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Book Details
Abstract
This issue of Cardiology Clinics, edited by Dr. Stephen Nicholls, focuses on Lipidology. Topics include, but are not limited to: Impact of lipoproteins on atherobiology; Lessons from genomic studies; Lipids and lipoproteins in risk prediction; Optimizing statins and ezetimibe in guideline focused management; Statin intolerance; Lipid lowering agents and diabetes risk; PCSK9 inhibitors; Bempedoic Acid; Triglyceride rich lipoproteins; Omega 3 Fatty Acids; Lipoprotein; CETP inhibitors; HDL infusions; and Targeting HDL functionality.
Table of Contents
Section Title | Page | Action | Price |
---|---|---|---|
Front Cover | Cover | ||
Lipidology\r | i | ||
Copyright\r | ii | ||
Contributors | iii | ||
EDITORIAL BOARD | iii | ||
EDITOR | iii | ||
AUTHORS | iii | ||
Contents | vii | ||
Preface: Lipidology | vii | ||
Impact of Lipoproteins on Atherobiology: Emerging Insights | vii | ||
Causal Effect of Lipids and Lipoproteins on Atherosclerosis: Lessons from Genomic Studies | vii | ||
Lipids and Lipoproteins in Risk Prediction | vii | ||
Optimizing Statins and Ezetimibe in Guideline-Focused Management | vii | ||
Statin Intolerance: Some Practical Hints | viii | ||
Treating Dyslipidemia in Type 2 Diabetes | viii | ||
Proprotein Convertase Subtilisin Kexin 9 Inhibitors | viii | ||
Bempedoic Acid (ETC-1002): A Current Review | viii | ||
Triglyceride-Rich Lipoproteins | ix | ||
Evolution of Omega-3 Fatty Acid Therapy and Current and Future Role in the Management of Dyslipidemia | ix | ||
Is Lipoprotein(a) Ready for Prime-Time Use in the Clinic? | ix | ||
Cholesteryl Ester Transfer Protein Inhibitors as Agents to Reduce Coronary Heart Disease Risk | ix | ||
High-Density Lipoprotein Infusions | ix | ||
High-Density Lipoproteins: Effects on Vascular Function and Role in the Immune Response | x | ||
Intravascular Ultrasound Studies of Plaque Progression and Regression: Impact of Lipid-Modifying Therapies | x | ||
CARDIOLOGY CLINICS\r | xi | ||
FORTHCOMING ISSUES | xi | ||
August 2018 | xi | ||
November 2018 | xi | ||
RECENT ISSUES | xi | ||
February 2018 | xi | ||
November 2017 | xi | ||
Preface:\rLipidology | xiii | ||
Impact of Lipoproteins on Atherobiology | 193 | ||
Key points | 193 | ||
INTRODUCTION | 193 | ||
FOCUS ON THE ATHEROBIOLOGY OF APOLIPOPROTEIN B–CONTAINING LIPOPROTEINS | 194 | ||
LIPOPROTEINS | 195 | ||
BIOLOGICAL ACTIVITIES OF HIGH-DENSITY LIPOPROTEIN RELEVANT TO PROTECTION OF THE ENDOTHELIUM AND ARTERIAL WALL | 196 | ||
INTERRELATIONSHIPS BETWEEN THE BIOLOGICAL ACTIVITIES AND INTRAVASCULAR METABOLISM OF HIGH-DENSITY LIPOPROTEIN | 196 | ||
PROTEINS AND LIPIDS IN HIGH-DENSITY LIPOPROTEIN ASSOCIATED WITH ATHEROPROTECTIVE ACTIVITIES | 197 | ||
DEFECTIVE HIGH-DENSITY LIPOPROTEIN BIOLOGICAL ACTIVITIES IN DYSLIPIDEMIAS ASSOCIATED WITH PREMATURE ATHEROSCLEROTIC CARDIOV ... | 197 | ||
WHICH FACTORS CAN UNDERLIE SUBNORMAL OR ELEVATED LEVELS OF HIGH-DENSITY LIPOPROTEIN CHOLESTEROL? | 198 | ||
SUMMARY | 198 | ||
REFERENCES | 199 | ||
