Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that...

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Robert A. Vogel, MD Clinical Professor of Medicine University of Colorado Denver Disclosures: Disclosures: National Coordinator: ODYSSEY Outcomes Study (Phase III – Sanofi) Speakers Bureau: Sanofi, Regeneron

Transcript of Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that...

Page 1: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Robert A. Vogel, MD

Clinical Professor of Medicine

University of Colorado Denver

Disclosures:Disclosures:

National Coordinator: ODYSSEY Outcomes Study(Phase III – Sanofi)

Speakers Bureau: Sanofi, Regeneron

Page 2: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Case Report

A 67y/odiabeticm anhasCHD andanEFof30%(AICD). Hehasbeenangina-freeafteranL AD(AICD). Hehasbeenangina-freeafteranL ADstenosisw astreatedw ithaDES oneyearago. T hreem onthsago,hepresentedw ithanginaago. T hreem onthsago,hepresentedw ithanginaandadenovolesionofhisR CA notpresentoneyearago. N ow hisL AD stentlesionhasalsore-stenosed. Hehasbeenon20m gofCrestor,10m gstenosed. Hehasbeenon20m gofCrestor,10m gofZetia,w ithT C 170,L DL -C 80,T G 150 andHgbA1C,6.5. Arew edoingasm uchasw ecandoforA1C,6.5. Arew edoingasm uchasw ecandoforhislipids?

Page 3: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

The LDL (lipid) hypothesis is the concept thatexcess LDL and other atherogenic lipoproteinsexcess LDL and other atherogenic lipoproteinsare the predominant causal factors in thedevelopment of atherosclerosis. This hypothesisalso assumes that reducing LDL, regardless ofalso assumes that reducing LDL, regardless ofthe means, should produce a correspondingreduction in cardiovascular events.reduction in cardiovascular events.

Adapted from Jarcho JA, Keaney,J Jr, NEJM 2015; 372:2448

Page 4: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Cell Division

Lipid

R udolfVirchow 1856

Lipid

Page 5: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Michael Brown

Joseph Goldstein Regulation of Cholesterol Metabolism via LDL Receptor – Nobel 1985

Page 6: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Details of the LDL Hypothesis

↑ Atherogenic particlesparticles

DepositionOxidationMɸ uptake → foam

VLDLRemnants Mɸ uptake → foam

cellsCellular proliferationMatrix production

Remnants

LDL

Matrix productionInflammationPlaque rupture &

Chylo (Apo-B48)Remnants

Plaque rupture &erosion

Thrombosis

Primary factorFacilitating factors

Page 7: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Boekholdt SM et al, JACC 2014;64:485

Cardiovascular Risk vs. Statin Treatment-achievedLDL-C in 8 RCTs (N = 38,153)LDL-C in 8 RCTs (N = 38,153)

Achieved LDL-C (mg/dl)

Page 8: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Nikpay M et al, Nature Genetics 2015;47:1121-32

1000 Genomes-based Genome-wide Association Analysis ofCHD (185K cases and controls, 6.7 M common and 2.7M rare variants)CHD (185K cases and controls, 6.7 M common and 2.7M rare variants)

Confirmed

LDLR PCSK9

Confirmedtraditionalrisk factors:

LDL• LDL• Lp(a)• RLPs• RLPs• TG• SBP

Page 9: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Ference BA et al, JACC 2012;60:2631

Mendelian Randomization Analysis:Genetically Lower LDL-C (9 variants) vs. CHD Risk in 312,321 Subjects

30%

Genetically Lower LDL-C (9 variants) vs. CHD Risk in 312,321 Subjects

30%

CH

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rs11591147

20%

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0 5 10 15LDL-C (mg/dl) Reduction

0%

Page 10: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Ference BA et al, JACC 2012;60:2631

Early vs. Late Cholesterol Lowering for Reducing CHD Risk: Statin Trialsvs. Mendelian Analysis (9 SNPs, 6 genes) in 312,321 Subjectsvs. Mendelian Analysis (9 SNPs, 6 genes) in 312,321 Subjects

