Second Department of Cardiology, University General Hospital Attikon, Athens, Greece.
Second Department of Cardiology, University General Hospital Attikon, Athens, Greece.
J Clin Lipidol. 2019 May-Jun;13(3):502-508. doi: 10.1016/j.jacl.2019.02.007. Epub 2019 Mar 11.
Heterozygous familial hypercholesterolemia (HeFH) and combined hyperlipidemia (CHL) phenotype are associated with premature myocardial infarction (MI).
To assess the prevalence of HeFH and CHL phenotype among young survivors of MI and compare patients' characteristics with these 2 lipid disorders.
We recruited 382 young survivors of MI (≤40 years). Fasting lipids, lipoprotein(a) [Lp(a)], apolipoprotein A-1, and apolipoprotein B (apoB) levels were determined. Using the Dutch Lipid Clinic Network (DLCN) algorithm, patients having definite or probable HeFH were identified. Patients with apoB levels >120 mg/dL and triglyceride levels >170 mg/dL (1.92 mmol/L) [>90th percentile of 326 age and sex-matched healthy controls] were classified as having CHL phenotype. Common carotid artery intima-media thickness (CCA-IMT) was measured by B-mode ultrasonography.
Eighty-one patients (21.2%) had definite/probable HeFH and 62 (16.2%) had CHL phenotype. Twenty-three patients fulfilled the criteria for both HeFH and CHL phenotype and were removed from further comparisons. Patients with HeFH (n = 58) had higher levels of total cholesterol, low-density lipoprotein (LDL)-cholesterol, Lp(a), and apoB, whereas patients with CHL phenotype (n = 39) had higher levels of triglycerides and lower high-density lipoprotein (HDL)-cholesterol levels. The prevalence of metabolic syndrome was higher in patients with CHL phenotype compared to those with HeFH (67.0% vs 16.4%, P < .001). Patients with HeFH had more extensive coronary artery disease (3-vessel disease: 36.2% vs 12.8%, P = .011) and greater right CCA-IMT (0.67 ± 0.11 mm vs 0.56 ± 0.09 mm, P < .001) and left CCA-IMT (0.68 ± 0.10 mm vs 0.56 ± 0.08 mm, P < .001) compared to CHL phenotype patients.
Both HeFH and CHL phenotype are common among patients with premature MI. CHL phenotype compared to HeFH is associated with less atheromatous burden in coronary and carotid arteries at the time of first MI.
杂合子家族性高胆固醇血症(HeFH)和混合性高脂血症(CHL)表型与早发性心肌梗死(MI)有关。
评估年轻 MI 幸存者中 HeFH 和 CHL 表型的患病率,并比较患者的特征与这两种脂质紊乱。
我们招募了 382 名≤40 岁的年轻 MI 幸存者。测定空腹血脂、脂蛋白(a)[Lp(a)]、载脂蛋白 A-1 和载脂蛋白 B(apoB)水平。使用荷兰血脂诊所网络(DLCN)算法,确定具有明确或可能 HeFH 的患者。apoB 水平>120mg/dL 和甘油三酯水平>170mg/dL(1.92mmol/L)[超过 326 名年龄和性别匹配的健康对照者的第 90 百分位数]的患者被归类为 CHL 表型。通过 B 型超声测量颈总动脉内膜-中层厚度(CCA-IMT)。
81 名患者(21.2%)具有明确/可能的 HeFH,62 名患者(16.2%)具有 CHL 表型。23 名患者同时符合 HeFH 和 CHL 表型标准,被排除在进一步比较之外。HeFH 患者(n=58)总胆固醇、低密度脂蛋白(LDL)-胆固醇、Lp(a)和 apoB 水平较高,而 CHL 表型患者(n=39)甘油三酯水平较高,高密度脂蛋白(HDL)-胆固醇水平较低。与 HeFH 患者相比,CHL 表型患者代谢综合征的患病率更高(67.0%比 16.4%,P<.001)。HeFH 患者的冠状动脉疾病更为广泛(3 支血管病变:36.2%比 12.8%,P=.011),右颈总动脉 IMT 更大(0.67±0.11mm 比 0.56±0.09mm,P<.001),左颈总动脉 IMT 更大(0.68±0.10mm 比 0.56±0.08mm,P<.001)。
早发性 MI 患者中 HeFH 和 CHL 表型均很常见。与 HeFH 相比,CHL 表型在首次 MI 时与冠状动脉和颈动脉的动脉粥样硬化负担较轻相关。