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NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies
Background: Initial observational studies and a systematic review published recently have suggested that non-steroidal anti-inflammatory drug (NSAID) use has the trend to be associated with reduced risk of Alzheimer's disease (AD), while results remain conflicting. Thus, we performed an updated...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882872/ https://www.ncbi.nlm.nih.gov/pubmed/29643804 http://dx.doi.org/10.3389/fnagi.2018.00083 |
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author | Zhang, Caixia Wang, Yan Wang, Dongyin Zhang, Jidong Zhang, Fangfang |
author_facet | Zhang, Caixia Wang, Yan Wang, Dongyin Zhang, Jidong Zhang, Fangfang |
author_sort | Zhang, Caixia |
collection | PubMed |
description | Background: Initial observational studies and a systematic review published recently have suggested that non-steroidal anti-inflammatory drug (NSAID) use has the trend to be associated with reduced risk of Alzheimer's disease (AD), while results remain conflicting. Thus, we performed an updated meta-analysis to reevaluate the evidence on this association. Methods: Data sources from PUBMED, Embase and Cochrane Library from inception through April 2017 were searched by two independent reviewers. Eligible cohort studies were selected according to predefined keywords. We did a meta-analysis of available study data using a random-effects model to calculate overall relative risks (RRs) for associations between NSAID exposure and AD risk. Results: From 121 potentially relevant studies, 16 cohort studies including 236,022 participants, published between 1995 and 2016, were included in this systematic review. Meta-analysis demonstrated that current or former NSAID use was significantly associated with reduced risk of AD (RR, 0.81, 95% CI0.70 to 0.94) compared with those who did not use NSAIDs. This association existed in studies including all NSAID types, but not in aspirin (RR, 0.89, 95% CI 0.70 to 1.13), acetaminophen (RR, 0.87, 95% CI 0.40 to 1.91) or non-aspirin NSAID (RR, 0.84, 95% CI 0.58 to 1.23). Conclusions: Current evidence suggests that NSAID exposure might be significantly associated with reduced risk of AD. However, further large-scale prospective studies are needed to reevaluate this association, especially the associations in individual NSAID type. |
format | Online Article Text |
id | pubmed-5882872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58828722018-04-11 NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies Zhang, Caixia Wang, Yan Wang, Dongyin Zhang, Jidong Zhang, Fangfang Front Aging Neurosci Neuroscience Background: Initial observational studies and a systematic review published recently have suggested that non-steroidal anti-inflammatory drug (NSAID) use has the trend to be associated with reduced risk of Alzheimer's disease (AD), while results remain conflicting. Thus, we performed an updated meta-analysis to reevaluate the evidence on this association. Methods: Data sources from PUBMED, Embase and Cochrane Library from inception through April 2017 were searched by two independent reviewers. Eligible cohort studies were selected according to predefined keywords. We did a meta-analysis of available study data using a random-effects model to calculate overall relative risks (RRs) for associations between NSAID exposure and AD risk. Results: From 121 potentially relevant studies, 16 cohort studies including 236,022 participants, published between 1995 and 2016, were included in this systematic review. Meta-analysis demonstrated that current or former NSAID use was significantly associated with reduced risk of AD (RR, 0.81, 95% CI0.70 to 0.94) compared with those who did not use NSAIDs. This association existed in studies including all NSAID types, but not in aspirin (RR, 0.89, 95% CI 0.70 to 1.13), acetaminophen (RR, 0.87, 95% CI 0.40 to 1.91) or non-aspirin NSAID (RR, 0.84, 95% CI 0.58 to 1.23). Conclusions: Current evidence suggests that NSAID exposure might be significantly associated with reduced risk of AD. However, further large-scale prospective studies are needed to reevaluate this association, especially the associations in individual NSAID type. Frontiers Media S.A. 2018-03-28 /pmc/articles/PMC5882872/ /pubmed/29643804 http://dx.doi.org/10.3389/fnagi.2018.00083 Text en Copyright © 2018 Zhang, Wang, Wang, Zhang and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Zhang, Caixia Wang, Yan Wang, Dongyin Zhang, Jidong Zhang, Fangfang NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title | NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title_full | NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title_fullStr | NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title_full_unstemmed | NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title_short | NSAID Exposure and Risk of Alzheimer's Disease: An Updated Meta-Analysis From Cohort Studies |
title_sort | nsaid exposure and risk of alzheimer's disease: an updated meta-analysis from cohort studies |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882872/ https://www.ncbi.nlm.nih.gov/pubmed/29643804 http://dx.doi.org/10.3389/fnagi.2018.00083 |
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