vp as2012 final.ppt [호환 모드]summitmd.com/pdf/pdf/2105_vp_as2012_final.pdf · rapid effects...
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Plaque Profilingq gPursuing VP Signatures & New Therapeutic Agents
Cheol Whan Lee, MDCheol Whan Lee, MD
Professor of Medicine, University of Ulsan College of Medicine,, y g ,Heart Institute, Asan Medical Center, Seoul, Korea
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iiPresentationPresentation
Established Targets• Established Targets- HMGCoA reductase- P2Y receptor- P2Y12 receptor
• Emerging TargetsEmerging Targets- Lipid metabolism- ECM proteases- ECM proteases- Inflammation
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T G t DKing
of CV Medicine
Two Great DrugsStatins and Anti-platelet AgentsStatins and Anti platelet Agents
HMGCoA reductase: statins
P2Y12 receptor: clopidogrel, prasugrel, ticagrelor
HMGCoA reductase: statins
12 ecepto : p g , p g , t g
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…the only proven medicine
Landmark Statin TrialsLandmark Statin TrialsLandmark Statin TrialsLandmark Statin Trials
So Luxurious …So Luxurious …So Luxurious …So Luxurious …Clinical EndClinical End--Point Trials: Point Trials: “The Only “The Only One_StatinOne_Statin Trials”Trials”yy __AFCAPS/AFCAPS/TexCapsTexCaps, WOSCOPS, ALLHAT, CARE, LIPID, PROSPER, 4S, HPS, A, WOSCOPS, ALLHAT, CARE, LIPID, PROSPER, 4S, HPS, A--toto--Z, Z, MIRACL, CARDS, PROVEIT, ALLIANCE, 4D, ASCOTLLA, IDEAL, TNT, SPARCL, MIRACL, CARDS, PROVEIT, ALLIANCE, 4D, ASCOTLLA, IDEAL, TNT, SPARCL, AURORA CORONA GISSIAURORA CORONA GISSI--HF JUPITER SEAS SHARP IMPROVEHF JUPITER SEAS SHARP IMPROVE--IT (ongoing)IT (ongoing)
StatinStatin is an antiis an anti‐‐atherosclerotic drug.atherosclerotic drug.AURORA, CORONA, GISSIAURORA, CORONA, GISSI HF, JUPITER, SEAS, SHARP, IMPROVEHF, JUPITER, SEAS, SHARP, IMPROVE IT (ongoing).IT (ongoing).
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Rapid Effects of Statin TherapyBackground
Rapid Effects of Statin Therapy
12 h12 h 11 4 th4 th 66 12 month12 month7 d7 d 15 d15 d 24 month24 month12 hour12 hour 11--4 month4 month 66--12 month12 month
Ultrafast
7 day7 day
Fast
15 day15 day
Very Early Early Late
24 month24 month
Very Late
ARMYDA - ACS ARMYDA PROVE-IT MIRACL A to Z
4S/HPS
HPS-DM
LIPIDARMYDA -RECAPTURE
NAPLES II
ARMYDA -CAMs
ARMYDA 3
ASCOT
AVERT/CARDS
4S/HPSWOSCOPS
PROSPER
LIPID
CARE
ALHATNAPLES II ARMYDA 3
LIPS
JUPITERCORONA
LRC-CPPTPOSCH
Mechanisms of early benefits are not fully understood.
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Inside Plaques
Expression of HMGExpression of HMG--CoAR in Human CoronaryCoAR in Human Coronaryxpxp yyPlaques & Plaques & RelationshipRelationship to Plaque Destabilizationto Plaque Destabilization
Heart 2011;97:715‐20
We investigated the expression of HMG‐CoAR We investigated the expression of HMG CoAR in coronary atherectomy tissues retrieved from 43 patients with unstable & stable angina, & examined p g ,the relationship of HMG‐CoAR with plaque instability.
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Results
ImmunohistochemistryImmunohistochemistry
Unstable angina(n=22)
Stable angina(n=21)
p-value( )
α-SM actin (%)
( )
21.4±18.7 33.6±28.7 0.103
CD31 (%) 3.4±4.1 0.3±0.5 0.002
CD68 (%)
HMG CoA R (%)
10.9±16.2
3 0±4 5
1.8±1.7
0 4±0 7
0.016
0 014HMG-CoA R (%) 3.0±4.5 0.4±0.7 0.014
Data are shown as % positive area (immunostaining area/total plaque area×100) Data are shown as % positive area (immunostaining area/total plaque area×100).
