4.7 Article

Biological and Neuroimaging Markers as Predictors of 5-Year Incident Frailty in Older Adults: A Secondary Analysis of the MAPT Study

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/gerona/glaa296

关键词

Biomarkers; Inflammation; Neuroimaging; Nutrition

资金

  1. Region Occitanie/Pyrenees-Mediterranee [1901175]
  2. European Regional Development Fund (ERDF) [MP0022856]
  3. Alzheimer Prevention in Occitania and Catalonia (APOC Chair of Excellence-Inspire Program)
  4. Gerontopole of Toulouse
  5. French Ministry of Health
  6. Pierre Fabre Research Institute
  7. ExonHit Therapeutics SA
  8. Avid Radiopharmaceuticals Inc.
  9. University Hospital Center of Toulouse
  10. Association Monegasque pour la Recherche sur la maladie d'Alzheimer (AMPA)
  11. INSERM-University of Toulouse III

向作者/读者索取更多资源

This study aimed to investigate the predictive value of biological and neuroimaging markers in determining incident frailty among older adults over a period of 5 years. Although some markers like 25-hydroxyvitamin D deficiency, homocysteine levels, and neuroimaging data were significantly associated with incident frailty in unadjusted models, these associations disappeared after adjustment for age, sex, and other confounders. Omega-3 index was the only marker that showed a trend of association with incident frailty.
Background: This study aims to investigate the predictive value of biological and neuroimaging markers to determine incident frailty among older people for a period of 5 years. Methods: We included 1394 adults aged 70 years and older from the Multidomain Alzheimer Preventive Trial, who were not frail at baseline (according to Fried's criteria) and who had at least 1 post-baseline measurement of frailty. Participants who progressed to frailty during the 5-year follow-up were categorized as incident frailty and those who remained non-frail were categorized as without frailty. The differences of baseline biochemical factors (25-hydroxyvitamin D, homocysteine, omega-3 index, C-reactive protein), other biological markers (Apolipoprotein E genotypes, amyloid-beta deposits), and neuroimaging data (gray matter volume, hippocampal volume, white matter hyperintensities) were compared between groups. Cox proportional hazard model was used to evaluate the associations between biomarkers and incident frailty. Results: A total of 195 participants (14.0%) became frail over 5 years. Although 25-hydroxyvitamin D deficiency, homocysteine levels, low-grade inflammation (persistently increased C-reactive protein 3-10 mg/L), gray matter, and hippocampal volume were significantly associated with incident frailty in unadjusted models, these associations disappeared after adjustment for age, sex, and other confounders. Omega-3 index was the sole marker that presented a trend of association with incident frailty (hazard ratio: 0.92; 95% confidence interval: 0.83-1.01; p = .082). Conclusions: This study failed to identify biomarkers able to predict frailty incidence in community-dwelling older adults for a period of 5 years. Further longitudinal research with multiple measurements of biomarkers and frailty is needed to evaluate the long-term relationships between changes in biomarkers levels and frailty evolution.

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