Unit Code 8158:
Immunoglobulin M (IgM), Serum
Useful For
Suggests clinical disorders or settings where the test may be helpful
Detecting or monitoring of monoclonal gammopathies and immune
deficiencies
Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test
The gamma-globulin band as seen in conventional serum protein
electrophoresis consists of 5 immunoglobulins. In normal serum,
about 5% is IgM.
Elevations of IgM may be due to polyclonal immunoglobulin production.
Monoclonal elevations of IgM occur in macroglobulinemia.
Monoclonal gammopathies of all types may lead to a spike in the
gamma-globulin zone seen on serum protein electrophoresis.
Decreased immunoglobulin levels are found in patients with congenital
deficiencies.
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.
Males
0-4 months: 14-142 mg/dL
5-8 months: 24-167 mg/dL
9-23 months: 35-200 mg/dL
2-3 years: 41-200 mg/dL
4-17 years: 47-200 mg/dL
> or = 18 years: 50-300 mg/dL
Females
0-4 months: 14-142 mg/dL
5-8 months: 24-167 mg/dL
9-23 months: 35-242 mg/dL
2-3 years: 41-242 mg/dL
4-17 years: 56-242 mg/dL
> or =18 years: 50-300 mg/dL
Interpretation
Provides information to assist in interpretation of the test results
Increased serum immunoglobulin concentrations occur due to
polyclonal or oligoclonal immunoglobulin proliferation in hepatic
disease (hepatitis, liver cirrhosis), connective tissue diseases, acute
and chronic infections, as well as in the cord blood of neonates with
intrauterine and perinatal infections.
Elevation of IgM may occur in monoclonal gammopathies such as
macroglobulinemia, primary systemic amyloidosis, monoclonal gamm-
opathy of undetermined significance, and related disorders.
Decreased levels are found in patients with primary or secondary
immune deficiencies.
Cautions
Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances
Electrophoresis is usually required to interpret an elevated
immunoglobulin class as polyclonal versus monoclonal.
Immunofixation is usually required to characterize
a monoclonal protein.
If there is a discrete M-peak, the monoclonal protein can be
monitored with quantitative immunoglobulins. If immunoglobulin
quantitation is used to monitor the size of a monoclonal protein
which is contained in a back-ground of polyclonal immunoglobulins,
however, changes in the immunoglobulin quantitation may reflect
changes in the background immunoglobulins, and serum protein
electrophoresis should therefore be used to monitor the monoclonal
protein.
Clinical Reference
Provides recommendations for further in-depth reading of a clinical nature
1. Webster ADB: Laboratory Investigation of primary deficiency
of the lymphoid system. In Clinics in Immunology and Allergy.
Vol. 5. 3rd edition. Philadelphia, WB Saunders Company, 1985,
pp 447-468
2. Pinching AJ: Laboratory investigation of secondary immunodeficiency.
In Clinics in Immunology and Allergy. Vol. 5. Third edition. Philadelphia,
WB Saunders Company, 1985, pp 469-490
3. Dispenzieri A, Gertz MA, Kyle RA: Distribution of diseases associated
with moderate polyclonal gammopathy in patients seen at Mayo
Clinic during 1991. Blood 1997;90:353
4. Kyle RA, Greipp PR: The laboratory investigation of monoclonal
gammopathies. Mayo Clin Proc 1978;53:719-739
5. Ballow M, O'Neil KM: Approach to the patient with recurrent
infections. In Allergy: Principles and Practice. Vol. 2. Fourth
edition. Edited by E Middleton Jr, CE Reed, EF Ellis, et al. St.
Louis, MO, Mosby-Year Book, Inc., 1993, pp 1027-1058
6. Kyle RA: Detection of quantitation of monoclonal proteins. Clin
Immunol Newsletter 1990;10:84-86


