Systematic Review of Longitudinal Evidence and Methodologies for Research on Neighborhood Characteristics and Brain Health

Public Health Rev. 2024 Mar 26:45:1606677. doi: 10.3389/phrs.2024.1606677. eCollection 2024.

Abstract

Objective: Synthesize longitudinal research evaluating neighborhood environments and cognition to identify methodological approaches, findings, and gaps. Methods: Included studies evaluated associations between neighborhood and cognition longitudinally among adults >45 years (or mean age of 65 years) living in developed nations. We extracted data on sample characteristics, exposures, outcomes, methods, overall findings, and assessment of disparities. Results: Forty studies met our inclusion criteria. Most (65%) measured exposure only once and a majority focused on green space and/or blue space (water), neighborhood socioeconomic status, and recreation/physical activity facilities. Similarly, over half studied incident impairment, cognitive function or decline (70%), with one examining MRI (2.5%) or Alzheimer's disease (7.5%). While most studies used repeated measures analysis to evaluate changes in the brain health outcome (51%), many studies did not account for any type of correlation within neighborhoods (35%). Less than half evaluated effect modification by race/ethnicity, socioeconomic status, and/or sex/gender. Evidence was mixed and dependent on exposure or outcome assessed. Conclusion: Although longitudinal research evaluating neighborhood and cognitive decline has expanded, gaps remain in types of exposures, outcomes, analytic approaches, and sample diversity.

Keywords: Alzheimer’s disease; adults; aging; cognition; longitudinal study; neighborhoods.

Publication types

  • Review

Grants and funding

The authors declare that members of the research team are supported by funding from the National Institute on Aging (R01AG072634) and the Urban Health Collaborative at Drexel University. LB is supported by NIH/NIA K01AG063895, NIH/NIA R21AG075291, and the Alzheimer’s Association (AARG-21-850963). TH and KH are supported by NIH/NIA R01AG058969.