Houston Methodist Academic Institute, TX.
Circulation. 2024 Aug 27;150(9):724-735. doi: 10.1161/CIRCULATIONAHA.123.067957. Epub 2024 Aug 26.
Familial hypercholesterolemia (FH) is a genetic disease that leads to elevated low-density lipoprotein cholesterol levels and risk of coronary heart disease. Current therapeutic options for FH remain relatively limited and only partially effective in both lowering low-density lipoprotein cholesterol and modifying coronary heart disease risk. The unique characteristics of nucleic acid therapies to target the underlying cause of the disease can offer solutions unachievable with conventional medications. DNA- and RNA-based therapeutics have the potential to transform the care of patients with FH. Recent advances are overcoming obstacles to clinical translation of nucleic acid-based medications, including greater stability of the formulations as well as site-specific delivery, making gene-based therapy for FH an alternative approach for treatment of FH.
家族性高胆固醇血症(FH)是一种遗传疾病,会导致低密度脂蛋白胆固醇水平升高,并增加患冠心病的风险。目前 FH 的治疗选择仍然相对有限,在降低低密度脂蛋白胆固醇和改变冠心病风险方面的效果也只是部分有效。针对疾病根本原因的核酸疗法具有独特的特点,可以提供传统药物无法实现的解决方案。基于 DNA 和 RNA 的疗法有可能改变 FH 患者的治疗方式。最近的进展克服了将核酸药物进行临床转化的障碍,包括制剂的稳定性更高以及特定部位的递药,使得 FH 的基因治疗成为 FH 治疗的一种替代方法。