Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA; University of Wisconsin Cardiovascular Research Center, 8503 Wisconsin Institutes for Medical Research, Madison, WI, USA.
Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
J Clin Lipidol. 2018 Nov-Dec;12(6):1445-1451. doi: 10.1016/j.jacl.2018.07.014. Epub 2018 Jul 31.
BACKGROUND: Low-density lipoprotein cholesterol (LDL-C) level and lipoprotein(a) [Lp(a)] ≥ 50 mg/dL predict atherosclerotic cardiovascular disease (ASCVD) risk in adults with familial hypercholesterolemia (FH), but their role for children with FH is less clear. OBJECTIVE: This study examined the relationship between elevated Lp(a) and LDL-C levels in a pediatric population with FH and onset of ASCVD in family members. METHODS: Retrospective review of pediatric patients with FH identified LDL-C, Lp(a), and family history of ASCVD. Logistic regression modeling evaluated the association between the child's Lp(a) and peak LDL-C level with earliest age of ASCVD onset in their family. RESULTS: One hundred twenty-nine children from 109 families were identified. Children from families with early-onset ASCVD were 3 times more likely to have high Lp(a) than those with a family history of late-onset ASCVD (OR: 3.77, 95% CI: 1.16-12.25, P = .027) but were not more likely to have highly elevated peak LDL-C (≥190 mg/dL) (OR: 0.45, 95% CI: 0.11-1.80, P = .26). CONCLUSION: Children with FH and family history of early-onset ASCVD were more likely to have Lp(a) ≥50 mg/dL than children with FH and family history of late-onset ASCVD. Family history of early-onset ASCVD was more predictive of a child's Lp(a) level than of a child's peak LDL-C. Measurement of Lp(a) in children with FH may better characterize their cardiovascular risk, particularly when knowledge of family history is limited. Lp(a) testing may also identify children with FH that could benefit from more aggressive management to reduce ASCVD risk.
背景:低密度脂蛋白胆固醇(LDL-C)水平和脂蛋白(a)[Lp(a)]≥50mg/dL 可预测家族性高胆固醇血症(FH)成人的动脉粥样硬化性心血管疾病(ASCVD)风险,但它们在 FH 儿童中的作用尚不清楚。 目的:本研究探讨了 FH 儿科人群中升高的 Lp(a) 与 LDL-C 水平与家族 ASCVD 发病之间的关系。 方法:回顾性分析 FH 患儿的 LDL-C、Lp(a) 和 ASCVD 家族史。Logistic 回归模型评估了患儿的 Lp(a)与 LDL-C 峰值与家族 ASCVD 发病最早年龄之间的相关性。 结果:共确定了 109 个家族的 129 名儿童。与家族 ASCVD 发病晚的患儿相比,家族 ASCVD 发病早的患儿 Lp(a) 更高的可能性是其三倍(OR:3.77,95%CI:1.16-12.25,P=0.027),但高度升高的 LDL-C 峰值(≥190mg/dL)的可能性并不更高(OR:0.45,95%CI:0.11-1.80,P=0.26)。 结论:FH 患儿且家族 ASCVD 发病早的患儿比 FH 患儿且家族 ASCVD 发病晚的患儿更有可能出现 Lp(a)≥50mg/dL。家族 ASCVD 发病早史比患儿的 LDL-C 峰值更能预测患儿的 Lp(a)水平。在家族史知识有限的情况下,FH 患儿的 Lp(a)测量可能更能反映其心血管风险。Lp(a)检测还可以识别出 FH 患儿,他们可能受益于更积极的管理,以降低 ASCVD 风险。
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