doi: 10.1161/CIRCULATIONAHA.105.579342
(Circulation. 2006;113:664-670.)
© 2006 American Heart Association, Inc.
Epidemiology |
Prognostic Value of Aortic Pulse Wave Velocity as Index of Arterial Stiffness in the General Population
From the Research Center for Prevention and Health, Copenhagen, Denmark (T.W.H.); Laboratory of Hypertension, Department of Molecular and Cardiovascular Research, University of Leuven, Leuven, Belgium (J.A.S., L.T.); Department of Cardiology, Bispebjerg University Hospital, Copenhagen, Denmark (C.T.-P., T.W.H.); and Medical Department M, Glostrup University Hospital, Copenhagen, Denmark (J.J., S.R., H.I.).
Correspondence to Tine Willum-Hansen, MD, PhD, Bispebjerg Hospital, Y-forskning bygning 40, Bispebjerg Bakke, DK-2400 Copenhagen NV, Denmark. E-mail tw{at}heart.dk
Received July 29, 2005; revision received October 23, 2005; accepted November 18, 2005.
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Abstract |
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Background— Few population studies addressed the prognostic significance of aortic pulse wave velocity (APWV) above and beyond other cardiovascular risk factors.
Methods and Results— We studied a sex- and age-stratified random sample of 1678 Danes aged 40 to 70 years. We used Cox regression to investigate the prognostic value of APWV, office pulse pressure (PP), and 24-hour ambulatory PP while adjusting for mean arterial pressure (MAP) and other covariates. Over a median follow-up of 9.4 years, the incidence of fatal and nonfatal cardiovascular end points, cardiovascular mortality, and fatal and nonfatal coronary heart disease amounted to 154, 62, and 101 cases, respectively. We adjusted for sex, age, body mass index, MAP measured in the office (conventional PP and APWV) or by ambulatory monitoring (24-hour PP), smoking, and alcohol intake. With these adjustments, APWV maintained its prognostic significance in relation to each end point (P<0.05), whereas office and 24-hour PP lost their predictive value (P>0.19), except for office PP in relation to coronary heart disease (P=0.02). For each 1-SD increment in APWV (3.4 m/s), the risk of an event increased by 16% to 20%. In sensitivity analyses, APWV still predicted all cardiovascular events after standardization to a heart rate of 60 beats per minute, after adjustment for 24-hour MAP instead of office MAP, and/or after additional adjustment for the ratio of total to HDL serum cholesterol and diabetes mellitus at baseline.
Conclusions— In a general Danish population, APWV predicted a composite of cardiovascular outcomes above and beyond traditional cardiovascular risk factors, including 24-hour MAP.
Key Words: arterial stiffness • cardiovascular diseases • epidemiology • pulse pressure • risk factors
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Introduction |
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During a person’s lifetime, as part of the aging process or as a consequence of hypertension, atherosclerosis, or other pathological processes, the aorta stiffens.1 Accordingly, the forward pulse wave travels faster, and the arterial waves reflected from the periphery reach the heart early during systole, which leads to higher systolic but lower diastolic blood pressure, an augmentation of the cardiac workload, and a decrease of the coronary perfusion pressure.2 The aortic pulse wave velocity (APWV) reflects central arterial stiffness.2 APWV is a predictor of cardiovascular outcome in patients with hypertension,3–5 diabetes,6 end-stage renal disease,7 and elderly hospitalized subjects.8 However, only 1 small Japanese survey9 and 1 study in an elderly population (mean age, 73.7 years)10 have studied the predictive value of APWV in the general population. Furthermore, pulse pressure, an indirect measure of increased arterial stiffness, predicts a poor prognosis in treated and untreated hypertensive subjects11–15 and in older subjects randomly selected from European16 or North American17,18 populations.
Editorial p 601
Clinical Perspective p 670
In 1993–1994, we recorded pulse pressure from office blood pressure readings and 24-hour ambulatory recordings as well as APWV in a sex- and age-stratified random sample of the general Danish population. Follow-up continued until October 2003. In the present analysis, we studied the extent to which the office and 24-hour pulse pressures and APWV predicted cardiovascular outcome above and beyond mean arterial pressure as an index of the blood pressure level.
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Methods |
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Study Population
The Ethics Committee of Copenhagen County approved the Monitoring of Trends and Determinants in Cardiovascular Disease (MONICA) health survey.19 The study was conducted in accordance with the Helsinki Declaration. Participants provided informed written consent. In 1982–1984, we selected a random sample of the residents of Glostrup County with the goal to recruit an equal number of women and men aged 30, 40, 50, and 60 years. At baseline, the participation rate was 82.6%. In 1993–1994, the 3785 former participants were invited for a follow-up examination at the Research Center for Prevention and Health in Glostrup, of whom 2656 (70.2%) renewed informed written consent and were examined.20 For the present analysis, we excluded 978 subjects because APWV had not been recorded (n=36), because they were unwilling to have their 24-hour ambulatory blood pressure measured (n=568), because they had <14 daytime or <7 nighttime blood pressure readings (n=232),21 because their ambulatory blood pressure had been recorded during nighttime shifts (n=13), or because they had a previous history of myocardial infarction or stroke (n=106) or were taking digoxin or nitrates (n=23). Thus, the number of subjects statistically analyzed totaled 1678 (63.2% of those with a follow-up examination).
