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Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease
INTRODUCTION: Neuroinflammation and cerebrovascular disease (CeVD) have been implicated in cognitive impairment and Alzheimer's disease (AD). The present study aimed to examine serum inflammatory markers in preclinical stages of dementia and in AD, as well as to investigate their associations w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318538/ https://www.ncbi.nlm.nih.gov/pubmed/28239640 http://dx.doi.org/10.1016/j.dadm.2017.01.001 |
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author | Zhu, Yanan Chai, Yuek Ling Hilal, Saima Ikram, M. Kamran Venketasubramanian, Narayanaswamy Wong, Boon-Seng Chen, Christopher P. Lai, Mitchell K.P. |
author_facet | Zhu, Yanan Chai, Yuek Ling Hilal, Saima Ikram, M. Kamran Venketasubramanian, Narayanaswamy Wong, Boon-Seng Chen, Christopher P. Lai, Mitchell K.P. |
author_sort | Zhu, Yanan |
collection | PubMed |
description | INTRODUCTION: Neuroinflammation and cerebrovascular disease (CeVD) have been implicated in cognitive impairment and Alzheimer's disease (AD). The present study aimed to examine serum inflammatory markers in preclinical stages of dementia and in AD, as well as to investigate their associations with concomitant CeVD. METHODS: We performed a cross-sectional case–control study including 96 AD, 140 cognitively impaired no dementia (CIND), and 79 noncognitively impaired participants. All subjects underwent neuropsychological and neuroimaging assessments, as well as collection of blood samples for measurements of serum samples interleukin (IL)-6, IL-8, and tumor necrosis factor α levels. Subjects were classified as CIND or dementia based on clinical criteria. Significant CeVD, including white-matter hyperintensities (WMHs), lacunes, and cortical infarcts, was assessed by magnetic resonance imaging. RESULTS: After controlling for covariates, higher concentrations of IL-8, but not the other measured cytokines, were associated with both CIND and AD only in the presence of significant CeVD (CIND with CeVD: odds ratios [ORs] 4.53; 95% confidence interval [CI] 1.5–13.4 and AD with CeVD: OR 7.26; 95% CI 1.2–43.3). Subsequent multivariate analyses showed that among the types of CeVD assessed, only WMH was associated with higher IL-8 levels in CIND and AD (WMH: OR 2.81; 95% CI 1.4–5.6). DISCUSSION: Serum IL-8 may have clinical utility as a biomarker for WMH in AD. Longitudinal follow-up studies would help validate these findings. |
format | Online Article Text |
id | pubmed-5318538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53185382017-02-26 Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease Zhu, Yanan Chai, Yuek Ling Hilal, Saima Ikram, M. Kamran Venketasubramanian, Narayanaswamy Wong, Boon-Seng Chen, Christopher P. Lai, Mitchell K.P. Alzheimers Dement (Amst) Special Section: Vascular Contributions to Alzheimer's Disease INTRODUCTION: Neuroinflammation and cerebrovascular disease (CeVD) have been implicated in cognitive impairment and Alzheimer's disease (AD). The present study aimed to examine serum inflammatory markers in preclinical stages of dementia and in AD, as well as to investigate their associations with concomitant CeVD. METHODS: We performed a cross-sectional case–control study including 96 AD, 140 cognitively impaired no dementia (CIND), and 79 noncognitively impaired participants. All subjects underwent neuropsychological and neuroimaging assessments, as well as collection of blood samples for measurements of serum samples interleukin (IL)-6, IL-8, and tumor necrosis factor α levels. Subjects were classified as CIND or dementia based on clinical criteria. Significant CeVD, including white-matter hyperintensities (WMHs), lacunes, and cortical infarcts, was assessed by magnetic resonance imaging. RESULTS: After controlling for covariates, higher concentrations of IL-8, but not the other measured cytokines, were associated with both CIND and AD only in the presence of significant CeVD (CIND with CeVD: odds ratios [ORs] 4.53; 95% confidence interval [CI] 1.5–13.4 and AD with CeVD: OR 7.26; 95% CI 1.2–43.3). Subsequent multivariate analyses showed that among the types of CeVD assessed, only WMH was associated with higher IL-8 levels in CIND and AD (WMH: OR 2.81; 95% CI 1.4–5.6). DISCUSSION: Serum IL-8 may have clinical utility as a biomarker for WMH in AD. Longitudinal follow-up studies would help validate these findings. Elsevier 2017-01-23 /pmc/articles/PMC5318538/ /pubmed/28239640 http://dx.doi.org/10.1016/j.dadm.2017.01.001 Text en © 2017 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 | Special Section: Vascular Contributions to Alzheimer's Disease Zhu, Yanan Chai, Yuek Ling Hilal, Saima Ikram, M. Kamran Venketasubramanian, Narayanaswamy Wong, Boon-Seng Chen, Christopher P. Lai, Mitchell K.P. Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title | Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title_full | Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title_fullStr | Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title_full_unstemmed | Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title_short | Serum IL-8 is a marker of white-matter hyperintensities in patients with Alzheimer's disease |
title_sort | serum il-8 is a marker of white-matter hyperintensities in patients with alzheimer's disease |
topic | Special Section: Vascular Contributions to Alzheimer's Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318538/ https://www.ncbi.nlm.nih.gov/pubmed/28239640 http://dx.doi.org/10.1016/j.dadm.2017.01.001 |
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