1.0 mmol/L

0.5 mmol/L

0.25 mmol/L0.25 mmol/L

0.125 mmol/L

CHD RiskGenetically lower

Statin trials

Page 11: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors
Page 12: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Case Study: 86 yoF,asym ptom aticw ithonnom eds,w antsherm am m ography resultsm eds,w antsherm am m ography results

P M H:negative,nevertookm eds

FH:Fatherhadearly CHD,Vineberg,diedat66FH:Fatherhadearly CHD,Vineberg,diedat66

P .E.:BP 152/78,P 78,BM I24N orm alN orm al

L abs:T C 316,L DL -C 210,HDL -C 54,T G 258ECG:W N LECG:W N L

ClinicalCourse:livedto96,diedof“ oldage”

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9Rodrigues F et al, JAMA Cardiol 2016, Nov 9.

“Statin Hypothesis”: Annual Mortality in 509,766Older VA Patients with ASCVD by Statin TreatmentOlder VA Patients with ASCVD by Statin Treatment

6%

7%

5%

6%

An

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3%

4%

An

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2%

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ort

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y

0%

1%

0%

No Statin Low-intensityStatin

M0d-intensityStatin

High-IntensityStatin

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• LDL-C, IDL-C• LDL-C, IDL-C

• Triglycerides, RLPs

• NO Availability

LDL Receptors

Endothelial F’n• NO Availability

• NF-

• CRP

Endothelial F’n

• CRP

• M, MMP-1,

MMP-3, MMP-9

Inflammation

MMP-3, MMP-9

• Platelet Activation

TF Clotting• TF Clotting

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Ridker et al, N Engl J Med Aug 27, 2017

CANTOS: Canakinumab (IL-1β inhibitor) 50, 150, and 300mg SC q3mo vs. Placebo in 10,061 Subjects with prior MI andSC q3mo vs. Placebo in 10,061 Subjects with prior MI and

CRP >2 on Lipid Lowering over 4 YearsMI, CVA, CVD with Canakinumab 150mg vs. Pbo

(Initial LDL-C 82 mg/dl)

Page 16: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

N EnglJM ed 2006;354:1264-72

Sequence variations in PCSK9, low

N atureGenetics2003;534:154

Sequence variations in PCSK9, lowLDL, and protection againstcoronary heart disease

CohenJC,Boerw inkleE,M osley T H Jr,HobbsHH

RESULTS:O fthe3363 blacksubjectsexam ined,2.6 percenthadO fthe3363 blacksubjectsexam ined,2.6 percenthadnonsensem utationsinP CS K9;thesem utationsw ereassociated w itha28 percentreductioninm eanL DLcholesterolandan88percentreductionintheriskofCHD(P =0.008 forthereduction;hazard ratio,0.11;95 percentconfidenceinterval,0.02 to0.81;P =0.03).O fthe9524confidenceinterval,0.02 to0.81;P =0.03).O fthe9524w hitesubjectsexam ined,3.2 percenthad asequencevariationinP CS K9 thatw asassociated w itha15 percentreductioninL DL cholesteroland a47 percentreductionintheriskofCHD (hazardratio,0.50;95 percentconfidenceinterval,0.32 to0.79;P =0.003).interval,0.32 to0.79;P =0.003).CONCLUSIONS:T hesedataindicatethatm oderatelifelongreductionintheplasm alevelofL DL cholesterolisassociated w ithasubstantialreductionintheincidenceofcoronary events,substantialreductionintheincidenceofcoronary events,eveninpopulationsw ithahighprevalenceofnon-lipid-related cardiovascularriskfactors.