Data Collection
At the research center, a trained nurse measured anthropometric characteristics. Body mass index was weight in kilograms divided by height in meters squared. After the subjects had rested for 5 minutes in the supine position, 2 consecutive blood pressure readings were obtained with a random zero mercury sphygmomanometer fitted with an appropriate cuff size. The 2 readings were averaged for analysis. Hypertension was defined as an office blood pressure of 
140 mm Hg systolic or 90 mm Hg diastolic22 or as the use of antihypertensive drugs. Heart rate was counted at the radial artery over 15 seconds. Immediately thereafter, the same trained nurse used 2 piezoelectric pressure transducers (Hellige GmbH) to record in all subjects the arterial wave simultaneously at the left common carotid and femoral arteries.23 APWV was the travel distance between the 2 transducers, measured on the body surface, divided by the transit time, determined manually by the foot-to-foot velocity method.23 For analysis, we averaged from 2 to 15 heart cycles. As reported by Asmar and colleagues,23 the intraobserver repeatability coefficient for the measurements of APWV, computed according to the method of Bland and Altman24 and expressed as a percentage of the maximal variation in APWV (4 times the standard deviation), was &9.0%.
We programmed validated25 Takeda TM-2421 recorders (A&D) to obtain blood pressure recordings at an interval of 15 minutes from 7 AM to 11 PM and every 30 minutes from 11 PM to 7 AM. For analysis we used only the oscillometric measurements. We computed the within-subject 24-hour means of the ambulatory measurements with weights according to the time interval between successive readings. Pulse pressure (the difference between systolic and diastolic blood pressure) and mean arterial pressure (diastolic blood pressure plus one third of pulse pressure) were computed from the office and the 24-hour ambulatory blood pressures.
Venous blood samples collected after overnight fasting were analyzed by standard automated methods for lipids and blood glucose. According to published criteria,26 diabetes mellitus was defined as a fasting blood glucose level of 7.0 mmol/L or as the use of oral antidiabetic drugs or insulin. The participants completed a self-administrated questionnaire inquiring into their past and current medical history, intake of medications, and lifestyle. A high alcohol intake was a consumption of >5 alcoholic beverages per day, and a low level of physical activity was <4 hours of exercise per week.27
Ascertainment of Events
For all enrolled subjects, we ascertained vital status via the Danish Civil Registration System, the cause of death from the blinded adjudication of the diseases on the death certificates, and nonfatal events from the Danish National Health Register, which has a high sensitivity and predictive value.28 The end points considered in the present analysis were cardiovascular mortality, fatal and nonfatal coronary heart disease, and a composite end point consisting of cardiovascular mortality, coronary heart disease (ICD-8 codes 410 to 414 or ICD-10 codes I20 to I25), and stroke (ICD-8 codes 431, 433, or 434 or ICD-10 codes I61 or I63).
Statistical Analysis
For statistical analysis, we used SAS software, version 9.1 (SAS Institute). To compare means, we used the standard normal Z test for large samples or ANOVA with Tukey test for multiple comparisons. For proportions, we used the 
2 statistic with Bonferroni correction of the probability values, if appropriate. In the analysis of outcome, for participants who experienced multiple events, we considered only the first event. We implemented Cox proportional hazard regression to calculate relative hazard ratios in relation to APWV and pulse pressure. First, in exploratory analyses, we calculated relative hazard ratios for the composite cardiovascular end point by quintiles of the distribution of APWV and the office and 24-hour pulse pressures, unadjusted or with adjustment for sex and age. We used the deviation from mean coding29,30 to compute hazard ratios in quintiles relative to the overall risk in the study population. This approach avoids any assumption about the shape of the association between outcome and APWV or pulse pressure.30 Next, to identify significant predictors of outcome, we used forward and backward selection in Cox regression with the probability value for independent covariates to enter or stay in the model set at 0.05. The baseline measurements considered as predictors were sex, age, body mass index, waist-to-hip ratio, mean arterial pressure, use of antihypertensive drugs, current smoking, alcohol intake, physical activity, ratio of total to HDL serum cholesterol, and diabetes mellitus. To test for heterogeneity between women and men in the associations between outcome and APWV, we forced the appropriate interaction term into the regression models. In a sensitivity analysis, we standardized each participant’s APWV to a heart rate of 60 beats per minute by means of regression analysis in women and men, separately.31 Statistical significance was a probability value of 
0.05 on 2-sided tests.
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Results |
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Baseline Characteristics of Participants
The 1678 participants included 800 women (47.7%), 608 hypertensive patients (36.2%), of whom 147 (24.2%) were takings antihypertensive drugs, and 48 diabetic subjects (2.8%), of whom 17 (35.4%) were on treatment with antidiabetic agents. Women compared with men had lower office and ambulatory blood pressures, lower APWV, and higher heart rate but similar pulse pressure on office and 24-hour ambulatory blood pressure measurement (Table 1). Alcohol intake in excess of 5 beverages per day was more frequent among men. In the total study population, average values (±SD) of mean arterial pressure were 97.8±12.1 and 91.6±9.9 mm Hg on office and 24-hour ambulatory measurement, respectively. The ratio of total to HDL serum cholesterol averaged 4.6±1.5 in all participants.
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The 978 subjects excluded from analysis compared with the 1678 included were older (40/50/60/70 years, 30%/26%/24%/20% versus 26%/29%/27%/18%; P=0.01), were more likely to be female (54.5% versus 47.8%; P<0.01), and were more likely to have lower systolic/diastolic levels of office blood pressure (129.6/80.0 versus 131.1/81.1 mm Hg; P<0.05).
