Clinical Background
Diabetes mellitus (DM) is a chronic illness that leads to significant morbidity and death in the U.S.
Disease Complications
- Acute
- Diabetic ketoacidosis - Type 1 DM
- Hyperosmolar nonketotic coma - Type 2 DM
- Long-term (Types 1 and 2 DM)
- Cardiac - coronary artery disease
- Immunologic - recurrent infections
- Neurologic - neuropathy
- Ophthalmic - retinopathy
- Renal - proteinuria with renal failure
- Vascular - small vessel disease with extremity loss
- A large body of evidence supports that structured care with appropriate clinical interventions may prevent acute complications and improve long-term outcomes in DM patients
See Also
Diagnosis
Diagnosis
| Criteria for the Diagnosis of Diabetes |
One of the following criteria:
|
| (Used with permission from Standards of Medical Care, 2007, S5) |
- Disease Monitoring
| Recommendations for Physical Examination |
|
| (Adapted with permission from Standards of Medical Care, 2007, S8) |
- Laboratory Testing
- Glycemic control
- Hemoglobin A1C
- Premise of testing
- Glycation of hemoglobin is non-linear over time and occurs over the whole lifespan of the red blood cell
- Correlates with risk of long term complications and with diabetes control over previous 2-3 months
- Target goal: <7% of glycated hemoglobin
- Laboratory testing recommendations
- 2 measurements per year for patients meeting goal of <7%
- If patient is not hypoglycemic, goal should be <6%
- More frequent monitoring in patients with HbA1c greater than or equal to 7%; however not more often than every 3 months
- Do not use for diagnosis for diabetes
- 2 measurements per year for patients meeting goal of <7%
- Premise of testing
- 1-5-Anhydroglucitol
- Premise of testing
- Renal reabsorption of 1,5-anhydroglucitol is competitively inhibited by glucose and is excreted in the urine when the concentration of plasma glucose exceeds its renal threshold (~180 mg/dL).
- Poor glycemic control leads to decreased concentrations of plasma 1,5-anhydroglucitol
- Less sensitive to small changes in glycemic control at high HbA1c levels
- Laboratory testing recommendations
- Not recommended as a standard test for monitoring DM
- May be useful for identifying post-prandial hyperglycemia and assessing glycemic control in patients with moderately controlled diabetes
- Premise of testing
- Fructosamine
- Premise of testing
- Intermediate marker of glycemia
- Carbonyl group of glucose reacts with an amino group of a protein
- Provides glycemia index over 20-day period
- Laboratory testing recommendations
- May be useful in monitoring gestational DM; not recommended as a standard to use for other types of DM
- May be used in patients with shortened red cell survival (eg, sickle cell disease)
- Premise of testing
- Albumin, glycated
- Premise of testing
- Intermediate marker of glycemia
- Measures glycation of serum albumin
- Provides glycemia index over 20-day period
- Laboratory testing recommendations
- May be useful in monitoring gestational DM; not recommended as a standard to use for other types of DM
- May be used in patients with shortened red cell survival (eg, sickle cell disease)
- Control in patients with moderately controlled diabetes
- Premise of testing
- Insulin
- Premise of testing
- Circulating levels of insulin may be prognostic for likelihood of progression to insulin dependence in diabetes
- Testing recommendations
- Not recommended as a standard test for monitoring DM
- Premise of testing
- C-peptide
- Premise of testing
- C-peptide connects the A& B chains of proinsulin
- Released in equimolar concentrations with insulin
- Reflects endogenous insulin production
- Laboratory testing recommendations
- Not recommended as a standard test for monitoring DM
- May be useful for assessing endogenous insulin production to confirm need for insulin therapy
- Premise of testing
- Hemoglobin A1C
- Dyslipidemia
- Lipid panel
- Premise of testing
- Patients with diabetes have an increased incidence of lipid abnormalities
