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cover of episode #334 - Cardiovascular disease, the number one killer: development, biomarkers, apoB, cholesterol, brain health, and more | Tom Dayspring, M.D.

#334 - Cardiovascular disease, the number one killer: development, biomarkers, apoB, cholesterol, brain health, and more | Tom Dayspring, M.D.

2025/2/3
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Tom Dayspring: 动脉粥样硬化性心血管疾病(ASCVD)是由于胆固醇沉积在动脉壁上引起的。胆固醇通过载脂蛋白B(ApoB)家族的脂蛋白颗粒运输到动脉壁。ApoB是动脉粥样硬化发展的关键指标,因为它决定了脂蛋白颗粒的数量。 测量ApoB比测量低密度脂蛋白胆固醇(LDL-C)更能有效评估心血管风险。 动脉粥样硬化是一个漫长的过程,需要几十年时间。在动脉壁中,ApoB颗粒会聚集并氧化,这会引发炎症反应,导致泡沫细胞的形成和斑块的积累。 高甘油三酯血症会加剧动脉粥样硬化,因为它会增加ApoB颗粒的浓度并促进斑块形成。 高密度脂蛋白胆固醇(HDL-C)水平不能可靠地预测心血管健康,因为HDL的功能与其胆固醇含量无关。 脑部胆固醇的代谢与身体其他部位不同。大脑自身合成大部分胆固醇,并且胆固醇在脑中的周转率很慢。 星形胶质细胞合成并向神经元提供胆固醇,而神经元则将胆固醇转化为24S-羟基胆固醇,并将其排出体外。 载脂蛋白E(ApoE)基因型会影响脑部胆固醇的代谢,ApoE4等位基因与阿尔茨海默病风险增加有关。 他汀类药物可能会影响脑部胆固醇的合成,但总体而言,它们对认知功能的影响很小。 降低甘油三酯和饱和脂肪的摄入量有助于降低ApoB水平。 Peter Attia: 动脉粥样硬化性心血管疾病是全球范围内男性和女性死亡的主要原因。 该疾病的发生是一个漫长的过程,可能从儿童时期就开始。 除了高血压、吸烟和血脂异常外,胰岛素抵抗和慢性肾脏疾病也是ASCVD的重要风险因素。 ApoB是ASCVD的一个关键因果因素,但它不是唯一因素。 降低ApoB水平是治疗ASCVD的关键目标,可以通过改变生活方式和药物治疗来实现。 血清脱氢胆固醇是脑部胆固醇合成的生物标志物,可用于评估阿尔茨海默病的风险。 他汀类药物可能对脑部胆固醇合成产生影响,但大型临床试验并未显示其会增加痴呆症的风险。 在未来几年,我们期待在ASCVD的治疗、诊断和生物标志物方面取得更多进展。

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Tom Dayspring is a world-renowned expert in clinical lipidology and a previous guest on The Drive. In this episode, Tom explores the foundations of atherosclerosis and why atherosclerotic cardiovascular disease (ASCVD) is the leading cause of death worldwide for both men and women. He examines how the disease develops from a pathological perspective and discusses key risk factors, including often-overlooked contributors such as insulin resistance and chronic kidney disease. He breaks down the complexities of cholesterol and lipoproteins—including LDL, VLDL, IDL, and HDL—with an in-depth discussion on the critical role of apolipoprotein B (apoB) in the development of atherosclerosis. Additionally, he covers the importance of testing various biomarkers, the impact of nutrition on lipid levels, and the vital role of cholesterol in brain health, including how cholesterol is synthesized and managed in the brain, how it differs from cholesterol regulation in the rest of the body, and how pharmacological interventions can influence brain cholesterol metabolism.

We discuss:

  • Defining atherosclerotic cardiovascular disease (ASCVD): development, risks, and physiological impact [2:45];
  • The pathogenesis of ASCVD: the silent development over decades, and the importance of early detection for prevention of adverse outcomes [10:45];
  • Risk factors versus risk markers for ASCVD, and how insulin resistance and chronic kidney disease contribute to atherosclerosis [17:30];
  • How hyperinsulinemia elevates cardiovascular risk [24:00];
  • How apoB-containing lipoproteins contribute to atherosclerosis, and why measuring apoB is a superior indicator of cardiovascular risk compared to LDL cholesterol [29:45];
  • The challenges of detecting early-stage atherosclerosis before calcification appears [46:15]; Lp(a): structure, genetic basis, and significant risks associated with elevated Lp(a) [55:30]; - How aging and lifestyle factors contribute to rising apoB and LDL cholesterol levels, and the lifestyle changes that can lower it [59:45];
  • How elevated triglycerides, driven by insulin resistance, increase apoB particle concentration and promote atherosclerosis [1:08:00];
  • How LDL particle size, remnant lipoproteins, Lp(a), and non-HDL cholesterol contribute to cardiovascular risk beyond apoB levels [1:21:45];
  • The limitations of using HDL cholesterol as a marker for heart health [1:29:00];
  • The critical role of cholesterol in brain function and how the brain manages its cholesterol supply [1:36:30];
  • The impact of ApoE genotype on brain health and Alzheimer's disease risk [1:46:00];
  • How the brain manages cholesterol through specialized pathways, and biomarkers to track cholesterol health of the brain [1:50:30];
  • How statins might affect brain cholesterol synthesis and cognitive function, and alternative lipid-lowering strategies for high-risk individuals [1:57:30];
  • Exciting advancements in therapeutics, diagnostics, and biomarkers coming in the next few years [2:09:30];
  • Recent consensus statements on apoB and Lp(a) from the National Lipid Association (NLA) [2:12:30]; and
  • More.

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