HANDBOOK OF DYSLIPIDEMIA AND ATHEROSCLEROSIS Part One Professor Jean-Charles Fruchart Department of Atherosclerosis (Inserm UR545) Pasteur Institute of Lille University of Lille II France
The global epidemic of modern living ATHEROSCLEROSIS
Cardiovascular disease is the leading cause of death among adults worldwide (1996) Coronary disease7.2 million Cancer6.3 Cerebrovascular disease4.6 Acute lower respiratory tract infections3.9 Tuberculosis3.0 COPD (chronic obstructive pulmonary disease)2.9 Diarrhea (including dysentery)2.5 Malaria2.1 AIDS1.5 Hepatitis B1.2
Coronary mortality: alarming worldwide forecasts
Atherosclerosis: a multifactorial disease
Main risk factors for coronary heart disease
Global projections for the diabetes epidemic:
Atherosclerosis
The stages of development of atherosclerosis PATHOPHYSIOLOGY
Arterial wall: structure and function
Different stages of atherosclerotic plaque development
Vascular endothelium modification in atherosclerosis
Plaque formation 1 — Fatty streak
Plaque formation 2 — Fibrous cap
Plaque formation 3 — Lipid core
From plaque to thrombosis, key event: plaque rupture
The role of the macrophage PATHOPHYSIOLOGY
Plaque vulnerability Key role of macrophages
Vulnerable plaque Key role of the macrophage in vascular wall inflammation
Fibrinogen is an independent risk factor for atherosclerosis
Vulnerable plaque Key role of the macrophage in the degradation of the fibrous cap
Thrombus formation The macrophages release coagulation factors
Tissue factor: the initiator of coagulation and thrombogenesis in vivo
Oxidized LDL and thrombogenesis
Plaque disruption (plaque cracking, fissuring, rupture – thrombosis start point)
The role of atherogenic lipoproteins PATHOPHYSIOLOGY
Lipid core constitution Activated macrophages accumulate lipids
Lipid core constitution LDL oxidation
Parietal vascular inflammation The activated macrophage produces inflammatory cytokines
Parietal vascular inflammation NF B action in the inflammation process
The influence of risk factors PATHOPHYSIOLOGY
Diabetes and atherosclerosis
Tobacco and atherosclerosis
Dyslipidemia and atherosclerosis
HTN, hemodynamic factor and atheroclerosis
How to reduce plaque formation Intervention on risk factors
The goals of treatment PATHOPHYSIOLOGY
How to reduce the risk of plaque rupture
How to reduce the risk of thrombosis
~10% Weight loss = ~30% Visceral adipose tissue loss
Characteristics of an unstable plaque
Plaque vulnerability factors Intrinsic factors
Modification of extrinsic vulnerability factors
Plaque rupture The main releasing factors
Synthesis and transport PHYSIOLOGY OF LIPIDS AND LIPOPROTEINS
Classification of lipids and lipoproteins
Characteristics of lipoproteins
Triglyceride-rich lipoproteins: size, structure and composition
Digestion and metabolism of dietary fat
HDL metabolism and reverse cholesterol transport
Cholesterol efflux and reverse cholesterol transport is modulated by two receptors
Atherogenicity of small dense LDL
Atherogenicity PHYSIOLOGY OF LIPIDS AND LIPOPROTEINS
Size and apolipoprotein composition are the main factors determining atherogenicity of triglyceride-rich particles
Apo C-III modulates VLDL
Apo C-III in apo B particles is atherogenic
Relationship between apo C-III in apo B containing lipoproteins and atherogenicity
PROCAM Study MI-Incidence according to LDL-cholesterol and triglycerides
PROCAM Study CHD risk according to LDL-C and TG increased TG confers raised CHD risk at all levels of LDL-C
HDL: an anti-atherogenic lipoprotein
HDL metabolism: 5 key genes
HDL: apo AI-rich particles
Apo A-I protects against atherosclerosis
Apo A-II protects against atherosclerosis The human apo A-II transgenic mouse model