4.7 Article

TNFR-1 and GDF-15 Are Associated With Plasma Neurofilament Light Chain and Progranulin Among Community-Dwelling Older Adults: A Secondary Analysis of the MAPT Study

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/gerona/glac244

关键词

Amyloid-beta; Cognitive decline; Inflammation; Neurodegeneration; Nutrition

资金

  1. French Ministry of Health
  2. University Hospital Center of Toulouse/Gerontopole
  3. Pierre Fabre Research Institute
  4. ExonHit Therapeutics
  5. University Hospital Center of Toulouse
  6. Association Monegasque pour la Recherche sur la maladie d'Alzheimer (AMPA)
  7. UMR 1027 Unit INSERM-University of Toulouse III
  8. National Institute on Aging grants NIH [R56AG061900, RF1AG061900]
  9. Saint Louis University
  10. Region Occitanie/Pyrenees-Mediterranee [1901175]
  11. European Regional Development Fund [MP0022856]
  12. Alzheimer Prevention in Occitania and Catalonia (APOC Chair of Excellence - Inspire Program)

向作者/读者索取更多资源

There is evidence of an association between inflammation pathways and plasma markers of neurodegeneration, highlighting the importance of monitoring this risk in older adults.
There is growing evidence that cognitive decline can be affected by both nutritional aspects and inflammation. Plasma neurodegenerative biomarkers stand out as minimally invasive useful measures to monitor the potential risk of cognitive decline. This study aimed to investigate the associations between biomarkers of neurodegeneration, nutrition, and inflammation among community-dwelling older adults, and to verify if associations differed according to apolipoprotein E (APOE) epsilon 4 status. This cross-sectional analysis included 475 participants >= 70 years old from the Multidomain Alzheimer Preventive Trial (MAPT), mean age 76.8 years (SD = 4.5), 59.4% women. Biomarkers of neurodegeneration (plasma amyloid-beta(42/40)-A beta(42/40), neurofilament light chain-NfL, progranulin), nutrition (erythrocyte docosahexaenoic acid, eicosapentaenoic acid, omega-3 index; plasma homocysteine-Hcy, 25 hydroxyvitamin D), inflammation (plasma tumor necrosis factor receptor 1-TNFR-1, monocyte chemoattractant protein 1-MCP-1, interleukin 6-IL-6), and cellular stress (plasma growth differentiation factor 15-GDF-15) were assessed. Linear regression analyses were performed to investigate the associations between nutritional and inflammatory biomarkers (independent variables) and neurodegenerative biomarkers (dependent variables), with adjustments for age, sex, education, body mass index, physical activity, allocation to MAPT groups, and APOE epsilon 4 status. After adjusting for confounders, A beta(42/40) was not associated with nutritional or inflammatory markers. NfL was positively associated with GDF-15, TNFR-1, IL-6, and Hcy. Progranulin was positively associated with GDF-15, TNFR-1, and MCP-1. Analyses restricted to APOE epsilon 4 carriers (n = 116; 26.9%) or noncarriers were mostly similar. Our cross-sectional study with community-dwelling older adults corroborates previous evidence that inflammatory pathways are associated to plasma markers of neurodegeneration.

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