- Research article
- Open Access
- Open Peer Review
Young smoker “ABCD” vascular assessment: a four-step ultrasound examination for detecting peripheral, extra and intra-cranial early arterial damage
© The Author(s). 2016
- Received: 22 December 2015
- Accepted: 7 June 2016
- Published: 8 July 2016
Cigarette smoking is known as a major risk factor in the pathogenic mechanisms of stroke, coronary and peripheral artery disease (CAD and PAD), even in young subjects. The aim of this study is the creation of a four-step ultrasound examination to evaluate and monitor the peripheral, the extra and the intra-cranial assessment of the arterial early damage in smokers. The evaluations of A, the Ankle-brachial index, ABI, B, the Breath holding index, BHI, C, the Carotid intima media thickness, CIMT, and D, the Diameter of the abdominal aorta represent the “ABCD” assessment.
Thirty-eight healthy smokers and 43 controls underwent A, calculated for each leg. B was calculated after determination of subjects’ flow velocity of middle cerebral artery (MCA) by trans-cranial colour Doppler (TCCD) before and after 30 s of apnoea at baseline and just after smoking a cigarette, to simulate the chronic and acute effects of smoking. Finally, C and D evaluation were assessed using a high-resolution B-mode ultrasound.
Smokers presented higher values of CIMT (mean and maximal), and lower BHI both at baseline and just after smoking (p < 0.01), though in the normal range. No significant differences were found for A and D between smokers and non- smokers.
Our results underline the importance of the assessment of B and C, that, though in the normal range, present significant differences between smokers and non-smokers. These data could drive the screening between smokers in age-related manner. Moreover, the “ABCD” examination could represent a valid method to detect and then monitor smokers’ vascular damage. Although it is far to be considered a screening and routine tool, it should be contemplated in a wider context of possible not-invasive practical screening and follow-up modalities. This would be designed to implement preventive strategies and tools aimed at discouraging tobacco addiction and monitoring cardiovascular risk patients.
- Ankle-brachial index
- Breath holding index
- Carotid intima-media thickness
- Abdominal aorta diameter
- Early arterial damage
PAD can be assessed with not invasive tests and the ankle-brachial index (ABI) is the most widely used measure to detect the presence of PAD . Originally described by Winsor , nowadays the ABI is an important indicator of atherosclerosis and a prognostic marker, even in absence of symptoms . An ABI of less than 0.90 is the threshold to define PAD, using the Doppler modality .
Several studies have confirmed a dose and time-dependent relationship between carotid intima media thickness (CIMT) and smoking in the context of subclinical atherosclerotic damage . In particular, our group  has recently demonstrated higher CIMT values in healthy young smokers than in age-sex matched non-smokers. CIMT, assessed by B-mode ultrasonography is a sensitive marker of atherosclerosis, also in the early stages, being an independent predictor of stroke and cardiovascular events .
Regarding the effects of smoking on the impairment of cerebral circulation, it is known that acute smoking reduces the cerebral vasodilator response to hypercapnia [10, 11], but the effects of chronic smoking are not well established. Cerebral vasomotor reactivity can be studied by measuring changes in flow velocity in response to vasodilatatory stimuli as such as CO2 inhalation, breath holding or acetazolamide administration [12, 13]. The breath-holding index (BHI) is considered the most practical, inexpensive, best-tolerated and easy to perform alternative to the previous methods .
Moreover, if a significant carotid stenosis or occlusion is considered as one of the most important factors affecting cerebral vasomotor reactivity, very recently an association between altered reactivity and CAD has been established, even in the absence of significant carotid stenosis .
Finally, it is well known for many years that smoking has also been emphasized as an independent risk factor for abdominal aortic aneurysm (AAA) , but precise worldwide-accepted recommendations for screening are still lacking .
This work intends to better define the vascular damage of smoking in young healthy people, creating a relatively easy ultrasound examination system, in order to provide evidence of the major impact of smoking on vascular assessment and to underline the importance of preventive strategies in the young population.
The same system (ABCD) could be the basis for future screening and follow up modalities also for older smokers and for the “vascular “risk patient.
Ethics statement: the study was conducted in accordance with the ethical standards laid down in the Helsinki Declaration of 1975 and its late amendments. Healthy volunteers were recruited among the students of Verona University School of Medicine and among the Internal Medicine certification board students of the same institution. All participants provided written consent prior to commencing the study and the local ethical committee approved the study.
The healthy volunteers were recruited according to the following criteria: male and female; aged 23–31; normal BMI; no use of antioxidant supplementation or anti-inflammatory medication during or for six months prior to commencing the study; no diagnosed cerebral or cardio or peripheral vascular disease, hypertension, hypercholesterolemia or diabetes mellitus or endocrine disorders.
Non-smokers included those who had never smoked or those who had not smoked for at least 3 years.
Smokers were described as individuals who smoked at least 3 cigarettes per day with a smoking duration period ≥ 6 months.