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PositiveControl
UnstableAngina
NegativeC t l
StableA i ControlAngina
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HMG-CoAR Mφ
Merge
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HMGCoAR Filipin staining
Negative control Colocalization
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R l ti hi B t CD68 P iti A
Results
Relationship Between CD68-Positive Areas& HMG-CoA Reductase-Positive Areas (mm2)
2 )
40
2 )
40
ctas
e (m
m2
30r= 0.018, p=0.937
tase
(mm
2
30r= 0.721, p<0.001
CoA
redu
c
10
20
CoA
redu
ct
10
20
0 20 40 60 80 100 120H
MG
C
0HM
GC
0
10
Unstable Angina Stable Angina
CD68 (mm2)
0 20 40 60 80 100 120
CD68 (mm2)
0 20 40 60 80 100 120
g g
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Beyond CholesterolSummary
Beyond Cholesterol
Statin
HMGCoA ReductaseLiver: cholesterol Plaque: inflammation
Plaque StabilizationPlaque Stabilization
These findings support a potential role of the HMGThese findings support a potential role of the HMG--CoARCoAR in the in the g pp pg pp ppathogenesis of ACS, and may help explain the early benefits of pathogenesis of ACS, and may help explain the early benefits of statinstatin therapy in patients with ACS. therapy in patients with ACS.
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T G t DKing
of CV Medicine
Two Great DrugsStatins and Anti-platelet AgentsStatins and Anti platelet Agents
HMGCoA reductase: statins
P2Y12 receptor: clopidogrel, prasugrel, ticagrelor
HMGCoA reductase: statins
12 ecepto : p g , p g , t g
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P2Y12 Receptor: A Key Player12 p y y
Curr Pharm Des 2006;12:1255Circulation 2010;121:171
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PLATO: Major Outcomesj
HR 0.84(0.77-0.92)P=.0003NNT=54
CV Death / MI / StrokeClopidogrel
9.8
11.7
%)
10
12
NNT 54
Ticagrelor
cide
nce(
%
8
HR 0.79(0 69-0 91)
CV deathClopidogrel
5.1
ativ
e In
c
6
(0.69-0.91)P=.001NNT=90Ticagrelor
4.0
Cum
ula
2
4
0
Definite ST33%p=0.009
Total death 22%↓ (NNT )
Days After Randomization120 1800 60 p<0.0001 (NNT70)
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Bleeding Tax4
) Non‐procedural Bleeding
g
3pe
r yea
r) Non procedural Bleeding
3.06Ticagrelor
2
rate
(%
2.31Clopidogrel
1
stim
ated
p g
0HR 1.31 (95% CI 1.08-1.60), p=0.006
K-M
es
0 60 120 180 240 300 360
No. at riskDays from first IP dose
TicagrelorClopidogrel
9,2359,186
7,6417,718
7,2477,371
6,9797,134
5,4965,597
4,0674,147
3,6983,764
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“More Bleeding = More Death”More Bleeding = More DeathImpact of Bleeding on Mortality after PCI
17,393 patients from REPLACE-2, ACUITY and Horizons
TIMI Bleed All 3 17 [2 51 4 0] <0 001
HR [95%CI] P-value
TIMI Bleed-All
TIMI Bleed-Nonaccess Site
3.17 [2.51-4.0]
3.94 [3.07-5.15]
<0.001
<0.001
TIMI Bleed-Access Site Only
[ ]
1.82 [1.17-2.83] 0.008
0.1 81
Adjusted Risk for 1-Year Mortality
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Inside Plaques
Differential Expression of P2YDifferential Expression of P2Y1212 Receptor in Culprit Receptor in Culprit Pl f P ti t ith AMI & St bl A iPl f P ti t ith AMI & St bl A iPlaques from Patients with AMI & Stable AnginaPlaques from Patients with AMI & Stable Angina
Am J ardiol 2011;108:799‐803
W d h i f P Y We compared the expression of P2Y12 receptors in coronary atherectomy tissues retrieved from i i h AMI ( ) bl i ( )54 patients with AMI (n=35) or stable angina (n=19).
