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Cardio IQ(R) Insulin Resistance Panel with Score

Test Summary

The determination of insulin in serum is primarily used for the diagnosis of glycemic disorders in diabetic and pre-diabetic patients in the assessment of insulin resistant syndromes. Insulin is synthesized by the pancreatic beta cell as a precursor, proinsulin. Proinsulin is processed to insulin and C-peptide, a contiguous peptide between the insulin A and B chains, as it passes through the cell. The C-peptide in the proinsulin ensures correct folding and processing of proinsulin as it passes through the cell. Both insulin and C-peptide are released together from the beta cells in response to increased glucose levels. Because of differences in half-life and hepatic clearance, peripheral blood levels of C-peptide and insulin are no longer equimolar but remain highly correlated. A steady-state plasma glucose test in individuals undergoing an insulin suppression test to assess insulin resistance found that the combination of insulin and C-peptide was a better indicator of insulin resistance than either one individually.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

0.5 mL serum

Minimum Volume

0.3 mL

Instructions

N/A

Patient Preparation

Overnight fasting is required

Storage

N/A

Transport Temperature

Refrigerated

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 7 days
  • Frozen: 28 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Hemolysis

Order Code

CIRPL

EPIC (Premier) Code

LAB6876

Includes

Insulin, Intact, LC/MS/MS, C-Peptide, LC/MS/MS, Insulin Resistance Score

CPT Code

  • 83525
  • 84681

Billing Code

  • 671335
  • 671336

CPT Statement

Methodology

Immunocapture Liquid Chromatography/Tandem Mass Spectrometry

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano CA, 92675

Department

Reference Testing

Reference Range

nsulin, Intact, LC/MS/MS ≤16 uIU/mL C-peptide, LC/MS/MS 0.68-2.16 ng/mL Insulin Resistance Score ≤66

Setup Schedule / Expected Turnaround Time

Sunday-Friday; Report available: 3 - 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

0.5 mL serum

Minimum Volume

0.3 mL

Instructions

N/A

Patient Preparation

Overnight fasting is required

Storage

N/A

Transport Temperature

Refrigerated

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 7 days
  • Frozen: 28 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Hemolysis

Billing

CPT Code

  • 83525
  • 84681

Billing Code

  • 671335
  • 671336

CPT Statement

Result Information

Methodology

Immunocapture Liquid Chromatography/Tandem Mass Spectrometry

Testing Laboratory

N/A

Reference Range

nsulin, Intact, LC/MS/MS ≤16 uIU/mL C-peptide, LC/MS/MS 0.68-2.16 ng/mL Insulin Resistance Score ≤66

Setup Schedule / Expected Turnaround Time

Sunday-Friday; Report available: 3 - 5 days