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Magnesium, Random Urine (with Creatinine), AA [19743X]
Test Code14460
CPT Codes
82570, 83735
Preferred Specimen
10 mL of a well-mixed, preserved random urine, submitted in a plastic, leak-proof container
Minimum Volume
0.5 mL
Instructions
Please submit 10 mL of a well-mixed random urine. Adjust pH to < 3.0 with 6N HCl before aliquoting for testing. Refrigerate during and after collection.
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: 4 days
Refrigerated: 7 days
Frozen: 90 days
Refrigerated: 7 days
Frozen: 90 days
Methodology
Inductively Coupled Plasma/Mass Spectrometry (ICP/MS)
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Tues-Sat; Report available: Same day
Reference Range
Magnesium, Random Urine
Creatinine, Random Urine
| Adult | 22-130 mg/g creat | |
| ≤6 Months | 2-28 mg/dL | |
| 7-11 Months | 2-31 mg/dL | |
| 1-2 Years | 2-110 mg/dL | |
| 3-8 Years | 2-130 mg/dL | |
| 9-12 Years | 2-160 mg/dL | |
| >12 Years Male | 20-320 mg/dL | |
| >12 Years Female | 20-275 mg/dL | |
Clinical Significance
This test may be used to investigate causes of abnormal serum magnesium levels. It may also be used to assess risk for renal stone formation and to evaluate for magnesium deficiency or excess. Measurement of total serum magnesium is generally considered sufficient for most clinical scenarios. However, measurement of magnesium in urine can provide additional useful information in some settings [1].
Magnesium is a trace element primarily acquired through dietary intake. Magnesium is stored within bones and intracellularly, where it binds to adenosine triphosphate (ATP) and serves as a cofactor for many cellular processes. Its level in the serum is tightly regulated [2].
Magnesium deficiency is uncommon in the general population. In hospitalized patients, magnesium deficiency may be caused by gastrointestinal losses (diarrhea, malabsorption, nasogastric drainage, etc) and urinary losses (diuretics use, prolonged parenteral fluid therapy, diabetes-induced osmotic diuresis, etc). It is also seen in the setting of chronic alcohol exposure and in certain endocrine and congenital disorders [2].
Magnesium excess generally results from excessive intake of antacid medications, enemas, and magnesium-containing parenteral fluids. However, it may also be seen in pregnant women and their neonates following magnesium therapy for preeclampsia [2].
The kidneys filter and reabsorb magnesium from circulating plasma. Magnesium excretion in the urine inhibits the development of calcium-containing urinary stones. When urine magnesium levels are low, the urine may become supersaturated by calcium phosphate and calcium oxalate crystals, contributing to a risk of urinary stone formation [3].
Results from patients receiving magnesium infusion products should be interpreted with caution. Urine magnesium should be interpreted alongside serum magnesium. Serum hypomagnesemia paired with elevated urine magnesium suggests renal magnesium losses. Decreased urine magnesium in the setting of hypomagnesemia suggests insufficient intake and/or gastrointestinal losses.
Test results should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. Ryan MF, et al. Ann Clin Biochem.1998;35:449-459.
2. Burtis C, et al. Amino acids and proteins. In: Tietz Fundamentals of Clinical Chemistry and Molecular Diagnostics. 7th ed. St Louis, Missouri: Elsevier;2015:310-314.
3. Sutton RA, et al. Miner Electrolyte Metab.1993;19:232-240.
Magnesium is a trace element primarily acquired through dietary intake. Magnesium is stored within bones and intracellularly, where it binds to adenosine triphosphate (ATP) and serves as a cofactor for many cellular processes. Its level in the serum is tightly regulated [2].
Magnesium deficiency is uncommon in the general population. In hospitalized patients, magnesium deficiency may be caused by gastrointestinal losses (diarrhea, malabsorption, nasogastric drainage, etc) and urinary losses (diuretics use, prolonged parenteral fluid therapy, diabetes-induced osmotic diuresis, etc). It is also seen in the setting of chronic alcohol exposure and in certain endocrine and congenital disorders [2].
Magnesium excess generally results from excessive intake of antacid medications, enemas, and magnesium-containing parenteral fluids. However, it may also be seen in pregnant women and their neonates following magnesium therapy for preeclampsia [2].
The kidneys filter and reabsorb magnesium from circulating plasma. Magnesium excretion in the urine inhibits the development of calcium-containing urinary stones. When urine magnesium levels are low, the urine may become supersaturated by calcium phosphate and calcium oxalate crystals, contributing to a risk of urinary stone formation [3].
Results from patients receiving magnesium infusion products should be interpreted with caution. Urine magnesium should be interpreted alongside serum magnesium. Serum hypomagnesemia paired with elevated urine magnesium suggests renal magnesium losses. Decreased urine magnesium in the setting of hypomagnesemia suggests insufficient intake and/or gastrointestinal losses.
Test results should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. Ryan MF, et al. Ann Clin Biochem.1998;35:449-459.
2. Burtis C, et al. Amino acids and proteins. In: Tietz Fundamentals of Clinical Chemistry and Molecular Diagnostics. 7th ed. St Louis, Missouri: Elsevier;2015:310-314.
3. Sutton RA, et al. Miner Electrolyte Metab.1993;19:232-240.
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153
