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Interpretive Handbook

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Test 60068 :
Electrophoresis, Protein, Random, Urine

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Urine proteins can be grouped into 5 fractions by protein electrophoresis:

-Albumin

-Alpha-1

-Alpha-2

-Beta-globulin

-Gamma globulin

 

The urine total protein concentration, the electrophoretic pattern, and the presence of a monoclonal immunoglobulin light chain may be characteristic of monoclonal gammopathies such as multiple myeloma, primary systemic amyloidosis, and light-chain deposition disease.

Useful For Suggests clinical disorders or settings where the test may be helpful

Identifying patients with a monoclonal M-spike

Interpretation Provides information to assist in interpretation of the test results

A characteristic monoclonal band (M-spike) is often found in the urine of patients with multiple myeloma (MM). The initial identification of an M-spike or an area of restricted migration should be followed by MPSU / Monoclonal Protein Study, 24 Hour, Urine, which includes immunofixation electrophoresis to identify the immunoglobulin heavy chain and/or light chain. Immunoglobulin heavy chain fragments as well as free light chains may be seen in the urine of patients with monoclonal gammopathies.

  

The presence of a monoclonal light chain M-spike of >1 g/24 hours is consistent with a diagnosis of MM or macroglobulinemia.

  

The presence of a small amount of monoclonal light chain and proteinuria (total protein >3 g/24 hours) that is predominantly albumin is consistent with primary systemic amyloidosis (AL) and light-chain deposition disease (LCDD). Because patients with AL and LCDD may have elevated urinary protein without an identifiable M-spike, urine protein electrophoresis is not considered an adequate screen for the disorder. MPSU / Monoclonal Protein Study, 24 Hour, Urine, which includes immunofixation electrophoresis, should be performed if the clinical suspicion is high.

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Urine protein electrophoresis (PEL) alone is not considered adequate screening for monoclonal gammopathies. Patients suspected of having a monoclonal gammopathy may have a normal urine protein electrophoretic pattern, and these patients should have immunofixation electrophoresis (MPSU / Monoclonal Protein Study, 24 Hour, Urine) performed.

 

Random urine specimens may be sufficient for identifying monoclonal proteins, but 24 hour specimens should be used to quantitate and monitor urinary abnormalities.

 

Monoclonal gammopathies are rarely seen in patients <30 years of age.

 

Hemolysis may cause a discrete band on PEL, which will be negative on immunofixation.

 

Penicillin may split the albumin band.

 

Radiographic agents may produce an uninterpretable pattern.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

ELECTROPHORESIS, PROTEIN

The following fractions, if present, will be reported as a percent of the total protein. 

Albumin

Alpha-1-globulin

Alpha-2-globulin

Beta-globulin

Gamma-globulin 

No reference values apply to random urines.

Clinical References Provides recommendations for further in-depth reading of a clinical nature

1. Kyle RA, Katzmann JA, Lust JA, Dispenziei A: Clinical indications and applications of electrophoresis and immunofixation. In Manual of Clinical Laboratory Immunology. Sixth edition. Edited by NR Rose, et al. Washington, DC. ASM Press, 2002, pp 66-67

2. Kyle RA, Katzmann JA, Lust JA, Dispernzieri A: Immunochemical characterization of immunoglobulins. In Manual of Clinical Laboratory Immunology. Sixth  edition. Edited by N.R. Rose, et al. Washington, DC. ASM Press, 2002, pp 71-91


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