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Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease

OBJECTIVE: To determine the key inflammatory pathways that are activated in the peripheral and CNS compartments at the mild cognitive impairment (MCI) stage of Alzheimer’s disease (AD). METHODS: A cross‐sectional study of patients with clinical and biomarker characteristics consistent with MCI‐AD in...

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Autores principales: Pillai, Jagan A., Maxwell, Sean, Bena, James, Bekris, Lynn M., Rao, Stephen M., Chance, Mark, Lamb, Bruce T., Leverenz, James B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649519/
https://www.ncbi.nlm.nih.gov/pubmed/31353852
http://dx.doi.org/10.1002/acn3.50827
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author Pillai, Jagan A.
Maxwell, Sean
Bena, James
Bekris, Lynn M.
Rao, Stephen M.
Chance, Mark
Lamb, Bruce T.
Leverenz, James B.
author_facet Pillai, Jagan A.
Maxwell, Sean
Bena, James
Bekris, Lynn M.
Rao, Stephen M.
Chance, Mark
Lamb, Bruce T.
Leverenz, James B.
author_sort Pillai, Jagan A.
collection PubMed
description OBJECTIVE: To determine the key inflammatory pathways that are activated in the peripheral and CNS compartments at the mild cognitive impairment (MCI) stage of Alzheimer’s disease (AD). METHODS: A cross‐sectional study of patients with clinical and biomarker characteristics consistent with MCI‐AD in a discovery cohort, with replication in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort. Inflammatory analytes were measured in the CSF and plasma with the same validated multiplex analyte platform in both cohorts and correlated with AD biomarkers (CSF Aβ42, total tau (t‐tau), phosphorylated tau (p‐tau) to identify key inflammatory pathway activations. The pathways were additionally validated by evaluating genes related to all analytes in coexpression networks of brain tissue transcriptome from an autopsy confirmed AD cohort to interrogate if the same pathway activations were conserved in the brain tissue gene modules. RESULTS: Analytes of the tumor necrosis factor (TNF) signaling pathway (KEGG ID:4668) in the CSF and plasma best correlated with CSF t‐tau and p‐tau levels, and analytes of the complement and coagulation pathway (KEGG ID:4610) best correlated with CSF Aβ42 levels. The top inflammatory signaling pathways of significance were conserved in the peripheral and the CNS compartments. They were also confirmed to be enriched in AD brain transcriptome gene clusters. INTERPRETATION: A cell‐protective rather than a proinflammatory analyte profile predominates in the CSF in relation to neurodegeneration markers among MCI‐AD patients. Analytes from the TNF signaling and the complement and coagulation pathways are relevant in evaluating disease severity at the MCI stage of AD.
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spelling pubmed-66495192019-07-31 Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease Pillai, Jagan A. Maxwell, Sean Bena, James Bekris, Lynn M. Rao, Stephen M. Chance, Mark Lamb, Bruce T. Leverenz, James B. Ann Clin Transl Neurol Research Articles OBJECTIVE: To determine the key inflammatory pathways that are activated in the peripheral and CNS compartments at the mild cognitive impairment (MCI) stage of Alzheimer’s disease (AD). METHODS: A cross‐sectional study of patients with clinical and biomarker characteristics consistent with MCI‐AD in a discovery cohort, with replication in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort. Inflammatory analytes were measured in the CSF and plasma with the same validated multiplex analyte platform in both cohorts and correlated with AD biomarkers (CSF Aβ42, total tau (t‐tau), phosphorylated tau (p‐tau) to identify key inflammatory pathway activations. The pathways were additionally validated by evaluating genes related to all analytes in coexpression networks of brain tissue transcriptome from an autopsy confirmed AD cohort to interrogate if the same pathway activations were conserved in the brain tissue gene modules. RESULTS: Analytes of the tumor necrosis factor (TNF) signaling pathway (KEGG ID:4668) in the CSF and plasma best correlated with CSF t‐tau and p‐tau levels, and analytes of the complement and coagulation pathway (KEGG ID:4610) best correlated with CSF Aβ42 levels. The top inflammatory signaling pathways of significance were conserved in the peripheral and the CNS compartments. They were also confirmed to be enriched in AD brain transcriptome gene clusters. INTERPRETATION: A cell‐protective rather than a proinflammatory analyte profile predominates in the CSF in relation to neurodegeneration markers among MCI‐AD patients. Analytes from the TNF signaling and the complement and coagulation pathways are relevant in evaluating disease severity at the MCI stage of AD. John Wiley and Sons Inc. 2019-07-04 /pmc/articles/PMC6649519/ /pubmed/31353852 http://dx.doi.org/10.1002/acn3.50827 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, 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.
spellingShingle Research Articles
Pillai, Jagan A.
Maxwell, Sean
Bena, James
Bekris, Lynn M.
Rao, Stephen M.
Chance, Mark
Lamb, Bruce T.
Leverenz, James B.
Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title_full Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title_fullStr Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title_full_unstemmed Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title_short Key inflammatory pathway activations in the MCI stage of Alzheimer’s disease
title_sort key inflammatory pathway activations in the mci stage of alzheimer’s disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649519/
https://www.ncbi.nlm.nih.gov/pubmed/31353852
http://dx.doi.org/10.1002/acn3.50827
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