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Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis

Objective: To test the hypothesis that olfactory (OF) and gustatory function (GF) is disturbed in patients with autoimmune encephalitides (AE). Methods: The orthonasal OF was tested in 32 patients with AE and 32 age- and sex-matched healthy controls (HC) with the standardized Threshold Discriminatio...

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Autores principales: Geran, Rohat, Uecker, Florian C., Prüss, Harald, Haeusler, Karl Georg, Paul, Friedemann, Ruprecht, Klemens, Harms, Lutz, Schmidt, Felix A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528690/
https://www.ncbi.nlm.nih.gov/pubmed/31156532
http://dx.doi.org/10.3389/fneur.2019.00480
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author Geran, Rohat
Uecker, Florian C.
Prüss, Harald
Haeusler, Karl Georg
Paul, Friedemann
Ruprecht, Klemens
Harms, Lutz
Schmidt, Felix A.
author_facet Geran, Rohat
Uecker, Florian C.
Prüss, Harald
Haeusler, Karl Georg
Paul, Friedemann
Ruprecht, Klemens
Harms, Lutz
Schmidt, Felix A.
author_sort Geran, Rohat
collection PubMed
description Objective: To test the hypothesis that olfactory (OF) and gustatory function (GF) is disturbed in patients with autoimmune encephalitides (AE). Methods: The orthonasal OF was tested in 32 patients with AE and 32 age- and sex-matched healthy controls (HC) with the standardized Threshold Discrimination Identification (TDI) score. This validated olfactory testing method yields individual scores for olfactory threshold (T), odor discrimination (D), and identification (I), along with a composite TDI score. The GF was determined by the Taste Strip Test (TST). Results: Overall, 24/32 (75%) of patients with AE, but none of 32 HC (p < 0.001) had olfactory dysfunction in TDI testing. The results of the threshold, discrimination and identification subtests were significantly reduced in patients with AE compared to HC (all p < 0.001). Assessed by TST, 5/19 (26.3%) of patients with AE, but none of 19 HC presented a significant limitation in GF (p < 0.001). The TDI score was correlated with the subjective estimation of the olfactory capacity on a visual analog scale (VAS; r(s) = 0.475, p = 0.008). Neither age, sex, modified Rankin Scale nor disease duration were associated with the composite TDI score. Conclusions: This is the first study investigating OF and GF in AE patients. According to unblinded assessment, patients with AE have a reduced olfactory and gustatory capacity compared to HC, suggesting that olfactory and gustatory dysfunction are hitherto unrecognized symptoms in AE. Further studies with larger number of AE patients would be of interest to verify our results.
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spelling pubmed-65286902019-05-31 Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis Geran, Rohat Uecker, Florian C. Prüss, Harald Haeusler, Karl Georg Paul, Friedemann Ruprecht, Klemens Harms, Lutz Schmidt, Felix A. Front Neurol Neurology Objective: To test the hypothesis that olfactory (OF) and gustatory function (GF) is disturbed in patients with autoimmune encephalitides (AE). Methods: The orthonasal OF was tested in 32 patients with AE and 32 age- and sex-matched healthy controls (HC) with the standardized Threshold Discrimination Identification (TDI) score. This validated olfactory testing method yields individual scores for olfactory threshold (T), odor discrimination (D), and identification (I), along with a composite TDI score. The GF was determined by the Taste Strip Test (TST). Results: Overall, 24/32 (75%) of patients with AE, but none of 32 HC (p < 0.001) had olfactory dysfunction in TDI testing. The results of the threshold, discrimination and identification subtests were significantly reduced in patients with AE compared to HC (all p < 0.001). Assessed by TST, 5/19 (26.3%) of patients with AE, but none of 19 HC presented a significant limitation in GF (p < 0.001). The TDI score was correlated with the subjective estimation of the olfactory capacity on a visual analog scale (VAS; r(s) = 0.475, p = 0.008). Neither age, sex, modified Rankin Scale nor disease duration were associated with the composite TDI score. Conclusions: This is the first study investigating OF and GF in AE patients. According to unblinded assessment, patients with AE have a reduced olfactory and gustatory capacity compared to HC, suggesting that olfactory and gustatory dysfunction are hitherto unrecognized symptoms in AE. Further studies with larger number of AE patients would be of interest to verify our results. Frontiers Media S.A. 2019-05-14 /pmc/articles/PMC6528690/ /pubmed/31156532 http://dx.doi.org/10.3389/fneur.2019.00480 Text en Copyright © 2019 Geran, Uecker, Prüss, Haeusler, Paul, Ruprecht, Harms and Schmidt. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Geran, Rohat
Uecker, Florian C.
Prüss, Harald
Haeusler, Karl Georg
Paul, Friedemann
Ruprecht, Klemens
Harms, Lutz
Schmidt, Felix A.
Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title_full Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title_fullStr Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title_full_unstemmed Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title_short Olfactory and Gustatory Dysfunction in Patients With Autoimmune Encephalitis
title_sort olfactory and gustatory dysfunction in patients with autoimmune encephalitis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528690/
https://www.ncbi.nlm.nih.gov/pubmed/31156532
http://dx.doi.org/10.3389/fneur.2019.00480
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