In vivo biomarkers of structural and functional brain development and aging in humans

Neurosci Biobehav Rev. 2020 Oct:117:142-164. doi: 10.1016/j.neubiorev.2017.11.002.

Abstract

Brain aging is a major determinant of aging. Along with the aging population, prevalence of neurodegenerative diseases is increasing, therewith placing economic and social burden on individuals and society. Individual rates of brain aging are shaped by genetics, epigenetics, and prenatal environmental. Biomarkers of biological brain aging are needed to predict individual trajectories of aging and the risk for age-associated neurological impairments for developing early preventive and interventional measures. We review current advances of in vivo biomarkers predicting individual brain age. Telomere length and epigenetic clock, two important biomarkers that are closely related to the mechanistic aging process, have only poor deterministic and predictive accuracy regarding individual brain aging due to their high intra- and interindividual variability. Phenotype-related biomarkers of global cognitive function and brain structure provide a much closer correlation to age at the individual level. During fetal and perinatal life, autonomic activity is a unique functional marker of brain development. The cognitive and structural biomarkers also boast high diagnostic specificity for determining individual risks for neurodegenerative diseases.

Keywords: Autonomous activity; Biomarkers; Brain aging; Brain maturation; BrainAGE; Cognition; Epigenetic clock; Fetal autonomic brain age; Fetal brain development; Telomere length; Visual attention; Visual information uptake.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aged
  • Aging*
  • Biomarkers
  • Brain
  • Cognition
  • Female
  • Humans
  • Neurodegenerative Diseases*
  • Pregnancy

Substances

  • Biomarkers