Blood TDP-43 Combined with Demographics Information Predicts Dementia Occurrence in Community Non-Dementia Elderly

J Alzheimers Dis. 2021;79(1):301-309. doi: 10.3233/JAD-201263.

Abstract

Background: TAR DNA-binding protein-43 (TDP-43) and neurofilament light chain (NfL) are promising fluid biomarkers of disease progression for various dementia.

Objective: We would explore whether blood levels of NfL and TDP-43 could predict the long-term progression to dementia, and the relationship of TDP-43 levels between cerebrospinal fluid (CSF) and blood.

Methods: A total of 86 non-dementia elderly received 7-year follow-up, and were divided into 49 stable normal control (NC)/mild cognitive impairment (MCI) subjects, 19 subjects progressing from NC to MCI, and 18 subjects progressing from NC/MCI to dementia. Blood TDP-43 and NfL levels, and cognitive functions were measured in all subjects. Furthermore, another cohort of 23 dementia patients, including 13 AD and 10 non-AD patients received blood and CSF measurements of TDP-43.

Results: In cohort 1, compared to stable NC/MCI group, there were higher levels of blood TDP-43 at baseline in subjects progressing from NC/MCI to dementia. The combination of baseline blood TDP-43 levels with demographics including age, education, and diabetes had the detection for dementia occurrence. Baseline blood levels of NfL are negatively associated with cognitive function at 7-year follow-up. In cohort 2, we found there were no relationship between CSF and blood levels of TDP-43. Moreover, the levels of TDP-43 in CSF was positively associated with the age of patients, especially in AD group.

Conclusion: Single blood TDP-43 could not estimate dementia occurrence; however, TDP-43 combined with demographics has the predictive effect for dementia occurrence and NfL level is associated with a decrease of cognitive function.

Keywords: Dementia; TDP-43; follow-up; mild cognitive impairment; neurofilament light chain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / blood*
  • Alzheimer Disease / cerebrospinal fluid
  • Alzheimer Disease / epidemiology
  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / cerebrospinal fluid
  • Case-Control Studies
  • Cognitive Dysfunction / blood*
  • Cognitive Dysfunction / cerebrospinal fluid
  • Cognitive Dysfunction / epidemiology
  • Cognitive Dysfunction / physiopathology
  • DNA-Binding Proteins / blood*
  • DNA-Binding Proteins / cerebrospinal fluid
  • Dementia / blood
  • Dementia / cerebrospinal fluid
  • Dementia / epidemiology
  • Dementia / physiopathology
  • Disease Progression
  • Educational Status
  • Female
  • Humans
  • Independent Living
  • Male
  • Middle Aged
  • Neurofilament Proteins / blood
  • Peptide Fragments / cerebrospinal fluid
  • Phosphorylation
  • Risk Assessment
  • tau Proteins / cerebrospinal fluid

Substances

  • Amyloid beta-Peptides
  • DNA-Binding Proteins
  • Neurofilament Proteins
  • Peptide Fragments
  • TARDBP protein, human
  • amyloid beta-protein (1-40)
  • amyloid beta-protein (1-42)
  • neurofilament protein L
  • tau Proteins