Test Summary
ACTH concentrations show a diurnal variation with high levels in the morning and low levels in the evening. Therefore, as with cortisol, it is important to know the collection time of the plasma sample for interpretation of the results. Plasma ACTH measurements are useful in the differential diagnosis of Cushing's disease (ACTH hypersecretion), autonomous ACTH producing pituitary tissue (e.g. Nelson's syndrome), hypopituitarism with ACTH deficiency and ectopic ACTH syndrome. In addition to cortisol measurements, ACTH determinations can be used together with suppression or stimulation tests to diagnose the origin of glucocorticoid overproduction. Similarly, ACTH measurements can be employed to facilitate differential diagnosis of adrenocortical insufficiency (Addison’s disease). ACTH not produced by the pituitary gland is known as ectopic ACTH; this is often associated with small cell carcinoma of the lung. In rare cases ectopic ACTH can be caused by thymic tumors, pancreatic adenocarcinomas, or bronchial carcinoids. These tumors often secrete ACTH precursors (POMC and pro-ACTH).
Aliases
- Adrenocorticotropic Hormone
- Corticotropin
Specimen Collection
Preferred Specimen
1.5 mL frozen plasma collected in an EDTA (lavender-top) tube
Instructions
Draw specimens between 7AM and 10AM. If drawn during any other time, the reference ranges do not apply. Only use pre-cooled sampling vials. After drawing the blood, put the vials immediately on ice. Use a cooled centrifuge to separate the plasma. Centrifuge immediately after collection to separate plasma from cells. Transfer plasma to a plastic specimen transport container and mark the specimen type as plasma on the container. Freeze immediately
Storage
Plastic screw-cap vial
Transport Temperature
Frozen
Specimen Stability
- Room temperature: unacceptable
- Refrigerated: unacceptable
- Frozen: 32 days
Limitations
ACTH measurement is not recommended for patients who have been administered cosyntropin (ACTH (1-24)) because the results may be falsely elevated or depressed. Reference: Siemens Healthcare Customer Notification IMC20-04.A.US March 25, 2020.
Other Acceptable Specimens
PPT potassium EDTA (white-top) tube
Unacceptable Specimens
Received thawed
Order Code
ACTH
EPIC (Premier) Code
LAB011
Includes
N/A
CPT Code
Billing Code
CPT Statement
Methodology
Electrochemiluminescence (ECLIA)
FDA Status
FDA Approved
Physician Attestation of Informed Consent
N/A
Testing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153
Department
Reference Testing
Reference Range
7.2 - 63.3 pg/mL
Setup Schedule / Expected Turnaround Time
Tuesday - Saturday; Report available: 1 - 2 days
Specimen Collection
Preferred Specimen
1.5 mL frozen plasma collected in an EDTA (lavender-top) tube
Instructions
Draw specimens between 7AM and 10AM. If drawn during any other time, the reference ranges do not apply. Only use pre-cooled sampling vials. After drawing the blood, put the vials immediately on ice. Use a cooled centrifuge to separate the plasma. Centrifuge immediately after collection to separate plasma from cells. Transfer plasma to a plastic specimen transport container and mark the specimen type as plasma on the container. Freeze immediately
Storage
Plastic screw-cap vial
Transport Temperature
Frozen
Specimen Stability
- Room temperature: unacceptable
- Refrigerated: unacceptable
- Frozen: 32 days
Limitations
ACTH measurement is not recommended for patients who have been administered cosyntropin (ACTH (1-24)) because the results may be falsely elevated or depressed. Reference: Siemens Healthcare Customer Notification IMC20-04.A.US March 25, 2020.
Other Acceptable Specimens
PPT potassium EDTA (white-top) tube
Unacceptable Specimens
Received thawed
Billing
CPT Code
Billing Code
CPT Statement
Result Information
Methodology
Electrochemiluminescence (ECLIA)
Testing Laboratory
N/A
Reference Range
7.2 - 63.3 pg/mL
Setup Schedule / Expected Turnaround Time
Tuesday - Saturday; Report available: 1 - 2 days