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A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China
The aim of this retrospective study was to derive and validate a reliable nomogram for predicting prognosis of autoimmune encephalitis (AE). A multi-center retrospective study was conducted in four hospitals in China, using a random split-sample method to allocate 173 patients into either a training...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060553/ https://www.ncbi.nlm.nih.gov/pubmed/33897585 http://dx.doi.org/10.3389/fneur.2021.612569 |
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author | Sun, Yueqian Ren, Guoping Ren, Jiechuan Shan, Wei Han, Xiong Lian, Yajun Wang, Tiancheng Wang, Qun |
author_facet | Sun, Yueqian Ren, Guoping Ren, Jiechuan Shan, Wei Han, Xiong Lian, Yajun Wang, Tiancheng Wang, Qun |
author_sort | Sun, Yueqian |
collection | PubMed |
description | The aim of this retrospective study was to derive and validate a reliable nomogram for predicting prognosis of autoimmune encephalitis (AE). A multi-center retrospective study was conducted in four hospitals in China, using a random split-sample method to allocate 173 patients into either a training (n = 126) or validation (n = 47) dataset. Demographic, radiographic and therapeutic presentation, combined with clinical features were collected. A modified Rankin Scale (mRS) at discharge was the principal outcome variable. A backward-stepwise approach based on the Akaike information criterion was used to test predictors and construct the final, parsimonious model. Multivariable analysis was conducted using logistic regression to develop a prognosis model and validate a nomogram using an independent dataset. The performance of the model was assessed using receiver operating characteristic curves and a Hosmer-Lemeshow test. The final nomogram model considered age, viral prodrome, consciousness impairment, memory dysfunction and autonomic dysfunction as predictors. Model validations displayed a good level of discrimination in the validation set: area under the Receiver operator characteristic curve = 0.72 (95% Confidence Interval: 0.56–0.88), Hosmer–Lemeshow analysis suggesting good calibration (chi-square: 10.33; p = 0.41). The proposed nomogram demonstrated considerable potential for clinical utility in prediction of prognosis in autoimmune encephalitis. |
format | Online Article Text |
id | pubmed-8060553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80605532021-04-23 A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China Sun, Yueqian Ren, Guoping Ren, Jiechuan Shan, Wei Han, Xiong Lian, Yajun Wang, Tiancheng Wang, Qun Front Neurol Neurology The aim of this retrospective study was to derive and validate a reliable nomogram for predicting prognosis of autoimmune encephalitis (AE). A multi-center retrospective study was conducted in four hospitals in China, using a random split-sample method to allocate 173 patients into either a training (n = 126) or validation (n = 47) dataset. Demographic, radiographic and therapeutic presentation, combined with clinical features were collected. A modified Rankin Scale (mRS) at discharge was the principal outcome variable. A backward-stepwise approach based on the Akaike information criterion was used to test predictors and construct the final, parsimonious model. Multivariable analysis was conducted using logistic regression to develop a prognosis model and validate a nomogram using an independent dataset. The performance of the model was assessed using receiver operating characteristic curves and a Hosmer-Lemeshow test. The final nomogram model considered age, viral prodrome, consciousness impairment, memory dysfunction and autonomic dysfunction as predictors. Model validations displayed a good level of discrimination in the validation set: area under the Receiver operator characteristic curve = 0.72 (95% Confidence Interval: 0.56–0.88), Hosmer–Lemeshow analysis suggesting good calibration (chi-square: 10.33; p = 0.41). The proposed nomogram demonstrated considerable potential for clinical utility in prediction of prognosis in autoimmune encephalitis. Frontiers Media S.A. 2021-04-08 /pmc/articles/PMC8060553/ /pubmed/33897585 http://dx.doi.org/10.3389/fneur.2021.612569 Text en Copyright © 2021 Sun, Ren, Ren, Shan, Han, Lian, Wang and Wang. https://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 Sun, Yueqian Ren, Guoping Ren, Jiechuan Shan, Wei Han, Xiong Lian, Yajun Wang, Tiancheng Wang, Qun A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title | A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title_full | A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title_fullStr | A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title_full_unstemmed | A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title_short | A Validated Nomogram That Predicts Prognosis of Autoimmune Encephalitis: A Multicenter Study in China |
title_sort | validated nomogram that predicts prognosis of autoimmune encephalitis: a multicenter study in china |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060553/ https://www.ncbi.nlm.nih.gov/pubmed/33897585 http://dx.doi.org/10.3389/fneur.2021.612569 |
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