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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6187651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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