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A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes

Neural implants offer solutions for a variety of clinical issues. While commercially available devices can record neural signals for short time periods, they fail to do so chronically, partially due to the sustained tissue response around the device. Our objective was to assess the correlation betwe...

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Autores principales: Stiller, Allison M., Black, Bryan J., Kung, Christopher, Ashok, Aashika, Cogan, Stuart F., Varner, Victor D., Pancrazio, Joseph J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187651/
https://www.ncbi.nlm.nih.gov/pubmed/30424376
http://dx.doi.org/10.3390/mi9090443
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author Stiller, Allison M.
Black, Bryan J.
Kung, Christopher
Ashok, Aashika
Cogan, Stuart F.
Varner, Victor D.
Pancrazio, Joseph J.
author_facet Stiller, Allison M.
Black, Bryan J.
Kung, Christopher
Ashok, Aashika
Cogan, Stuart F.
Varner, Victor D.
Pancrazio, Joseph J.
author_sort Stiller, Allison M.
collection PubMed
description Neural implants offer solutions for a variety of clinical issues. While commercially available devices can record neural signals for short time periods, they fail to do so chronically, partially due to the sustained tissue response around the device. Our objective was to assess the correlation between device stiffness, a function of both material modulus and cross-sectional area, and the severity of immune response. Meta-analysis data were derived from nine previously published studies which reported device material and geometric properties, as well as histological outcomes. Device bending stiffness was calculated by treating the device shank as a cantilevered beam. Immune response was quantified through analysis of immunohistological images from each study, specifically looking at fluorescent markers for neuronal nuclei and astrocytes, to assess neuronal dieback and gliosis. Results demonstrate that the severity of the immune response, within the first 50 µm of the device, is highly correlated with device stiffness, as opposed to device modulus or cross-sectional area independently. In general, commercially available devices are around two to three orders of magnitude higher in stiffness than devices which induced a minimal tissue response. These results have implications for future device designs aiming to decrease chronic tissue response and achieve increased long-term functionality.
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spelling pubmed-61876512018-11-01 A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes Stiller, Allison M. Black, Bryan J. Kung, Christopher Ashok, Aashika Cogan, Stuart F. Varner, Victor D. Pancrazio, Joseph J. Micromachines (Basel) Article Neural implants offer solutions for a variety of clinical issues. While commercially available devices can record neural signals for short time periods, they fail to do so chronically, partially due to the sustained tissue response around the device. Our objective was to assess the correlation between device stiffness, a function of both material modulus and cross-sectional area, and the severity of immune response. Meta-analysis data were derived from nine previously published studies which reported device material and geometric properties, as well as histological outcomes. Device bending stiffness was calculated by treating the device shank as a cantilevered beam. Immune response was quantified through analysis of immunohistological images from each study, specifically looking at fluorescent markers for neuronal nuclei and astrocytes, to assess neuronal dieback and gliosis. Results demonstrate that the severity of the immune response, within the first 50 µm of the device, is highly correlated with device stiffness, as opposed to device modulus or cross-sectional area independently. In general, commercially available devices are around two to three orders of magnitude higher in stiffness than devices which induced a minimal tissue response. These results have implications for future device designs aiming to decrease chronic tissue response and achieve increased long-term functionality. MDPI 2018-09-06 /pmc/articles/PMC6187651/ /pubmed/30424376 http://dx.doi.org/10.3390/mi9090443 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stiller, Allison M.
Black, Bryan J.
Kung, Christopher
Ashok, Aashika
Cogan, Stuart F.
Varner, Victor D.
Pancrazio, Joseph J.
A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title_full A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title_fullStr A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title_full_unstemmed A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title_short A Meta-Analysis of Intracortical Device Stiffness and Its Correlation with Histological Outcomes
title_sort meta-analysis of intracortical device stiffness and its correlation with histological outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187651/
https://www.ncbi.nlm.nih.gov/pubmed/30424376
http://dx.doi.org/10.3390/mi9090443
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