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Test Code MCM24 Mast Cell Mediators, 24 Hour, Urine


Ordering Guidance


Random urine collections are preferred for patients with episodic symptoms, for example in the context of allergic reactions brought on by specific environmental factors. For random urine collections, order MCMRU / Mast Cell Mediators, Random, Urine.



Specimen Required


Patient Preparation:

1. Patient must not be taking monoamine oxidase inhibitors (MAOI) or aminoguanidine, as these medications increase N-methylhistamine (NMH) levels.

2. Patients taking aspirin or nonsteroidal anti-inflammatory drugs (NSAID) may have decreased concentrations of prostaglandin F2 alpha (23BP). If possible, the patient should discontinue use for 2 weeks or 72 hours, respectively, before specimen collection.

Supplies: Urine Container, 60 mL (T313)

Collection Container/Tube: Plastic urine container

Submission Container/Tube: Plastic, 60-mL urine bottle

Specimen Volume: 20 mL

Collection Instructions:

1. Collect urine for 24 hours.

2. No preservative.

3. Aliquot urine into plastic tube and send to lab.

Additional Information: See Urine Preservatives-Collection and Transportation for 24-Hour Urine Specimens for multiple collections.


Secondary ID

608378

Useful For

Evaluating patients at risk for mast cell activation syndrome (eg, systemic mastocytosis) using 24-hour urine collections

Profile Information

Test ID Reporting Name Available Separately Always Performed
CRT2F Creatinine, 24 HR, U No Yes
TLTE1 Leukotriene E4, 24 Hr, U Yes Yes
T23B1 2,3-dinor 11B-Prostaglandin F2a Yes Yes
TNMH1 N-Methylhistamine, 24 Hr, U Yes Yes

Method Name

CRT2F: Enzymatic Colorimetric Assay

TLTE1, T23B1, TNMH1: Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Specimen Type

Urine

Specimen Minimum Volume

10 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Frozen 28 days

Reject Due To

  All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Reference Values

N-METHYLHISTAMINE:

0-5 years: 120-510 mcg/g creatinine

6-16 years: 70-330 mcg/g creatinine

>16 years: 30-200 mcg/g creatinine

 

2,3-DINOR 11B-PROSTAGLANDIN F2a:

<1802 pg/mg creatinine

 

LEUKOTRIENE E4:

≤104 pg/mg creatinine

 

CREATININE:

Males: 930-2955 mg/24 h

Females: 603-1783 mg/24 h

Reference values have not been established for patients who are younger than 18 years.

Interpretation

Analytical reports within the scope of the individual assays will be provided when testing is complete.

Method Description

N-methylhistamine is extracted from urine using solid-phase extraction. The elute is analyzed using liquid chromatography tandem mass spectrometry (LC-MS/MS) and quantified using a stable isotope labeled internal standard.(Martens-Lobenhoffer J, Neumann HJ. Determination of 1-methylhistamine and 1-methylimidazoleacetic acid in human urine as a tool for the diagnosis of mastocytosis. J Chromatogr B Biomed Sci Appl. 1999;721[1]:135-140; Lueke AJ, Meeusen JW, Donato LJ, Gray AV, Butterfield JH, Saenger AK. Analytical and clinical validation of an LC-MS/MS method for urine leukotriene E4: A marker of systemic mastocytosis. Clin Biochem. 2016;49[13-14]:979-982. doi:10.1016/j.clinbiochem.2016.02.007)

 

2,3-Dinor-11beta-prostaglandin F2alpha:

2,3-Dinor-11beta-prostaglandin F2alpha (23BPG) is quantified in urine by LC-MS/MS. Deuterium-labeled 23BPG internal standard (d4-11BPGF2a) is added to all controls and specimens, which are then liquid/liquid extracted. The eluent is evaporated, and samples/QC are then reconstituted prior to LC-MS/MS analysis.(Unpublished Mayo method)

 

Leukotriene E4:

Leukotriene E4 (LTE4) is quantified in urine via multiplexed LC-MS/MS. Deuterium-labeled LTE4 internal standard is added to all standards/controls/samples, which are then filtered. After additional sample clean-up, this eluent is analyzed by LC-MS/MS.(Unpublished Mayo method)

 

Creatinine:

The enzymatic method is based on the determination of sarcosine from creatinine with the aid of creatininase, creatinase, and sarcosine oxidase. The liberated hydrogen peroxide is measured via a modified Trinder reaction using a colorimetric indicator. Optimization of the buffer system and the colorimetric indicator enables the creatinine concentration to be quantified both precisely and specifically.(Package insert: Creatinine plus ver 2. Roche Diagnostics; V15.0, 03/2019)

Day(s) Performed

Monday, Tuesday, Thursday

Report Available

3 to 7 days

Specimen Retention Time

See individual Test IDs

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

82542

84150

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MCM24 Mast Cell Mediators, 24 Hour, U In Process

 

Result ID Test Result Name Result LOINC Value
CR_AF Creatinine, 24 HR, U 2162-6
620242 2,3-dinor 11B-Prostaglandin F2a 94381-1
620244 N-Methylhistamine, 24 Hr 44340-8
620240 Leukotriene E4, U 101115-4
TM10F Collection Duration (h) 13362-9
VL8F Urine Volume (mL) 3167-4
CRF24 Creatinine Concentration, 24 HR, U 20624-3

Urine Preservative Collection Options

Note: The addition of preservative or application of temperature controls must occur within 4 hours of completion of the collection.

Ambient (No additive)

No

Refrigerate (No additive)

No

Frozen (No additive)

Preferred

50% Acetic Acid

OK

Boric Acid

OK

Diazolidinyl Urea

No

6M Hydrochloric Acid

No

6M Nitric Acid

No

Sodium Carbonate

OK

Thymol

No

Toluene

No