Studies were conducted in a quiet, temperature-controlled laboratory (25 °C), in the morning. Subjects were asked to retrain from caffeine and alcohol-containing a beverages for at least 8 h before the examination. The examinations were conducted at baseline for the non-smokers and both at the baseline and within maximum of 10 min after smoking a cigarette for the smokers (based on previous data about the peak of blood nicotine concentrations in the systemic circulation after smoking ).
Subjects were tested as “with regular sinus rhythm clinically” (no history of arrhythmia or any cardiovascular disease was reported).
Ultrasound examinations were performed by the same examiner (CM) who was unaware of the subjects’ smoking habits before performing the A, baseline B, C and D.
The following steps constitute the ABCD examination.
A: the ABI assessment
According to a recent review statement about its measurement , the ABI was determined from blood pressure measurement in both upper limbs and ankles, with the subject in supine position. Systolic blood pressure from the brachial artery in the antecubital fossa was measured using a blood pressure cuff and high-resolution B-mode ultrasound (HC Envisor, Philips) equipped with continuous –wave Doppler 5 MHz probe. In the lower limbs, systolic blood pressure from the posterior tibial or dorsalis pedis arteries was measured with Doppler detection by placing a blood pressure cuff at the ankle. ABI was calculated as the ratio of the higher systolic blood pressure measured at the ankle to the systolic blood pressure measured at the brachial artery. The interpretation of the ABI was made according to the current classification and interpretation recommendations .
B: the BHI assessment
The subjects were examined while supine, with their head hyperextended and turned away from the side being scanned. The trans-temporal approach was used to detect continuous measurements of flow signals from the M1 segment of the middle cerebral artery (MCA), 45–65 mm depth  Pulsed-wave TCCD (2 MHz probe, Envisor, Philips) was used.
Cerebrovascular reactivity to hypercapnia was evaluated by means of the BHI . The BHI has been calculated according to the following formula: BHI% = [(MFV apnea—MFV rest)/MFV rest x30] x 100.
The breath holding indices from the two sides were averaged within one subject.
Mean flow velocity (MFV) was calculated according to the formula: MFV = [PSV+(EDV x2)]/3.
It was obtained at rest by the continuous recording of 1-min period of normal breathing, then the subjects were asked to hold their breath for 30 s following a normal inspiration in order to avoid a Valsalva effect . A normal BHI was considered if ≥0.69, an impaired BHI if <0.69 . Subjects were preliminary instructed on how to perform BHI and they test the procedure before starting the recordings.
Three subjects were excluded because with poor insonation of the temporal bone window.
C: the CIMT assessment
CIMT was evaluated as distance between the leading edge of the lumen-intima interface and the leading edge of the media adventitia interface, according to the recommendations of the Mannheim Carotid Intima-Media thickness Consensus . The investigator performed not invasive measurements of CIMT using a high-resolution B-mode ultrasound (Envisor, Philips) equipped with a 7.5-to 12-MHz probe. For all subjects, CIMT was measured in the far wall of the common carotid artery proximal to the bifurcation, at the bulb and the origin of the internal carotid artery of both sides . On each arterial site, mean CIMT values (as averaged across the entire distance) and maximal CIMT values were recorded using Carotid Studio, a validated real-time automatic technique for CIMT measurement . These 6 combined mean and maximal CIMT far-wall measurements from left and right side were averaged.
D: the diameter of the abdominal aorta
The examination took place with the subject in the supine position, using a 5 MHz phased-array probe. Aorta was visualized in the longitudinal plane and was examined from the diaphragm to the bifurcation. Aorta was then examined in the axial plane with scans perpendicular to the longitudinal plane. Aortic diameters were measured 1 cm distal to the renal arteries level.
A Shapiro Wilk test was used to test the null-hypotesis that the population was normally distributed.
Because of the fact that BHI, mean and max IMT resulted not normally distributed, the non-parametric Mann- Whitney's U test was used for these data.
For the other data, differences between two groups were analysed by a two-tailed unpaired Student’s t-test.
Normally distributed continuous variables (ABI and Diameter of the abdominal aorta) are expressed as mean ± SD while non-normally distributed variables (BHI, C-IMT mean and max) are presented as median and interquartile range (IQR), according to the formula: IQR = xU-xL, where xU is the Upper quartile and xL is the Lower quartile (25th -75 th percentile).
Statistical significance was inferred at p values < 0.05. All data were analysed with StatView (SaS).
Both groups of non-smokers and smokers were comparable with respect to age and gender; moreover body mass index (BMI), systolic and diastolic blood pressure (SBP and DBP) and heart rate (HR) were within normal range and similar in both groups (p not significantly different).
None of the subjects had significant stenosis or occlusion of the extra and intra-cranial arteries.
No differences in MCA MFV (cm/s) at rest were observed between smokers and non-smokers (p not significantly different).
Substantially, groups baseline differences referred only about the current smoking habit (present or absent, number of cigarettes/day and smoking duration in years) (p < 0.01).
The examiner spent a mean of 8 min for the total examination of the non-smoker subjects, and a mean of 8 min plus the 10 min after smoking for the smoker ones.
