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Peripheral inflammation is associated with brain atrophy and cognitive decline linked to mild cognitive impairment and Alzheimer's disease.
Liang, Nuanyi; Nho, Kwangsik; Newman, John W; Arnold, Matthias; Huynh, Kevin; Meikle, Peter J; Borkowski, Kamil; Kaddurah-Daouk, Rima.
Afiliação
  • Liang N; West Coast Metabolomics Center, Genome Center, University of California-Davis, Davis, CA, 95616, USA.
  • Nho K; Department of Radiology and Imaging Sciences and the Indiana Alzheimer Disease Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
  • Newman JW; West Coast Metabolomics Center, Genome Center, University of California-Davis, Davis, CA, 95616, USA.
  • Arnold M; Department of Nutrition, University of California-Davis, Davis, CA, 95616, USA.
  • Huynh K; Western Human Nutrition Research Center, United States Department of Agriculture-Agriculture Research Service, Davis, CA, 95616, USA.
  • Meikle PJ; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, 27708, USA.
  • Borkowski K; Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Kaddurah-Daouk R; Baker Heart and Diabetes Institute, Melbourne, VIC, 3004, Australia.
Sci Rep ; 14(1): 17423, 2024 07 29.
Article em En | MEDLINE | ID: mdl-39075118
ABSTRACT
Inflammation is an important factor in Alzheimer's disease (AD). An NMR measurement in plasma, glycoprotein acetyls (GlycA), captures the overall level of protein production and glycosylation implicated in systemic inflammation. With its additional advantage of reducing biological variability, GlycA might be useful in monitoring the relationship between peripheral inflammation and brain changes relevant to AD. However, the associations between GlycA and these brain changes have not been fully evaluated. Here, we performed Spearman's correlation analyses to evaluate these associations cross-sectionally and determined whether GlycA can inform AD-relevant longitudinal measurements among participants in the Alzheimer's Disease Neuroimaging Initiative (n = 1506), with additional linear models and stratification analyses to evaluate the influences of sex or diagnosis status and confirm findings from Spearman's correlation analyses. We found that GlycA was elevated in AD patients compared to cognitively normal participants. GlycA correlated negatively with multiple concurrent regional brain volumes in females diagnosed with late mild cognitive impairment (LMCI) or AD. Baseline GlycA level was associated with executive function decline at 3-9 year follow-up in participants diagnosed with LMCI at baseline, with similar but not identical trends observed in the future decline of memory and entorhinal cortex volume. Results here indicated that GlycA is an inflammatory biomarker relevant to AD pathogenesis and that the stage of LMCI might be relevant to inflammation-related intervention.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia / Encéfalo / Doença de Alzheimer / Disfunção Cognitiva / Inflamação Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia / Encéfalo / Doença de Alzheimer / Disfunção Cognitiva / Inflamação Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article