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Results
ImmunohistochemistryImmunohistochemistryAMI
(n=35)Stable angina
(n=19)p-
value
α-SM actin (%) 2.9±2.7 12.3±14.4 0.011
CD31 (%)
CD68 (%)
1.1±1.6
15 5±13 6
0.2±0.2
7 0±14 6
0.001
0 038CD68 (%)
P2Y12 Receptor (%)
15.5±13.6
1.1±0.9
7.0±14.6
0.5±0.4
0.038
<0.001P2Y12 Receptor (%) 1.1±0.9 0.5±0.4 0.001
Data are shown as % positive area (immunostaining area/total plaque area×100).AMI STEMI NSTEMI AMI: STEMI 27, NSTEMI 8
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AMIP2Y12R SMC CD31
P2Y12R SMC CD31
Stable anginaStable angina
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Beyond PlateletsSummary
Beyond Platelets
ADP
P2Y12 ReceptorpPlatelets Endothelial Cells VSMCs
Acute Coronary SyndromeAcute Coronary Syndrome
P2Y12 receptor inhibitors may have a dual antiP2Y12 receptor inhibitors may have a dual anti--ischemic effectischemic effectP2Y12 receptor inhibitors may have a dual antiP2Y12 receptor inhibitors may have a dual anti ischemic effect ischemic effect by inhibiting both platelet activation and plaque destabilization.by inhibiting both platelet activation and plaque destabilization.
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iiPresentationPresentation
Established Targets• Established Targets- HMGCoA reductase- P2Y receptor- P2Y12 receptor
• Emerging TargetsEmerging Targets- Lipid metabolism- ECM proteases- ECM proteases- Inflammation
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Residual CV Risk in Statin Treated PatientsUnmet Medical Need
Residual CV Risk in Statin-Treated Patients
0
161615
272431
24 22
ction,
%
10
20
30
363737
3137
Ris
k Reduc
40
50
60
Rela
tive
R
60
70
80
90
Despite optimal treatment the residual risk of another
90
100
Despite optimal treatment, the residual risk of another MACE in these patients is estimated to be 70–80%.
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On-Treatment HDL-C and CV RiskRed Flag Sign?
HDL: not predictive of residual vascular risk
On Treatment HDL C and CV Riskp
- JUPITER: Lancet2010;376:333- TNT: NEJM2007; 357: 1301- PROVEIT: ATVB2009; 29: 424
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Futile Strategies?The Story So Far …HDL-Targeted Therapies
We have reached the limit of what we can do by lowering LDL-C?
The Story So Far …
Estrogen (↑15%): WHI trialFibrates (↑15%): ACCORD Lipid trial
We have reached the limit of what we can do by lowering LDL-C?.
Fibrates (↑15%): ACCORD Lipid trial
Nicotinic acids (↑20%)Nicotinic acids (↑20%)Extended release niacin: AIM‐HIGH trialTredaptive (nicotinic acid/laropiprant) : HPS‐2 trialTredaptive (nicotinic acid/laropiprant) : HPS 2 trial
CETP inhibitors (↑30%-140%)(↑ )Torcetrapib: Illuminate trial (↑death: discarded) Anacetrapib: Define trial (safe), HPS‐3 (REVEAL) trialDalcetrapib: Dal‐Plaque (promising), Dal‐Outcomes trial
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New TargetsA Potential Game Changer
Biologic Wows for LDL-C Lowering
PCSK9: a key regulator of the LDL receptorGain-of-function mutations result in hypercholesterolemiaGain of function mutations result in hypercholesterolemiaLoss-of-function mutations associated with low LDL-C & low prevalence of CHD events
SAR236553/REGN727 is a highly specific, fully human monoclonal antibody (mAb) to PCSK9
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Monoclonal Antibody to PCSK9, SAR236553/REGN727, Adjunct to Statin
0S
Monoclonal Antibody to PCSK9, SAR236553/REGN727, in Patients with Primary Hypercholesterolemia
Baselin
e
20
-10
BASELINE WEEK 2 WEEK 4 WEEK 6 WEEK 8 WEEK 10 WEEK 12∆ - 5.1%
ange fro
m
-30
-20
±SE)
% C
h
-50
-40
∆ - 47.7%
∆ - 39.6%
∆ - 43.2%
-C
Mean (±
-70
-60
∆ - 64.2%
∆ 47.7%
LD
L
-80
-70
Placebo SAR236553 50 mg Q2W SAR236553 100 mg Q2WSAR236553 200 mg Q4W SAR236553 300 mg Q4W SAR236553 150 mg Q2W
∆ - 72.4%
It was generally safe & well tolerated. SQ every two weeks dropped LDL by 40% to 72%There is some risk of immunity with an agent like this & we need longer-term outcome studies.
