how should one decide whom to treat for hypertension? how should one decide whom to treat for...
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How Should One Decide Whom to Treat for Hypertension?
Jay N. Cohn, M.D.
Professor of Medicine
Director, Rasmussen Center for Cardiovascular Disease Prevention
University of Minnesota Medical School
Minneapolis, MN
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CV Mortality Risk Doubles withCV Mortality Risk Doubles withEach 20/10 mm Hg BP Increment*Each 20/10 mm Hg BP Increment*
*Individuals aged 40-69 years, starting at BP 115/75 mm Hg.CV, cardiovascular; SBP, systolic blood pressure; DBP, diastolic blood pressureLewington S, et al. Lancet. 2002; 60:1903-1913.JNC VII. JAMA. 2003.
CVmortality
risk
SBP/DBP (mm Hg)
0
1
2
3
4
5
6
7
8
115/75 135/85 155/95 175/105
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Impact of “High-Normal” BP on Impact of “High-Normal” BP on CV RiskCV Risk
Data from the Framingham Heart StudyData from the Framingham Heart Study
16
12
8
4
0
Optimal BP
Normal BP
12
8
4
00 2 4 6 8 10 12
Years
Optimal BP
Normal BP
High-normal BPWomen
Men
Cumulative
incidence of CV events
(%)
High-normal BP
Vasan et al. N Engl J Med. 2001;345:1291-7.
Optimal BP: <120/80Normal BP: 120-129/80-84High-normal BP: 130-139/85-89
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Lower Is BetterLower Is BetterIHD Rates by SBP, DBP, and AgeIHD Rates by SBP, DBP, and Age
A: Systolic Blood Pressure
40-49 years
50-59 years
60-69 years
70-79 years
80-89 yearsAge at risk:
IHD
Mo
rtal
ity
(Flo
atin
g A
bso
lute
Ris
k a
nd
95
% C
I) 256
128
64
32
16
8
4
2
1
120 140 160 180
Usual SBP (mm Hg)
B: Diastolic Blood Pressure
IHD
Mo
rtal
ity
(Flo
atin
g A
bso
lute
Ris
k a
nd
95
% C
I) 256
128
64
32
16
8
4
2
1
70 80 90 100 110
Usual DBP (mm Hg)
Lewington et al. Lancet. 2002;360:1903-1913.
Age at risk:
40-49 years
50-59 years
60-69 years
70-79 years
80-89 years
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Hypothesis
The apparent linear relationship between blood pressure and ischemic disease events as well as age and ischemic disease events does not necessarily mean that age or blood pressure cause events but that both markers capture a progressively higher proportion of people with early disease.
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Blood Pressure and Likelihood of Disease
100
Frequency in
Population (%)
50
0
75 100 125 150 175 200
Systolic Blood Pressure (mmHg)
No Disease
Possible Disease
Likely Disease
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Systolic BP Reduction Systolic BP Reduction and CVD Mortality and CVD Mortality
Systolic BP (control - experimental, mm Hg)
Car
dio
vas
cula
r M
ort
alit
y O
dd
s R
atio
Staessen JA et al. Lancet. 2001;358:1305 -1315.
1.50
1.25
1. 00
0.75
0.50
0.25
-5 0 5 10 15 20 25
P =.003
MIDAS/NICS/VHASUKPDS C vs A
INSIGHTHOT L vs H
HOT M vs HMRC1
MRC2
SHEPHEP
EWPHE
RCT70-80
Syst-Eur
STONE
Syst-ChinaUKPDS L vs H
HOPE
PART2/SCATATMH
STOP1
CAPPP
STOP2/CCBs
STOP2/ACEIs
NORDIL
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SBP Reductions as Little as SBP Reductions as Little as 2 mm Hg Reduce the Risk of CV Events by 2 mm Hg Reduce the Risk of CV Events by
Up to 10%Up to 10%
• Meta-analysis of 61 prospective, observational studies• 1 million adults• 12.7 million person-years
Lewington S et al. Lancet. 2002;360:1903-1913.
2 mm Hg decrease in mean SBP
10% reduction in risk of stroke mortality
7% reduction in risk of ischemic heart disease mortality
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Pg 9
CCOZ_18815_Giles_DT2
Benefits of Intensive BP ReductionHOT Study
**Mean BP from 6 months of follow-up to end of study. Hansson L et al. Lancet. 1998;351:1755-1762.
**Mean BP from 6 months of follow-up to end of study. Hansson L et al. Lancet. 1998;351:1755-1762.
Achieved DBP* (mm Hg)
85.2 83.2 81.1
100
80
40
0
20
60
P=0.05 for trend
Nu
mb
er o
f M
Is
90 143.7 85.2
85 141.4 83.2
80 138.7 81.1
TargetDBP
(mm Hg)
AchievedSBP
(mm Hg)
AchievedDBP*
(mm Hg)
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HypothesisThe apparent linear relationship
between the magnitude of drug-induced BP fall and the reduction of morbid events does not necessarily indicate that blood pressure reduction prevents events but that the drugs protect the arteries and heart (while also lowering blood pressure). A corollary: the greater the BP reduction from a drug the less the vascular disease - i.e., BP fall identifies a low-risk population.
