AHA Issues Advice on Incidentally Identified CVD Gene Variants

"The scope and use of genetic testing have expanded greatly in the past decade with the increasing ease and reduced cost of DNA sequencing," Andrew P. Landstrom, MD, PhD, chair of the scientific statement writing committee, says in a news release.

The new AHA statement is the first to focus on monogenic CVD genes which can be passed on within families, such a hypertrophic cardiomyopathy and long QT syndrome. Reevaluate the specific genetic variant periodically to ensure that the CVD link remains accurate. As knowledge about a variant evolves over time, its link to disease may be reclassified.

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