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Brain‐clinical signatures for vagus nerve stimulation response
AIM: Vagus nerve stimulation (VNS) is a valuable treatment for drug‐resistant epilepsy (DRE) without the indication of surgical resection. The clinical heterogeneity of DRE has limited the optimal indication of choice and diagnosis prediction. The study aimed to explore the correlations of brain‐cli...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928539/ https://www.ncbi.nlm.nih.gov/pubmed/36415145 http://dx.doi.org/10.1111/cns.14021 |
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author | Guo, Zhihao Mo, Jiajie Zhang, Chao Zhang, Jianguo Hu, Wenhan Zhang, Kai |
author_facet | Guo, Zhihao Mo, Jiajie Zhang, Chao Zhang, Jianguo Hu, Wenhan Zhang, Kai |
author_sort | Guo, Zhihao |
collection | PubMed |
description | AIM: Vagus nerve stimulation (VNS) is a valuable treatment for drug‐resistant epilepsy (DRE) without the indication of surgical resection. The clinical heterogeneity of DRE has limited the optimal indication of choice and diagnosis prediction. The study aimed to explore the correlations of brain‐clinical signatures with the clinical phenotype and VNS responsiveness. METHODS: A total of 89 DRE patients, including VNS‐ (n = 44) and drug‐treated (n = 45) patients, were retrospectively recruited. The brain‐clinical signature consisted of demographic information and brain structural deformations, which were measured using deformation‐based morphometry and presented as Jacobian determinant maps. The efficacy and presurgical differences between these two cohorts were compared. Then, the potential of predicting VNS response using brain‐clinical signature was investigated according to the different prognosis evaluation approaches. RESULTS: The seizure reduction was higher in the VNS‐treated group (42.50%) as compared to the drug‐treated group (12.09%) (p = 0.11). Abnormal imaging representation, showing encephalomalacia (p (corrected) = 0.03), was commonly observed in the VNS‐treated group (p = 0.04). In the patients treated with VNS, the mild/subtle brain abnormalities indicated higher seizure frequency (p = 0.03) and worse VNS response (p = 0.04). The partial least square regression analysis showed a moderate prediction potential of brain‐clinical signature for VNS response (p < 0.01). The increase in the pre‐VNS seizure frequency and structural etiology could indicate a worse prognosis (higher McHugh classification). CONCLUSION: The brain‐clinical signature illustrated its clinical potential in predicting the VNS response, which might allow clinicians to personalize treatment decisions for DRE patients. |
format | Online Article Text |
id | pubmed-9928539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99285392023-02-16 Brain‐clinical signatures for vagus nerve stimulation response Guo, Zhihao Mo, Jiajie Zhang, Chao Zhang, Jianguo Hu, Wenhan Zhang, Kai CNS Neurosci Ther Original Articles AIM: Vagus nerve stimulation (VNS) is a valuable treatment for drug‐resistant epilepsy (DRE) without the indication of surgical resection. The clinical heterogeneity of DRE has limited the optimal indication of choice and diagnosis prediction. The study aimed to explore the correlations of brain‐clinical signatures with the clinical phenotype and VNS responsiveness. METHODS: A total of 89 DRE patients, including VNS‐ (n = 44) and drug‐treated (n = 45) patients, were retrospectively recruited. The brain‐clinical signature consisted of demographic information and brain structural deformations, which were measured using deformation‐based morphometry and presented as Jacobian determinant maps. The efficacy and presurgical differences between these two cohorts were compared. Then, the potential of predicting VNS response using brain‐clinical signature was investigated according to the different prognosis evaluation approaches. RESULTS: The seizure reduction was higher in the VNS‐treated group (42.50%) as compared to the drug‐treated group (12.09%) (p = 0.11). Abnormal imaging representation, showing encephalomalacia (p (corrected) = 0.03), was commonly observed in the VNS‐treated group (p = 0.04). In the patients treated with VNS, the mild/subtle brain abnormalities indicated higher seizure frequency (p = 0.03) and worse VNS response (p = 0.04). The partial least square regression analysis showed a moderate prediction potential of brain‐clinical signature for VNS response (p < 0.01). The increase in the pre‐VNS seizure frequency and structural etiology could indicate a worse prognosis (higher McHugh classification). CONCLUSION: The brain‐clinical signature illustrated its clinical potential in predicting the VNS response, which might allow clinicians to personalize treatment decisions for DRE patients. John Wiley and Sons Inc. 2022-11-22 /pmc/articles/PMC9928539/ /pubmed/36415145 http://dx.doi.org/10.1111/cns.14021 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Guo, Zhihao Mo, Jiajie Zhang, Chao Zhang, Jianguo Hu, Wenhan Zhang, Kai Brain‐clinical signatures for vagus nerve stimulation response |
title | Brain‐clinical signatures for vagus nerve stimulation response |
title_full | Brain‐clinical signatures for vagus nerve stimulation response |
title_fullStr | Brain‐clinical signatures for vagus nerve stimulation response |
title_full_unstemmed | Brain‐clinical signatures for vagus nerve stimulation response |
title_short | Brain‐clinical signatures for vagus nerve stimulation response |
title_sort | brain‐clinical signatures for vagus nerve stimulation response |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928539/ https://www.ncbi.nlm.nih.gov/pubmed/36415145 http://dx.doi.org/10.1111/cns.14021 |
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