Causal Effect of Lipids and Lipoproteins on Atherosclerosis | 203 | ||
Key points | 203 | ||
INTRODUCTION | 203 | ||
MENDELIAN RANDOMIZATION | 204 | ||
LOW-DENSITY LIPOPROTEIN CHOLESTEROL | 204 | ||
What is the Causal Effect of Lowering Low-Density Lipoprotein Cholesterol by Inhibiting HMG-CoA Reductase? | 205 | ||
What is the Causal Effect of Lowering Low-Density Lipoprotein Cholesterol by Inhibiting NPC1L1? | 205 | ||
What is the Causal Effect of Lowering Low-Density Lipoprotein Cholesterol by Inhibiting PCSK9? | 206 | ||
Does the Mechanism of Lowering Low-Density Lipoprotein Cholesterol Matter? | 206 | ||
Is Atherosclerosis Caused by Low-Density Lipoprotein Cholesterol or Low-Density Lipoprotein Particles? | 207 | ||
TRIGLYCERIDE-RICH VERY LOW-DENSITY LIPOPROTEINS AND THEIR REMNANTS | 207 | ||
HIGH-DENSITY LIPOPROTEINS | 208 | ||
LIPOPROTEIN(A) | 209 | ||
SUMMARY | 210 | ||
REFERENCES | 210 | ||
Lipids and Lipoproteins in Risk Prediction | 213 | ||
Key points | 213 | ||
INTRODUCTION | 213 | ||
TRADITIONAL LIPID RISK FACTORS | 215 | ||
Non–High-Density Lipoprotein Cholesterol | 215 | ||
Triglycerides | 215 | ||
High-Density Lipoprotein Cholesterol | 216 | ||
Total Cholesterol to High-Density Lipoprotein Cholesterol Ratio | 216 | ||
EMERGING RISK FACTORS | 216 | ||
Apolipoproteins | 216 | ||
Lipoprotein(a) | 217 | ||
Lipoprotein Particles | 217 | ||
SUMMARY | 217 | ||
REFERENCES | 218 | ||
Optimizing Statins and Ezetimibe in Guideline-Focused Management | 221 | ||
Key points | 221 | ||
INTRODUCTION | 221 | ||
DISCUSSION | 222 | ||
SUMMARY | 223 | ||
REFERENCES | 223 | ||
Statin Intolerance | 225 | ||
Key points | 225 | ||
DEFINITION AND PREVALENCE | 225 | ||
SYMPTOMS AND CAUSALITY | 226 | ||
FOUR-STEP DIAGNOSIS | 227 | ||
TREATMENT CHALLENGES | 228 | ||
SUMMARY | 229 | ||
REFERENCES | 229 | ||
Treating Dyslipidemia in Type 2 Diabetes | 233 | ||
Key points | 233 | ||
INTRODUCTION | 233 | ||
DYSLIPIDEMIA IN DIABETES | 233 | ||
STATINS AND DIABETES | 234 | ||
ADDITIONAL LOW-DENSITY LIPOPROTEIN CHOLESTEROL-LOWERING AGENTS AND DIABETES | 234 | ||
FIBRIC ACID DERIVATIVES | 235 | ||
ADDITIONAL TRIGLYCERIDE-LOWERING STRATEGIES | 235 | ||
HIGH-DENSITY LIPOPROTEIN TARGETED THERAPIES | 236 | ||
SUMMARY | 236 | ||
REFERENCES | 236 | ||
Proprotein Convertase Subtilisin Kexin 9 Inhibitors | 241 | ||
Key points | 241 | ||
INTRODUCTION | 241 | ||
PROPROTEIN CONVERTASE SUBTILISIN KEXIN 9 | 242 | ||
CLINICAL STUDIES ON EVOLOCUMAB AND ALIROCUMAB | 242 | ||
Evolocumab | 243 | ||
Alirocumab | 247 | ||
OTHER MONOCLONAL ANTIBODIES TO PROPROTEIN CONVERTASE SUBTILISIN KEXIN 9 | 251 | ||
Bococizumab | 251 | ||
LY3015014 | 251 | ||
NEW APPROACHES FOR THE INHIBITION OF PROPROTEIN CONVERTASE SUBTILISIN KEXIN 9 | 252 | ||
Adnectins | 252 | ||
Inclisiran | 252 | ||
Anti–Proprotein Convertase Subtilisin Kexin 9 Vaccines | 252 | ||
SUMMARY | 253 | ||
REFERENCES | 253 | ||
Bempedoic Acid (ETC-1002) | 257 | ||
Key points | 257 | ||
INTRODUCTION | 257 | ||
MECHANISM OF ACTION | 258 | ||
POTENTIAL MECHANISM OF LOWERING MYOTOXICITY AND ATHEROSCLEROSIS | 259 | ||
