Test ID RLTE4 Leukotriene E4, Random, Urine
Ordering Guidance
Random urine collections are preferred for patients with episodic symptoms, (eg, in the context of allergic reactions brought on by specific environmental factors or mast cell activation syndrome).
Additional Testing Requirements
For an optimal evaluation, testing for urinary leukotriene E4 should be accompanied by laboratory investigations for the presence of serum tryptase (TRYPT / Tryptase, Serum), urinary 2,3-dinor 11 beta-prostaglandin F2 alpha (23BPR / 2,3-Dinor 11 Beta-Prostaglandin F2 Alpha, Random, Urine) and urinary N-methylhistamine (NMHR / N-Methylhistamine, Random, Urine).
Specimen Required
Patient Preparation: Patients taking 5-lipoxygenase inhibitor zileuton (Zyflo) may have decreased concentrations of leukotriene E4. If medically feasible, the patient should not take zileuton for 48 hours before specimen collection.
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Container/Tube: Plastic vial
Specimen Volume: 5 mL
Collection Instructions:
1. Within a few hours of symptom onset, collect a random urine specimen.
2. No preservative.
3. Aliquot urine into a plastic vial and send frozen.
Secondary ID
606354Useful For
Aiding in the evaluation of patients at-risk for mast cell disorders (eg, systemic mastocytosis, IgE-mediated allergies, or aspirin-exacerbated respiratory disease) using random urine collections
Specimen Type
UrineSpecimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Urine | Frozen (preferred) | 28 days |
| Refrigerated | 72 hours | |
| Ambient | 8 hours |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
LEUKOTRIENE E4
≤104 pg/mg creatinine
CREATININE
<18 years: Not established
≥18 years: 16-326 mg/dL
Day(s) Performed
Monday, Tuesday, Thursday
Report Available
2 to 9 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
82542
82570