Test ID NMHR N-Methylhistamine, Random, Urine
Advisory Information
Patients with chronic mast cell activation often have chronically elevated N-methylhistamine (NMH) levels and will sometimes have intermittent NMH elevations. In these cases, a 24-hour urine collection is preferred. See NMH24 / N-Methylhistamine, 24 Hour, Urine.
Specimen Required
Patient Preparation: Patient must not be taking monoamine oxidase inhibitors (MAOIs) or aminoguanidine as these medications increase N-methylhistamine (NMH) levels.
Supplies: Aliquot Tube, 5 mL (T465)
Container/Tube: Plastic vial, 5-mL
Specimen Volume: 5 mL
Collection Instructions:
1. Collect a random urine specimen within a few hours of symptom onset.
2. No preservative.
Useful For
Screening for and monitoring of mastocytosis and disorders of systemic mast-cell activation, such as anaphylaxis and other forms of severe systemic allergic reactions using random urine specimens
Monitoring therapeutic progress in conditions that are associated with secondary, localized, low-grade persistent, mast-cell proliferation and activation such as interstitial cystitis
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
NMHR1 | N-Methylhistamine, Random | No | Yes |
CRETR | Creatinine, Random, U | No | Yes |
Special Instructions
Method Name
NMHR1: Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
CRETR: Enzymatic Colorimetric Assay
Reporting Name
N-Methylhistamine, Random, USpecimen Type
UrineSpecimen Minimum Volume
3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 28 days | |
Frozen | 28 days | ||
Ambient | 14 days |
Reference Values
0-5 years: 120-510 mcg/g creatinine
6-16 years: 70-330 mcg/g creatinine
>16 years: 30-200 mcg/g creatinine
Day(s) and Time(s) Performed
Tuesday, Thursday; 10 a.m.
Performing Laboratory

Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.CPT Code Information
82542
82570
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
NMHR | N-Methylhistamine, Random, U | 13781-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
605015 | N-Methylhistamine, Random, U | 13781-0 |
CRETR | Creatinine, Random, U | 2161-8 |