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Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis

PURPOSE: This study aimed to investigate whether the impaired ciliary length and aberrant ciliary ultrastructure marker, dynein axonemal intermediate chain 1 (DNAI1), are important pathological characteristics in nasal mucosa from patients with allergic rhinitis (AR). PATIENTS AND METHODS: Biopsies...

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Autores principales: Zhou, Suizi, Liu, Yitong, Yang, Yueying, Huang, Hongming, Qiu, Qianhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896970/
https://www.ncbi.nlm.nih.gov/pubmed/36741287
http://dx.doi.org/10.2147/JIR.S393025
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author Zhou, Suizi
Liu, Yitong
Yang, Yueying
Huang, Hongming
Qiu, Qianhui
author_facet Zhou, Suizi
Liu, Yitong
Yang, Yueying
Huang, Hongming
Qiu, Qianhui
author_sort Zhou, Suizi
collection PubMed
description PURPOSE: This study aimed to investigate whether the impaired ciliary length and aberrant ciliary ultrastructure marker, dynein axonemal intermediate chain 1 (DNAI1), are important pathological characteristics in nasal mucosa from patients with allergic rhinitis (AR). PATIENTS AND METHODS: Biopsies were taken from the inferior turbinate (IT) of controls (n = 20) and patients with AR (n = 20). The ciliary length and the DNAI1 location patterns were assessed by using immunofluorescent staining. Three patterns of DNAI1 localization were defined using a semi-quantitative scoring system: normal (N), partial (P) and absence (A). Every individual section was assigned a score between 0 and 2 in each high-power field (5 fields per sample). The score of 0 = pattern N >70%; 1 = patterns N + P >70%; and 2 = pattern A ≥30%. The receiver operating characteristic (ROC) curve was used to evaluate the predicted value of DNAI1 score for AR. RESULTS: The ciliary length was reduced by 33.3% in patients with AR compared with controls (P < 0.0001). The higher DNAI1 score was found in the AR group, with a median (first and third quartile) of 0.9 (0.4 and 1.08), which was 0.1 (0 and 0.76) in the control group (P = 0.0071). The ROC of DNAI1 was calculated based on the area under the curve of 0.74 (P = 0.0094). The cutoff value of ROC was 0.5833, with a sensitivity and specificity of 70%. CONCLUSION: These results suggested that the shorter ciliary length and aberrant localization of DNAI1 are potentially important pathological characteristics of the allergic nasal mucosa. The aberrant localization of DNAI1 may provide a novel candidate target for clinical management of AR.
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spelling pubmed-98969702023-02-04 Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis Zhou, Suizi Liu, Yitong Yang, Yueying Huang, Hongming Qiu, Qianhui J Inflamm Res Original Research PURPOSE: This study aimed to investigate whether the impaired ciliary length and aberrant ciliary ultrastructure marker, dynein axonemal intermediate chain 1 (DNAI1), are important pathological characteristics in nasal mucosa from patients with allergic rhinitis (AR). PATIENTS AND METHODS: Biopsies were taken from the inferior turbinate (IT) of controls (n = 20) and patients with AR (n = 20). The ciliary length and the DNAI1 location patterns were assessed by using immunofluorescent staining. Three patterns of DNAI1 localization were defined using a semi-quantitative scoring system: normal (N), partial (P) and absence (A). Every individual section was assigned a score between 0 and 2 in each high-power field (5 fields per sample). The score of 0 = pattern N >70%; 1 = patterns N + P >70%; and 2 = pattern A ≥30%. The receiver operating characteristic (ROC) curve was used to evaluate the predicted value of DNAI1 score for AR. RESULTS: The ciliary length was reduced by 33.3% in patients with AR compared with controls (P < 0.0001). The higher DNAI1 score was found in the AR group, with a median (first and third quartile) of 0.9 (0.4 and 1.08), which was 0.1 (0 and 0.76) in the control group (P = 0.0071). The ROC of DNAI1 was calculated based on the area under the curve of 0.74 (P = 0.0094). The cutoff value of ROC was 0.5833, with a sensitivity and specificity of 70%. CONCLUSION: These results suggested that the shorter ciliary length and aberrant localization of DNAI1 are potentially important pathological characteristics of the allergic nasal mucosa. The aberrant localization of DNAI1 may provide a novel candidate target for clinical management of AR. Dove 2023-01-30 /pmc/articles/PMC9896970/ /pubmed/36741287 http://dx.doi.org/10.2147/JIR.S393025 Text en © 2023 Zhou et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhou, Suizi
Liu, Yitong
Yang, Yueying
Huang, Hongming
Qiu, Qianhui
Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title_full Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title_fullStr Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title_full_unstemmed Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title_short Shorter Cilia Length and Aberrant Ciliated Marker DNAI1 in Allergic Rhinitis
title_sort shorter cilia length and aberrant ciliated marker dnai1 in allergic rhinitis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896970/
https://www.ncbi.nlm.nih.gov/pubmed/36741287
http://dx.doi.org/10.2147/JIR.S393025
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