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iiPresentationPresentation
Established Targets• Established Targets- HMGCoA reductase- P2Y receptor- P2Y12 receptor
• Emerging TargetsEmerging Targets- Lipid metabolism- ECM proteases- ECM proteases- Inflammation
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ECM Proteases Hypothesis f Pl R tof Plaque Rupture
M i l i (MMP )Matrix metaloproteinases (MMPs)Elevated: MMP1, MMP2, MMP3, MMP8, MMP9, MMP10, MMP13
ADAMTS proteasesOthers: serine proteases (elastase) cysteine proteases (cathepsins)Others: serine proteases (elastase), cysteine proteases (cathepsins)
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Tragic Failure
MMP-Based Therapy
MMPs have been heralded as promising targets for cancer therapy on the basis of their massive up-regulation in malignant tissues and their
i bili d d ll f h ll l iunique ability to degrade all components of the extracellular matrix.
Many of these trials turned out to be major failures. y jOwing to serious complications, the trials were terminated early.
MMPs are vital for immune regulation. Some MMPs are the good guysMMPs are vital for immune regulation. Some MMPs are the good guys in disease. To overcome the danger of off-target effects, it is essential to either thoroughly characterize the biological roles or understand the degree of cross-reactivity of inhibitors before drug developmentdegree of cross-reactivity of inhibitors before drug development.
Science 2002;295:2387
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ADAMTS ProteasesAMI Stable Angina AMI Stable Angina
ADMTS1 ADMTS2
ADMTS4 ADMTS3
ADMTS5 ADMTS13
J Clin Pathol 2011;64:399 J Thromb Thrombolysis 2012 (in press)
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Target for futuredrug development
LimitationsIt remains uncertain whether ADAMTS It remains uncertain whether ADAMTS It remains uncertain whether ADAMTS It remains uncertain whether ADAMTS proteases are a cause or consequence of proteases are a cause or consequence of plaque instability plaque instability plaque instability. plaque instability.
Y fi fi ht t fl i Y fi fi ht t fl i You can see firefighters at every flaming You can see firefighters at every flaming building, but they did not set the blazes.building, but they did not set the blazes.
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iiPresentationPresentation
Established Targets• Established Targets- HMGCoA reductase- P2Y receptor- P2Y12 receptor
• Emerging TargetsEmerging Targets- Lipid metabolism- ECM proteases- ECM proteases- Inflammation
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Inflammation AKey Player
The contribution of inflammation to the development of atherosclerotic plaques is now well-understood and several promising targets have been identified.
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Nonspecific Inflammatory Genes
I fl t G t R t d PlThe proper study of mankind is man
Inflammatory Genes at Ruptured PlaquesThe proper study of mankind is man.
HG-U133 Plus 254,675 probes
Inflammation is caused by complex interactions involving multiple cell types & multiple mediators. It is not yet clear which targets will yield the greatest effect in atherosclerosis.
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PLA2 i hibit ↓ d d l lAnti-inflammatory Drugs Cooling Down
Burning Plaques
PLA2 inhibitors (↓ oxidized LDL, multiple isozymes) Darapladib (Lp‐PLA2): STABILITY trial (Phase 3)Varespladib (sPLA2): VISTA 16 trial (Phase 3)Varespladib (sPLA2): VISTA‐16 trial (Phase 3)
Experimental DrugsA ii flAntiinflammatory agents‐Methotrexate: Cardiovascular Inflammation Reduction Trial ‐ Others:Others:
It is not yet clear which anti-inflammatory targets will yield the greatest effect in preventing, reversing or delaying this process.
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Strong DesireLittle Hope
Summary
There are no therapies specifically to target • e e a e o t e ap es spec ca y to ta getthe inflammatory component of atherosclerosis.
There is a critical need to identify key markers & local mediators of the atherosclerotic process
•& local mediators of the atherosclerotic process so that new therapeutics can be developed.