The relevance of VGKC positivity in the absence of LGI1 and Caspr2 antibodies

Autor: Maarten J. Titulaer, Roland D. Thijs, Peter A. E. Sillevis Smitt, Mariska M.P. Nagtzaam, Agnes van Sonderen, Esther Hulsenboom, Paul W. Wirtz, Marienke A.A.M. de Bruijn, Marco W.J. Schreurs, Roelien H. Enting, Sanae Boukhrissi
Přispěvatelé: Neurology, Immunology
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
CREUTZFELDT-JAKOB-DISEASE
Encephalomyelitis
COMPLEX ANTIBODIES
0302 clinical medicine
Medicine
Young adult
Child
Aged
80 and over

MORVANS-SYNDROME
biology
CHANNEL ANTIBODIES
Limbic encephalitis
Intracellular Signaling Peptides and Proteins
Radioimmunoassay
Middle Aged
Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3]
Titer
Treatment Outcome
Potassium Channels
Voltage-Gated

Child
Preschool

Female
Antibody
Adult
Adolescent
Nerve Tissue Proteins
Young Adult
03 medical and health sciences
Autoimmune Diseases of the Nervous System
ACQUIRED NEUROMYOTONIA
Humans
Clinical significance
LIMBIC ENCEPHALITIS
Aged
Retrospective Studies
business.industry
Autoantibody
Infant
Membrane Proteins
Proteins
medicine.disease
030104 developmental biology
Immunology
biology.protein
AUTOANTIBODIES
Neurology (clinical)
business
Biomarkers
030217 neurology & neurosurgery
Zdroj: EUR Research Portal
Neurology, 86(18), 1692-1699. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 86(18), 1692-1699
Neurology, 86(18), 1692-1699. Lippincott Williams & Wilkins
Neurology, 86, 1692-1699
Neurology, 86, 18, pp. 1692-1699
ISSN: 1526-632X
0028-3878
DOI: 10.1212/wnl.0000000000002637
Popis: Item does not contain fulltext OBJECTIVE: To assess the clinical relevance of a positive voltage-gated potassium channel (VGKC) test in patients lacking antibodies to LGI1 and Caspr2. METHODS: VGKC-positive patients were tested for LGI1 and Caspr2 antibodies. Patients lacking both antibodies were matched (1:2) to VGKC-negative patients. Clinical and paraclinical criteria were used to blindly determine evidence for autoimmune inflammation in both groups. Patients with an inconclusive VGKC titer were analyzed in the same way. RESULTS: A total of 1,455 patients were tested by VGKC radioimmunoassay. Fifty-six patients tested positive, 50 of whom were available to be included. Twenty-five patients had antibodies to LGI1 (n = 19) or Caspr2 (n = 6) and 25 patients lacked both antibodies. Evidence for autoimmune inflammation was present in 7 (28%) of the VGKC-positive patients lacking LGI1 and Caspr2, compared to 9 (18%) of the VGKC-negative controls (p = 0.38). Evidence for autoimmune inflammation was mainly found in patients with limbic encephalitis/encephalomyelitis (57%), but not in other clinical phenotypes (5%, p < 0.01). VGKC titers were significantly higher in patients with antibodies to LGI1 or Caspr2 (p < 0.001). However, antibodies to Caspr2 could also be detected in patients with inconclusive low VGKC titer, while many VGKC-positive patients had no evidence for autoimmune inflammation. CONCLUSIONS: VGKC positivity in the absence of antibodies to LGI1 and Caspr2 is not a clear marker for autoimmune inflammation and seems not to contribute in clinical practice. No cutoff value for the VGKC titer was appropriate to discriminate between patients with and without autoimmune inflammation. 8 p.
Databáze: OpenAIRE