Research

Cerebrovascular disease is one of the leading causes of death in the US and is the number one cause of adult disability. The onset of disease can be strongly influenced by environmental factors, however, it is well established that a family history of disease can dramatically increase the risk, depending on the pattern of inheritance.

Identifying the genetic factors that influence susceptibility and progression of cerebrovascular disease will help identify at risk individuals, guide the selection of candidates for targeted clinical trials and play a crucial role in the era of Precision Medicine.

We aim to develop a sample collection, processing, storage, genomics and multi-omics pipeline for Florida investigators to aid in future research studies and move the field of cerebrovascular genetics forward.

Recruitment

The Southeastern United States, often referred to as the "Stroke Belt," is a region with significantly higher rates of stroke and cardiovascular disease compared to the national average. By focusing our cerebrovascular disease biorepository in Florida, we're addressing a critical need within this high-risk region. Florida's inclusion in the Stroke Belt makes it an ideal location for studying the unique environmental, genetic, and lifestyle factors that contribute to cerebrovascular diseases. This focus not only allows for targeted research but also provides an opportunity to develop region-specific interventions and improve outcomes for communities disproportionately affected by these conditions.