Luthra Gaurav, Shahbaz Mahrukh, Almatooq Halah, Foucambert Paul, Esbrand Faith, Zafar Sana, Panthangi Venkatesh, Cyril Kurupp Adrienne R, Raju Anjumol, Khan Safeera
Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Dermatology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Cureus. 2022 Sep 8;14(9):e28930. doi: 10.7759/cureus.28930. eCollection 2022 Sep.
Patients with familial hypercholesterolemia (FH) have an increased risk of having abnormally high low-density lipoprotein cholesterol (LDL-C) levels. One of the main groups of drugs used for FH is statins. However, even with statins, most patients with FH do not achieve their pre-defined therapeutic LDL-C goals. Therefore, proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) serve to decrease LDL-C levels in that population. A total of 838 articles were found after searching the databases of PubMed, MEDLINE, and Cochrane Library. After including only full-text peer-reviewed articles published in the last 10 years, 67 articles remained. Thirteen articles were put through the Cochrane bias assessment tool to screen for bias. After a strict quality assessment based on the criteria, eight articles were extracted and included in this systematic review. The data extraction from these studies showed that alirocumab and evolocumab were efficacious in decreasing LDL-C levels and achieving the pre-defined LDL-C goals. Many parameters influenced the strength of the LDL-C reduction: sample size of the population, genetic structure of the patients affected by FH, length of the trial, or baseline lipid-lowering therapy used. Therefore, one must consider several other factors while evaluating the percent reduction of PCSK9i. This review is limited because it did not comment on these drugs' cardiovascular outcomes or mortality benefits. In addition, some of the articles used in this systematic review have small sample sizes and short trial times, limiting the long-term evaluation of these drugs.
家族性高胆固醇血症(FH)患者出现低密度脂蛋白胆固醇(LDL-C)水平异常升高的风险增加。用于FH的主要药物类别之一是他汀类药物。然而,即便使用了他汀类药物,大多数FH患者仍未达到预先设定的LDL-C治疗目标。因此,前蛋白转化酶枯草溶菌素/克新9型抑制剂(PCSK9i)有助于降低该人群的LDL-C水平。在检索PubMed、MEDLINE和Cochrane图书馆数据库后,共找到838篇文章。仅纳入过去10年发表的全文同行评审文章后,还剩下67篇。13篇文章通过Cochrane偏倚评估工具进行偏倚筛查。根据标准进行严格的质量评估后,提取了8篇文章并纳入本系统评价。这些研究的数据提取表明,阿利西尤单抗和依洛尤单抗在降低LDL-C水平和实现预先设定的LDL-C目标方面是有效的。许多参数影响LDL-C降低的强度:人群样本量、受FH影响患者的基因结构、试验时长或使用的基线降脂治疗。因此,在评估PCSK9i的降低百分比时,必须考虑其他几个因素。本综述存在局限性,因为它未对这些药物的心血管结局或死亡率获益进行评论。此外,本系统评价中使用的一些文章样本量小且试验时间短,限制了对这些药物的长期评估。