低密度脂蛋白胆固醇体操:探索弗里德瓦尔德、马丁-霍普金斯和桑普森公式在个性化血脂管理中的优势和局限性。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Journal of Personalized Medicine Pub Date : 2024-09-20 DOI:10.3390/jpm14091000
Ion Bogdan Mănescu, Liliana Demian, Minodora Dobreanu
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引用次数: 0

摘要

背景:低密度脂蛋白胆固醇(LDL-C)最常用的估算方法是弗里德瓦尔德方程,该方程有明显的局限性。然而,人们提出了更精确的方法。本研究调查了这些方法的优点和局限性,并确定了每种方程最适用或最不适用的情况:方法:一组 222 人接受了标准血脂轮廓评估,包括直接测量他们的低密度脂蛋白胆固醇(dLDL-C)。还使用弗里德瓦尔德方程、马丁-霍普金斯方程和桑普森方程估算了 LDL-C。结果分析了估测的 LDL-C 和测量的 LDL-C 之间的差异(%Delta)与 dLDL-C、高密度脂蛋白胆固醇(HDL-C)和甘油三酯水平的关系:与弗里德瓦尔德方程(-12.2 ± 9.2)相比,马丁-霍普金斯方程(-8.8 ± 9.8)和桑普森方程(-9.5 ± 9.2)的 Delta 百分比明显较低(p < 0.0001)。随着 dLDL-C 水平的降低,所有方程都越来越低估 LDL-C。马丁-霍普金斯方程的%Delta与dLDL-C(≤130 mg/dL)和甘油三酯呈显著正相关,与HDL-C呈显著负相关。在 30 个具有极端 %Delta 值的亚组中,观察到严重低估的模式,特别是当低密度脂蛋白胆固醇、低甘油三酯和高密度脂蛋白胆固醇同时出现时:马丁-霍普金斯方程是估算低密度脂蛋白胆固醇的优越方法,也是精准医疗的重要工具。然而,临床医生和实验室专业人员必须意识到它的局限性,并识别可能导致严重低估 LDL-C 的模式。我们提出了一种算法,供临床实验室提供个性化的低密度脂蛋白胆固醇评估。
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Low-Density Lipoprotein Cholesterol Gymnastics: Exploring the Advantages and Limitations of the Friedewald, Martin-Hopkins, and Sampson Equations for Personalized Lipid Management.

Background: The most commonly used method for low-density lipoprotein cholesterol (LDL-C) estimation is the Friedewald equation, which has notable limitations. However, more accurate methods have been proposed. This study investigates the advantages and limitations of these methods and identifies the contexts in which each equation is the most or least applicable.

Methods: A cohort of 222 individuals underwent a standard lipid profile assessment, including directly measuring their LDL-C (dLDL-C). LDL-C was also estimated using the Friedewald, Martin-Hopkins, and Sampson equations. The differences (%Delta) between the estimated and measured LDL-C were analyzed in relation to dLDL-C, high-density lipoprotein cholesterol (HDL-C), and triglyceride levels.

Results: The %Delta was significantly lower (p < 0.0001) for the Martin-Hopkins (-8.8 ± 9.8) and Sampson (-9.5 ± 9.2) equations compared to Friedewald (-12.2 ± 9.2). All equations increasingly underestimated LDL-C as the dLDL-C levels decreased. The %Delta of the Martin-Hopkins equation showed significant positive correlations with dLDL-C (≤130 mg/dL) and triglycerides and a significant negative correlation with HDL-C. In a subgroup of 30 individuals with extreme %Delta values, patterns of gross underestimation were observed, particularly when low LDL-C, low triglycerides, and high HDL-C coincided.

Conclusions: The Martin-Hopkins equation is a superior method for LDL-C estimation and a valuable tool in precision medicine. However, clinicians and laboratory professionals must be aware of its limitations and recognize patterns that could lead to significant LDL-C underestimation. We propose an algorithm for clinical laboratories to provide personalized LDL-C assessments.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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