Test ID HBA1C Hemoglobin A1c, Blood
Useful For
Evaluating the long-term control of blood glucose concentrations in diabetic patients
Diagnosing diabetes
Identifying patients at increased risk for diabetes (prediabetes)
Method Name
Ion-Exchange Chromatography Quantitative
Reporting Name
Hemoglobin A1c, BSpecimen Type
Whole Blood EDTAContainer/Tube: Lavender top (EDTA)
Specimen Volume: 3 mL
Collection Instructions: Send specimen in original tube.
Specimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Whole Blood EDTA | Refrigerated (preferred) | 7 days |
Ambient | 24 hours |
Clinical Information
Diabetes mellitus is a chronic disorder associated with disturbances in carbohydrate, fat, and protein metabolism characterized by hyperglycemia. It is one of the most prevalent diseases, affecting approximately 24 million individuals in the United States. Long-term treatment of the disease emphasizes control of blood glucose levels to prevent the acute complications of ketosis and hyperglycemia. In addition, long-term complications such as retinopathy, neuropathy, nephropathy, and cardiovascular disease can be minimized if blood glucose levels are effectively controlled.
Hemoglobin A1c (HbA1c) is a result of the nonenzymatic attachment of a hexose molecule to the N-terminal amino acid of the hemoglobin molecule. The attachment of the hexose molecule occurs continually over the entire life span of the erythrocyte and is dependent on blood glucose concentration and the duration of exposure of the erythrocyte to blood glucose. Therefore, the HbA1c level reflects the mean glucose concentration over the previous period (approximately 8-12 weeks, depending on the individual) and provides a much better indication of long-term glycemic control than blood and urinary glucose determinations. Diabetic patients with very high blood concentrations of glucose have from 2 to 3 times more HbA1c than normal individuals.
Diagnosis of diabetes includes 1 of the following:
-Fasting plasma glucose ≥126 mg/dL
-Symptoms of hyperglycemia and casual plasma glucose >or =200 mg/dL
-Two-hour glucose ≥200 mg/dL during oral glucose tolerance test unless there is unequivocal hyperglycemia, confirmatory testing should be repeated on a different day
In addition, recommendations from the American Diabetes Association (ADA) include the use of HbA1c to diagnose diabetes, using a cutpoint of 6.5%.(1) The cutpoint was based upon sensitivity and specificity data from several studies. Advantages to using HbA1c for diagnosis include:
-HbA1c provides an assessment of chronic hyperglycemia
-Assay standardization efforts from the National Glycohemoglobin Standardization Program have been largely successful and the accuracy of HbA1c is closely monitored by manufacturers and laboratories
-No fasting is necessary
-Intraindividual variability is very low (critical value of <2%)
-A single test could be used for both diagnosing and monitoring diabetes
When using HbA1c to diagnose diabetes, an elevated HbA1c should be confirmed with a repeat measurement, except in those individuals who are symptomatic and also have an increased plasma glucose >200 mg/dL. Patients who have an HbA1c between 5.7 and 6.4 are considered at an increased risk for developing diabetes in the future. (The terms prediabetes, impaired fasting glucose, and impaired glucose tolerance will eventually be phased out by the ADA to eliminate confusion.)
The ADA recommends measurement of HbA1c (typically 3-4 times per year for type 1 and poorly controlled type 2 diabetic patients, and 2 times per year for well-controlled type 2 diabetic patients) to determine whether a patient's metabolic control has remained continuously within the target range.
Reference Values
≥18 years: 4.0-6.0%
Reference values have not been established for patients who are <18 years of age.
Cautions
Most common hemoglobin (Hb) variants (HbF <15%, heterozygous HbC, heterozygous HbS) do not interfere with this HPLC method. Other variants of Hb may show interference with this method. The known variants that fall into this category are HbE, HbD, Hb Fukuoka, Hb Philadelphia, and Hb Raleigh.
If the specimen cannot be analyzed using the Biorad Variant II cation exchange HPLC method due to a hemoglobinopathy or other interference, a second-tier test will be performed on the Trinity Biotech ultra-2 HPLC method utilizing boronate-affinity chromatography, which is least affected by Hb variants. Most specimens from patients with hemoglobinopathies can be accurately monitored with the boronate-affinity method. If the specimen cannot be analyzed using either method due to a hemoglobinopathy or other interference, measurement of serum fructosamine may be helpful to monitor glycemic control. See FRUCT / Fructosamine, Serum.
In patients with rare homozygous forms of abnormal Hb (eg, CC, SS, EE, SC), there is no HbA present and thus no hemoglobin A1c (HbA1c) value can be quantitated using this method. In these patients, the RBC lifespan is often variable and although an HbA1c could be reported using a boronate-affinity method, it is likely not providing a true measurement of the patient's glycemic control and could lead to misinterpretation. In such situations, fructosamine should be used as an alternate measurement of glycemia and is recommended for monitoring these patients. Fructosamine is a stable ketoamine that represents intermediate-term glycemic control (2-3 weeks). See FRUCT / Fructosamine, Serum.
In cases of hemolytic anemia, the lifetime of erythrocytes is shortened and will result in decreased glycated hemoglobin results. This effect will depend upon the severity of the anemia. Specimens from patients with polycythemia or postsplenectomy may exhibit increased glycated hemoglobin values due to a somewhat longer lifespan of the RBCs. Caution should be exercised when interpreting the HbA1c results from patients with these conditions.
This assay is not useful in determining day-to-day glucose control and should not be used to replace daily home testing of blood glucose.
Day(s) Performed
Monday through Sunday; Continuously
Report Available
Same day/1 dayPerforming Laboratory

Test Classification
This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
83036