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Mayo Clinic Laboratories

Epic Test Code LAB1005 Glucagon, Plasma

Additional Codes

MML Code: GLP

 

NY State Approved

Yes

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Reporting Name

Glucagon, P

Method Name

Enzyme-Linked Immunosorbent Assay (ELISA)

Specimen Stability Information

Specimen Type Temperature Time
Plasma EDTA Frozen 90 days


Specimen Required


Patient Preparation: Patient should fast for 8 hours before specimen collection.

Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube: Lavender top (EDTA)

Submission Container/Tube: Plastic vial

Specimen Volume: 2 mL

Collection Instructions:

1. Pre-chill lavender top (EDTA) tube at 4° C before drawing the specimen.

2. Draw blood into the pre-chilled tube and process as follows:

 a. Chill filled tube in wet ice for 10 minutes.

 b. Centrifuge in a refrigerated centrifuge or in a pre-chilled centrifuge carrier.

 c. Immediately after centrifugation, aliquot plasma into a plastic vial and freeze.


Specimen Type

Plasma EDTA

Specimen Minimum Volume

0.45 mL

Reference Values

≥1 year of age: ≤159 pg/mL

<1 year of age: No reference interval established.

 

For International System of Units (SI) for Reference Values, see www.mayocliniclabs.com/order-tests/si-unit-conversion.html.

Report Available

3 to 7 days

Day(s) Performed

Tuesday, Friday

CPT Code Information

82943

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Useful For

Diagnosis and follow-up of glucagonomas and other glucagon-producing tumors

 

Assessing diabetic patients with problematic hyper- or hypoglycemic episodes (extremely limited utility)

Clinical Information

Glucagon is a single-chain polypeptide of 29 amino acids that is derived from a larger precursor peptide (big plasma glucagon), which is cleaved upon secretion. The main sites of glucagon production are the hypothalamus and pancreatic alpha-islet cells. The function of hypothalamic glucagon is incompletely understood and currently no clinical disorders of hypothalamic glucagon function have been defined. Pancreatic islet glucagon is secreted in response to hypoglycemia, with resultant increases in blood glucose concentration. Glucagon's hyperglycemic effect is produced by stimulating hepatic glycogenolysis and gluconeogenesis; it has no effect on muscle glycogen. Once blood glucose levels have normalized, glucagon secretion ceases.

 

Excessive glucagon secretion can lead to hyperglycemia. Excessive and inappropriate glucagon secretion can sometimes be observed in diabetes, particularly during ketoacidosis, and can complicate management of the disorder. In rare cases, it also can occur in tumors of the pancreatic islets (glucagonoma), hepatocellular carcinomas, carcinoid tumors, and other neuroendocrine neoplasms. Patients with glucagon-secreting tumors may present with classic glucagonoma syndrome, consisting of necrolytic migratory erythema, diabetes, and diarrhea, but can also have more subtle symptoms and signs.

 

Decreased or absent glucagon response to hypoglycemia can be seen in type I diabetes (insulin-dependent diabetes) and can contribute to severe and prolonged hypoglycemic responses.

 

Glucagon is routinely measured along with serum glucose, insulin, and C-peptide levels during the mixed-meal test employed in the diagnostic workup of suspected postprandial hypoglycemia. However, it plays only a minor role in the interpretation of this test.

Interpretation

Elevated glucagon concentrations in the absence of hypoglycemia may indicate the presence of a glucagon-secreting tumor. Successful treatment of a glucagon-secreting tumor is associated with normalization of glucagon levels.

 

Inappropriate elevations in glucagon concentrations in patients who are hyperglycemic and have type I diabetes indicate that paradoxical glucagon release may contribute to disease severity. This can be observed if insulin treatment is inadequate and patients are ketotic. However, glucagon measurement plays little, if any, role in the diagnostic workup of diabetic ketoacidosis.

 

In patients with diabetes, low glucagon concentrations (undetectable or in the lower quartile of the normal range) in the presence of hypoglycemia indicate impairment of hypoglycemic counter regulation. These patients may be particularly prone to recurrent hypoglycemia. This can be a permanent problem due to islet alpha-cell destruction or other, less well understood processes (eg, autonomous neuropathy). It can also be functional, most often due to over-tight blood glucose control and may be reversible after decreasing insulin doses.

Cautions

Results obtained with different glucagon assays can differ. This can be caused by use of different calibration standards or variable cross-reactivity with different isoforms of glucagon, not all of which are biologically active.

 

The monoclonal antibodies used in this assay only detect the full-length glucagon (amino acids1-29) and do not cross react with glucagon fragments or closely related peptides such as glicentin, oxyntomodulin, glucagon-like peptide-1 (GLP-1), GLP-2, or glicentin-related pancreatic polypeptide.

 

Glucagon serial measurements should always be performed using the same assay.

 

Patients with diabetes, acromegaly, or Cushing syndrome or who are obese have higher glucagon levels.

 

Tumor marker tests, including glucagon, are not specific for malignancy. All immunometric assays can, on rare occasions, be subject to hooking at extremely high analyte concentrations (false-low results), heterophilic antibody interference (false-high results), or autoantibody interference (unpredictable effects). If the laboratory result does not fit the clinical picture, these possibilities should be considered.

 

In rare cases, some individuals can develop antibodies to mouse or other animal antibodies (often referred to as human anti-mouse antibodies [HAMA] or heterophile antibodies), which may cause interference in some immunoassays. Caution should be used in interpretation of results, and the laboratory should be alerted if the result does not correlate with the clinical presentation.

Specimen Retention Time

2 weeks

Forms

If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.