BioAge: toward a multi-determined, mechanistic account of cognitive aging

Ageing Res Rev. 2014 Nov:18:95-105. doi: 10.1016/j.arr.2014.09.003. Epub 2014 Sep 30.

Abstract

The search for reliable early indicators of age-related cognitive decline represents a critical avenue for progress in aging research. Chronological age is a commonly used developmental index; however, it offers little insight into the mechanisms underlying cognitive decline. In contrast, biological age (BioAge), reflecting the vitality of essential biological systems, represents a promising operationalization of developmental time. Current BioAge models have successfully predicted age-related cognitive deficits. Research on aging-related cognitive function indicates that the interaction of multiple risk and protective factors across the human lifespan confers individual risk for late-life cognitive decline, implicating a multi-causal explanation. In this review, we explore current BioAge models, describe three broad yet pathologically relevant biological processes linked to cognitive decline, and propose a novel operationalization of BioAge accounting for both moderating and causal mechanisms of cognitive decline and dementia. We argue that a multivariate and mechanistic BioAge approach will lead to a greater understanding of disease pathology as well as more accurate prediction and early identification of late-life cognitive decline.

Keywords: Biological age; Cognitive aging; Early identification; Inflammation; Oxidative stress; Vascular health.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Age Factors
  • Aging / pathology
  • Aging / psychology*
  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Brain / physiopathology*
  • Cognition Disorders / diagnosis
  • Cognition Disorders / etiology*
  • Cognition Disorders / metabolism
  • Cognition Disorders / physiopathology
  • Cognition Disorders / psychology
  • Cognition*
  • Health Status
  • Humans
  • Inflammation / complications
  • Oxidative Stress
  • Risk Factors
  • Vascular Diseases / complications