Incidence of End Points in Exploratory Analyses
During follow-up (median, 9.4 years; 5th to 95th percentile interval, 4.0 to 10.1 years), 14 838 person-years accrued. Of 171 deaths, 62 (36.3%) were due to cardiovascular illnesses. The incidence of the composite cardiovascular outcome totaled 154 events, including 43 cardiovascular deaths, 88 coronary events, and 23 strokes. Coronary heart disease consisted of 22 fatal and 79 nonfatal events, including 18 fatal and 35 nonfatal cases of acute myocardial infarction.
Table 2 lists the baseline characteristics according to the quintiles of APWV. The explanatory analysis unadjusted or adjusted for sex and age (Figure 1) revealed strong associations of the risk of the composite cardiovascular end point with APWV and office and 24-hour pulse pressures (Figure 1).
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Cox Regression
Using Cox regression, we computed the relative hazard ratios associated with a 1-SD increase in APWV and the office and 24-hour pulse pressures, first without any adjustment, next with adjustment for sex and age, and then additionally adjusted for body mass index, mean arterial pressure, current smoking, and alcohol intake (Table 3). In the fully adjusted models, mean arterial pressure was derived from the office measurements for office pulse pressure and APWV and from the ambulatory recordings for the 24-hour pulse pressure.
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In Cox models unadjusted or only adjusted for sex and age, APWV and the office and 24-hour pulse pressures consistently predicted each of the 3 outcomes under study. In the fully adjusted models, APWV maintained its prognostic significance in relation to each end point, whereas the office and 24-hour pulse pressures no longer predicted outcome, except for the office pulse pressure in relation to coronary heart disease. Figure 2 shows the absolute risk in women and men associated with APWV at different levels of mean arterial pressure in the office, while controlling for age, body mass index, current smoking, and alcohol intake.
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Sensitivity Analysis of APWV as Predictor of Outcome
The relative hazards ratios relating the 3 end points to APWV were higher in women than men (Table 4). At any level of mean arterial pressure, the absolute risk of a composite cardiovascular outcome in relation to APWV also increased more in women than men (Figure 2). However, when we formally tested the interaction between APWV and sex for the 3 end points, none of the probability values reached significance, irrespective of whether (P>0.48) or not (P>0.23) the Cox models were adjusted for other covariates. Furthermore, exclusion of subjects on antihypertensive drugs at the time of the APWV measurement weakened the relative hazard ratio reported for cardiovascular mortality from 1.20 (P=0.03; Table 3) to 1.08 (P=0.53; Table 4).
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Standardizing APWV to a heart rate of 60 beats per minute, adjustment for the 24-hour mean arterial pressure instead of the office measurement at the time of APWV registration, additional adjustment for the ratio of total to HDL serum cholesterol and diabetes mellitus at baseline, and the combination of the 3 former adjustments did not materially change the point estimates of relative hazard ratios reported for APWV in Table 3 but widened the CIs. However, in all instances, APWV remained a significant and independent predictor of the composite cardiovascular end point (Table 4).
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Discussion |
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The key finding of our study was that in middle-aged and elderly individuals randomly recruited from a Western European population, APWV measured over a few seconds in the office was a significant predictor of cardiovascular complications, above and beyond mean arterial pressure and other risk factors, including sex, age, body mass index, current smoking, and alcohol intake. With similar adjustments applied, the office and 24-hour pulse pressures lost their prognostic value with the exception of office pulse pressure in relation to coronary heart disease. For each 1-SD increment in APWV, the risk of an event increased by 16% to 20%. In sensitivity analyses, APWV still predicted all cardiovascular events after standardization to a heart rate of 60 beats per minute, after adjustment for 24-hour instead of office mean arterial pressure, and/or after additional adjustment for the ratio of total to HDL serum cholesterol and diabetes mellitus at baseline.
Most previous studies on the role of APWV as cardiovascular risk factor involved patients with hypertension,3–5 diabetes mellitus,6 or end-stage renal disease7 or elderly hospitalized subjects.8 Among patients with hypertension, the relative hazard ratios associated with a 3.4-m/s increase in APWV were 1.34 for stroke,4 1.38 for coronary complications,5 and 1.23 for cardiovascular mortality.3 The hazard ratios for a similar increase in APWV were 1.80 for cardiovascular mortality in elderly patients8 and 1.30 and 3.06 for total mortality in patients with diabetes6 or end-stage renal disease,7 respectively. Boutouyrie and colleagues5 reported relative hazard ratios for coronary heart disease in low-risk hypertensive patients by tertiles of APWV and adjusted for the Framingham risk score.32 With the bottom tertile as referent group, these ratios were 2.37 (95% CI, 1.45 to 3.86) and 5.60 (95% CI, 2.10 to 14.9) for the middle and top tertiles.5 In similarly informed calculations in our own cohort, the corresponding relative risks were 2.49 (95% CI, 1.09 to 5.70) and 3.77 (95% CI, 1.58 to 9.04), respectively. These findings suggest that the relative hazard ratios in our population-based study are smaller than those in patients because we excluded subjects with previous cardiovascular disease. Moreover, the more extensive adjustment for additional risk factors also weakened the hazard ratios in our study compared with those in the patient cohorts.3,6–8
To our knowledge, only 2 population-based studies9,10 previously examined the role of APWV as an independent predictor of cardiovascular outcomes. Shokawa and colleagues9 followed a cohort of 492 Japanese Americans, including 272 women (55.3%) living in Hawaii. Their mean age was 63.7 years. Over 10 years of follow-up, all-cause and cardiovascular mortality amounted to 43 and 14 deaths, respectively. The authors determined the receiver operating characteristics curve of APWV, which best discriminated subjects who died from those who survived. They observed that the optimal threshold was 9.9 m/s. In multivariate analyses adjusted for sex, age, systolic blood pressure, diabetes mellitus, hyperlipidemia, and ECG abnormalities, the relative risk associated with an elevated APWV was 1.42 (95% CI, 0.96 to 2.11) for all-cause mortality and 4.24 (95% CI, 1.39 to 12.9) for cardiovascular mortality. However, the small number of events and the post hoc determination of the threshold value for APWV render the results of this study difficult to interpret.
