<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fu P</submitter><funding>The Canadian Institutes of Health Research</funding><funding>Janssen Alzheimer Immunotherapy Research &amp;amp; Development, LLC</funding><funding>Lumosity</funding><funding>DOD ADNI</funding><funding>Merck &amp;amp; Co., Inc.</funding><funding>Pfizer Inc.</funding><funding>NIA NIH HHS</funding><funding>Cogstate</funding><funding>IXICO Ltd.</funding><funding>Meso Scale Diagnostics, LLC</funding><funding>Eisai Inc.</funding><funding>National Institutes of Health</funding><funding>GE Healthcare</funding><funding>National Institute on Aging</funding><funding>Eli Lilly and Company</funding><funding>CereSpir, Inc.</funding><funding>Fujirebio</funding><funding>Transition Therapeutics</funding><funding>Novartis Pharmaceuticals Corporation</funding><funding>Takeda Pharmaceutical Company</funding><funding>EuroImmun</funding><funding>Foundation for the National Institutes of Health</funding><funding>Alzheimer&amp;apos;s Disease Neuroimaging Initiative</funding><funding>Araclon Biotech</funding><funding>Servier</funding><funding>Alzheimer’s Drug Discovery Foundation</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><funding>Elan Pharmaceuticals, Inc.</funding><funding>Neurotrack Technologies</funding><funding>BioClinica, Inc.</funding><funding>AbbVie</funding><funding>Bristol-Myers Squibb Company</funding><funding>CIHR</funding><funding>Piramal Imaging</funding><funding>NeuroRx Research</funding><funding>Alzheimer’s Association</funding><funding>Genentech, Inc.</funding><funding>Biogen</funding><funding>Johnson &amp;amp; Johnson Pharmaceutical Research &amp;amp; Development LLC</funding><funding>F. Hoffmann-La Roche Ltd</funding><funding>Lundbeck</funding><pagination>e0274503</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9604923</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(10)</volume><pubmed_abstract>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.</pubmed_abstract><journal>PloS one</journal><pubmed_title>CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia.</pubmed_title><pmcid>PMC9604923</pmcid><funding_grant_id>U01 AG024904</funding_grant_id><funding_grant_id>W81XWH-12-2-0012</funding_grant_id><pubmed_authors>Peng F</pubmed_authors><pubmed_authors>Fu P</pubmed_authors><pubmed_authors>Alzheimer’s Disease Neuroimaging Initiative</pubmed_authors></additional><is_claimable>false</is_claimable><name>CSF TNF α levels were associated with conversion from mild cognitive impairment to dementia.</name><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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-03T21:29:41.412Z</modification><creation>2025-04-03T21:29:41.412Z</creation></dates><accession>S-EPMC9604923</accession><cross_references><pubmed>36288380</pubmed><doi>10.1371/journal.pone.0274503</doi></cross_references></HashMap>