creatinine<br />

Clinical References: 1. Fenton TR, Eliasziw M, Lyon AW, et al: Low 5-year stability of<br />

within-patient ion excretion and urine pH in fasting-morning-urine specimens. Nutr Res 2009<br />

May;29(5):320-326 2. Mircetic RN, Dodig S, Raos M, et al: Magnesium concentration in plasma,<br />

leukocytes and urine of children with intermittent asthma. Clin Chim Acta 2001 Oct;312(1-2):197-203<br />

Malaria Antibody Screen (P. falciparum, P. vivax, P. malariae, P.<br />

ovale), IFA<br />

Reference Values:<br />

Reference Range: Pos = > 1:64 Neg 64 - In U.S. citizens (brief exposure) may reflect recent infection; in some areas of the world,<br />

may be maximum titer demonstratable even in clinical cases.<br />

In U.S. citizens with brief exposure to infection, a PLASMODIUM FALCIPARUM titer of =>1:64<br />

may reflect recent infection. Speciation of the infecting malaria parasite is made by using four IFA slides<br />

prepared with P. FALCIPARUM, P. VIVAX, P. MALARIAE and P. OVALE, respectively. Antibody<br />

titers in U.S. citizens rarely persist more than six (6) months after chemotherapeutic cure. Titers in people<br />

with prolonged exposure and in people native to malaria endemic areas may persist for years because of<br />

relapses. Due to the increased volume of diagnostic specimens and to maximize the use of our malaria<br />

slides, we now titrate specimens at dilutions of 1:16 and 1:64. We will report immunofluorescence results<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 1156

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