Insulin Resistance and Gray Matter Volume in Neurodegenerative Disease
dc.contributor.author | Morris, J. K. | |
dc.contributor.author | Vidoni, Eric D. | |
dc.contributor.author | Perea, R. D. | |
dc.contributor.author | Rada, R. | |
dc.contributor.author | Johnson, David K. | |
dc.contributor.author | Lyons, Kelly E. | |
dc.contributor.author | Pahwa, Rajesh | |
dc.contributor.author | Burns, Jeffrey M. | |
dc.contributor.author | Honea, Robyn A. | |
dc.date.accessioned | 2017-02-16T20:46:24Z | |
dc.date.available | 2017-02-16T20:46:24Z | |
dc.date.issued | 2014-06-13 | |
dc.identifier.citation | MORRIS, J. K., VIDONI, E. D., PEREA, R. D., RADA, R., JOHNSON, D. K., LYONS, K., … HONEA, R. A. (2014). INSULIN RESISTANCE AND GRAY MATTER VOLUME IN NEURODEGENERATIVE DISEASE. Neuroscience, 270, 139–147. http://doi.org/10.1016/j.neuroscience.2014.04.006 | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/23199 | |
dc.description.abstract | The goal of this study was to compare insulin resistance in aging and aging-related neurodegenerative diseases, and to determine the relationship between insulin resistance and gray matter volume (GMV) in each cohort using an unbiased, voxel-based approach. Insulin resistance was estimated in apparently healthy elderly control (HC, n = 21) and neurodegenerative disease (Alzheimer’s disease (AD), n = 20; Parkinson’s disease (PD), n = 22) groups using Homeostasis Model Assessment of Insulin Resistance 2 (HOMA2) and intravenous glucose tolerance test (IVGTT). HOMA2 and GMV were assessed within groups through General Linear Model multiple regression. We found that HOMA2 was increased in both AD and PD compared to the HC group (HC vs. AD, p = 0.002, HC vs. PD, p = 0.003), although only AD subjects exhibited increased fasting glucose (p = 0.005). Furthermore, our voxel-based morphometry analysis revealed that HOMA2 was related to GMV in all cohorts in a region-specific manner (p < 0.001, uncorrected). Significant relationships were observed in the medial prefrontal cortex (HC), medial temporal regions (AD), and parietal regions (PD). Finally, the directionality of the relationship between HOMA2 and GMV was disease-specific. Both HC and AD subjects exhibited negative relationships between HOMA2 and brain volume (increased HOMA2 associated with decreased brain volume), while a positive relationship was observed in PD. This cross-sectional study suggests that insulin resistance is increased in neurodegenerative disease, and that individuals with AD appear to have more severe metabolic dysfunction than individuals with PD or PD dementia. | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 3.0 (CC BY-NC-ND 3.0 US), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Insulin resistance | en_US |
dc.subject | Alzheimer’s disease | en_US |
dc.subject | Parkinson’s disease | en_US |
dc.subject | Dementia | en_US |
dc.subject | Metabolism | en_US |
dc.subject | Glucose tolerance | en_US |
dc.title | Insulin Resistance and Gray Matter Volume in Neurodegenerative Disease | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Johnson, D.K. | |
kusw.kudepartment | Psychology | en_US |
kusw.oanotes | Per SHERPA/RoMEO 2/16/2017: Author's Pre-print: green tick author can archive pre-print (ie pre-refereeing) Author's Post-print: green tick author can archive post-print (ie final draft post-refereeing) Publisher's Version/PDF: cross author cannot archive publisher's version/PDF General Conditions: Authors pre-print on any website, including arXiv and RePEC Author's post-print on author's personal website immediately Author's post-print on open access repository after an embargo period of between 12 months and 48 months Permitted deposit due to Funding Body, Institutional and Governmental policy or mandate, may be required to comply with embargo periods of 12 months to 48 months Author's post-print may be used to update arXiv and RepEC Publisher's version/PDF cannot be used Must link to publisher version with DOI Author's post-print must be released with a Creative Commons Attribution Non-Commercial No Derivatives License | en_US |
dc.identifier.doi | 10.1016/j.neuroscience.2014.04.006 | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-0496-1445 | |
kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.rights.accessrights | openAccess |
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Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 3.0 (CC BY-NC-ND 3.0 US), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.