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CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia

We aimed to examine the association of CSF tumor necrosis factor-alpha (TNFα) with conversion from mild cognitive impairment (MCI) to dementia. At baseline, there were a total of 129 participants with MCI in this study. The association of CSF TNFα levels with the incidence of dementia were evaluated...

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Detalles Bibliográficos
Autores principales: Fu, Pan, Peng, Feifei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604923/
https://www.ncbi.nlm.nih.gov/pubmed/36288380
http://dx.doi.org/10.1371/journal.pone.0274503
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author Fu, Pan
Peng, Feifei
author_facet Fu, Pan
Peng, Feifei
author_sort Fu, Pan
collection PubMed
description We aimed to examine the association of CSF tumor necrosis factor-alpha (TNFα) with conversion from mild cognitive impairment (MCI) to dementia. At baseline, there were a total of 129 participants with MCI in this study. The association of CSF TNFα levels with the incidence of dementia were evaluated using Cox proportional hazards regression analysis adjusted for potential confounders. Individuals were categorized into groups based on the CSF TNFα tertiles. Compared to the low group (the reference group), the intermediate group progressed more rapidly to dementia [HR (95% CI) = 2.2 (1.15–4.1); p = 0.016] after adjusting for other covariates. However, the high group did not progress faster than the low group [HR (95% CI) = 1.5 (0.79–2.8); p = 0.214]. Our study suggested a potential non-relationship between CSF TNFα levels and the risk of development of dementia among MCI older people.
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spelling pubmed-96049232022-10-27 CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia Fu, Pan Peng, Feifei PLoS One Research Article We aimed to examine the association of CSF tumor necrosis factor-alpha (TNFα) with conversion from mild cognitive impairment (MCI) to dementia. At baseline, there were a total of 129 participants with MCI in this study. The association of CSF TNFα levels with the incidence of dementia were evaluated using Cox proportional hazards regression analysis adjusted for potential confounders. Individuals were categorized into groups based on the CSF TNFα tertiles. Compared to the low group (the reference group), the intermediate group progressed more rapidly to dementia [HR (95% CI) = 2.2 (1.15–4.1); p = 0.016] after adjusting for other covariates. However, the high group did not progress faster than the low group [HR (95% CI) = 1.5 (0.79–2.8); p = 0.214]. Our study suggested a potential non-relationship between CSF TNFα levels and the risk of development of dementia among MCI older people. Public Library of Science 2022-10-26 /pmc/articles/PMC9604923/ /pubmed/36288380 http://dx.doi.org/10.1371/journal.pone.0274503 Text en © 2022 Fu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fu, Pan
Peng, Feifei
CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title_full CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title_fullStr CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title_full_unstemmed CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title_short CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia
title_sort csf tnf α levels were associated with conversion from mild cognitive impairment to dementia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604923/
https://www.ncbi.nlm.nih.gov/pubmed/36288380
http://dx.doi.org/10.1371/journal.pone.0274503
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