Cystine, Quantitative, Random Urine
Test Summary
This quantitative test may be useful for evaluation of individuals with clinically suspected cystinuria, including those with symptoms of kidney stones or cystine crystals detected in urinalysis [1]. Although 24-hour urine testing is generally preferred for diagnostic evaluation and monitoring of cystinuria [2], random or first-morning void urine collection may be helpful for diagnosis when 24-hour urine collection is not feasible (eg, for young children) [3].
Cystinuria, an autosomal recessive genetic disorder that can cause kidney stones, is characterized by excessive excretion of cystine and dibasic amino acids in the urine. Around 1% to 2% of all kidney stones, and 6% to 8% of kidney stones in children, are caused by cystinuria [1]. Approximately 83% of patients with cystinuria who develop a kidney stone will have a recurrence within 5 years [1]. Common complications of cystinuria include chronic kidney disease and hypertension [1].
This test does not differentiate between free and bound cystine in patients taking cystine-binding thiol drugs [1]. This test alone is not sufficient to predict risk of kidney stones in individuals with cystinuria [1].
The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. Daga S, et al. Urology. 2021;149:70-75.
2. Williams JC Jr, et al. Urolithiasis. 2021;49(1):1-16.
3. Servais A, et al. Kidney Int. 2021;99(1):48-58.
Aliases
- N/A
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
Instructions
Do not thaw. Patient age is required for correct reference range.
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: Unacceptable
- Refrigerated: Unacceptable
- Frozen: 60 days
Limitations
Other Acceptable Specimens
Unacceptable Specimens
Order Code
EPIC (Premier) Code
Includes
CPT Code
- 82131
- 82570
Billing Code
- 670248
- 670249
CPT Statement
Methodology
FDA Status
Physician Attestation of Informed Consent
Testing Laboratory
33608 Ortega Highway
San Juan Capistrano CA, 92675
Department
Reference Range
Pediatric (<18 Years) | 3.2-12.6 mmol/mol creat | ||||
Adult | 3.4-16.4 mmol/mol creat |
Creatinine, Random Urine
0-6 Months | 0.18-2.48 mmol/L |
7-11 Months | 0.18-2.74 mmol/L |
1-2 Years | 0.18-9.72 mmol/L |
3-8 Years | 0.18-11.49 mmol/L |
9-12 Years | 0.18-14.14 mmol/L |
>12 Years | 1.77-23.31 mmol/L |
Setup Schedule / Expected Turnaround Time
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
Instructions
Do not thaw. Patient age is required for correct reference range.
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: Unacceptable
- Refrigerated: Unacceptable
- Frozen: 60 days
Limitations
Other Acceptable Specimens
Unacceptable Specimens
Result Information
Methodology
Testing Laboratory
Reference Range
Pediatric (<18 Years) | 3.2-12.6 mmol/mol creat | ||||
Adult | 3.4-16.4 mmol/mol creat |
Creatinine, Random Urine
0-6 Months | 0.18-2.48 mmol/L |
7-11 Months | 0.18-2.74 mmol/L |
1-2 Years | 0.18-9.72 mmol/L |
3-8 Years | 0.18-11.49 mmol/L |
9-12 Years | 0.18-14.14 mmol/L |
>12 Years | 1.77-23.31 mmol/L |