• Does cardiovascular risk and pathogenic mechanisms in CHIP vary with the gene mutated or the specific mutation? |
• Can therapeutic interventions (e.g. lifestyle modification, medications) alter cardiovascular risk in CHIP, and do so in a mutation dependent manner? |
• Should the VAF of the mutant gene in CHIP be used in clinical decision making? |
• To what degree does CHIP interact with other risk factors for cardiovascular disease, including genetic predisposition. |
• What populations can benefit for screening for CHIP? |
• At what intervals should individuals with CHIP have follow-up from a clinical effectiveness perspective? |
• What pathways prove most clinically effective for CHIP carriers with a known/prior malignancy? Should these pathways differ from patients without a cancer diagnosis? |