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Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome

BACKGROUND: To investigate the sensitivity and specificity of corneal confocal microscopy (CCM) in the diagnosis of immune-related motor neuron disease syndrome and evaluation of the response to immunosuppressive therapy. METHODS: Seventy-two patients with clinical manifestations of motor neuron dis...

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Autores principales: Jiao, Lin, Zhang, Yuanjin, Wang, Haikun, Fan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996532/
https://www.ncbi.nlm.nih.gov/pubmed/35410142
http://dx.doi.org/10.1186/s12883-022-02667-5
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author Jiao, Lin
Zhang, Yuanjin
Wang, Haikun
Fan, Dongsheng
author_facet Jiao, Lin
Zhang, Yuanjin
Wang, Haikun
Fan, Dongsheng
author_sort Jiao, Lin
collection PubMed
description BACKGROUND: To investigate the sensitivity and specificity of corneal confocal microscopy (CCM) in the diagnosis of immune-related motor neuron disease syndrome and evaluation of the response to immunosuppressive therapy. METHODS: Seventy-two patients with clinical manifestations of motor neuron disease (MND) were analysed. According to whether they had concomitant rheumatic immune disease or rheumatic immune antibody abnormalities, they were divided into an MND group (33 patients) and an immune-related MND syndrome group (39 patients). Another 10 healthy adults were selected as the control group. All individuals were examined by CCM. RESULTS: For Langerhans cell(LC) density, the area under the receiver operating characteristic(ROC)curve was 0.8, the best cut-off was 67.7 cells/mm2, the sensitivity was 79.5%, and the specificity was 72.7%. For inferior whorl length (IWL), the area under the ROC curve was 0.674, the best cut-off was 17.41 mm/mm(2), the sensitivity was 69.2%, and the specificity was 66.7%. After immunosuppressive therapy in 5 patients with immune-related MND syndrome, the LCD was significantly reduced (P < 0.05), and there was no statistically significant change in the IWL (P > 0.05). CONCLUSION: The LC density and IWL are ideal for distinguishing MND from immune-related MND syndrome. The LC density reflects the immunotherapy response sensitively.
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spelling pubmed-89965322022-04-12 Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome Jiao, Lin Zhang, Yuanjin Wang, Haikun Fan, Dongsheng BMC Neurol Research BACKGROUND: To investigate the sensitivity and specificity of corneal confocal microscopy (CCM) in the diagnosis of immune-related motor neuron disease syndrome and evaluation of the response to immunosuppressive therapy. METHODS: Seventy-two patients with clinical manifestations of motor neuron disease (MND) were analysed. According to whether they had concomitant rheumatic immune disease or rheumatic immune antibody abnormalities, they were divided into an MND group (33 patients) and an immune-related MND syndrome group (39 patients). Another 10 healthy adults were selected as the control group. All individuals were examined by CCM. RESULTS: For Langerhans cell(LC) density, the area under the receiver operating characteristic(ROC)curve was 0.8, the best cut-off was 67.7 cells/mm2, the sensitivity was 79.5%, and the specificity was 72.7%. For inferior whorl length (IWL), the area under the ROC curve was 0.674, the best cut-off was 17.41 mm/mm(2), the sensitivity was 69.2%, and the specificity was 66.7%. After immunosuppressive therapy in 5 patients with immune-related MND syndrome, the LCD was significantly reduced (P < 0.05), and there was no statistically significant change in the IWL (P > 0.05). CONCLUSION: The LC density and IWL are ideal for distinguishing MND from immune-related MND syndrome. The LC density reflects the immunotherapy response sensitively. BioMed Central 2022-04-11 /pmc/articles/PMC8996532/ /pubmed/35410142 http://dx.doi.org/10.1186/s12883-022-02667-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jiao, Lin
Zhang, Yuanjin
Wang, Haikun
Fan, Dongsheng
Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title_full Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title_fullStr Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title_full_unstemmed Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title_short Corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
title_sort corneal confocal microscopy in the evaluation of immune-related motor neuron disease syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996532/
https://www.ncbi.nlm.nih.gov/pubmed/35410142
http://dx.doi.org/10.1186/s12883-022-02667-5
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