Dementia, Autoimmune/Paraneoplastic Evaluation, Serum

Alphabetical Test listing

Dementia, Autoimmune/Paraneoplastic Evaluation, Serum-12688

  
Dementia, Autoimmune/Paraneoplastic Evaluation, Serum
  
12688
  
LAB12688
  
DMS1
  
Cognitive decline
Cognitive impairment
DEMES
Dipeptidyl aminopeptidase-like protein 6
Leucine-Rich Glioma Inactivated Protein-1 IgG
  
Dementia, Interpretation, S
AMPA-R Ab CBA, S
Amphiphysin Ab, S
Anti-Glial Nuclear Ab, Type 1
Anti-Neuronal Nuclear Ab, Type 1
Anti-Neuronal Nuclear Ab, Type 2
Anti-Neuronal Nuclear Ab, Type 3
CASPR2-IgG CBA, S
CRMP-5-IgG, S
DPPX Ab IFA, S
GABA-B-R Ab CBA, S
GAD65 Ab Assay, S
GFAP IFA, S
IgLON5 IFA, S
LGI1-IgG CBA, S
mGluR1 Ab IFA, S
Neurochondrin IFA, S
NIF IFA, S
NMDA-R Ab CBA, S
Purkinje Cell Cytoplasmic Ab Type 2
Purkinje Cell Cytoplasmic Ab Type Tr

For reflex tests see algorithm on Clinical and Interpretive info tab
  

 

Useful for investigating new onset dementia and cognitive impairment plus 1 or more of the following:

  • Rapid onset and progression
  • Fluctuating course
  • Psychiatric accompaniments (psychosis, hallucinations)
  • Movement disorder (myoclonus, tremor, dyskinesias)
  • Headache
  • Autoimmune stigmata (personal history or family history or signs of diabetes mellitus, thyroid disorder, vitiligo, poliosis [premature graying], myasthenia gravis, rheumatoid arthritis, systemic lupus erythematosus)
  • Smoking history (20+ pack years) or other cancer risk factors
  • History of cancer
  • Inflammatory cerebral spinal fluid
  • Neuroimaging findings atypical for degenerative etiology
  
  • For optimal antibody detection, specimen collection is recommended prior to initiation of immunosuppressant medication
  • This test should not be requested in patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed, or canceled if radioactivity remains
  • Patient should have no general anesthetic or muscle-relaxant drugs in the previous 24 hours
  
Serum
  
  
4.0 mL
  
2.5 mL
  
  1. Allow sample to clot
  2. Spin
  3. Transfer serum to a Screw cap transfer vial/tube (Mayo T914), labelled as serum, within two (2) hours of sample collection
  
  
  

Immediately following collection, thoroughly mix sample by gently inverting 5 times

  
  1. Allow sample to clot for a minimum of 30 minutes
  2. Spin within two (2) hours of sample collection
  3. Transfer serum to a Screw cap transfer vial/tube (Mayo T914), labelled as serum
  

Refrigerated (preferred) - 28 days

Frozen - 28 days

Ambient - 72 hours

  
Mayo Clinic Laboratories (DMS2): R-MM
  
Daily
  
8 - 12 days
  

Immunofluorescence assay (IFA)

Cell-binding assay (CBA)

Western blot (WB)

Radioimmunoassay (RIA)

Immunoblot (IB)

  

See report

  
86255 x 19
86341

Additional CPT codes (if appropriate):
84182-AGNBS
86256 AGNTS
86255-AINCS
86256-AMPIS
84182-AMIBS
84182-AN1B
86256-AN1TS
84182-AN2BS
86256-AN2TS
86256-AN3TS
86256-APHTS
86256-CRMTS
84182-CRMWS
86255-DPPCS
86256-DPPTS
86256-GABIS
86255-GFACS
86256-GFATS
86255-IG5CS
86256-IG5TS
86255-GL1CS
86256-GL1TS
86255-NCDCS
86256-NCDTS
86255-NFHCS
86256-NIFTS
86255-NFLCS
86256-NMDIS
86256-PC2TS
84182-PCTBS
86256-PCTTS
  
11/18/2014
  
02/14/2023
  
02/14/2023