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Test Code LDAI Progentec aiSLE DX Lupus Disease Activity 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 current systemic lupus erythematosus disease activity when used in conjunction with standard clinical assessment

Method Name

Immunoassay

Reporting Name

Lupus Disease Activity 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

C-X-C Motif Chemokine Ligand 10 (CXCL10/IP-10): 37-343 pg/mL

Interferon gamma (IFN-y): 0.34-7.80 pg/mL

Interleukin-15 (IL-15): 1.00-4.30 pg/mL

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

Interferon alpha-2 (IFNa-2): 3.600-8.300 pg/mL

Interleukin-10 (IL-10): 1.20-9.50 pg/mL

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

TNF-Related Apoptosis-Inducing Ligand (TRAIL): 26-120 pg/mL

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

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

Day(s) Performed

Thursday

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

0446U

LOINC Code Information

Test ID Test Order Name Order LOINC Value
LDAI Lupus Disease Activity Index, P Not Provided

 

Result ID Test Result Name Result LOINC Value
DA1 CXC Motif Ligand 10 (CXCL10)(IP-10) Not Provided
DA2 Interferon gamma (IFN-g) Not Provided
DA3 Interleukin 15 (IL-15) Not Provided
DA4 Interleukin 4 (IL-4) Not Provided
DA5 Interferon alpha 2 (IFN-a2) Not Provided
DA6 Interleukin 10 (IL-10) Not Provided
DA7 Interleukin 7 (IL-7) Not Provided
DA8 TNF-Relat Apop-Induc Ligand (TRAIL) Not Provided
DA9 B Lymphocyte Stimulator (BAFF) BLyS Not Provided
DA10 Osteopontin (OPN) Not Provided
DA11 aiSLE DX DAI Score Not Provided
DA12 Comments Not Provided