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Metanephrines (urine)

Test Background

Metanephrines are the 3-O-methylated metabolites of catecholamines. They are formed in chromaffin cells by the action of catechol-O-methyl transferase which produces metanephrine (MN) from adrenaline; normetanephrine (NMN) from noradrenaline; and 3-methoxytyramine (3-MT) from dopamine.

Measurement of metanephrines is used to demonstrate elevated production of catecholamines and is recommended as a first line investigation for the diagnosis of phaeochromocytoma and paraganglioma (PPGL).

PPGL are rare neuroendocrine tumours arising from adrenal chromaffin cells (phaeochromocytoma) and extra-adrenal chromaffin cells of the sympathetic paravertebral ganglia (paraganglioma). Rarely these tumours are biochemically silent but commonly they produce excessive levels of one or more catecholamines. The presence of membrane-bound catechol-O-methyl transferase in tumour cells results in the metabolism of secreted catecholamines to their respective metanephrines. This occurs in a continuous manner, independent of catecholamine release, thus providing a diagnostic advantage of metanephrines measurement over catecholamines.

Diagnosis of phaeochromocytoma depends on a high index of clinical suspicion and biochemical confirmation of excessive metanephrine secretion.

Clinical Indications

24 hour urine metanephrine measurement may be considered when signs and symptoms of catecholamine excess are present, particularly if paroxysmal. These include:

- Hypertension
- Sweating
- Anxiety
- Palpitations
- Headache

Other clinical settings where plasma metanephrine testing is indicated include:

- PPGL symptoms provoked by use of medications associated with adverse effects*
- Adrenal incidentaloma, with or without hypertension
- Hereditary predisposition or syndromic features suggesting hereditary PPGL

(MEN-2, Von Hippel-Lindau syndrome, Neurofibromatosis type-1)
- Previous history of PPGL

*dopamine D2 receptor antagonists, βadrenergic receptor blockers, sympathomimetics, opioid analgesics, norepinephrine reuptake inhibitors (including tricyclic antidepressants), serotonin reuptake inhibitors, monoamine oxidase inhibitors, corticosteroids, peptides (ACTH, glucagon), neuromuscular blocking agents.

Reference Range

Reference intervals will be given with the report

Sample volume
24 hour urine collection
Turnaround time
3 weeks
Sample & Container Required
24 hour urine collection acidified
Transport Storage
Stable at 2-8°C however freezing pending dispatch recommended. Sample can be sent by first class post.
Notes

Random urine samples are accepted where it is difficult to provide 24 hour collections.

These must be acidified on their initial receipt in the laboratory specimen reception.
Samples with pH>3.0 are unsuitable for this assay.

Not currently performed in house; this is a referred test. Referral laboratory is Synnovis.

Record last updated
September 8, 2025

Sample Container

24hr Urine Bottle (with acid warning label)

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Test Results

Yes, we have a Pathology User Guide

Yes. Please email your request to Imperial.nwlpcustomerservice@nhs.net

Results are communicated to clinical staff and are normally not communicated direct to patients either on telephone requests or in written report. If you need to contact us please click here to view the contact details page

Please contact the Customer Service Team Monday to Friday from 8:30am – 6:00pm on 0203 313 5353. Alternatively, see the Pathology User Guide for how to contact the relevant department. If advice is not urgent you can also email your query to Imperial.nwlpcustomerservice@nhs.net

Additional tests may be added by discussion with the relevant laboratory. The time limit for adding additional tests to a sample already received in the laboratory will depend on the type of sample and the department it was sent to.

Information on the repertoire of tests performed by pathology, including reference ranges, turnaround times and specimen requirements, can be found in the test directory.

NWLP operates UKAS accredited medical laboratories as per the references below. The current scope of accreditation for all NWLP’s laboratories can be found on the UKAS website.

See the following UKAS ref numbers:

  • Clinical Biochemistry Ref: 8673
  • Haematology and Blood Transfusion Ref: 8674
  • Infection & Immunity Sciences (Including Immunology, Virology, Microbiology and Histocompatibility and Immunogenetics ) Ref: 8659
  • Cellular Pathology (Including Histopathology, Cytology and Molecular Pathology) Ref: 9615

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UKAS requires the laboratories to be accredited for a particular repertoire/scope (ISO15189), any changes or additions to repertoire require assessment by UKAS (extension to scope).

The BD Hospital Tube GuideBD GP Tube Guide and BD Paediatric Tube Guide provide visual references to the correct tube types and collection instructions.

Home testing

INSTRUCTION SHEET FOR BLOOD SAMPLE COLLECTION 

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VIDEO ON BLOOD SAMPLE COLLECTION (without subtitles)

VIDEO ON BLOOD SAMPLE COLLECTION (with subtitles)

Our accreditations

Upholding excellence in diagnostic standards

Our laboratories are accredited by the UK Accreditation Service (UKAS) against the international standard ISO15189:2022. UKAS is the accreditation body for the UK that assesses medical laboratories.

Find out more about our accreditations on the UKAS website.

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