Role of imaging in risk assessment models: the example of CIMT

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Role of imaging in risk assessment models: the example of CIMT Diederick E. Grobbee, MD, PhD, FESC Professor of Clinical Epidemiology Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands

Disclosure I report being on an advisory boards for Organon, Pfizer, Roche, and Takeda; receiving consulting, lecture fees, and travel reimbursements from Roche, Takeda, Organon/Merck Schering Plough, AstraZeneca, and Servier; and research grants from Pfizer, AstraZeneca, Novartis, Organon/Merck Schering Plough, Wyeth, Unilever, GlaxoSmithKline, and Solvay.

Phases and Faces of Cardiovascular Disease

Schematic presentation of how atherosclerosis develops Foam Cell Fatty Streak Intermediate Lesions Atheroma FibrousPl aque Complicated Lesion/Rupture Exposure to time and unfavourable risk factors

Imaging allows assessment of atherosclerosis progression Endothelial Dysfunction Carotid IMT Plaque Stenosis Calcification Composition

Monitoring atherosclerosis: options Flow-mediated dilatation (FMD) Arterial compliance/ elasticity Pulse wave velocity Carotid artery intima-media thickness(cimt) IVUS Coronary artery calcification Clinical signs and symptoms Early Late

Carotid IMT measurement: a window on the disease process

Carotid ultrasound imaging (CIMT)

Carotid scan: anatomy and images

Starting in the Rotterdam Study, early nineties: Common far wall Picture from PhD thesis Michiel Bots, currently professor of cardiovascular disease epidemiololgy Utrecht Univerisity

Carotid IMT and Risk Factors: Age and Gender Bots ML, Grobbee DE. Carotid artery intima-media thickness as an indicator of generalized atherosclerosis. J Intern Med. 1994;236:567-73 JuliusCenter.NL

Carotid IMT and Risk Factors: Smoking Bots ML, Grobbee DE. Carotid artery intima-media thickness as an indicator of generalized atherosclerosis. J Intern Med. 1994;236:567-73 JuliusCenter.NL

Rotterdam Study and ARIC showed that Age, sex, smoking, total cholesterol, LDL, HDL, fibrinogen, CRP, blood pressure, alcohol. are all consistently related to thickness of carotid intima-media Note: even if not measure of local atherosclerosis, it is a measure of total atherosclerotic burden Bots ML, Grobbee DE. Carotid artery intima-media thickness as an indicator of generalized atherosclerosis. J Intern Med. 1994;236:567-73

CIMT and angiographic coronary atherosclerosis Kablak at al. Heart 2004;90:1286

Carotid Disease as a Marker of Cardiovascular Risk : IHD Bots, Grobbee, et al. Circulation 1997

Carotid IMT Measured Using B-mode Ultrasound: Progress in reproducibility since the early days 1989 1994 1999 2001 2001 2002 2002 2003

JuliusCenter.NL Arterioscler Thromb Vasc Biol. 2008;28:2296-2302

CIMT today: Many options to chose from Stroke 2003;34:2985-2994

180 150 120 90 probe carotid bulb internal carotid artery common carotid artery blood flow external carotid artery carotid flow divider carotid dilatation JuliusCenter.NL

Use of CIMT measurements enables to detect effects on atherosclerosis earlier with smaller sample sizes Can indicate value (or lack thereof) of new compounds faster Examples Rosuvastatin (METEOR) Torcetrapib (Radiance) JuliusCenter.NL

Measurement of change in CIMT over time (example for Meteor)

Meteor - Study design Patients Asymptomatic for CHD Maximum IMT 1.2 <3.5 mm Modest hypercholesterolaemia Men (aged 45-70) Women (aged 55-70) Rosuvastatin 40 mg Placebo Visit: Week: 1 6 2 4 3 2 4 0 5 6 6 13 7 26 8 39 9 52 10 65 11 78 12 91 13 104 Run in / eligibility Lipids Safety Lipids Safety CIMT Safety CIMT Safety Lipids Safety CIMT Safety CIMT Lipids Safety CIMT= carotid intima media thickness Adapted from Crouse JR, Bots ML, Grobbee DE, et al. Cardiovasc Drugs Ther 2004; 18: 231 8

Change in IMT of 12 carotid sites (mm) METEOR primary endpoint: Rate of change of maximum IMT Rosuvastatin vs placebo Progression Regression JAMA 2007;297:1344-1353 +0.03 +0.02 Placebo +0.0131 mm/yr (n=252) +0.01 P<0.0001 (Rosuvastatin vs. placebo) 0.00 1 2 Time (years) -0.01 Rosuvastatin 40 mg -0.0014 mm/yr (n=624) P=NS (Rosuvastatin vs. zero slope Placebo; Change in CIMT (95% CI) JAMA 2007;297:1344-1353 Rosuvastatin 40 mg; Change in CIMT (95% CI)

Radiance: the end of a bright future for Torcetrapib 80 75 70 65 60 55 50 45 40 HDL (mg/dl) 68.5 65.2 47.6 75.5 76.2 77.3 73.6 71.5 72.6 71.7 T/A A 110 105 100 95 90 85 80 47.4 46.8 46.3 46.5 45.8 44.5 44.3 45.2 45.3 46.6 75 70 LDL (mg/dl) 105.1 106.6 106.1 105.1 105.3103.1 102.7 100.9 100.4 100.8 100.2 T/A A 84.5 84.0 84.6 83.7 86.4 85.9 83.0 83.8 81.5 BL 1 3 6 9 12 15 18 21 24 BL 1 3 6 9 12 15 18 21 24 1.80 1.60 1.40 1.20 1.3002 1.3150 1.3079 1.3319 1.3469 1.3680 1.3260 1.3210 1.3592 1.3634 1.00 0.80 0.60 Baseline Month 6 Means +/- SD Month 12 Month 18 Month 24 Treatment Period Lancet 2007

