Department of Medicine, Centre for Heart Lung Innovation, Providence Health Care, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Eur Heart J. 2024 Sep 14;45(35):3231-3250. doi: 10.1093/eurheartj/ehae417.
Familial hypercholesterolaemia (FH) is a highly prevalent monogenic disorder characterized by elevated LDL cholesterol (LDL-C) levels and premature atherosclerotic cardiovascular disease. Sex disparities in diagnosis, lipid-lowering therapy, and achieved lipid levels have emerged worldwide, resulting in barriers to care in FH. A systematic review was performed to investigate sex-related disparities in treatment, response, and lipid target achievement in FH (PROSPERO, CRD42022353297).
MEDLINE, Embase, The Cochrane library, PubMed, Scopus, PsycInfo, and grey literature databases were searched from inception to 26 April 2023. Records were eligible if they described sex differences in the treatment of adults with FH.
Of 4432 publications reviewed, 133 met our eligibility criteria. In 16 interventional clinical trials (eight randomized and eight non-randomized; 1840 participants, 49.4% females), there were no differences between males and females in response to fixed doses of lipid-lowering therapy, suggesting that sex was not a determinant of response. Meta-analysis of 25 real-world observational studies (129 441 participants, 53.4% females) found that females were less likely to be on lipid-lowering therapy compared with males (odds ratio .74, 95% confidence interval .66-.85). Importantly, females were less likely to reach an LDL-C < 2.5 mmol/L (odds ratio .85, 95% confidence interval .74-.97). Similarly, treated LDL-C levels were higher in females. Despite this, male sex was associated with a two-fold greater relative risk of major adverse cardiovascular events including myocardial infarction, atherosclerotic cardiovascular disease, and cardiovascular mortality.
Females with FH were less likely to be treated intensively and to reach guideline-recommended LDL-C targets. This sex bias represents a surmountable barrier to clinical care.
家族性高胆固醇血症(FH)是一种常见的单基因疾病,其特征是 LDL 胆固醇(LDL-C)水平升高和早发动脉粥样硬化性心血管疾病。全球范围内已出现 FH 患者在诊断、降脂治疗和血脂达标方面的性别差异,导致 FH 患者的治疗存在障碍。本系统评价旨在调查 FH 患者在治疗、反应和血脂达标方面的性别差异(PROSPERO,CRD42022353297)。
从建库至 2023 年 4 月 26 日,检索 MEDLINE、Embase、The Cochrane 图书馆、PubMed、Scopus、PsycInfo 和灰色文献数据库。如果记录描述了 FH 成年患者治疗方面的性别差异,则符合纳入标准。
在 4432 篇综述中,有 133 篇符合纳入标准。在 16 项干预性临床试验(8 项随机对照试验和 8 项非随机对照试验;1840 名参与者,49.4%为女性)中,固定剂量降脂治疗的反应在男性和女性之间没有差异,这表明性别不是反应的决定因素。对 25 项真实世界观察性研究(129441 名参与者,53.4%为女性)的荟萃分析发现,与男性相比,女性接受降脂治疗的可能性较低(比值比.74,95%置信区间.66-.85)。重要的是,女性达到 LDL-C<2.5mmol/L 的可能性较低(比值比.85,95%置信区间.74-.97)。同样,女性的 LDL-C 水平也较高。尽管如此,男性的性别与主要不良心血管事件(包括心肌梗死、动脉粥样硬化性心血管疾病和心血管死亡率)的相对风险增加两倍相关。
FH 女性患者接受强化治疗和达到指南推荐的 LDL-C 目标的可能性较低。这种性别差异是 FH 患者临床治疗的一个可克服的障碍。