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Insulin and C-Peptide

Code:9060|CPT:83525, 84681|LOINC:20448-7, 1986-9

Synonyms
Гормон поджелудочной железы, регулятор обмена углеводов.C-Peptide and InsulinInsulinPancreatic hormone, regulator of carbohydrate metabolism
IncludesInsulin C-Peptide, Serum

Analysis details

Methodology

  • Electrochemiluminescence immunoassay (ECLIA)
  • Chemiluminescent immunoassay (CLIA)

Expected Turnaround Time

1 day

Special Instructions

  • Fast for at least 12 hours; water is permitted.
  • If clinically appropriate and approved by the clinician, hold medications for 24 hours before collection.
  • Do not smoke during the 3 hours preceding specimen collection.
  • Stop high‑dose biotin for a minimum of 72 hours before collection and record any biotin use.

How to use

The Insulin and C‑Peptide test (also known as the C‑peptide and insulin profile) assesses endogenous insulin secretion and pancreatic beta‑cell function by comparing paired insulin and C‑peptide concentrations. When reviewed alongside plasma glucose, the profile aids evaluation of hypoglycemia and supports the diagnosis of insulinoma. It is used to monitor endogenous insulin production in diabetes, to gauge insulin resistance, and to inform treatment choices in type 2 diabetes, including whether to initiate insulin therapy or oral hypoglycemic agents. C‑peptide is not affected by insulin antibodies and remains informative when patients are receiving exogenous insulin.

Limitations

Pancreatic beta cells synthesize insulin, and secretion rises as blood glucose increases after meals. Insulin facilitates cellular uptake of glucose and promotes hepatic glycogen formation; when glucose is abundant, surplus substrate is directed toward lipogenesis. Inadequate insulin production or impaired action reduces cellular glucose use and produces hyperglycemia, which over time contributes to complications affecting the kidneys, cardiovascular system, nervous system, and vision. Type 1 diabetes reflects absolute insulin deficiency, while type 2 diabetes is characterized predominantly by insulin resistance with a relative impairment in secretion. Hyperinsulinemia can precipitate or accompany hypoglycemia and may result from exogenous insulin administration or from autonomous secretion by an insulinoma.

UnitµIU/mL
Reference interval
IndicationsWorkup of confirmed or suspected hypoglycemia with autonomic and neuroglycopenic features (eg, diaphoresis, palpitations, confusion, visual disturbance, dizziness, weakness), Diagnosis of insulinoma and postoperative surveillance for recurrence, Assessment of islet cell transplant graft function over time

Possible Causes of Abnormal Results

Decreased levels

  • biotin (high dose)

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume1 mL (min 0.5 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen