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Test Code NSAI Neurosyphilis IgG, Antibody Index, Spinal Fluid


Specimen Required


Only orderable as part of a profile. For more information see NSAIP / Neurosyphilis IgG Antibody Index with VDRL, Serum and Spinal Fluid.

 

Both spinal fluid (CSF) and serum are required for this test. CSF and serum must be collected within a maximum of 24 hours of each other.

 

Specimen Type: Spinal fluid

Container/Tube: Sterile vial

Specimen Volume: 2.2 mL

Collection Instructions:

1. The spinal fluid (CSF) specimen must be collected within 24 hours of the serum specimen, preferably at the same time.

2. The CSF aliquot should be from the second, third, or fourth CSF vial collected during the lumbar puncture. Do not submit CSF from the first vial due to the possibility of blood contamination, which will cause specimen rejection.

3. Label vial as spinal fluid or CSF.

4. Band CSF specimen together with the serum sample.

 

Specimen Type: Serum

Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 2.2 mL

Collection Instructions:

1. Within 24 hours of collection of the spinal fluid specimen, a serum specimen must also be collected, preferably at the same time.

2. Centrifuge and aliquot serum into a plastic vial.

3. Label tube as serum.

4. Band serum specimen together with the CSF sample.


Secondary ID

621141

Useful For

Aid in the diagnosis of neuroinvasive syphilis as part of a profile

Method Name

Only orderable as part of a profile. For more information see NSAIP / Neurosyphilis IgG Antibody Index with VDRL, Serum and Spinal Fluid.

 

Enzyme-Linked Immunosorbent Assay (ELISA)

Specimen Type

CSF

Specimen Minimum Volume

Spinal fluid: 1.5 mL; Serum: 1.5 mL

Specimen Stability Information

Specimen Type Temperature Time
CSF Refrigerated (preferred) 10 days
  Frozen  10 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Spinal fluid (CSF) contaminated with blood Reject

Reference Values

Only orderable as part of a profile. For more information see NSAIP / Neurosyphilis IgG Antibody Index with VDRL, Serum and Spinal Fluid.

 

Antibody Index: 0.6-1.2

 

Reference values apply to all ages.

Interpretation

Negative:

Results indicate lack of intrathecal antibody synthesis to syphilis (Treponema pallidum). This suggests the absence of neurosyphilis. The initial screen reactive result may be due to anti-syphilis antibodies present in the cerebrospinal fluid (CSF) due to increased permeability of the blood-brain barrier or transient introduction during lumbar puncture.

 

Equivocal:

Possible intrathecal antibody synthesis to syphilis (T pallidum) detected. Results should be correlated with exposure history and clinical presentation to establish a diagnosis of neurosyphilis. Sample has been reflexed for VDRL testing to establish a titer. False positive results may occur in patients with other spirochete infections (eg, Borrelia, Leptospira).

 

Positive:

Results indicate the presence of intrathecal antibody synthesis to syphilis (T pallidum), suggesting neurosyphilis. Results should be correlated with exposure history and clinical presentation to establish the diagnosis. Sample has been reflexed to VDRL testing to establish a titer. False positive results may occur in patients with other spirochete infections (eg, Borrelia, Leptospira).

 

Invalid:

Result is due to abnormally elevated total IgG levels in CSF. This may be due to passive diffusion through the blood-brain barrier or contamination of the CSF with blood during a traumatic lumbar puncture. Consider repeat testing if clinically indicated.

Method Description

The test kit contains microtiter strips with break-off reagent wells coated with purified recombinant Treponema pallidum antigens. In the first reaction step, diluted patient samples are incubated in the wells. In the case of positive samples, T pallidum-specific IgG antibodies will bind to the antigens. To detect the bound antibodies, a second incubation is carried out using an enzyme-labelled antihuman IgG (enzyme conjugate), followed by a third incubation using chromogen/substrate, which catalyzes a color reaction that is then measured for optical density (OD) using spectrophotometry. The obtained OD values of the paired patient serum and cerebrospinal fluid (CSF) samples are compared against a 4-level calibration curve to quantitatively determine the relative anti-T pallidum IgG antibody titers.(Unpublished Mayo method)

 

The quantitative test results obtained on paired serum and CSF specimens using the T pallidum IgG enzyme-linked immunosorbent assay are expressed as relative units (U/mL) and must be used along with the total IgG and albumin levels in the patient's paired serum and CSF samples to calculate the anti-T pallidum antibody index (AI), which determines the absence or presence of intrathecal anti-T pallidum IgG antibody synthesis. Total IgG and albumin testing on serum and CSF is performed using the Siemens BN II nephelometric testing system.(Instruction manual: Siemens Nephelometer II Operations. Siemens V 2.3, 2008; Addendum to the Instruction Manual 2.3, 08/2017)

 

To detect an infection of the central nervous system, it is necessary to differentiate between intrathecally produced antibodies and antibodies passed from blood into the CSF. The AI is the value of intrathecal pathogen-specific antibody production. This AI value represents the portion of pathogen-specific antibodies in total IgG of CSF and the portion of pathogen-specific antibodies in total IgG of serum. The patient's AI is calculated using the Reiber and Lange method.(Reiber H, Lange P. Quantification of virus-specific antibodies in cerebrospinal fluid and serum: sensitive and specific detection of antibody synthesis in brain. Clin Chem. 1991;37(7):1153-1160)

Day(s) Performed

Monday through Friday

Report Available

2 to 4 days

Specimen Retention Time

2 weeks

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

82784 x 2

82040

86780 x 2

82042

LOINC Code Information

Test ID Test Order Name Order LOINC Value
NSAI Neurosyphilis IgG, Ab Index 105193-7

 

Result ID Test Result Name Result LOINC Value
NSY3 Neurosyphilis IgG Ab Index Value 105193-7
NSY4 Neurosyphilis IgG Ab Index Interp 69048-7