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Antihypertensive Drugs that Slow Disease Progression in Known Doses
Vascular CardiacRamipril EnalaprilPerindopril Captopril?other ACEIs Carvedilol
Amlodipine MetoprololValsartan BucindololLosartan ValsartanHydrochlorothiazide Candesartan
SpironolactoneEplerenoneISDN/hydralazine
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Old Paradigm
BP Cholesterol
Disease Disease
Treatment Treatment
Normal Normal
GOAL: Target Response
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Current Paradigm
DISEASE
BP Cholesterol
GOAL: ?Target Response
TR
EA
TM
EN
T
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Pathophysiology of CV ContinuumGenes EnvironmentEthnicity DietFamily Hx ExercisePolymorphisms StressProteomics Smoking
Blood Vessel/ Heart
AngiotensinNitric Oxide
Progression AldosteroneNorepinephrineCytokines
Structural Remodeling
CAD Cerebrovascular DiseaseHeart Failure Renal FailurePVD Dementia
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Genes, Ethnicity, Diet, Exercise, Smoking, Obesity, Lipids
Small Artery Arterial Structural Cardiac Elasticity Abnormalities Abnormalities (Endothelial Microalbumin LVM Dysfunction) IMT BNP BP Retinal Vasculopathy ECG PNE Large Artery Elasticity AngII Exercise BP
Resting BP
Disease
Drug TherapyRAAS Blockade StatinsNO Enhancers Antihypertensives Antioxidants ?Antiinflammatories
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ASH Writing Group: ASH Writing Group: Proposed New Definition of HypertensionProposed New Definition of Hypertension
Hypertension is a progressive cardiovascular syndrome arising from complex and interrelated etiologies. Early markers of the syndrome are often present before blood pressure elevation is sustained; therefore, hypertension cannot be classified solely by discrete blood pressure thresholds. Progression is strongly associated with functional and structural cardiac and vascular abnormalities that damage the heart, kidneys, brain, vasculature and other organs and lead to premature morbidity and death.
ASH Writing Group 2005.
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†CVD designation is determined by the constellation of risk factors, early disease markers, and target-organ disease. CVD, cardiovascular disease.
ASH Writing Group Definition and ASH Writing Group Definition and Classification of HypertensionClassification of Hypertension
Classification Normal Stage 1 hypertension
Stage 2 hypertension
Stage 3 hypertension
Descriptive Category
Normal BP or rare blood pressure
elevationsAND
No identifiable CVD†
Occasional or intermittent BP
elevationsOR
Early CVD†
Sustained BPelevations
ORProgressive
CVD†
Marked and sustained BP
elevationsOR
Advanced CVD†
Cardiovascular Risk Factors
None or few Several Many Many
Early Disease Markers
None Usually present Overtly present Overtly present with progression
Target-organ Disease
None None Early signs present
Overtly present with or without
CVD events
ASH Writing Group 2005.
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Early Markers for Hypertensive Vascular Disease
Blood Pressure-Exaggerated response to exercise-Widened pulse pressure
Vascular-Reduced small artery elasticity-Reduced large artery elasticity-Endothelial dysfunction-Increased pulsewave velocity-Increased carotid intima-medial thickness-Retinal vascular changes-Microalbuminuria
Cardiac-Increased LV wall thickness -Increased LV volume-Increased LV mass -Abnormal ECG-B-type natriuretic peptide
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R A S M U S S E NC E N T E R
forCARDIOVASCULAR
DISEASE PREVENTION
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RASMUSSEN CENTER
Screening Tests for Early Detection
• Arterial Elasticity (Pulse Contour Analysis)
- Small Artery (C2)
- Large Artery (C1)
• Rest and exercise BP (3-minute treadmill)
• Retinal digital photograph
• Urine for microalbumin/creatinine ratio
• Carotid intimal-medial thickness
Vascular Evaluation
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RASMUSSEN CENTER
Screening Tests for Early Detection
Cardiac Evaluation
• Electrocardiogram
• Cardiac ultrasound (LVID & LVWT)
• Plasma BNP (Biosite)
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RASMUSSEN CENTER
Screening Tests for Early Detection
Modifiable Disease Contributors
• Fasting lipids (LDL, HDL, Trig)
• Fasting blood sugar
• hsCRP
• Homocysteine
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Results of Rasmussen Center Screening
