Gary S. Mintz,, MD. IVUS Observations in Acute (vs Chronic) Coronary Artery Disease: Structure vs Function
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1 Gary S. Mintz,, MD IVUS Observations in Acute (vs Chronic) Coronary Artery Disease: Structure vs Function
2 Important IVUS Observations: Remodeling Originally used (first by Glagov) ) to explain atherosclerosis in the absence of lumen compromise - mostly in reference segments Regardless of the definition, assessing lesion remodeling requires a comparison to the reference segment Positive (outward) remodeling in ACS Negative (constrictive or inward) remodeling in stenosis formation in chronic stable angina
3 Reference Segments Lesions Positive remodeling Intermediate remodeling Negative remodeling Mintz et al, J Am Coll Cardiol 1995;25: Nishioka et al. J Am Coll Cardiol 1996; 27:
4 1) Glagov.. N Engl J Med 1987;316: ) Mintz.. Circulation 1997;95: ) Nishioka.. JACC 1996;27: ) Lim. Circulation. 1997;95: ) Tauth.. AJC 1997;8: ) Kornowski.. AJC 1998; 81: ) Schwarzacher.. Circulation 1998;98:I ) Schoenhagen.. Circulation 2;11: ) Sabate.. AJC 1999;84: ) von Birgelen.. JACC 21;37: ) Kawagoe.. Circulation 1998;98:I ) Mintz.. JACC 1995;25: ) Dangas.. Circulation1999;99: ) Weissman.. AJC 1999;84: ) Hong. Am Heart J 2;14: ) Abizaid.. JACC 1999;33:53A 17) Wexberg.. JACC 2;36: ) Mehran.. Circulation 2;11: ) Taylor. JACC 1999;34:76-7 2) Nakamura. JACC 21;37: ) Pethig.. Am Heart J 1998;135: ) Kobashigawa.. J Heart Lung Transplant 2;19: ) Endo. JACC 21;37:7-5 24) Okura. JACC 21 (in press) 25) Nishioka.. AJC 21;87: ) Gyongyosi. Coron Artery Dis 1999;1: ) Ward. Atherosclerosis 21;154: Rem Intermediate -Rem Plaque burden Plaque burden Reference segment disease (12) Advanced fibrocalcific Early atherosclerosis (1) disease (2,5,9) Soft plaques (9) Chronic stable angina or old MI (2,3,5,14,17,2) Acute coronary syndromes (7,8,1,11,16,2) Hypercholesterolemia (5) High HDL-cholesterol (19) Increased restenosis and CK-MB post-pci (13,17,18,23,24) New stenosis in another location (17) Advanced age (26) Smoking (5,14) Insulin-treated DM (6) Vasospastic angina (15) Transplant atherosclerosis (4,21,22) Proximal disease, eccentric Ostial,, distal disease, lesions surrounded by eccentric lesions surrounded pericardium (9,25) by myocardium (9,25,27)
5 Remodeling in Acute Coronary Syndromes Proximal reference EEM CSA (mm 2 ) Lumen CSA (mm 2 ) ACS 15.2±5, 5, 2 9.1±3.6 Stable 14.2± ±2.8 p ACS Stable P=.1 P&M CSA (mm 2 ) 6.1± ± Lesion EEM CSA (mm 2 ) Lumen CSA (mm 2 ) 16.1± ± ± ± P&M CSA (mm 2 ) Remodeling Index 13.9± ± ±4.8.94± Positive No Negative Remodeling Schoenhagen et al. Circulation 2;11:598-63
6 Diabetes Modulates Remodeling in ACS and Stable Angina (n=927) Frequency of Positive Remodeling Acute Coronary Syndrome Stable Angina DM 59/183 (32.%) 17/88 (19.6%) No DM 225/469 (48.%) 42/187 (22.3%) Abizaid,, unpublished observations
7 In Some Patients with Chronic Stable Angina Negative Remodeling Appears to Occur Early During Stenosis Formation 14 intermediate stenoses 274 RCA stenoses, stratified (QCA DS<6%) according to reference disease 6 5 Negative remodeling Intermediate remodeling 5 45 Positive remodeling Negative Remodeling Intermediate Remodeling Positive Remodeling <2% (n=91) 2-4% (n=91) 4-6% (n=92) Reference plaque burden Hirose M, AJC in press Hong M-K, M JACC in press
8 244 Patients with Stable Angina and Single Vessel Intervention 5 Positive Pre-PCI Remodeling (n=7) Intermediate Pre-PCI Remodeling (n=11) Negative Pre-PCI Remodeling (n=64) 4 3 p=.24 p=.36 p= MACE (%) Target Lesion Restenosis (%) New Stenosis Formation (%) Wexberg et al. J Am Coll Cardiol 2;36:186-9
