Test Code LSDS Lysosomal Disorders Screen, Random, Urine
Ordering Guidance
This test is the recommended screening test for the initial workup of a suspected lysosomal disorder (LD) when the patient's clinical features are not suggestive of any specific LD.
Necessary Information
1. Patient's age is required.
2. 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:
1. Do not administer low-molecular weight heparin before specimen collection.
2. Baby wipes or wipes containing soaps or lotions should not be used before specimen collection because these may interfere with results.
Supplies: Urine Container, 60 mL (T313)
Container/Tube: Clean, plastic urine container with no metal cap or glued insert
Specimen Volume: 12 mL
Pediatric Volume: 3.5 mL
Collection Instructions:
1. Collect a random urine specimen (early morning preferred).
2. No preservative.
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.
Useful For
Screening patients suspected of having a lysosomal disorder
Genetics Test Information
This is a general urine screening test for a broad array of lysosomal and related disorders (LD). Not all LD are detectable by this method.
Disease States
- Sialidosis
- Galactosialidosis
Profile Information
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| CTS02 | Ceramide Trihex and Sulfatide, U | Yes, (Order CTSU) | Yes |
| MPS02 | Mucopolysaccharides Quant, U | Yes, (Order MPSQU) | Yes |
| OLI02 | Oligosaccharide Screen, U | Yes, (Order OLIGU) | Yes |
| SAU02 | Sialic Acid, Free and Total, U | Yes, (Order SAU) | Yes |
| BG721 | Lysosomal Disorders Interpretation | No | Yes |
Testing Algorithm
For information see:
-Lysosomal Disorders Diagnostic Algorithm, Part 1
-Lysosomal Disorders Diagnostic Algorithm, Part 2
-Lysosomal Disorders Screen Interpretive Algorithm
-Epilepsy: Unexplained Refractory and/or Familial Testing Algorithm
Special Instructions
Reporting Name
Lysosomal Disorders Scrn, USpecimen Type
UrineSpecimen Minimum Volume
3.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Urine | Refrigerated (preferred) | 15 days |
| Frozen | 90 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
Free Sialic Acid:
≤4 weeks: ≤208 mmol/mol creatinine
5 weeks-12 months: ≤104 mmol/mol creatinine
13 months-18 years: ≤100 mmol/mol creatinine
≥19 years: ≤38 mmol/mol creatinine
Total Sialic Acid:
≤4 weeks: ≤852 mmol/mol creatinine
5 weeks-12 months: ≤656 mmol/mol creatinine
13 months-18 years: ≤335 mmol/mol creatinine
≥19 years: ≤262 mmol/mol creatinine
Total/Free Ratio:
≤4 weeks: 1.94-18.68
5 weeks-12 months: 2.34-13.85
13 months-18 years: 2.63-9.18
≥19 years: 3.35-15.81
Ceramide Trihexosides:
Negative
Sulfatides:
Negative
Oligosaccharides:
Negative
An interpretive report will be provided.
Method Description
Ceramide trihexosides and sulfatides are determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. Urine specimens are centrifuged, and most of the supernatant is discarded from the pellet. Reagent including internal standards is added, and then ceramide trihexosides and sulfatides are extracted. After centrifugation, the bottom layer is spotted onto a MALDI plate, matrix is added and allowed to air dry. The plate is then analyzed using a MALDI TOF/TOF 5800 Analyzer.(Unpublished Mayo method)
Dermatan sulfate (DS), heparan sulfate (HS), keratan sulfate (KS) and chondroitin-6-sulfate (C6S) are enzymatically digested from urine. The reaction mixture is centrifuged and analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS). The ratio of the extracted peak area of DS, HS, KS and C6S to internal standard as determined by LC-MS/MS is used to calculate the concentration of DS, HS, KS and C6S in the sample.(Unpublished Mayo method)
Oligosaccharides in urine samples are extracted using Oasis HLB and carbograph columns and lyophilized overnight. Oligosaccharides are permethylated, the tubes centrifuged, and the supernatant removed. The supernatant is quenched with water, neutralized with acetic acid, extracted, eluted, and again lyophilized overnight. Specimens are resuspended, mixed 1:1 with a matrix solution, spotted onto a MALDI plate and allowed to air dry. The plate is then analyzed using a MALDI TOF/TOF 5800 Analyzer.(Xia B, Asif G, Arthur L, et al. Oligosaccharide analysis in urine by MALDI-TOF mass spectrometry for the diagnosis of lysosomal storage diseases. Clin Chem 2013;59[9]:1357-1368, Hall PL, Lam C, Alexander JJ. Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency. Mol Genet Metab. 2018;124[1]:82-86)
Sialic acid in urine samples is measured twice to obtain free sialic acid and total sialic acid values. Free sialic acid is dried down and butylated in 3M hydrochloric acid in butanol. Total sialic acid is hydrolyzed with hydrochloric acid and butylated in 3M hydrochloric acid in butanol. Both samples are reconstituted in eluent and analyzed by LC-MS/MS. The free and total sialic acid samples are quantitated using an internal standard calibration curve.(Tebani A, Schlemmer D, Imbard A, et al. Measurement of free and total sialic acid by isotopic dilution liquid chromatography tandem mass spectrometry method. J. Chromatogr. B Analyt Technol Biomed Life Sci. 2011;879[31]:3694-3699, Li J, Wu T, Zhang X, et al. Clinical application of liver diseases diagnosis using ultrahigh-sensitive liquid chromatography-mass spectrometry for sialic acids detection. J. Chromatogr. A. 2022;1666:462837)
Day(s) Performed
Varies
Report Available
8 to 14 daysSpecimen Retention Time
1 monthPerforming Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
83789
83864
84377
84275
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| LSDS | Lysosomal Disorders Scrn, U | 105125-9 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 621077 | Dermatan Sulfate | 94692-1 |
| 621078 | Heparan Sulfate | 94693-9 |
| 621079 | Chondroitin-6 Sulfate | 94690-5 |
| 621080 | Keratan Sulfate | 92806-9 |
| 621074 | Free Sialic Acid | In Process |
| 621075 | Total Sialic Acid | In Process |
| 621076 | Total/Free Sialic Acid Ratio | In Process |
| 621081 | Ceramide Trihexosides | 34680-9 |
| 621082 | Sulfatides | 34646-0 |
| 621083 | Oligosaccharides | 49284-3 |
| 606773 | Lysosomal Disorders Interpretation | 94423-1 |
| 606772 | Reviewed By | 18771-6 |