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脂质测量在心血管疾病管理中的应用:实用建议——国家脂质协会写作组的科学声明。

Lipid measurements in the management of cardiovascular diseases: Practical recommendations a scientific statement from the national lipid association writing group.

机构信息

Emory University School of Medicine, Atlanta, GA, United States; Atlanta Veterans Affairs Medical Center, Atlanta, GA, United States.

Emory University School of Medicine, Atlanta, GA, United States.

出版信息

J Clin Lipidol. 2021 Sep-Oct;15(5):629-648. doi: 10.1016/j.jacl.2021.09.046. Epub 2021 Sep 24.

DOI:10.1016/j.jacl.2021.09.046
PMID:34802986
Abstract

Lipoprotein measurements are pivotal in the management of patients at risk for atherosclerotic coronary heart disease (CHD) with myocardial infarction and coronary death as the main outcomes, and for atherosclerotic cardiovascular disease (ASCVD), which includes CHD and stroke. Recent developments and changes in guidelines affect optimization of using lipid measures as cardiovascular biomarkers. This scientific statement reviews the pre-analytical, analytical, post-analytical, and clinical aspects of lipoprotein measurements. Highlights include the following: i) It is acceptable to screen with nonfasting lipids. ii) non-high-density lipoprotein HDL-cholesterol (non-HDL-C) is measured reliably in either the fasting or the nonfasting state and can effectively guide ASCVD prevention. iii) low density lipoprotein cholesterol (LDL-C) can be estimated from total cholesterol, high density lipoprotein cholesterol (HDL-C), and triglyceride (TG) measurements. For patients with LDL-C>100 mg/dL and TG ≤150 mg/dL it is reasonable to use the Friedewald formula. However, for those with TG 150-400 mg/dL the Friedewald formula for LDL-C estimation is less accurate. The Martin/Hopkins method is recommended for LDL-C estimation throughout the range of LDL-C levels and up to TG levels of 399 mg/dL. For TG levels ≥400 mg/dL LDL-C estimating equations are currently not recommended and newer methods are being evaluated. iv) When LDL-C or TG screening results are abnormal the clinician should consider obtaining fasting lipids. v) Advanced lipoprotein tests using apolipoprotein B (apoB), LDL Particle Number (LDL-P) or remnant cholesterol may help to guide therapeutic decisions in select patients, but data are limited for patients already on lipid lowering therapy with low LDL-C levels. Better harmonization of advanced lipid measurement methods is needed. Lipid measurements are recommended 4-12 weeks after a change in lipid treatment. Lipid laboratory reports should denote desirable values and specifically identify extremely elevated LDL-C levels (≥190 mg/dL at any age or ≥160 mg/dL in children) as severe hypercholesterolemia. Potentially actionable abnormal lipid test results, including fasting triglycerides (TG) ≥500 mg/dL, should be reported as hypertriglyceridemia. Appropriate use and reporting of lipid tests should improve their utility in the management of persons at high risk for ASCVD events.

摘要

脂蛋白测量在管理有发生动脉粥样硬化性冠心病(CHD)风险的患者中至关重要,这些患者的主要结局是心肌梗死和冠状动脉死亡,以及发生动脉粥样硬化性心血管疾病(ASCVD),其包括 CHD 和中风。最近的指南发展和变化影响了脂质测量作为心血管生物标志物的优化使用。本科学声明审查了脂蛋白测量的分析前、分析中、分析后和临床方面。重点包括以下内容:i)用非空腹脂质进行筛查是可以接受的。ii)非高密度脂蛋白胆固醇(非 HDL-C)在空腹或非空腹状态下均可可靠测量,并能有效指导 ASCVD 预防。iii)低密度脂蛋白胆固醇(LDL-C)可通过总胆固醇、高密度脂蛋白胆固醇(HDL-C)和甘油三酯(TG)测量值估算。对于 LDL-C>100mg/dL 和 TG≤150mg/dL 的患者,使用 Friedewald 公式估算 LDL-C 是合理的。然而,对于 TG 150-400mg/dL 的患者,Friedewald 公式估算 LDL-C 的准确性较低。建议在 LDL-C 水平范围内和 TG 水平高达 399mg/dL 时使用 Martin/Hopkins 方法估算 LDL-C。对于 TG 水平≥400mg/dL,目前不建议使用 LDL-C 估算方程,正在评估新方法。iv)当 LDL-C 或 TG 筛查结果异常时,临床医生应考虑进行空腹脂质检测。v)使用载脂蛋白 B(apoB)、低密度脂蛋白颗粒数(LDL-P)或残余胆固醇的先进脂蛋白检测可能有助于指导特定患者的治疗决策,但对于已经接受降脂治疗且 LDL-C 水平较低的患者,数据有限。需要更好地协调先进的脂质测量方法。建议在改变脂质治疗后 4-12 周进行脂质检测。脂质实验室报告应注明理想值,并特别识别出极高的 LDL-C 水平(任何年龄≥190mg/dL 或儿童≥160mg/dL),作为严重高胆固醇血症。应将异常脂质检测结果(包括空腹甘油三酯(TG)≥500mg/dL)报告为高甘油三酯血症。适当使用和报告脂质检测结果可提高其在管理 ASCVD 高危人群中的效用。

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