Test Results For:
Free Light Chains Kappa/Lambda Ratio
Test Overview
- Test Name
-
Free Light Chains Kappa/Lambda Ratio
- Test Code
- FLCR
Short Description
Free Light Chains Kappa/Lambda Ratio
Test Name
Free Light Chains Kappa/Lambda Ratio
Test Code
FLCR
Category
Biochemistry
TAT
Main Lab:
6
Hour(s)
Family Site:
<6hrs
Specimen(s)
1 x N/A - mL - - N/A
Specimen Type
N/A
Specimen Format
-
Specimen Colour
-
Specimen Volume
- mL
Sampling Order
-
Origin
N/A
Collection Time after baseline
-
Transport Temperature
-
Accepted Other Specimens
-
TAT
Main Lab:
6
Hour(s)
Family Site:
<6hrs
Test Stability
Room Temp:
-
2–8°C:
-
Methodology
-
Specimen Type
N/A
Delay before pre-treatment
-
Transport temperature
-
Test stability at room temperature
-
Test stability at 2–8°C
- -
Haemolysis interference
No
Clinical Interest
The kappa (κ) and lambda (λ) free light chains are produced by plasma cells, and their abnormal production is a hallmark of several hematological diseases.
In multiple myeloma, malignant plasma cells often produce excessive amounts of one type of free light chain, either kappa or lambda, leading to an abnormal kappa/lambda ratio. The measurement of FLCs can detect monoclonal production of light chains, which is crucial for diagnosing both typical and atypical forms of multiple myeloma.
A subtype of myeloma, light chain multiple myeloma, predominantly secretes light chains rather than intact immunoglobulins. FLC assays are essential for diagnosing this form, as traditional serum protein electrophoresis might not detect the monoclonal proteins effectively.
Some cases of multiple myeloma, known as nonsecretory myeloma, do not produce detectable levels of monoclonal proteins in serum or urine by standard methods. FLC measurement can often reveal the presence of monoclonal free light chains, thus aiding in diagnosis.
FLC levels are monitored during treatment to assess the effectiveness of therapy. A significant reduction in abnormal FLCs suggests a good response to treatment, whereas rising levels may indicate disease progression or relapse.
Clinical Information Required
-
Patient Collection Note
-
LOINC Code
88-4, 6788-4
Outwork
No