Repas Thomas B, Tanner J Ross
Regional Medical Clinic - Endocrinology, 640 Flormann St, Rapid City, SD 57701-4649.
J Am Osteopath Assoc. 2014 Feb;114(2):99-108. doi: 10.7556/jaoa.2014.023.
Familial hypercholesterolemia (FH) is an autosomal dominant disorder resulting in severe elevation of total and low-density lipoprotein cholesterol levels. There are more than 600,000 individuals in the United States with FH. Individuals with FH tend to experience premature cardiovascular disease and often die from sudden cardiac death at a young age. Statins alone or in combination with other lipid-lowering medications are effective in managing FH and preventing cardiovascular events. For patients who do not respond to or are intolerant of pharmacotherapy, low-density lipoprotein apheresis is available as a nonpharmacologic treatment option. Despite the prevalence of FH, it is undiagnosed and untreated in the majority of patients. Screening, combined with appropriate drug therapy, can save lives. The authors review the screening, diagnosis, and management of FH.
家族性高胆固醇血症(FH)是一种常染色体显性疾病,会导致总胆固醇和低密度脂蛋白胆固醇水平严重升高。美国有超过60万人患有FH。FH患者往往会过早出现心血管疾病,并且常常在年轻时死于心源性猝死。单独使用他汀类药物或与其他降脂药物联合使用,对于控制FH和预防心血管事件是有效的。对于那些对药物治疗无反应或不耐受的患者,低密度脂蛋白去除法可作为一种非药物治疗选择。尽管FH很常见,但大多数患者未被诊断和治疗。筛查加上适当的药物治疗,可以挽救生命。作者回顾了FH的筛查、诊断和管理。