Genetic Determinants of Vascular Dementia.

Can J Cardiol

Population Health Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada; Department of Pathology and Molecular Medicine, McMaster University, Michael G. DeGroote School of Medicine, Hamilton, Ontario, Canada; Thrombosis and Atherosclerosis Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, Ontario, Canada. Electronic address:

Published: August 2024

AI Article Synopsis

  • Vascular dementia (VaD) is a common type of cognitive impairment linked to vascular issues, and recent genetic research using various methods has revealed its complex nature.
  • Genetic associations and risk factors like stroke and hypertension are crucial for understanding and preventing VaD, highlighting the need for a multifaceted approach.
  • Collaborations and advanced scientific techniques can enhance our understanding of VaD’s genetics, leading to improved diagnostics and treatments based on its underlying molecular mechanisms.

Article Abstract

Vascular dementia (VaD) is a prevalent form of cognitive impairment with underlying vascular etiology. In this review, we examine recent genetic advancements in our understanding of VaD, encompassing a range of methodologies including genome-wide association studies, polygenic risk scores, heritability estimates, and family studies for monogenic disorders revealing the complex and heterogeneous nature of the disease. We report well known genetic associations and highlight potential pathways and mechanisms implicated in VaD and its pathological risk factors, including stroke, cerebral small vessel disease, and cerebral amyloid angiopathy. Moreover, we discuss important modifiable risk factors such as hypertension, diabetes, and dyslipidemia, emphasizing the importance of a multifactorial approach in prevention, treatment, and understanding the genetic basis of VaD. Last, we outline several areas of scientific advancements to improve clinical care, highlighting that large-scale collaborative efforts, together with an integromics approach can enhance the robustness of genetic discoveries. Indeed, understanding the genetics of VaD and its pathophysiological risk factors hold the potential to redefine VaD on the basis of molecular mechanisms and to generate novel diagnostic, prognostic, and therapeutic tools.

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Source
http://dx.doi.org/10.1016/j.cjca.2024.03.025DOI Listing

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