GENETIC DATA ON ATP CITRATE LYASE INHIBITION | 259 | ||
PHASE 1 AND 2 STUDIES | 259 | ||
PHASE 3 STUDIES | 261 | ||
SUMMARY | 262 | ||
REFERENCES | 262 | ||
Triglyceride-Rich Lipoproteins | 265 | ||
Key points | 265 | ||
INTRODUCTION | 265 | ||
TRIGLYCERIDE METABOLISM | 265 | ||
CAUSES OF HYPERTRIGLYCERIDEMIA | 266 | ||
APPROACH TO THE CONVENTIONAL TREATMENT OF ELEVATED TRIGLYCERIDES | 267 | ||
OTHER AND NOVEL THERAPIES TARGETING ELEVATED TRIGLYCERIDES | 268 | ||
Triglycerides Production | 268 | ||
TARGETING CLEARANCE OF TRIGLYCERIDE-RICH LIPOPROTEINS | 270 | ||
Lipoprotein Lipase | 270 | ||
ApolipoproteinCII | 270 | ||
ApolipoproteinAV | 271 | ||
ApolipoproteinCIII | 271 | ||
Angiopoietin-Like Proteins | 271 | ||
Glycosylphosphatidylinositol-Anchored High-Density Lipoprotein Binding Protein-1 | 272 | ||
Lipase Maturation Factor-1 | 272 | ||
SUMMARY | 272 | ||
REFERENCES | 272 | ||
Evolution of Omega-3 Fatty Acid Therapy and Current and Future Role in the Management of Dyslipidemia | 277 | ||
Key points | 277 | ||
INTRODUCTION | 277 | ||
AVAILABLE OMEGA-3 FATTY ACID FORMULATIONS | 278 | ||
OMEGA-3 FATTY ACIDS’ BENEFITS AND MECHANISM OF ACTION | 278 | ||
DYSLIPIDEMIA SUBGROUPS WITH THE GREATEST ANTICIPATED BENEFIT | 280 | ||
RESIDUAL RISK DESPITE STATIN THERAPY | 280 | ||
CURRENT AND FUTURE ROLE OF OMEGA-3 FATTY ACID THERAPY | 280 | ||
RISKS OF OMEGA-3 FATTY ACID THERAPY | 282 | ||
SUMMARY | 282 | ||
REFERENCES | 283 | ||
Is Lipoprotein(a) Ready for Prime-Time Use in the Clinic? | 287 | ||
Key points | 287 | ||
INTRODUCTION | 287 | ||
BIOLOGY AND EPIDEMIOLOGY OF LIPOPROTEIN(A) | 287 | ||
CAUSAL ROLE OF LIPOPROTEIN(A) IN ATHEROSCLEROTIC CARDIOVASCULAR DISEASE | 289 | ||
THERAPEUTIC LOWERING OF LIPOPROTEIN(A): TOWARD WIDER CLINICAL USE OR CLINICAL TRIALS? | 289 | ||
Niacin, Aspirin, and Estrogen | 290 | ||
Lipoprotein Apheresis | 290 | ||
Newer Therapies, Nonspecific Lowering of Lipoprotein(a): Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors, Mipomers ... | 290 | ||
Proprotein convertase subtilisin/kexin type 9 inhibitors | 290 | ||
Mipomersen | 291 | ||
Microsomal triglyceride transfer protein inhibitors | 291 | ||
Cholesteryl ester transfer protein inhibitors | 291 | ||
Others agents: thyromimetics, interleukin-6 receptor monoclonal antibodies, and farnesoid X receptor agonists | 291 | ||
Selective lowering of lipoprotein(a): apolipoprotein(a) antisense and silencing agents | 292 | ||
PRACTICAL CONSIDERATIONS FOR A FUTURE MODEL OF CARE | 292 | ||
International Guidelines: Is There Consensus and How Strong Is the Evidence? | 292 | ||
Detection: Targeted and Systematic Screening | 292 | ||
Analytical caveats: a thorny issue | 292 | ||
Risk Assessment: Toward Precision Medicine | 294 | ||
Lifestyle and Pharmacotherapy: Is It All About Low-Density Lipoprotein Cholesterol? | 294 | ||
SUMMARY: PRIME-TIME USE? | 295 | ||
REFERENCES | 296 | ||
Cholesteryl Ester Transfer Protein Inhibitors as Agents to Reduce Coronary Heart Disease Risk | 299 | ||
Key points | 299 | ||
INTRODUCTION | 299 | ||
