Is the Relationship Between Cardiovascular Disease and Alzheimer's Disease Genetic? A Scoping Review

Anni Moore1, Marylyn D Ritchie1,2,3

  • 1Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Genes
|January 8, 2025
PubMed

Insights

Cardiovascular disease (CVD) and Alzheimer's disease (AD) share genetic links and biological pathways, increasing risk for both conditions. Understanding these overlaps, particularly in lipid metabolism and blood pressure, is key to managing aging-related diseases.

Area of Science:

  • Genetics and Aging Research
  • Neuroscience
  • Cardiology

Background:

  • Cardiovascular disease (CVD) and Alzheimer's disease (AD) frequently co-occur in aging populations.
  • Epidemiological data suggest a bidirectional relationship between CVD and AD risk.
  • The precise genetic underpinnings of this comorbidity remain incompletely understood.

Purpose of the Study:

  • To conduct a scoping review of identified overlapping genetics between CVD and AD.
  • To examine shared genetic risk at the individual gene and pathway levels.
  • To synthesize current evidence on the genetic relationship between these prevalent aging diseases.

Main Methods:

  • Systematic literature search of PubMed and Scopus databases (1990-October 2024).
  • Adherence to PRISMA-ScR guidelines for scoping reviews.
  • Inclusion criteria focused on studies analyzing genetic relationships between CVD and AD using statistical methods.

Main Results:

  • 274 articles were selected from 2918 initial results, categorized into shared genetic risk and mechanisms.
  • Genes such as APOE, PSEN1, and PSEN2 demonstrate effects across both AD and CVD.
  • Key shared pathways include lipid metabolism, blood pressure regulation, and blood-brain barrier (BBB) integrity.

Conclusions:

  • Familial genes with high penetrance can simultaneously elevate risk for both CVD and AD.
  • Dysregulation in broader pathways like lipid metabolism, blood pressure control, and BBB function significantly contributes to the comorbidity and progression of AD and CVD.
  • Further research requires diverse populations and longitudinal data to fully elucidate genetic contributions.
Abstract

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