The investigators of the Health, Aging, and Body Composition (Health ABC) study10 measured APWV in 2488 older subjects (age range, 70 to 79 years), including 1002 blacks (40.3%) and 1302 women (52.3%). Over 4.6 years, 265 deaths occurred, 111 as a result of cardiovascular causes. The incidence of fatal and nonfatal events amounted to 341 cases of coronary heart disease, 94 strokes, and 181 cases of heart failure. The Health ABC team10 presented their results by quartiles of the distribution of APWV because, in contrast to the present findings (Figure 1), they noticed a threshold effect between the first and second quartile. From the lowest to the highest quartile, the relative risk gradually and significantly increased 2- to 3-fold for all-cause and cardiovascular mortality, coronary heart disease, and stroke. APWV remained predictive after adjustment for race, sex, age, systolic blood pressure, and previous cardiovascular disease.
Our observation that office pulse pressure was a significant predictor of coronary heart disease is in agreement with the Framingham findings. Indeed, Franklin and colleagues18 demonstrated that in subjects aged <50 years, diastolic blood pressure was a strong predictor of coronary heart disease. Age 50 to 59 years was a transition period when systolic, diastolic, and pulse pressures were similar predictors of cardiovascular risk, whereas from 60 years on, diastolic pressure was negatively related to the risk of coronary events so that pulse pressure became a better predictor than systolic pressure. We assume that in our study population with a median age of 51.1 years, these age-related trends18 contributed to the prognostic significance of pulse pressure.
The present study must be interpreted within the context of its potential limitations and the choices that we made in our epidemiological and statistical approach. First, at baseline, we did not determine the reproducibility of the APWV measurements. However, only 1 trained observer acquired and read all APWV recordings. Asmar and colleagues23 reported an intraobserver repeatability of 9.0%. If reproducibility would not have been within state-of-the-art standard limits, this would have weakened rather than strengthened the current estimates of the predictive value of APWV. Second, the number of strokes was too small to include cerebrovascular accidents as a separate end point in our analyses. On the other hand, in contrast to several other reports,3,4,6–9 our analysis included fatal as well as nonfatal hard cardiovascular outcomes. This is a crucial issue for the external validity of our observations because in this era of high-technology medicine, the case-fatality rate of major cardiovascular complications is declining quickly in developed countries so that solely reporting fatal outcomes is falling short of current clinical practice. Third, we deliberately chose to exclude 129 participants with a previous history of myocardial infarction or stroke or who were taking digoxin or nitrates. The exclusion from analysis of participants with a previous history of cardiovascular disease lends support to the concept that stiffening of the central arteries is already prognostically relevant in relatively healthy subjects.2 Fourth, whether or not APWV should be standardized for heart rate remains a matter of debate. In the present study, heart rate did not behave as a significant forerunner of a worse cardiovascular outcome. When we standardized APWV to a heart rate of 60 beats per minute, our results were consistent. Finally, we chose to adjust APWV and the office and 24-hour pulse pressures for mean arterial pressure rather than for systolic blood pressure. In keeping with published evidence,33 we viewed blood pressure as being composed of a steady component (mean arterial pressure) and a pulsatile component (pulse pressure). These measurements are statistically independent from one another.33 In our data, pulse pressure was more tightly correlated with systolic blood pressure (r2=0.50) than with mean arterial pressure (r2=0.29). For APWV, the r2 values were 0.24, 0.30, and 0.22 for pulse pressure, systolic blood pressure, and mean arterial pressure, respectively.
Our present observations in a population sample without previous cardiovascular complications extend previous reports on the prognostic value of APWV.3–10 APWV, a simple and noninvasive measurement obtained over a few heart cycles, significantly refined the risk stratification above and beyond classic risk factors. Even when adjusted for mean arterial pressure determined from 24-hour ambulatory blood pressure recordings, APWV kept its prognostic value in relation to the composite of all cardiovascular events. The present findings highlight the need to develop more sensitive techniques to measure the stiffness of various compartments of the arterial tree, which can be readily applied in routine clinical practice for risk stratification. Moreover, further molecular, clinical, and epidemiological research should clarify the genetic mechanisms, environmental factors, and their interaction that lead to premature stiffening of the arterial wall.34 Figure 2 suggests that for the same level of mean arterial pressure, APWV might behave as a stronger risk predictor in women than men. Given the age distribution of our study population, this observation might be due to the fact that most of the age-related increase in systolic blood pressure occurs after age 50 years in women, whereas the opposite is true in men.1 However, when we formally tested the interaction terms between APWV and sex in relation to the 3 outcomes, none reached statistical significance, possibly because of a lack of power.35
In conclusion, in a general population of Western European extraction, APWV predicted a composite of cardiovascular outcomes above and beyond 24-hour mean arterial pressure and traditional risk factors. In combination with the previous studies in patients3–8 and populations,9,10 our present findings support the notion that measurement of arterial stiffness is useful in clinical practice for risk stratification.