- Lipid lowering therapies have been demonstrated to reduce macrovascular disease
- Premise of testing
- Target goal: LDL <70 mg/dL (particularly if there is evidence or risk of CVD); HDL >40 mg/dL, triglycerides <150 mg/dL
- Recommended laboratory testing
- Initial evaluation and every year if goals are met
- More often if goals are not met
- Treat aggressively with statins if goals not met
- Initial evaluation and every year if goals are met
- Recommended laboratory testing
- Lipid panel
- Hepatic function
- Liver function tests (SGOT, SGPT, alkaline phosphatase, bilirubin)
- Premise of testing
- Patients with DM are at-risk for steatohepatitis
- Recommend testing - initial and annually thereafter if values are normal on initial testing
- Premise of testing
- Liver function tests (SGOT, SGPT, alkaline phosphatase, bilirubin)
- Renal function
- Creatinine
- Premise of testing
- Many drugs will require adjusted dosing based on creatinine, creatinine clearance or estimated glomerular filtration rates (eGFR)
- Absolute creatinine values do not reflect glomerular filtration rates in many patients
- Diabetic nephropathy diminishes creatinine
- Renal function thereby diminishes clearance and glomerular filtration rate
- Creatinine and eGFR are broad measures of renal function
- Target goal
- Normal ranges
- Males - 97-113 mL/min
- Females - 88-128 mL/min
- Recommended laboratory testing
- Serum creatinine and eGFR (calculated) annually
- Normal ranges
- Premise of testing
- Creatinine
- Microalbumin (urine)
- Premise of testing
- Diabetic nephropathy occurs in 20-40% of patients with diabetes and is the single leading cause of end stage renal disease
- Microalbuminuria (persistent albuminuria) (range 30-299 mg/g creatinine, 30-299 mg/24 hours) signifies the earliest stage of diabetic nephropathy
- Target goal
- <30 mg/g creatinine, <30 mg/24 hour urine
- Recommended laboratory testing
- Spot urine or 24-hour urine for microalbumin annually
- Addition of angiotensin converting enzyme inhibitors to diabetes regimen is renoprotective if microalbuminuria is present
- Premise of testing
- Thyroid function
- TSH
- Premise of testing
- Autoimmune thyroid disease occurs more frequently in patients with DM
- Recommend testing initially and, if normal, every 3 years thereafter
- Premise of testing
- TSH
- Glycemic control
| Tests |
Tests generally appear in the order most useful for common clinical situations
| Test name: Hemoglobin A1c |
| ARUP #: 0081335 |
| Methodology: Method: High Performance Liquid Chromatography/Boronate Affinity |
| Use: Monitor diabetes |
| Limitations: Unstable hemoglobins or hemolytic anemia may yield falsely low results Iron deficiency anemia may yield falsely high results |
| Test name: Microalbumin, Urine |
| ARUP #: 0050203 |
| Methodology: Immunoturbidimetric |
| Use: Monitor diabetic nephropathy in insulin-dependent diabetes mellitus |
| Test name: Lipid Panel |
| ARUP #: 0020421 |
| Methodology: Refer to individual components |
| Use: Monitor levels of LDL, HDL and triglycerides |
| Test name: Glomerular Filtration Rate, Estimated |
| ARUP #: 0020725 |
| Methodology: Spectrophotometry |
| Use: Monitor renal function (Test includes serum creatinine) |
| Test name: Hepatic Function Panel |
| ARUP #: 0020416 |
| Methodology: Refer to individual components. |
| Use: Assess liver function |
| Limitations: |
| Follow-up: |
| Test name: Thyroid Stimulating Hormone |
| ARUP #: 0070145 |
| Methodology: Electrochemiluminescent Immunoassay |
| Use: Assess and monitor thyroid function |
| Limitations: |
| Follow-up: |
| Test name: Albumin, Glycated |
| ARUP #: 0080700 |
| Methodology: Boronate Affinity Chromatography/Immunoturbidimetric |
| Use: Useful in gestational DM monitoring or in patients with shortened red cell survival |
| Limitations: |
| Follow-up: |
| Test name: 1,5 Anhydroglucitol (GlycoMark) |
| ARUP #: 0080453 |
| Methodology: Enzymatic |
| Use: Assess glycemic control in patient with moderately controlled diabetes Useful marker for postprandial hyperglycemia Complementary marker to Hemoglobin A1C |
