Screening for anti-titin antibodies in patients with various paraneoplastic neurological syndromes

Anti-titin antibodies indicate a paraneoplastic etiology pointing towards a thymoma in myasthenia gravis (MG), but their seroprevalence and potential diagnostic value in patients with other paraneoplastic neurological syndromes (PNS) is unknown. Therefore, we screened the sera of 44 PNS patients wit...

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Bibliographic Details
Main Authors: Berger, Benjamin (Author) , Labeit, Siegfried (Author)
Format: Article (Journal)
Language:English
Published: 15 June-15 July 2016
In: Journal of neuroimmunology
Year: 2016, Volume: 295, Pages: 18-20
ISSN:1872-8421
DOI:10.1016/j.jneuroim.2016.04.004
Online Access:Verlag, Volltext: https://doi.org/10.1016/j.jneuroim.2016.04.004
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0165572816300741
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Author Notes:Benjamin Berger, Oliver Stich, Siegfried Labeit, Sebastian Rauer
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Summary:Anti-titin antibodies indicate a paraneoplastic etiology pointing towards a thymoma in myasthenia gravis (MG), but their seroprevalence and potential diagnostic value in patients with other paraneoplastic neurological syndromes (PNS) is unknown. Therefore, we screened the sera of 44 PNS patients with well-characterized onconeural antibodies (anti-Hu, Yo, Ri, CV2/CRMP5, Ma1, Ma2/Ta, or amphiphysin) for anti-titin reactivity. Two patients (4.5%) were positive for anti-titin antibodies: both patients differed regarding the PNS (sensorimotor neuropathy and subacute cerebellar degeneration vs. chorea), well-characterized onconeural antibodies (CV2/CRMP5 vs. Ri), and malignoma (small cell lung cancer vs. breast cancer). However, retrospectively, the patients neither showed any symptoms of MG nor a thymoma on a computed tomographic (CT) scan. The results of this study indicate that anti-titin antibodies without a predictive relevance for MG or thymoma may be present in a small proportion of patients with PNS.
Item Description:Gesehen am 14.06.2019
Laut Vorlage Volume 295-296
Physical Description:Online Resource
ISSN:1872-8421
DOI:10.1016/j.jneuroim.2016.04.004