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Acknowledgments |
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This study was supported by grants from the Danish Heart Foundation (grant 01-2-9-9A-22914), Danish Medical Association Research Fund/Volten, and Danish Pharmaceutical Association. The authors gratefully acknowledge the clerical assistance of Sandra Covens (Leuven, Belgium).
Disclosures
None.
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CLINICAL PERSPECTIVE
Aortic pulse wave velocity is easily acquired at the bedside and reflects central arterial stiffness. Accordingly, we investigated this as a predictor of outcome in 1678 Danes, aged 40 to 70 years, randomly recruited from the population of Copenhagen. Over a median follow-up of 9.4 years, the incidence of fatal and nonfatal cardiovascular end points, cardiovascular mortality, and fatal and nonfatal coronary heart disease amounted to 154, 62, and 101 cases, respectively. We adjusted for sex, age, body mass index, mean arterial pressure measured in the office or by ambulatory monitoring, smoking, and alcohol intake. With these adjustments, aortic pulse wave velocity maintained its prognostic significance in relation to each end point, whereas office and 24-hour pulse pressure lost their predictive value with the exception of office pulse pressure in relation to coronary heart disease. In conclusion, aortic pulse wave velocity acquired in a few seconds predicted cardiovascular outcomes over and beyond 24-hour ambulatory blood pressure and traditional risk factors. These findings highlight the potential of indexes of arterial stiffness in risk stratification and the need to introduce such measurements into clinical practice.
Circulation 2006 113: 597.
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  J. D. Maclay, D. A. McAllister, N. L. Mills, F. P. Paterson, C. A. Ludlam, E. M. Drost, D. E. Newby, and W. MacNee Vascular Dysfunction in Chronic Obstructive Pulmonary Disease Am. J. Respir. Crit. Care Med., September 15, 2009; 180(6): 513 - 520. [Abstract] [Full Text] [PDF]
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 F. J. He, M. Marciniak, E. Visagie, N. D. Markandu, V. Anand, R. N. Dalton, and G. A. MacGregor Effect of Modest Salt Reduction on Blood Pressure, Urinary Albumin, and Pulse Wave Velocity in White, Black, and Asian Mild Hypertensives Hypertension, September 1, 2009; 54(3): 482 - 488. [Abstract] [Full Text] [PDF]
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 N. C. Edwards, R. P. Steeds, P. M. Stewart, C. J. Ferro, and J. N. Townend Effect of spironolactone on left ventricular mass and aortic stiffness in early-stage chronic kidney disease: a randomized controlled trial. J. Am. Coll. Cardiol., August 4, 2009; 54(6): 505 - 512. [Abstract] [Full Text] [PDF]
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H. P. Kuhl Hypertrophic cardiomyopathy, fibrosis, and aortic stiffness an unidentified association unraveled by magnetic resonance imaging. J. Am. Coll. Cardiol., July 14, 2009; 54(3): 263 - 264. [Full Text] [PDF]
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 C. E Bolton, J. R Cockcroft, R. Sabit, M. Munnery, C. M McEniery, I. B Wilkinson, S. Ebrahim, J. E Gallacher, D. J Shale, and Y. Ben-Shlomo Lung function in mid-life compared with later life is a stronger predictor of arterial stiffness in men: The Caerphilly Prospective Study Int. J. Epidemiol., June 1, 2009; 38(3): 867 - 876. [Abstract] [Full Text] [PDF]
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S. G. Anderson, T. A.B. Sanders, and J. K. Cruickshank Plasma Fatty Acid Composition as a Predictor of Arterial Stiffness and Mortality Hypertension, May 1, 2009; 53(5): 839 - 845. [Abstract] [Full Text] [PDF]
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 K. V. Tarasov, S. Sanna, A. Scuteri, J. B. Strait, M. Orru, A. Parsa, P.-I Lin, A. Maschio, S. Lai, M. G. Piras, et al. COL4A1 Is Associated With Arterial Stiffness by Genome-Wide Association Scan Circ Cardiovasc Genet, April 1, 2009; 2(2): 151 - 158. [Abstract] [Full Text] [PDF]
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S. Sakuragi, K. Abhayaratna, K. J. Gravenmaker, C. O'Reilly, W. Srikusalanukul, M. M. Budge, R. D. Telford, and W. P. Abhayaratna Influence of Adiposity and Physical Activity on Arterial Stiffness in Healthy Children: The Lifestyle of Our Kids Study Hypertension, April 1, 2009; 53(4): 611 - 616. [Abstract] [Full Text] [PDF]
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 J. A. Chirinos, S. S. Franklin, R. R. Townsend, and L. Raij Body Mass Index and Hypertension Hemodynamic Subtypes in the Adult US Population Arch Intern Med, March 23, 2009; 169(6): 580 - 586. [Abstract] [Full Text] [PDF]
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 C. A. Peralta, R. Katz, M. Madero, M. Sarnak, H. Kramer, M. H. Criqui, and M. G. Shlipak The Differential Association of Kidney Dysfunction With Small and Large Arterial Elasticity: The Multiethnic Study of Atherosclerosis Am. J. Epidemiol., March 15, 2009; 169(6): 740 - 748. [Abstract] [Full Text] [PDF]
