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The power of representation: Statistical analysis of diversity in US Alzheimer's disease genetics data.

Diane XueElizabeth E BlueMatthew P ConomosAlison E Fohner
Published in: Alzheimer's & dementia (New York, N. Y.) (2024)
AD genetics datasets are largely representative of US ADRD burden. However, there is a wide discrepancy between proportional representation and statistically meaningful representation. Most variation identified in GWAS of non-Hispanic White individuals have low to moderate effects. Comparable risk variants in non-White populations are not detectable given current sample sizes, which could lead to disparities in future studies and drug development. We urge AD genetics researchers and institutions to continue investing in recruiting diverse participants and use community-based participatory research practices.
Keyphrases
  • healthcare
  • primary care
  • neural network
  • electronic health record
  • copy number
  • cognitive decline
  • big data
  • risk factors
  • machine learning
  • african american
  • case control
  • dna methylation
  • health insurance