| Limitations: Will be decreased in individuals with renal glucose thresholds that are markedly different from 180 mg/dL (e.g., chronic renal failure, pregnancy, dialysis) and in those undergoing steroid therapy |
| Test name: Fructosamine |
| ARUP #: 0099012 |
| Methodology: Spectrophotometry |
| Use: Can be used to monitor gestational diabetes or a patient with shortened red cell survival |
| Limitations: Variations in levels of serum proteins can affect results High levels of ascorbic acid interfere with the assay |
| Follow-up: |
Additional Tests Available
| Test name: C-Peptide, Serum or Plasma |
| ARUP #: 0070103 |
| Methodology: Chemiluminescent Immunoassay |
| Comments: Not useful in diabetes mellitus monitoring |
| Test name: Insulin, Free & Total |
| ARUP #: 0070155 |
| Methodology: Chemiluminescent Immunoassay |
| Comments: Not useful in diabetes mellitus monitoring |
References
Guidelines
American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Diabetes and pregnancy. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 5 pages. NGC:005858American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Glycemic management. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 19 pages. NGC:005853American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Hypertension management. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 6 pages. NGC:005854American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Lipid management. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 8 pages. NGC:005855American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Microvascular complications. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 6 pages. NGC:005857American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Nutrition and diabetes. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 4 pages. NGC:005856American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Prevention of type 2 diabetes mellitus. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 4 pages. NGC:005852American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus. Screening and diagnosis. American Association of Clinical Endocrinologists - Medical Specialty Society
American College of Endocrinology - Medical Specialty Society. 2000 Jan (revised 2007). 3 pages. NGC:005851Qaseem A, Vijan S, Snow V, Cross JT, Weiss KB, Owens DK. Glycemic control and type 2 diabetes mellitus: the optimal hemoglobin A1c targets. A guidance statement from the American College of Physicians. Ann Intern Med . 2007 ;147 (6 ):417-422 . Snow V, Aronson MD, Hornbake ER, Mottur-Pilson C, Weiss KB. Lipid control in the management of type 2 diabetes mellitus: a clinical practice guideline from the American College of Physicians. Ann Intern Med . 2004 ;140 (8 ):644-649 . Consensus statement on the worldwide standardization of the hemoglobin A1C measurement: the American Diabetes Association, European Association for the Study of Diabetes, International Federation of Clinical Chemistry and Laboratory Medicine, and the International Diabetes Federation. Diabetes Care . 2007 ;30 (9 ):2399-2400 . Standards of medical care in diabetes--2008. Diabetes Care . 2008 ;31 Suppl 1 :S12-S54 .
Cited References
General References
References from the ARUP Institute for Clinical and Experimental Pathology Research®
Medical Reviewers
Grenache, David G., Ph.D. Medical Director, Special Chemistry at ARUP Laboratories; Assistant Professor, Clinical Pathology, University of Utah
Lehman, Christopher M., M.D. Co-Medical Director, University Hospital Clinical Laboratory; Associate Professor, Clinical Pathology, University of Utah
Meikle, A. Wayne, M.D. Medical Director, RIA and Endocrinology at ARUP Laboratories; Professor of Internal Medicine and Pathology, University of Utah
Roberts, William L. , M.D., Ph.D. Medical Director, Automated Core Laboratory at ARUP Laboratories; Professor, Pathology, University of Utah
Comprehensive Review: May 2008
Last Update: September 2008

