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 N. Bjarnegard, H. J Arnqvist, T.;r. Lindstro;m, L. Jonasson, and T. Lanne Long-term hyperglycaemia impairs vascular smooth muscle cell function in women with type 1 diabetes mellitus Diabetes and Vascular Disease Research, January 1, 2009; 6(1): 25 - 31. [Abstract] [PDF]
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 F. Antonini-Canterin, S. Carerj, V. Di Bello, G. Di Salvo, S. La Carrubba, O. Vriz, D. Pavan, A. Balbarini, G. L. Nicolosi, and On behalf of the Research Group of the Italian Soc Arterial stiffness and ventricular stiffness: a couple of diseases or a coupling disease? A review from the cardiologist's point of view Eur J Echocardiogr, January 1, 2009; 10(1): 36 - 43. [Abstract] [Full Text] [PDF]
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 J. Andrade, L. Er, A. Ignaszewski, and A. Levin Exploration of Association of 1,25-OH2D3 with Augmentation Index, a Composite Measure of Arterial Stiffness Clin. J. Am. Soc. Nephrol., November 1, 2008; 3(6): 1800 - 1806. [Abstract] [Full Text] [PDF]
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 R. D. Smith and P. J. Levy Review: New techniques for assessment of vascular function Therapeutic Advances in Cardiovascular Disease, October 1, 2008; 2(5): 373 - 385. [Abstract] [PDF]
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 D. Nyhan and D. E. Berkowitz Perioperative Blood Pressure Management: Does Central Vascular Stiffness Matter? Anesth. Analg., October 1, 2008; 107(4): 1103 - 1106. [Full Text] [PDF]
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G. Schillaci, G. V.L. De Socio, G. Pucci, M. R. Mannarino, J. Helou, M. Pirro, and E. Mannarino Aortic Stiffness in Untreated Adult Patients With Human Immunodeficiency Virus Infection Hypertension, August 1, 2008; 52(2): 308 - 313. [Abstract] [Full Text] [PDF]
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 A. G. Ruitenbeek, T. J.M. van der Cammen, A. H. van den Meiracker, and F. U.S. Mattace-Raso Age and Blood Pressure Levels Modify the Functional Properties of Central but Not Peripheral Arteries Angiology, July 1, 2008; 59(3): 290 - 295. [Abstract] [PDF]
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 G. Grassi, F. Quarti-Trevano, and G. Mancia Review: Cardioprotective effects of telmisartan in uncomplicated and complicated hypertension Journal of Renin-Angiotensin-Aldosterone System, June 1, 2008; 9(2): 66 - 74. [Abstract] [PDF]
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 R Schutte, T Nawrot, T Richart, L Thijs, H A Roels, L M Van Bortel, H Struijker-Boudier, and J A Staessen Arterial structure and function and environmental exposure to cadmium Occup. Environ. Med., June 1, 2008; 65(6): 412 - 419. [Abstract] [Full Text] [PDF]
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 M Saito, H Okayama, K Nishimura, A Ogimoto, T Ohtsuka, K Inoue, G Hiasa, T Sumimoto, and J Higaki Possible link between large artery stiffness and coronary flow velocity reserve Heart, June 1, 2008; 94(6): e20 - e20. [Abstract] [Full Text] [PDF]
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J. Karalliedde, A. Smith, L. DeAngelis, V. Mirenda, A. Kandra, J. Botha, P. Ferber, and G. Viberti Valsartan Improves Arterial Stiffness in Type 2 Diabetes Independently of Blood Pressure Lowering Hypertension, June 1, 2008; 51(6): 1617 - 1623. [Abstract] [Full Text] [PDF]
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S. S. Najjar, A. Scuteri, V. Shetty, J. G. Wright, D. C. Muller, J. L. Fleg, H. P. Spurgeon, L. Ferrucci, and E. G. Lakatta Pulse Wave Velocity Is an Independent Predictor of the Longitudinal Increase in Systolic Blood Pressure and of Incident Hypertension in the Baltimore Longitudinal Study of Aging J. Am. Coll. Cardiol., April 8, 2008; 51(14): 1377 - 1383. [Abstract] [Full Text] [PDF]
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 M. Delahousse, M. Chaignon, L. Mesnard, P. Boutouyrie, M. E. Safar, T. Lebret, M. Pastural-Thaunat, L. Tricot, A. Kolko-Labadens, A. Karras, et al. Aortic Stiffness of Kidney Transplant Recipients Correlates with Donor Age J. Am. Soc. Nephrol., April 1, 2008; 19(4): 798 - 805. [Abstract] [Full Text] [PDF]
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G. F. Mitchell, V. Gudnason, L. J. Launer, T. Aspelund, and T. B. Harris Hemodynamics of Increased Pulse Pressure in Older Women in the Community-Based Age, Gene/Environment Susceptibility-Reykjavik Study Hypertension, April 1, 2008; 51(4): 1123 - 1128. [Abstract] [Full Text] [PDF]
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G. Mancia and G. Grassi Editorial: The new European Society of Hypertension/European Society of Cardiology (ESH/ESC) Guidelines Therapeutic Advances in Cardiovascular Disease, February 1, 2008; 2(1): 5 - 12. [PDF]
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M. E. Safar Review: Pulse pressure, arterial stiffness and wave reflections (augmentation index) as cardiovascular risk factors in hypertension Therapeutic Advances in Cardiovascular Disease, February 1, 2008; 2(1): 13 - 24. [Abstract] [PDF]
