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Test Code LFRI Progentec aiSLE DX Lupus Flare Risk Index, Plasma


Ordering Guidance


This test is intended to be ordered for adult patients. If the test is ordered for a patient younger than 18 years testing will be canceled.



Shipping Instructions


Specimen must be shipped frozen. Testing will be canceled if received ambient or refrigerated.



Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube: Yellow top (ACD solution A)

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions:

1. Centrifuge at 1500 x g for 20 minutes.

2. Aliquot plasma into plastic vial.

3. Freeze specimen within 2 hours of collection.

Note: Critical frozen. Separate specimens must be submitted when multiple tests are ordered.


Useful For

Aiding in the assessment of risk of flare in lupus patients when used in conjunction with standard clinical assessment

Method Name

Immunoassay

Reporting Name

Lupus Flare Risk Index, P

Specimen Type

Plasma

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Frozen 74 days

Reference Values

Monocyte chemoattractant protein-1 (MCP1)/CCL2: 54-368 pg/mL

Interleukin-5 (IL-5): 0.260-2.000 pg/mL

Interleukin-17A (IL-17A): 2.100-11.000 pg/mL

Interleukin-7 (IL-7): 1.10-12.00 pg/mL

Interleukin-4 (IL-4): 1.000-3.200 pg/mL

Tumor necrosis factor-a (TNF-a): 1.80-12.00pg/mL

Monocyte chemoattractant protein-3 (MCP3)/CCL7: 0.82-16.00pg/mL

B Lymphocyte Stimulator (BAFF)/BLys: 370-995 pg/mL

Osteopontin (OPN): 14,958-95,972 pg/mL

Tumor necrosis factor receptor 1 (TNFR1)/TNFRSF1A: 617-1595 pg/mL

Tumor necrosis factor receptor 2 (TNFR2)/TNFRSF1B: 1079-3589 pg/mL

Day(s) Performed

Wednesday

Report Available

1 to 7 days

Performing Laboratory

Progentec Diagnostics, Inc

Test Classification

Progentec Diagnostics developed and characterized this test. It is intended for clinical use and the reported results should be interpreted in relation to each patient's clinical condition and medical history. This test is a laboratory developed test (LDT) and is not cleared by the US Food and Drug Administration (FDA). Progentec Diagnostics Clinical Laboratory is certified under the Clinical Laboratory Improvement Amendment (CLIA) of 1988 and accredited by the College of American Pathologists to perform high complexity clinical testing.

CPT Code Information

0447U

LOINC Code Information

Test ID Test Order Name Order LOINC Value
LFRI Lupus Flare Risk Index, P Not Provided

 

Result ID Test Result Name Result LOINC Value
FR1 Mono chemoattrac prot-1 (MCP1) CCL2 Not Provided
FR2 Interleukin 5 (IL-5) Not Provided
FR3 Interleukin 17A (IL-17A) Not Provided
FR4 Interleukin 7 (IL-7) Not Provided
FR5 Interleukin 4 (IL-4) Not Provided
FR6 Tumor necrosis factor alpha Not Provided
FR7 Mono chemoattrac prot-3 (MCP3) CCL7 Not Provided
FR8 B Lymphocyte Stimulator (BAFF) BLyS Not Provided
FR9 Osteopontin (OPN) Not Provided
FR10 Tumor necrosis factor receptor 1 Not Provided
FR11 Tumor necrosis factor receptor 2 Not Provided
FR12 aiSLE DX FRI Score Not Provided
FR13 Comments Not Provided