EM2210G "From Reading the Genome for Risk to Rewriting it for Cardiovascular Health" (IM GR 102822)
Purpose and Overview
Atherosclerotic cardiovascular disease (ASCVD) is a heritable, common, complex disease and the leading cause of death in the world. Dr. Kathiresan will review progress in our understanding of the inherited basis for risk as well resistance to ASCVD. He will then turn to approaches to “rewrite” the genome using gene editing to treat ASCVD.
Target Audience
UT Southwestern faculty, fellows, residents and medical students, community physicians, nurse clinicians, physician assistants and nurses.
Learning Objectives
At the conclusion of this activity, the participant should be able to:
- To understand the two major genetic models for myocardial infarction risk – monogenic and polygenic.
- To describe how natural resistance mutations lower plasma apoB-containing lipoproteins lifelong in some people and lead to protection against atherosclerotic cardiovascular disease.
- To understand the development of a new class of medicines, which can edit the genome in an adult and potentially lead to permanent lowering of LDL cholesterol after a single dose.
Sekar Kathiresan, M.D.
Co-Founder and CEO
Verve Therapeutics
Available Credit
- 1.00 AMA
- 1.00 Attendance
Price
Required Hardware/software
Activities should be run with recent versions of common browsers, including Internet Explorer, Firefox and Google Chrome

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