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Test Code AN1TS Antineuronal Nuclear Antibody-Type 1 (ANNA-1) Titer, Serum (Non-Orderable)


Specimen Required


Only orderable as a reflex. For more information see:

AIAES / Axonal Neuropathy, Autoimmune/Paraneoplastic Evaluation, Serum

DMS2 / Dementia, Autoimmune/Paraneoplastic Evaluation, Serum

DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

ENS2 / Encephalopathy, Autoimmune/Paraneoplastic Evaluation, Serum

EPS2 / Epilepsy, Autoimmune/Paraneoplastic Evaluation, Serum

GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

MAS1 / Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum

MDS2 / Movement Disorder, Autoimmune/Paraneoplastic Evaluation, Serum

PCDES / Pediatric Autoimmune Encephalopathy/CNS Disorder Evaluation, Serum


Useful For

Only orderable as a reflex. For more information see:

AIAES / Axonal Neuropathy, Autoimmune/Paraneoplastic Evaluation, Serum

DMS2 / Dementia, Autoimmune/Paraneoplastic Evaluation, Serum

DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

ENS2 / Encephalopathy, Autoimmune/Paraneoplastic Evaluation, Serum

EPS2 / Epilepsy, Autoimmune/Paraneoplastic Evaluation, Serum

GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

MAS1 / Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum

MDS2 / Movement Disorder, Autoimmune/Paraneoplastic Evaluation, Serum

PCDES / Pediatric Autoimmune Encephalopathy/CNS Disorder Evaluation, Serum

 

Serological evaluation of patients who present with a subacute neurological disorder of undetermined etiology, especially those with risk factors for primary lung carcinoma

 

Directing a focused search for cancer

 

Investigating neurological symptoms that appear during, or after, cancer therapy, and are not explainable my metastasis

 

Reporting an end titer result from serum specimens

Testing Algorithm

If the indirect immunofluorescence pattern suggests antineuronal nuclear antibody type 1 (ANNA-1), then this test will be performed at an additional charge.

Method Name

Only orderable as a reflex. For more information see:

AIAES / Axonal Neuropathy, Autoimmune/Paraneoplastic Evaluation, Serum

DMS2 / Dementia, Autoimmune/Paraneoplastic Evaluation, Serum

DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

ENS2 / Encephalopathy, Autoimmune/Paraneoplastic Evaluation, Serum

EPS2 / Epilepsy, Autoimmune/Paraneoplastic Evaluation, Serum

GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

MAS1 / Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum

MDS2 / Movement Disorder, Autoimmune/Paraneoplastic Evaluation, Serum

PCDES / Pediatric Autoimmune Encephalopathy/CNS Disorder Evaluation, Serum

 

Indirect Immunofluorescence Assay (IFA)

Reporting Name

ANNA-1 Titer, S

Specimen Type

Serum

Specimen Minimum Volume

Serum: 0.6 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 28 days
  Frozen  28 days
  Ambient  72 hours

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Clinical Information

A spectrum of paraneoplastic neurologic disorders is associated with antineuronal nuclear antibody type1 (ANNA-1), also known as anti-Hu. ANNA-1 autoimmunity often manifests with multifocal neurological presentations. Typical presentations include neuropathies (mixed sensorimotor, sensory neuronopathy, autonomic neuropathy including gastrointestinal dysmotility/pseudo-obstruction or others), limbic encephalitis, cerebellar ataxia, encephalomyelitis, and myelopathy.

 

Small-cell lung carcinoma (SCLC) or other neuroendocrine tumors are almost always present in older adults, often as limited-stage disease. Extrapulmonary primary small-cell carcinoma, such as tumors of the skin, larynx, tongue, breast, cervix, prostate, endocrine, or pancreas, should be considered, especially in patients who do not smoke. Autopsy sometimes reveals SCLC in patients who lack evidence of tumor in life. In pediatric populations, neuroblastoma is sometimes encountered as the pertinent neoplasm. Other malignancies have also rarely been reported; in 15% of patients with confirmed SCLC, an unrelated and more apparent primary malignancy coexists with SCLC.

Reference Values

Only orderable as a reflex. For more information see:

AIAES / Axonal Neuropathy, Autoimmune/Paraneoplastic Evaluation, Serum

DMS2 / Dementia, Autoimmune/Paraneoplastic Evaluation, Serum

DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

ENS2 / Encephalopathy, Autoimmune/Paraneoplastic Evaluation, Serum

EPS2 / Epilepsy, Autoimmune/Paraneoplastic Evaluation, Serum

GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

MAS1 / Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum

MDS2 / Movement Disorder, Autoimmune/Paraneoplastic Evaluation, Serum

PCDES / Pediatric Autoimmune Encephalopathy/CNS Disorder Evaluation, Serum

 

<1:240

Day(s) Performed

Monday through Sunday

Report Available

6 to 8 days

Specimen Retention Time

2 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

86256

LOINC Code Information

Test ID Test Order Name Order LOINC Value
AN1TS ANNA-1 Titer, S 94342-3

 

Result ID Test Result Name Result LOINC Value
43431 ANNA-1 Titer, S 94342-3