Test Code MPSQU Mucopolysaccharides Quantitative, Random, Urine
Reporting Name
Mucopolysaccharides Quant, UPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Supporting the biochemical diagnosis of one of the mucopolysaccharidoses: types I, II, III, IV, VI, or VII
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Ordering Guidance
This test alone is not appropriate for the diagnosis of a specific mucopolysaccharidosis (MPS). Follow-up enzymatic or molecular genetic testing must be performed to confirm a diagnosis of an MPS.
Necessary Information
1. Patient's age is required.
2. Reason for testing is required.
3. Biochemical Genetics Patient Information (T602) is recommended. This information aids in providing a more thorough interpretation of results. Send information with specimen.
Specimen Required
Patient Preparation: Do not administer low-molecular weight heparin prior to collection
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Container/Tube: Plastic, 5-mL urine tube
Specimen Volume: 2 mL
Pediatric Volume: 1 mL
Collection Instructions: Collect a random urine specimen (early morning preferred).
Specimen Type
UrineSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 90 days | |
Frozen | 365 days | ||
Ambient | 7 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
DERMATAN SULFATE
≤1.00 mg/mmol creatinine
HEPARAN SULFATE
≤4 years: ≤0.50 mg/mmol creatinine
≥5 years: ≤0.25 mg/mmol creatinine
CHONDROITIN-6 SULFATE
≤24 months: ≤10.00 mg/mmol creatinine
25 months-10 years: ≤2.50 mg/mmol creatinine
≥11 years: ≤1.50 mg/mmol creatinine
KERATAN SULFATE
≤12 months: ≤2.00 mg/mmol creatinine
13-24 months: ≤1.50 mg/mmol creatinine
25 months-4 years: ≤1.00 mg/mmol creatinine
5-18 years: ≤0.50 mg/mmol creatinine
≥19 years: ≤0.30 mg/mmol creatinine
Interpretation
Elevations of dermatan sulfate, heparan sulfate, keratan sulfate, and/or chondroitin-6-sulfate may be indicative of one of the mucopolysaccharidoses types I, II, III, IV, VI, or VII.
Elevations of any or all sulfate species may be indicative of multiple sulfatase deficiency or mucolipidosis II/III.
Rarely, an elevation of keratan sulfate may be indicative of alpha-fucosidosis.
Day(s) Performed
Monday
Report Available
8 to 15 daysTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
83864
82570
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
MPSQU | Mucopolysaccharides Quant, U | 94691-3 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
BG716 | Reason for Referral | 42349-1 |
605986 | Dermatan Sulfate | 94692-1 |
605987 | Heparan Sulfate | 94693-9 |
605988 | Chondroitin-6 Sulfate | 94690-5 |
605989 | Keratan Sulfate | 92806-9 |
605990 | Interpretation | 59462-2 |
605985 | Reviewed By | 18771-6 |
Forms
1. Biochemical Genetics Patient Information (T602)
2. If not ordering electronically, complete, print, and send a Biochemical Genetics Test Request (T798) with the specimen.
Testing Algorithm
For more information see the following:
-Lysosomal Storage Disorders Diagnostic Algorithm, Part 1
-Newborn Screening Follow up for Mucopolysaccharidosis type II
If the patient has abnormal newborn screening result for mucopolysaccharidosis type I, immediate action should be taken. Refer to the appropriate American College of Medical Genetics and Genomics Newborn Screening ACT Sheet.(1)