Test ID LPCBS Lysophosphatidylcholines, LC MS/MS, Blood Spot
Useful For
Second-tier newborn screen for X-linked adrenoleukodystrophy
This test is not intended for metabolic screening of symptomatic patients.
This test is supplemental and not intended to replace state mandated newborn screening.
Genetics Test Information
This test is used as a second-tier newborn screen for X-linked adrenoleukodystrophy (X-ALD).
Highlights
Testing for C24:0 lysophosphatidylcholines (LPC) and C26:0 LPC can aid in the diagnosis of X-linked adrenoleukodystrophy (XALD) as well as other types of peroxisomal disorders.
Analysis of LPC in a blood spot test is a useful second-tier newborn screen test for XALD.
Special Instructions
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Reporting Name
LysoPC by LC MS/MS, BSSpecimen Type
Whole bloodSpecimen Required
Supplies: Card-Blood Spot Collection (Filter Paper) (T493)
Container/Tube:
Preferred: Blood Spot Collection Card
Acceptable: PerkinElmer 226 filter paper, Munktell filter paper, Whatman Protein Saver 903 Paper, local newborn screening card, or blood collected in tubes containing ACD or EDTA, and then spotted and dried on filter paper
Specimen Volume: 2 Blood spots
Collection Instructions:
1. An alternative blood collection option for a patient older than 1 year is a fingerstick. For detailed instructions, see How to Collect Dried Blood Spot Samples.
2. Completely fill at least 2 circles on the filter paper card (approximately 100 microliters blood per circle).
3. Let blood dry on the filter paper at ambient temperature in a horizontal position for a minimum of 3 hours.
4. Do not expose specimen to heat or direct sunlight.
5. Do not stack wet specimens.
6. Keep specimen dry.
Additional Information:
1. For collection instructions, see Blood Spot Collection Instructions.
2. For collection instructions in Spanish, see Blood Spot Collection Card-Spanish Instructions (T777).
3. For collection instructions in Chinese, see Blood Spot Collection Card-Chinese Instructions (T800.
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.
Specimen Minimum Volume
1 Blood spot
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole blood | Refrigerated (preferred) | 90 days | FILTER PAPER |
Frozen | 90 days | FILTER PAPER | |
Ambient | 28 days | FILTER PAPER |
Reference Values
Analyte |
Normal Range (nmol/mL) |
C20 Lysophosphatidylcholine |
Not applicable |
C22 Lysophosphatidylcholine |
Not applicable |
C24 Lysophosphatidylcholine |
≤0.41 |
C26 Lysophosphatidylcholine |
≤0.31 |
Day(s) Performed
Monday through Saturday
Performing Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
82542
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LPCBS | LysoPC by LC MS/MS, BS | 105457-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
34865 | Interpretation (LPCBS) | 59462-2 |
34860 | C20 Lysophosphatidylcholine | 90920-0 |
34861 | C22 Lysophosphatidylcholine | 90921-8 |
34862 | C24 Lysophosphatidylcholine | 90922-6 |
34863 | C26 Lysophosphatidylcholine | 90923-4 |
34864 | Reviewed By | 18771-6 |
Test 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.NY State Approved
YesReport Available
2 daysForms
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 Newborn Screen Follow-up for X-linked Adrenoleukodystrophy.
If the patient has an abnormal newborn screening result for X-linked adrenoleukodystrophy, immediate action should be taken. Refer to the appropriate ACMG Newborn Screening ACT Sheet.(1)