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B/E Receptor)

LDL, IDL,RLPs

CholesterolCholesterol

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HMGHMG--CoACoA--RR

(Sterol regulating element(Sterol regulating element--binding protein)binding protein)

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PCSK9 Regulation of LDL Receptor Expression

Forillustrationpurposesonly

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Cohen JC, et al. NEJM 2006; 354: 1264–72

Loss-of-Function PCSK9 Genetic Variants areAssociated with ↓ LDL-C and ↓↓ CHD

CHD ↓88% CHD ↓47%

Associated with ↓ LDL-C and ↓↓ CHD

LDL-C LDL-C↓15%

LDL-C↓28% ↓15%

Black Subjects White Subjects

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Hooper AJ et al, Atherosclerosis 2007;193:445

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Sabatine MS et al, N Engl J Med 3/17/17

Page 22: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors
Page 23: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

N EnglJM ed3/17/17

FOURIER Trial: Adverse Events

Page 24: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors
Page 25: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors
Page 26: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors
Page 27: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Ridker PM et al, N Engl J Med 3/17/17

Bococizumab in 27K Subjects with ASCVD, DM, or CKD with >1RF

SPIRE 1SPIRE 1LDL-C >707 Months

SPIRE 2SPIRE 2LDL-C >10012 Months

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Statin vs. Pbo, Statin vs. Statin, IMPROVE-IT, and FOURIERTrials: Relationship of LDL-C Lowering to CVE Reduction

CTT Collaboration. Lancet 2005; 366:1267; Lancet 2010;376:1670. Wiviott SD et al. JACC 2005;46:1411 Pedersen T et al, JAMA 2005;294:2437

Trials: Relationship of LDL-C Lowering to CVE Reduction

IMPROVE-IT PROVE-IT TNT St FOURIER Statin vs. PboIMPROVE-IT PROVE-IT TNT St FOURIER Statin vs. Pbo(simva 40/80 + eze) (prava 40 vs. atorva 80) (atorva 10 vs. 80) (simva + evolocumab)

Page 29: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Hepatic CellHepatic Cell

LDL-RLDL-R

PCSK9

EGF-A Domain Catalytic Site

Monoclonal antibodies:Fully andpartly hum anm Ab(FDA-approved)

PCSK9

Monoclonal antibodies:Fully andpartly hum anm Ab(FDA-approved)

Peptide mimics:P eptidesthatm im ictheEGF-A dom ainoftheL DL receptor

Gene silencing:m R N A antisenseoligonucleotides

Anti-cleavage (furin) compounds

Anti-PCSK9 vaccine

Page 30: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

Case Report

A 67y/odiabeticm anhasCHD andanEFof30%(AICD). Hehasbeenangina-freeafteranL AD(AICD). Hehasbeenangina-freeafteranL ADstenosisw astreatedw ithaDES oneyearago. T hreem onthsago,hepresentedw ithanginaago. T hreem onthsago,hepresentedw ithanginaandadenovolesionofhisR CA notpresentoneyearago. N ow hisL AD stentlesionhasalsore-stenosed. Hehasbeenon20m gofCrestor,10m gstenosed. Hehasbeenon20m gofCrestor,10m gofZetia,w ithT C 170,L DL -C 80,T G 150 andHgbA1C,6.5. Arew edoingasm uchasw ecandoforA1C,6.5. Arew edoingasm uchasw ecandoforhislipids?

Page 31: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

ACC and NLA Guidelines on PCSK9-I Use

Page 32: Robert A. Vogel, MD Clinical Professor of Medicine ...The LDL (lipid) hypothesis is the concept that excess LDL and other atherogenic lipoproteins are the predominant causal factors

• PCSK9 induces LDL receptor degradation• PCSK9 induces LDL receptor degradation

• mAb PCSK9 inhibitors reduce LDL-C 50-70%in patients on/off statins and in HeFH

Initial two-year data demonstrates a 20%• Initial two-year data demonstrates a 20%reduction in major CVEs in CHD subjects onstatinsstatins

• The early safety profile appears good

• Initial annual retail cost is ≈ $15K• Initial annual retail cost is ≈ $15K

• Other approaches to ↓PCSK9 are ac� vely being investigatedbeing investigated