Family history of coronary artery disease is an established risk factor that, alongside emerging genetic and imaging tools, is increasingly utilized for cardiovascular risk stratification.
How does family history, along with emerging genetic and imaging tools, impact cardiovascular risk stratification and screening for coronary artery disease?
This review highlights the growing importance of integrating family history, genetic profiling, and advanced imaging into cardiovascular risk stratification for early detection of coronary artery disease.
Family history for CAD (coronary artery disease) is an established cardiovascular (CV) risk factor and it is progressively acquiring importance in patients' CV risk stratification. Numerous studies have demonstrated that individuals with a first-degree relative affected by CAD have a significantly higher risk of developing the condition themselves; in particular, when CAD occurs at an early age in relatives. Indeed, recently published CCS (chronic coronary syndrome) ESC (European Society of Cardiology) guidelines include family history (FH) as a risk factor to consider when calculating pre-test risk for CAD. ESC guidelines on preventive cardiology (2021) only suggested CV risk assessment in the presence of a positive FH for CV disease, not considering it in the actual risk scores. Evidence suggests that positive anamnesis for relatives affected by CAD correlates with ACS (acute coronary syndrome) and CAD, with slight differences in relative risk as far as the degree of kinship is concerned. Genetic factors contribute to this correlation by influencing key processes that affect heart health, such as cholesterol metabolism, blood pressure regulation, and inflammatory responses. New technologies in the genetics field are increasing the availability of genome sequencing, and new polymorphism panels are being tested as predictive for CAD, objectifying familiarity. Advances in imaging techniques allow the assessment of coronary atherosclerosis and its composition, and these are acquiring strength in evidence and recommendations in ESC guidelines as a way to define coronary disease in low and low-to-intermediate risk patients and to guide medical therapy and interventional procedures. Use of these emerging tools to guide screening is likely to be extended, beyond high CV risk patients, to individuals with FH for early CAD and/or specific genetic profiles, as recent evidence in the literature is suggesting.
Lenarda et al. (Mon,) conducted a review in Coronary Artery Disease. Family history assessment and screening was evaluated. Family history of coronary artery disease is an established risk factor that, alongside emerging genetic and imaging tools, is increasingly utilized for cardiovascular risk stratification.