CIMT: Established measure of atherosclerosis Use of CIMT in cohort studies showed Consistent relations between risk factors and CIMT Already early in life Consistent relations between CIMT at various segments and future risk of MI and stroke Use of CIMT in trials (OPAL, Meteor, Facit, Radiance, etc.) showed Changes in thickness of time can be reproducibly measured Changes in CIMT over time reflect changes in risk Differential effects of drugs and diet on CIMT progression

CIMT in risk assessment Very often papers end with CIMT measurements may help to further characterise the patient CIMT measurements may help us in risk stratification Meaning that the value of CIMT alters the treatment strategy (risk stratification)

Recommendations 2000 AHA working group on identifying the high-risk patient for primary prevention: noninvasive tests of atherosclerotic burden (Circulation 2000;101:e12-e15) 2003 ESH/ESC guidelines for management of arterial hypertension (J Hypertens 2003, 21:1011) 2003 European guidelines on cardiovascular disease prevention in clinical practice (Eur Heart J 2003; 24:1601) 2004 & 2007 Mannheim Intima-media thickness consensus (Cerebro Dis 2007;23:75) 2006 SHARP statement (Am J Cardiol)

The issue is Does the result of the imaging test for atherosclerosis in one individual lead to a shift from one risk function category to another and is this shift indeed followed by different treatment consequences for that individual? -> Increased risk or decreased risk!

Incremental value of CIMT on top of risk factors in the prediction of CVD events Literature review on studies addressing incremental value Not relative risk / odds ratios But, Area under the receiver operating curve C-statistic Prediction rule Plantinga Y, et al. European Journal of Cardiovascular Prevention and Rehabilitation 2009, 16:639 644

Incremental value of CIMT on top of risk factors in the prediction of CVD events 380 hits 29 studies IMT & follow-up events 6 studies dealt with incremental value 3 in diabetes or known CVD included Remaining: Del Sol, Stroke 2001 Folsom, Diabetes Care 2003 Bernard, Diabetes Care 2006

The added value of CIMT measurements in risk stratification: Rotterdam Study Contribution of Different IMT Measures to Model 1 in the Prediction of Coronary Heart Disease and Stroke Model ROC * Area (95%CI) Model 1 0.72 (0.67 0.77) Model 1+maximum CCA IMT 0.74 (0.69 0.78) Model 1+maximum BIF IMT 0.74 (0.69 0.78) Model 1+maximum ICA IMT 0.75 (0.70 0.79) Model 1+combined IMT 0.75 (0.71 0.80) Adding CIMT to conventional risk factors for coronary heart disease and stroke does not result in a material increase in the predictive value when used as a screening tool Iglesias del Sol et al. Stroke 2001; 32:1532 1539

The added value of CIMT measurements in risk stratification: ARIC Combined (N=13,145) Women (N=7,463) Men (N=5,682) AUC using traditional risk factors only AUC using traditional risk factors and CIMT >75th percentile 0.748 0.757 0.802 0.809 0.684 0.703 CIMT 75 th percentile: 0.78 mm entire population, 0.73 mm women, 0.84 mm men Nambi V et al. Presented at AHA 2007

The added value of CIMT measurements in risk stratification Small effects: Change of 0.01 0.03 in AUC ROC But is AUC the most appropriate measure of performance in clinical practice? Alternative: Can CIMT measurement lead to a change in risk category and thereby trigger a different treatment approach?

Incidence of cardiovascular events (%) 50 40 30 Predicted incidence by the Framingham Risk Score Observed incidence 24 events only Hyperlipidaemia No data on size of groups 20 Threshold for drug therapy 10 0 Max-IMT<BTV Max-IMT BTV Max-IMT<BTV Max-IMT>BTV Low risk patients (FRS<10%) Intermediate risk patients (10% FRS<20%) Baldassarre D et al. Atherosclerosis 2007;191(2):403 408

ARIC: observed risk in various risk categories classified by CIMT Observed risk 2% yr threshold 1% yr threshold Courtesy Dr Ballantyne, 2008

Conclusions Carotid IMT measurements offer a well established method for imaging atherosclerosis in observational research Carotid IMT measurements can validly be used as a proxy marker for disease progression and regression in clinical trials

Conclusions Carotid IMT measurements integrate the effects of conventional risk factors on atherosclerosis occurrence and progression and therefore add little overall improvement of risk prediction models In patients in intermediate categories of risk Carotid IMT measurements may improve risk classification and assist in selecting those that have an indication for risk factor modification but the evidence is limited and additional research is needed to position their utility in clinical practice

Acknowledgements: my team Michiel L. Bots, Yolanda van der Graaf, Arno W. Hoes, Albert Hofman, Petra P.H. Peeters, Yvonne Plantinga, Yvonne T. van der Schouw, Ronald P. Stolk, Cuno S.P.M. Uiterwaal, Jacqueline C.M. Witteman, Frank Visseren + a group of excellent PhD fellows + numerous participants