Clinical and genetic diagnosis of familial hypercholesterolaemia in patients undergoing coronary angiography: the Ludwigshafen Risk and Cardiovascular Health Study.

IF 4.8 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Stefan Molnar, Hubert Scharnagl, Graciela E Delgado, Bernhard K Krämer, Ulrich Laufs, Winfried März, Marcus E Kleber, Julius L Katzmann
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引用次数: 0

Abstract

Aims: To investigate the prevalence of familial hypercholesterolaemia (FH) and compare the performance of clinical criteria and genetic testing in patients undergoing coronary angiography.

Methods and results: The prevalence of FH was determined with the Dutch Lipid Clinical Network (DLCN), US 'Make Early Diagnosis to Prevent Early Death' (US-MEDPED), Simon Broome (SB) criteria, the 'familial hypercholesterolaemia case ascertainment tool' (FAMCAT), and a clinical algorithm. Genetic screening was conducted with a custom array from Affymetrix (CARRENAL array) harbouring 944 FH mutations.The study cohort consisted of 3267 patients [78.6% with coronary artery disease (CAD)]. FH was diagnosed in 2.8%, 2.2%, 3.9%, and 7.9% using the DLCN, US-MEDPED, SB criteria, and the FAMCAT. The clinical algorithm identified the same patients as the SB criteria. Pathogenic FH mutations were found in 1.2% (1.2% in patients with CAD, 1.0% in patients without CAD). FH was more frequently diagnosed in younger patients. With genetic testing as reference, the clinical criteria achieved areas under the ROC curve [area under the curves (AUCs)] in the range of 0.56-0.68. Using only low-density lipoprotein cholesterol (LDL-C) corrected for statin intake, an AUC of 0.68 was achieved.

Conclusion: FH is up to four-fold more prevalent in patients undergoing coronary angiography than in contemporary cohorts representing the general population. Different clinical criteria yield substantially different diagnosis rates, overestimating the prevalence of FH compared with genetic testing. LDL-C testing alone may be sufficient to raise the suspicion of FH, which then needs to be corroborated by genetic testing.

Lay summary: In this study, we investigated the frequency of familial hypercholesterolaemia-a common genetic condition leading to markedly elevated low-density lipoprotein (LDL) cholesterol and increased risk of atherosclerosis-in 3267 patients undergoing coronary angiography according to commonly used diagnostic scoring systems and genetic testing.

冠状动脉造影术患者家族性高胆固醇血症的临床和基因诊断:路德维希港风险和心血管健康研究。
目的:研究家族性高胆固醇血症(FH)的患病率,并比较临床标准和基因检测在冠状动脉造影患者中的应用效果:根据荷兰血脂临床网络(DLCN)、US-MEDPED、Simon Broome(SB)标准、"家族性高胆固醇血症病例确定工具"(FAMCAT)和临床算法确定家族性高胆固醇血症的患病率。利用Affymetrix公司的定制阵列(CARRENAL阵列)对944个FH基因突变进行了基因筛查:研究队列包括 3267 名患者(78.6% 患有冠状动脉疾病 [CAD])。使用 DLCN、US-MEDPED、SB 标准和 FAMCAT 诊断出 FH 的比例分别为 2.8%、2.2%、3.9% 和 7.9%。临床算法确定的患者与 SB 标准确定的患者相同。在 1.2% 的患者中发现了致病性 FH 基因突变(1.2% 的患者患有 CAD,1.0% 的患者未患有 CAD)。年轻患者更常被诊断为 FH。以基因检测为参考,临床标准的 ROC 曲线下面积(AUC)在 0.56-0.68 之间。仅使用根据他汀类药物摄入量校正的低密度脂蛋白胆固醇,其AUC为0.68:结论:在接受冠状动脉造影术的患者中,FH 的发病率比代表普通人群的现代队列高出四倍。与基因检测相比,不同的临床标准得出的诊断率大相径庭,高估了 FH 的患病率。仅低密度脂蛋白胆固醇检测可能就足以引起对 FH 的怀疑,然后还需要通过基因检测加以证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.40
自引率
3.80%
发文量
76
期刊介绍: European Heart Journal - Quality of Care & Clinical Outcomes is an English language, peer-reviewed journal dedicated to publishing cardiovascular outcomes research. It serves as an official journal of the European Society of Cardiology and maintains a close alliance with the European Heart Health Institute. The journal disseminates original research and topical reviews contributed by health scientists globally, with a focus on the quality of care and its impact on cardiovascular outcomes at the hospital, national, and international levels. It provides a platform for presenting the most outstanding cardiovascular outcomes research to influence cardiovascular public health policy on a global scale. Additionally, the journal aims to motivate young investigators and foster the growth of the outcomes research community.
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