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MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes
INTRODUCTION: MCP-1 and eotaxin-1 are encoded on chromosome 17 and have been shown to reduce hippocampal neurogenesis in mice. We investigated whether these chemokines selectively associate with memory in individuals with mild cognitive impairment (MCI) and Alzheimer's disease (AD) dementia. ME...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941041/ https://www.ncbi.nlm.nih.gov/pubmed/27453930 http://dx.doi.org/10.1016/j.dadm.2016.05.004 |
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author | Bettcher, Brianne M. Fitch, Ryan Wynn, Matthew J. Lalli, Matthew A. Elofson, Jonathan Jastrzab, Laura Mitic, Laura Miller, Zachary A. Rabinovici, Gil D. Miller, Bruce L. Kao, Aimee W. Kosik, Kenneth S. Kramer, Joel H. |
author_facet | Bettcher, Brianne M. Fitch, Ryan Wynn, Matthew J. Lalli, Matthew A. Elofson, Jonathan Jastrzab, Laura Mitic, Laura Miller, Zachary A. Rabinovici, Gil D. Miller, Bruce L. Kao, Aimee W. Kosik, Kenneth S. Kramer, Joel H. |
author_sort | Bettcher, Brianne M. |
collection | PubMed |
description | INTRODUCTION: MCP-1 and eotaxin-1 are encoded on chromosome 17 and have been shown to reduce hippocampal neurogenesis in mice. We investigated whether these chemokines selectively associate with memory in individuals with mild cognitive impairment (MCI) and Alzheimer's disease (AD) dementia. METHODS: MCP-1 and eotaxin-1 were assayed in controls, MCI, and AD dementia patients with varying phenotypes (n = 171). A subset of 55 individuals had magnetic resonance imaging (MRI) scans available. Composite scores for cognitive variables were created, and medial temporal lobe volumes were obtained. RESULTS: An interaction was noted between MCP-1 and eotaxin-1, such that deleterious associations with memory were seen when both chemokines were elevated. These associations remained significant after adding APOE genotype and comparison (non-chromosome 17) chemokines into the model. These chemokines predicted left medial temporal lobe volume and were not related to other cognitive domains. DISCUSSION: These results suggest a potentially selective role for MCP-1 and eotaxin-1 in memory dysfunction in the context of varied MCI and AD dementia phenotypes. |
format | Online Article Text |
id | pubmed-4941041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49410412016-07-22 MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes Bettcher, Brianne M. Fitch, Ryan Wynn, Matthew J. Lalli, Matthew A. Elofson, Jonathan Jastrzab, Laura Mitic, Laura Miller, Zachary A. Rabinovici, Gil D. Miller, Bruce L. Kao, Aimee W. Kosik, Kenneth S. Kramer, Joel H. Alzheimers Dement (Amst) Blood-Based Biomarkers INTRODUCTION: MCP-1 and eotaxin-1 are encoded on chromosome 17 and have been shown to reduce hippocampal neurogenesis in mice. We investigated whether these chemokines selectively associate with memory in individuals with mild cognitive impairment (MCI) and Alzheimer's disease (AD) dementia. METHODS: MCP-1 and eotaxin-1 were assayed in controls, MCI, and AD dementia patients with varying phenotypes (n = 171). A subset of 55 individuals had magnetic resonance imaging (MRI) scans available. Composite scores for cognitive variables were created, and medial temporal lobe volumes were obtained. RESULTS: An interaction was noted between MCP-1 and eotaxin-1, such that deleterious associations with memory were seen when both chemokines were elevated. These associations remained significant after adding APOE genotype and comparison (non-chromosome 17) chemokines into the model. These chemokines predicted left medial temporal lobe volume and were not related to other cognitive domains. DISCUSSION: These results suggest a potentially selective role for MCP-1 and eotaxin-1 in memory dysfunction in the context of varied MCI and AD dementia phenotypes. Elsevier 2016-06-22 /pmc/articles/PMC4941041/ /pubmed/27453930 http://dx.doi.org/10.1016/j.dadm.2016.05.004 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Blood-Based Biomarkers Bettcher, Brianne M. Fitch, Ryan Wynn, Matthew J. Lalli, Matthew A. Elofson, Jonathan Jastrzab, Laura Mitic, Laura Miller, Zachary A. Rabinovici, Gil D. Miller, Bruce L. Kao, Aimee W. Kosik, Kenneth S. Kramer, Joel H. MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title | MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title_full | MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title_fullStr | MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title_full_unstemmed | MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title_short | MCP-1 and eotaxin-1 selectively and negatively associate with memory in MCI and Alzheimer's disease dementia phenotypes |
title_sort | mcp-1 and eotaxin-1 selectively and negatively associate with memory in mci and alzheimer's disease dementia phenotypes |
topic | Blood-Based Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941041/ https://www.ncbi.nlm.nih.gov/pubmed/27453930 http://dx.doi.org/10.1016/j.dadm.2016.05.004 |
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