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 P. Ou, D. S. Celermajer, O. Raisky, O. Jolivet, F. Buyens, A. Herment, D. Sidi, D. Bonnet, and E. Mousseaux Angular (Gothic) aortic arch leads to enhanced systolic wave reflection, central aortic stiffness, and increased left ventricular mass late after aortic coarctation repair: Evaluation with magnetic resonance flow mapping J. Thorac. Cardiovasc. Surg., January 1, 2008; 135(1): 62 - 68. [Abstract] [Full Text] [PDF]
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 S. Steigerwalt Management of Hypertension in Diabetic Patients With Chronic Kidney Disease Diabetes Spectr, January 1, 2008; 21(1): 30 - 36. [Abstract] [Full Text] [PDF]
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H Senzaki, Y Iwamoto, H Ishido, T Matsunaga, M Taketazu, T Kobayashi, H Asano, T Katogi, and S Kyo Arterial haemodynamics in patients after repair of tetralogy of Fallot: influence on left ventricular after load and aortic dilatation Heart, January 1, 2008; 94(1): 70 - 74. [Abstract] [Full Text] [PDF]
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S. R. Waldstein, S. C. Rice, J. F. Thayer, S. S. Najjar, A. Scuteri, and A. B. Zonderman Pulse Pressure and Pulse Wave Velocity Are Related to Cognitive Decline in the Baltimore Longitudinal Study of Aging Hypertension, January 1, 2008; 51(1): 99 - 104. [Abstract] [Full Text] [PDF]
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 M. J. Roman and J. E. Salmon Cardiovascular Manifestations of Rheumatologic Diseases Circulation, November 13, 2007; 116(20): 2346 - 2355. [Full Text] [PDF]
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 M. F. O'Rourke Arterial aging: pathophysiological principles Vascular Medicine, November 1, 2007; 12(4): 329 - 341. [Abstract] [PDF]
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M. Yoshida, H. Tomiyama, J. Yamada, Y. Koji, K. Shiina, M. Nagata, and A. Yamashina Relationships among Renal Function Loss within the Normal to Mildly Impaired Range, Arterial Stiffness, Inflammation, and Oxidative Stress Clin. J. Am. Soc. Nephrol., November 1, 2007; 2(6): 1118 - 1124. [Abstract] [Full Text] [PDF]
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 F. Verbeke, W. Van Biesen, P. Peeters, L. M. Van Bortel, and R. C. Vanholder Arterial stiffness and wave reflections in renal transplant recipients Nephrol. Dial. Transplant., October 1, 2007; 22(10): 3021 - 3027. [Abstract] [Full Text] [PDF]
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N. Cheung, A. R. Sharrett, R. Klein, M. H. Criqui, F.M. A. Islam, K. J. Macura, M. F. Cotch, B. E.K. Klein, and T. Y. Wong Aortic Distensibility and Retinal Arteriolar Narrowing: The Multi-Ethnic Study of Atherosclerosis Hypertension, October 1, 2007; 50(4): 617 - 622. [Abstract] [Full Text] [PDF]
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A. Benjo, R. E. Thompson, D. Fine, C. W. Hogue, D. Alejo, A. Kaw, G. Gerstenblith, A. Shah, D. E. Berkowitz, and D. Nyhan Pulse Pressure Is an Age-Independent Predictor of Stroke Development After Cardiac Surgery Hypertension, October 1, 2007; 50(4): 630 - 635. [Abstract] [Full Text] [PDF]
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M. F. O'Rourke and J. Hashimoto Mechanical Factors in Arterial Aging: A Clinical Perspective J. Am. Coll. Cardiol., July 3, 2007; 50(1): 1 - 13. [Abstract] [Full Text] [PDF]
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M. J. Roman, R. B. Devereux, J. R. Kizer, E. T. Lee, J. M. Galloway, T. Ali, J. G. Umans, and B. V. Howard Central Pressure More Strongly Relates to Vascular Disease and Outcome Than Does Brachial Pressure: The Strong Heart Study Hypertension, July 1, 2007; 50(1): 197 - 203. [Abstract] [Full Text] [PDF]
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R. Sabit, C. E. Bolton, P. H. Edwards, R. J. Pettit, W. D. Evans, C. M. McEniery, I. B. Wilkinson, J. R. Cockcroft, and D. J. Shale Arterial Stiffness and Osteoporosis in Chronic Obstructive Pulmonary Disease Am. J. Respir. Crit. Care Med., June 15, 2007; 175(12): 1259 - 1265. [Abstract] [Full Text] [PDF]
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 Authors/Task Force Members:, G. Mancia, G. De Backer, A. Dominiczak, R. Cifkova, R. Fagard, G. Germano, G. Grassi, A. M. Heagerty, S. E. Kjeldsen, et al. 2007 Guidelines for the Management of Arterial Hypertension: The Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC) Eur. Heart J., June 11, 2007; (2007) ehm236v1. [Full Text] [PDF]
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M. M.H. Hermans, R. Henry, J. M. Dekker, J. P. Kooman, P. J. Kostense, G. Nijpels, R. J. Heine, and C. D.A. Stehouwer Estimated Glomerular Filtration Rate and Urinary Albumin Excretion Are Independently Associated with Greater Arterial Stiffness: The Hoorn Study J. Am. Soc. Nephrol., June 1, 2007; 18(6): 1942 - 1952. [Abstract] [Full Text] [PDF]
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S. Laurent and P. Boutouyrie Recent Advances in Arterial Stiffness and Wave Reflection in Human Hypertension Hypertension, June 1, 2007; 49(6): 1202 - 1206. [Full Text] [PDF]