9 Important IVUS Observations: Lesion Morphology Acute Acute coronary syndromes Hypoechoic plaque Eccentric lesions Ruptured plaques Thrombus-containing plaques in ACS Fibrocalcific plaque in chronic stable angina in association with negative remodeling Positive Positive remodeling and unstable lesion morphologies - i.e., ruptured and thrombus-containing plaques - tend to occur together in ACS
10 Plaque Composition in Acute Coronary Syndromes p=.2 ACS Stable p=ns p=ns p=ns Echolucent Echodense Mixed Calcific Schoenhagen et al. Circulation 2;11:598-63
11 Comparison of Patients with ACS, no MI within 3 weeks, Single de novo Culprit Lesion Troponin (+) vs Troponin (-) p=.4 Plaque rupture (%) Troponin + (n=4) Troponin - (n=45) p=.3 p=.48 p=.17 Dissection (%) Thrombus (%) Any unstable morphology (%) Fuchs et al. Am J Cardiol 22;89:1111-3
12 Three Vessel IVUS Imaging in 24 Pts with ACS and Positive Tn 5 ruptured plaques 9 culprit lesion 41 nonculprit lesion 19 pts had at least 1 nonculprit plaque rupture 17 pts had 1 plaque rupture in a second artery 3 pts had plaque ruptures in all 3 arteries Rioufol et al Circulation 22;16: % # of Ruptured Plaques
13 3 plaque ruptures in 257 arteries of 254 pts Asymptomatic Stable angina Peri MI USA 46% 11% 11% 32% The frequency of stable angina or no symptoms in patients with plaque rupture suggests that asymptomatic rupture and healing are common and may be one of the mechanisms of progression of CAD Thrombus in 46% more frequent in pts with USA or peri-mi, p=.2 more frequent in arteries with multiple rupture sites, p=.4 Ca ++ in 55%, arc=36±47 located at the base of the rupture in 86% Tear in fibrous cap identified in 59%, at shoulder of plaque in 68% in center of plaque in 32% Multiple rupture sites in 14% of ACS patients Maehara et al J Am Coll Cardiol 22;4:94-1
14 22 patients with single de novo lesions studied using angioscopy and IVUS showed a relationship between thrombus and remodeling Complex lesions (irregular surface ±thrombus) Simple lesions (smooth surface w/o thrombus) Positive Remodeling (Lesion EEM>1.5 Reference) 8 1 Negative Remodeling (Lesion EEM<.95 Reference) 2 5 Smits et al. Cardiovasc Res 1999;41: p=.35
15 Culprit Lesion Morphology vs Remodeling in 6 Patients with Unstable Angina 1 Frequency of Plaque Rupture 1 Frequency of Thrombus Positive Intermediate Remodeling Negative Positive Intermediate Negative Remodeling Gyongyosi et al. Heart 1999;82:68-74
16 Remodeling vs plaque composition IVUS & histology in 29 patients (17 stable angina, 12 ACS) treated with DCA Remodeling index 1.2 IVUS & OCT in 82 lesions in 5 patients Remodeling index Inflammatory Lipid score cells Lipid rich* Mixed Fibrous *Remodeling also correlated with quadrants of lipid (p=.1) Uemura et al. ACC 23 Mac Neill et al. ACC 23
17 Calcium Does Not Increase the Biomechanical Instability of Atherosclerotic Plaques! Stable (n=1) Ruptured (n=1) p Ca ++ CSA (%) Lipid CSA (%) Calcium Lipid Maximal stress (kpa( kpa) x=stable x=ruptured kpa 16 x x x x x xx x x x x x x x p=ns x x x 3 % area of calcium Huang. Circulation 21;13:151-6 kpa 16 x x x xx x x x x x x p=.24 x x x x x x x 6 % area of lipid When fibrous plaque was replaced with calcium, stress changed insignificantly (p=.85). In contrast, stress decreased by 26% (p=.2) when lipid was replaced with fibrous plaque.
18 Multiple studies have shown that EBCT calcium score predicts acute coronary events at 1 year follow-up # with no events (n=1155) # with events (n=18) MACE (n=1172) Specificity Sensitivity Square Root of Calcium Score Death/MI (n=1172) Specificty Specificity Square Root of Calcium Score Arad et al. Circulation 1996;93: Sensitivity Square Root of Calcium Score 6 Arad et al. J Am Coll Cardiol 2;36:
19 Important IVUS Observations: Calcium If calcium is uncommon in ACS lesions and if calcium does not affect plaque vulnerability and instability, why does the EBCT calcium score predict acute events?
