Why the study?
Does CRISPR-Cas9 genome editing targeting lipid-related genes provide long-term protection against atherosclerosis?
Does CRISPR-Cas9 genome editing targeting lipid-related genes provide long-term protection against atherosclerosis?
CRISPR-Cas9 genome editing represents a potential novel therapeutic paradigm for achieving lifelong protection against atherosclerosis by permanently altering lipid-related genes.
CRISPR may enable durable lipid gene editing without lifelong dosing; leaves open its safety and efficacy for atherosclerotic disease prevention.
Although human genetics has resulted in the identification of novel lipid-related genes that can be targeted for the prevention of atherosclerotic vascular disease, medications targeting these genes or their protein products have short-term effects and require frequent administration during the course of the lifetime for maximal benefit. Genome-editing technologies, such as CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats-CRISPR-associated 9) have the potential to permanently alter genes in the body and produce long-term and even lifelong protection against atherosclerosis. In this review, we discuss recent advances in genome-editing technologies and early proof-of-concept studies of somatic in vivo genome editing in mice that highlight the potential of genome editing to target disease-related genes in patients, which would establish a novel therapeutic paradigm for atherosclerosis.
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Chadwick et al. (2017) studied this question.
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