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G. F. Mitchell, M. E. Dunlap, W. Warnica, A. Ducharme, J. M. O. Arnold, J.-C. Tardif, S. D. Solomon, M. J. Domanski, K. A. Jablonski, M. M. Rice, et al. Long-Term Trandolapril Treatment Is Associated With Reduced Aortic Stiffness: The Prevention of Events With Angiotensin-Converting Enzyme Inhibition Hemodynamic Substudy Hypertension, June 1, 2007; 49(6): 1271 - 1277. [Abstract] [Full Text] [PDF]
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G. F. Mitchell, C.-Y. Guo, E. J. Benjamin, M. G. Larson, M. J. Keyes, J. A. Vita, R. S. Vasan, and D. Levy Cross-Sectional Correlates of Increased Aortic Stiffness in the Community: The Framingham Heart Study Circulation, May 22, 2007; 115(20): 2628 - 2636. [Abstract] [Full Text] [PDF]
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 L. F. Drager, L. A. Bortolotto, A. C. Figueiredo, B. C. Silva, E. M. Krieger, and G. Lorenzi-Filho Obstructive Sleep Apnea, Hypertension, and Their Interaction on Arterial Stiffness and Heart Remodeling Chest, May 1, 2007; 131(5): 1379 - 1386. [Abstract] [Full Text] [PDF]
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 J. Roquer, A. Ois, A. Rodriguez-Campello, M. Gomis, E. Munteis, J. Jimenez-Conde, E. Cuadrado-Godia, and J. E. Martinez-Rodriguez Atherosclerotic Burden and Early Mortality in Acute Ischemic Stroke Arch Neurol, May 1, 2007; 64(5): 699 - 704. [Abstract] [Full Text] [PDF]
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C. Shirodaria, C. Antoniades, J. Lee, C. E. Jackson, M. D. Robson, J. M. Francis, S. J. Moat, C. Ratnatunga, R. Pillai, H. Refsum, et al. Global Improvement of Vascular Function and Redox State With Low-Dose Folic Acid: Implications for Folate Therapy in Patients With Coronary Artery Disease Circulation, May 1, 2007; 115(17): 2262 - 2270. [Abstract] [Full Text] [PDF]
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I. J. Kullo and A. R. Malik Arterial Ultrasonography and Tonometry as Adjuncts to Cardiovascular Risk Stratification J. Am. Coll. Cardiol., April 3, 2007; 49(13): 1413 - 1426. [Abstract] [Full Text] [PDF]
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 M. Kikuya, J. A. Staessen, T. Ohkubo, L. Thijs, H. Metoki, K. Asayama, T. Obara, R. Inoue, Y. Li, E. Dolan, et al. Ambulatory Arterial Stiffness Index and 24-Hour Ambulatory Pulse Pressure as Predictors of Mortality in Ohasama, Japan Stroke, April 1, 2007; 38(4): 1161 - 1166. [Abstract] [Full Text] [PDF]
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 C. Meyer, B. P. McGrath, and H. J. Teede Effects of Medical Therapy on Insulin Resistance and the Cardiovascular System in Polycystic Ovary Syndrome Diabetes Care, March 1, 2007; 30(3): 471 - 478. [Abstract] [Full Text] [PDF]
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K. Noma, C. Goto, K. Nishioka, D. Jitsuiki, T. Umemura, K. Ueda, M. Kimura, K. Nakagawa, T. Oshima, K. Chayama, et al. Roles of Rho-Associated Kinase and Oxidative Stress in the Pathogenesis of Aortic Stiffness J. Am. Coll. Cardiol., February 13, 2007; 49(6): 698 - 705. [Abstract] [Full Text] [PDF]
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G. Schillaci, M. R. Mannarino, G. Pucci, M. Pirro, J. Helou, G. Savarese, G. Vaudo, and E. Mannarino Age-Specific Relationship of Aortic Pulse Wave Velocity With Left Ventricular Geometry and Function in Hypertension Hypertension, February 1, 2007; 49(2): 317 - 321. [Abstract] [Full Text] [PDF]
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 J. Cameron Ageing and central aortic pulse wave analysis. Commentary on 'Is Augmentation Index a Good Measure of Vascular Stiffness in the Elderly?' by Fantin et al. Age Ageing, January 1, 2007; 36(1): 3 - 5. [Full Text] [PDF]
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S. Laurent, J. Cockcroft, L. Van Bortel, P. Boutouyrie, C. Giannattasio, D. Hayoz, B. Pannier, C. Vlachopoulos, I. Wilkinson, H. Struijker-Boudier, et al. Expert consensus document on arterial stiffness: methodological issues and clinical applications Eur. Heart J., November 1, 2006; 27(21): 2588 - 2605. [Abstract] [Full Text] [PDF]
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 N.C. Edwards, R.P. Steeds, C.J. Ferro, and J.N. Townend The treatment of coronary artery disease in patients with chronic kidney disease QJM, November 1, 2006; 99(11): 723 - 736. [Abstract] [Full Text] [PDF]
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M. Zureik, S. Czernichow, D. Courbon, J. Blacher, P. Ducimetiere, S. Hercberg, M. E. Safar, and P. Galan Parental Longevity, Carotid Atherosclerosis, and Aortic Arterial Stiffness in Adult Offspring Stroke, November 1, 2006; 37(11): 2702 - 2707. [Abstract] [Full Text] [PDF]
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J. N. Cohn Arterial Stiffness, Vascular Disease, and Risk of Cardiovascular Events Circulation, February 7, 2006; 113(5): 601 - 603. [Full Text] [PDF]
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