20 Volumetric IVUS analysis of 19 RCA's with 1 or 2 focal de novo stenoses EEM vol (mm 3 ) Lumen vol (mm 3 ) P&M vol (mm 3 ) Length (mm) Lesion 119 ± ±3 9 ± ±7.6 Non- Stenotic Segment 459 ± ± ± ±13.5 p <.1 <.1 <.1 <.1 72±12% of the plaque volume (range 46-86%) is in nonstenotic segments. Plaque volume l t ith l i Volumetric index of total calcium r=.57, p= Total plaque volume (mm 3 ) Tinana et al. Am J Cardiol 22;89:757-6
21 Proximal 3mm 12mm EEM CSA = 21.mm 2 Lumen CSA = 9.5mm 2 P+M CSA = 11.5mm 2 EEM CSA = 23.5mm 2 Lumen CSA = 5.5mm 2 P+M CSA = 18.mm 2 EEM CSA = 13.7mm 2 Lumen CSA = 9.3mm 2 P+M CSA = 4.4mm 2
22 1mm 4mm
23 2mm 6mm
24 Important IVUS Observations: Lumen Compromise What What separates lesions with asymptomatic plaque rupture from plaque ruptures that cause acute symptoms?
25 Clinical Follow up in 357 intermediate lesions in 3 pts deferred intervention after IVUS imaging IVUS MLD (mm) 4 3 Death/MI/TLR TLR DM no-dm r= QCA MLD (mm) IVUS MLA (mm 2 ) Independent predictors of death/mi/tlr was IVUS MLA (p=.41) Independent predictors of TLR were DM (p=.493) and IVUS MLA (p=.42) Although the number of patients with death and MI was small (n=6), the only independent predictor was IVUS MLD (p=.498). 1 5 IVUS MLA (mm 2 )
26 42 Consecutive Pts with Angiography Both Before and After MI Risk of MI 29 patients had a newly 14 occluded artery 12 In 19 pts, the artery 1 previously had a <5% DS 8 In only 1 pts the 6 occlusion was at the 4 site of the most severe 2 stenosis Little et al. Circulation 1988;78: Pts in CASS after Baseline Angiography Risk of Anterior MI within 3 years (%) Baseline QCA DS (%) Ellis et al. J Am Coll Cardiol 1988;11: "Because the aggregate risk of rupture associated with many non-significant lesions (each with an admitedly lower individual risk potential) exceeds that of the fewer significant lesions, an MI will more likely originate from a nonsignificant lesion." Kern and Meier. Circulation 21;13:3142-9
27 Comparison of Culprit and Non-Culprit Rupture Sites in ACS Patients with Rupture Sites in Non-ACS Patients ACS Culprit Plaque Ruptures (N=35) ACS Non-Culprit Plaque Ruptures (N=2) Non-ACS Plaque Ruptures (N=27) p= p= p= Rupture Site Remodeling Index Minimum Lumen Area (mm 2 ) Thrombus (%) Independent predictors of ACS were MLA and thrombus (both p=.1) Fuji et al. Unpublished Observations
28 Limitations of IVUS Measurement of fibrous cap Histologic studies suggest that the fibrous cap in vulnerable plaques measures <65 microns IVUS resolution is >1 microns Assessment of plaque composition
29 IVUS Can Measure Fibrous Cap Thickness In Vitro, but NOT In Vivo Hiro et al. Circulation 21;13:
30 Virtual Histology db MHz Fibrous, Fibrofatty, Lipidic-necrotic, Calcium
31 Predictive Accuracies of Training and Test Datasets Fibrous (n=11) Fibro-Lipidic (n=56) Calcified (n=5) Lipidic-Necrotic (n=7) Training Test Training Test Training Test Training Test FFT^ Welch AR
32 Ex-Vivo Validation Virtual Histology Fibrous, Fibro-lipidic, Lipidic-necrotic, Calcium
33 Ex-Vivo Validation Virtual Histology Fibrous, Fibro-lipidic, Lipidic-necrotic, Calcium
34 What about IVUS compared with other invasive diagnostic modalities? IVUS Structure + Plaque Composition Fibrous Cap Function Safe Validated in vivo Practical Available + IVUS+Virtual Histology + + OCT Thermography + Palpography + +
35 Conclusions Almost everything that we know about IVUS and vulnerable plaque has come from extrapolating studies of IVUS in ACS - NOT from prospective correlative studies Culprit lesions in ACS are, in general, characterized by Positive Positive remodeling Hypoechoic,, eccentric, ruptured plaques with evidence of thrombus With With a complex interaction between remodeling and plaque composition and instability in ACS. Positive remodeling Prevents lumen compromise "Paradoxically" may contribute to ACS and to MACE after PCI May May be less common in diabetics with ACS Negative remodeling Contributes to lumen compromise Probably can occur both early and late Calcium is a marker of plaque mass, not a determinant of instability
36 But... The relationship between ACS/MI, positive remodeling, "vulnerable" le" plaques, and ruptured plaques may not be so simple. Frequency of an MI is related to the severity of the underlying stenosis Not Not all pts with ACS/MI have positive remodeling Not Not all pts with ACS/MI have plaque rupture Not Not all ruptured plaques cause ACS/MI. In some pts plaque rupture re is asymptomatic and may be followed by healing, negative remodeling, calcification, and disease progression. In other patients the development of a thrombus (superimposed on plaque rupture) decreased lumen dimensions and results in ACS/MI While While the concept of using multiple complementary imaging techniques may seem attractive, any clinical approach must be practical and safe.
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