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.
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.
Background/Objectives:
Cardiovascular disease (CVD) and Alzheimer's disease (AD) are two diseases highly prevalent in the aging population and often co-occur. The exact relationship between the two diseases is uncertain, though epidemiological studies have demonstrated that CVDs appear to increase the risk of AD and vice versa. This scoping review aims to examine the current identified overlapping genetics between CVDs and AD at the individual gene level and at the shared pathway level.
Methods:
Following PRISMA-ScR guidelines for a scoping review, we searched the PubMed and Scopus databases from 1990 to October 2024 for articles that involved (1) CVDs, (2) AD, and (3) used statistical methods to parse genetic relationships.
Results:
Our search yielded 2918 articles, of which 274 articles passed screening and were organized into two main sections: (1) evidence of shared genetic risk; and (2) shared mechanisms. The genes APOE, PSEN1, and PSEN2 reportedly have wide effects across the AD and CVD spectrum, affecting both cardiac and brain tissues. Mechanistically, changes in three main pathways (lipid metabolism, blood pressure regulation, and the breakdown of the blood-brain barrier (BBB)) contribute to subclinical and etiological changes that promote both AD and CVD progression. However, genetic studies continue to be limited by the availability of longitudinal data and lack of cohorts that are representative of diverse populations.
Conclusions:
Highly penetrant familial genes simultaneously increase the risk of CVDs and AD. However, in most cases, sets of dysregulated genes within larger-scale mechanisms, like changes in lipid metabolism, blood pressure regulation, and BBB breakdown, increase the risk of both AD and CVDs and contribute to disease progression.
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