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Sorted By Test Name - Mayo Medical Laboratories

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IGG<br />

8160<br />

multiple myeloma (LCMM), Waldenstromâ€s macroglobulinemia (WM), nonsecretory myeloma<br />

(NSMM), smoldering multiple myeloma (SMM), monoclonal gammopathy of undetermined significance<br />

(MGUS), primary systemic amyloidosis (AL), and light chain deposition disease (LCDD). Monoclonal<br />

proteins are typically detected by serum protein electrophoresis (SPEP) and immunofixation (IF).<br />

However, the monoclonal light chain diseases (LCMM, AL, LCDD) and NSMM often do not have serum<br />

monoclonal proteins in high enough concentration to be detected and quantitated by SPEP. A sensitive<br />

nephelometric assay specific for kappa free light chain (FLC) that doesnâ€t recognize light chains<br />

bound to Ig heavy chains has recently been described. This automated, nephelometric assay is reported to<br />

be more sensitive than IF for detection of monoclonal FLC. In some patients with NSMM, AL, or LCDD<br />

the FLC assay provides a positive identification of a monoclonal serum light chain when the serum IF is<br />

negative. In addition, the quantitation of FLC has been correlated with disease activity in patients with<br />

NSMM and AL. See Laboratory Approach to the Diagnosis of Amyloidosis and Laboratory Screening<br />

<strong>Test</strong>s for Suspected Multiple Myeloma in Special Instructions.<br />

Useful For: Monitoring patients with monoclonal light chain diseases but no M-spike on protein<br />

electrophoresis<br />

Interpretation: The specificity of this assay for detection of monoclonal light chains relies on the ratio<br />

of free kappa and lambda light chains. Once an abnormal free light chain (FLC) K/L ratio has been<br />

demonstrated and a diagnosis has been made, the quantitation of the monoclonal light chain is useful for<br />

monitoring disease activity. Changes in FLC quantitation reflect changes in the size of the monoclonal<br />

plasma cell population. Our experience to date is limited, but changes of >25% or trending of multiple<br />

specimens are needed to conclude biological significance.<br />

Reference Values:<br />

KAPPA-FREE LIGHT CHAIN<br />

0.33-1.94 mg/dL<br />

LAMBDA-FREE LIGHT CHAIN<br />

0.57-2.63 mg/dL<br />

KAPPA/LAMBDA FLC RATIO<br />

0.26-1.65<br />

Clinical References: Drayson M, Tang LX, Drew R, et al: Serum free light chain measurements for<br />

identifying and monitoring patients with nonsecretory multiple myeloma. Blood 2001;97(9):2900-2902<br />

Immunoglobulin G (IgG), Serum<br />

Clinical Information: The gamma globulin band as seen in conventional serum protein<br />

electrophoresis consists of 5 immunoglobulins. In normal serum, about 80% is immunoglobulin G (IgG).<br />

Elevations of IgG may be due to polyclonal immunoglobulin production. Monoclonal elevation of IgG<br />

characterize multiple myeloma. Monoclonal gammopathies of all types may lead to a spike in the gamma<br />

globulin zone seen on serum protein electrophoresis. Decreased immunoglobulin levels are found in<br />

patients with congenital deficiencies.<br />

Useful For: Detecting or monitoring of monoclonal gammopathies and immune deficiencies<br />

Interpretation: Increased serum immunoglobulin concentrations occur due to polyclonal or<br />

oligoclonal immunoglobulin proliferation in hepatic disease (hepatitis, liver cirrhosis), connective tissue<br />

diseases, acute and chronic infections, as well as in the cord blood of neonates with intrauterine and<br />

perinatal infections. Elevation of immunoglobulin G may occur in monoclonal gammopathies such as<br />

multiple myeloma, primary systemic amyloidosis, monoclonal gammopathy of undetermined<br />

significance, and related disorders. Decreased levels are found in patients with primary or secondary<br />

immune deficiencies.<br />

Reference Values:<br />

0-

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