WHAT IS CHOLESTERYL ESTER TRANSFER PROTEIN, AND WHAT DOES IT DO? | 299 | ||
EFFECTS OF CHOLESTERYL ESTER TRANSFER PROTEIN ON PLASMA LIPOPROTEINS | 300 | ||
IMPACT OF CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY ON ATHEROSCLEROTIC CARDIOVASCULAR DISEASE | 301 | ||
Studies in Animals | 301 | ||
Genetic Studies in People | 302 | ||
EFFECT OF CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITORS IN HUMAN CLINICAL TRIALS | 302 | ||
Torcetrapib | 302 | ||
Dalcetrapib | 303 | ||
Evacetrapib | 303 | ||
Anacetrapib | 304 | ||
TA-8995 (AMG-8995) | 307 | ||
REASONS FOR THE CONFLICTING RESULTS IN HUMAN CLINICAL OUTCOME TRIALS OF CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITORS | 307 | ||
Harm Caused by Torcetrapib | 307 | ||
No Reduction in Cardiovascular Events with Dalcetrapib | 307 | ||
No Reduction in Cardiovascular Events with Evacetrapib | 307 | ||
EFFECT OF CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITION ON THE RISK OF DEVELOPING DIABETES | 307 | ||
SUMMARY | 308 | ||
REFERENCES | 308 | ||
High-Density Lipoprotein Infusions | 311 | ||
Key points | 311 | ||
INTRODUCTION | 311 | ||
HIGH-DENSITY LIPOPROTEIN AND PROTECTION | 311 | ||
HIGH-DENSITY LIPOPROTEIN EFFECTS OF EXISTING LIPID THERAPIES | 312 | ||
APOA-I MILANO | 312 | ||
CER | 312 | ||
CSL | 313 | ||
IMPLICATIONS OF THESE FINDINGS | 313 | ||
SUMMARY | 313 | ||
REFERENCES | 313 | ||
High-Density Lipoproteins | 317 | ||
Key points | 317 | ||
HIGH-DENSITY LIPOPROTEIN CHOLESTEROL HYPOTHESIS | 317 | ||
POTENTIAL ATHEROPROTECTIVE EFFECTS OF HIGH-DENSITY LIPOPROTEIN IN ENDOTHELIAL CELLS | 317 | ||
POTENTIAL REGULATORY FUNCTIONS OF HIGH-DENSITY LIPOPROTEIN IN INFECTION CONTROL AND (AUTO-) IMMUNE DISORDERS | 318 | ||
REGULATORY PROPERTIES OF HIGH-DENSITY LIPOPROTEIN IN INNATE AND ADAPTIVE IMMUNITY: THE ROLE OF LIPID RAFTS | 318 | ||
HIGH-DENSITY LIPOPROTEIN CHOLESTEROL AS THERAPEUTIC TARGET: RESULTS FROM RANDOMIZED, CONTROLLED CLINICAL TRIALS | 319 | ||
DYSFUNCTIONAL HIGH-DENSITY LIPOPROTEIN IN PATIENTS WITH CARDIOVASCULAR DISEASE | 321 | ||
ALTERATION AND MODIFICATION OF HIGH-DENSITY LIPOPROTEIN PROTEIN CARGO: A DETERMINANT OF ITS FUNCTIONAL VASCULAR PROPERTIES | 322 | ||
ALTERED PROPERTIES OF HIGH-DENSITY LIPOPROTEIN UNDER INFLAMMATORY CONDITIONS | 322 | ||
THE SHIFT IN HIGH-DENSITY LIPOPROTEIN FUNCTION IS LINKED TO INFLAMMATORY PATHWAYS | 322 | ||
MODIFICATIONS OF HIGH-DENSITY LIPOPROTEIN CONTRIBUTING TO THE SHIFT IN HIGH-DENSITY LIPOPROTEIN FUNCTION IN RESPONSE TO INF ... | 323 | ||
SUMMARY | 324 | ||
ACKNOWLEDGMENTS | 324 | ||
REFERENCES | 324 | ||
Intravascular Ultrasound Studies of Plaque Progression and Regression | 329 | ||
Key points | 329 | ||
INTRODUCTION | 329 | ||
EARLY IMAGING CLINICAL TRIALS | 329 | ||
INTRAVASCULAR ULTRASOUND | 330 | ||
STATIN ADMINISTRATION | 330 | ||
LOW-DENSITY LIPOPROTEIN LOWERING BEYOND STATINS | 331 | ||
ADDITIONAL ATHEROGENIC LIPID TARGETS | 331 | ||
HIGH-DENSITY LIPOPROTEIN AS A THERAPEUTIC TARGET | 331 | ||
IMPLICATIONS AND FUTURE STEPS | 332 | ||
SUMMARY | 332 | ||
REFERENCES | 332 |