0
20
40
60
80
100
120
140
0 2 4 6 8 10 12 14 16
3-D Column 1
Fre
qu
ency
Rasmussen Score
Low Risk
33%
Modest Risk
36%
High Risk
31%
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Patient: 60-year-old female registered nursePast History: negative except high cholesterolFamily History: both parents smoked, no significant CV disease
Physical Exam: Height 5’4” Weight 126 lb.HR 64 b/min BP 132/66 mmHg
Screening Results: C1 = 8.5 ml/mmHg x10 (abnormal)
C2 = 2.4 ml/mmHg x100 (abnormal)Exercise BP = 173/64 mmHg (abnormal)Retinal photo = A:V nicking (abnormal)Microalbumin = 0.86 mg/mmol (abnormal)LV ultrasound = increased mass (abnormal)Rasmussen score = 12 points
Blood Chemistry: LDL 187 mg/dl; HDL 70 mg/dl
Interpretation: Advanced CV DiseaseTreatment: Antihypertensive, statin
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Patient: 62-year-old female floristPast History: Asymptomatic, plays tennis and golf
Elevated cholesterol: Atorvastatin, 10 mgFamily History: Negative
Physical Exam: Height 5’5” Weight 128 lb.HR 74 b/min BP 140/80 mmHg
Screening Results: C1 = 8.7 ml/mmHg x10 (abnormal)
C2 = 1.6 ml/mmHg x100 (abnormal)Exercise BP = 182/80 mmHg (abnormal)Retinal photo = decreased A:V ratio (borderline)Microalbumin = 1.98 mg/mmol (abnormal)Rasmussen score = 9 points
Blood Chemistry: LDL 137 mg/dl; HDL 129 mg/dl; CRP 0.13 mg/dl
Interpretation: Advancing CV DiseaseTreatment: ACE/ARB; BP Control; Increase atorvastatin
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Patient: 49-year-old male executivePast History: Overweight, elevated BP, asymptomatic, no therapy
Family History: Hypertension, coronary disease
Physical Exam: Height 5’8” Weight 240 lb.HR 76 b/min BP 144/84 mmHg
Screening Results: C1 = 16.1 ml/mmHg x10 (normal)
C2 = 6.4 ml/mmHg x100 (normal)Exercise BP = 154/74 mmHg (normal)All other tests normalRasmussen score = 2 points (BP only)
Blood Chemistry: LDL 172 mg/dl; HDL 38 mg/dl; FBS 108 mg/dl; CRP 1.0 mg/dl
Interpretation: No CV DiseaseTreatment: Diet, ?statin
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Strategies for Aggressive Treatment
PRIMARY PREVENTION•Primary Prevention (global)
–Polypill–Everyone >55 years old
•Impractical•Inefficient•Benefit: risk ratio untested
•Primary Prevention (targeted)–Risk factor identification–Treatment targets risk factor
•Misses many at-risk•Risk factor levels?•Benefit: risk?
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Strategies for Aggressive Treatment
SECONDARY PREVENTION•Secondary Prevention (early)
–Detect markers for early disease–Treat disease not risk factor
•Sensitivity/specificity of detection?•Benefit: risk better?•Prolonged event-free survival•Reduced health care costs
•Secondary Prevention (late)–Patients with symptomatic disease–Treatment can prevent events/prolong life–Increased burden of health care costs
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Risk Factors
Biomarkers
Cardiac and VascularStructural Abnormalities
DeathNon-Fatal
MorbidEvents
RecurrenceProgression
Primary Prevention
Secondary Prevention
Tertiary Prevention
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Who to Treat with Antihypertensives (Pressure Orientation)
•SBP>160 mmHg most of the time
•SBP>140 mmHg most of the time & evidence for vascular or cardiac functional/structural abnormalities
•SBP>130 mmHg with symptomatic vascular or cardiac disease or diabetes
•?SBP>130 mmHg with evidence for vascular or cardiac functional/structural abnormalities
•GOAL: Lower Blood Pressure
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Who to Treat with Antihypertensives (Pathophysiologic Orientation)
•Anyone with symptomatic atherosclerotic vascular or cardiac disease
•?Anyone with vascular or cardiac functional/structural abnormalities and BP >120/80 mmHg
GOAL: Slow Disease Progression
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Future Paradigm
Early Disease
Statin
RAAS Blockade
Antihypertensives
NO donor/enhancer
Innovative Therapy
Slow Progression
GOAL: ?Target Dose
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Strategies to Identify At-Risk Population
•Blood pressure level–Which measurement?–What level?
•Cholesterol level–Which fraction?–Reproducibility?
•Blood pressure + cholesterol (BP + Ch)–Sensitivity, specificity
•BP + Ch + other “risk factors”–Sensitivity, specificity
•Early disease detection–Endothelial dysfunction–Vascular functional/structural abnormalities–Cardiac functional/structural abnormalities