Demographic and clinical characteristics of the study population setting
(n = 43)
(n = 38)
27 ± 4
26 ± 3
23 ± 2
23 ± 2
Number of cigarettes/day
0 ± 0
11 ± 5
Smoking duration (years)
0 ± 0
8 ± 2
SBP at rest (mmHg)
115 ± 15
117 ± 5
DBP at rest (mmHg)
69 ± 8
70 ± 5
Heart rate at rest (bpm)
65 ± 4
66 ± 4
SBP 1 min after smoking (mmHg)
127 ± 4
DBP 1 min after smoking (mmHg)
75 ± 4
Heart rate 1 min after smoking (bpm)
74 ± 2
SBP 10 min after smoking (mmHg)
120 ± 4
DBP 10 min after smoking (mmHg)
70 ± 4
Heart rate 10 min after smoking (bpm)
68 ± 2
MCA MFV at rest (cm/s)
63 ± 4
63 ± 5
the “ABCD” assessment in the study population setting
(n = 43)
(n = 38)
1.1 ± 0.05
1.1 ± 0.8
BHI baseline (MCA)
BHI 1 min after smoking (MCA)
1 ± 0.2
BHI 10 min after smoking (MCA)
1.1 ± 0.1
C-IMT (mean, mm)
C-IMT (max, mm)
Diameter of the abdominal aorta (mm)
15 ± 2
15 ± 1
As depicted in table 2, smokers presented higher values of CIMT (mean and maximal), and lower BHI in MCA at baseline (p < 0.01) with respect to non-smokers, though in the normal range.
No significant differences were found for A and D between smokers and non- smokers.
To our best knowledge, this is the first study aimed to create an easy to perform four-step ultrasound examination to evaluate the peripheral, the extra and the intra-cranial assessment of the arterial damage in young, otherwise healthy smokers. The ABCD consists in an easy to remember formula not only for physicians but also in an educational context. The results of this study could be the basis for detecting the same ultrasound parameters also in older populations of smokers (or with other cardiovascular risk factors) in order to create an “ultrasound score system” both for screening and follow-up.
The finding that acute cigarette smoking increased HR, SBP and DBP are consistent with previous ones .
Previous studies report different results about ABI assessment in smokers compared to non-smokers. In fact, in Korean adolescents (14–16 years old) there were no significant differences in ABI values between smokers compared to non-smokers , while in older subjects, but not elderly, current smokers had a lower mean ABI , showing the significant effect of smoking in the PAD development, with a tendency of lower ABI in the oldest age group.
Variations of method of ABI measurement could affect the values, while comparing Doppler method to oscillometric or auscultation ones or plethysmography, but the recent recommendation consider the Doppler method of choice, as the most reliable method with the best reproducibly, as recently reviewed .
BHI is proved to be effective and reproducible in the study of the cerebral hemodynamic with TCCD and has the advantage of being more rapid and well-tolerated than carbon dioxide inhalation and acetazolamide injection . The approach consisting of a fixed period of apnoea of 30 s following a normal inspiration can be considered sufficient to avoid a Valsalva effect.
Our data about BHI are in accordance with previous findings : in that paper Authors found the long-term impairment of vasodilator ability of cerebral vessels in young chronic smokers, also after smoking cessation and without CIMT impairment. Nevertheless, a previous study  found the acute effects of smoking in reducing the cerebrovascular reactivity to hypercapnia, suggesting a failure of cerebrovascular regulation that, in this case, was observed only a short time after smoking.
The lack of differences in BHI between males and females is in accordance with previous studies , but the velocity measurements by TCCD seems to be affected by the gender in some cases with not definitive explanations [28, 29].
The demonstration of higher CIMT values in healthy smokers than in age-sex matched non-smokers (though in the normal range) is in accordance with our previous one , with consistent results both in older subjects, [30, 31] and also in even younger healthy university students .
The debate about CIMT remains still open: although it was a widely accepted ultrasound marker of subclinical atherosclerosis, recently it has been shown that the traditional cardiovascular risk factors, and so also smoking, can explain only a small proportion of its variance . Moreover, there are no international guidelines on how precisely this measurement should be applied as a research tool, as recently reviewed in , and technical issues associated with CIMT measurements are still open.
As regards the evaluation of D, this is an important point. Atherosclerosis and AAA share risk factors, such as smoking, obviously, and also hypertension, and hypercholesterolemia , but many patients with advanced atherosclerosis do not develop AAA, whereas many patients without evidence of atherosclerosis present AAA. Cigarette smoking is surely the strongest risk factor for AAA. The strength of association between smoking and AAA is 2.5 times greater than the association between smoking and CAD, and 3.5 times greater than the association between smoking and cerebrovascular disease .
This is the first study that take together into account the indexes considered in the “ABCD” assessment, in particular in young healthy subjects.
The attempt to consider different parameters to assess the risk for smokers has been done in previous reports: for example, the Multi-Ethnic Study of Atherosclerosis (MESA)  considered coronary artery calcification, CIMT and ABI, in conjunction with circulating markers of inflammation in older patients.
It is reasonable that smoke affects MFV and, as reported in previous studies [37–39] also the vasomotor activity. It is possible that a subtle increase in MFV reflects a more subtle and generalized arterial narrowing caused by atherosclerosis. MFV increase could substantially represent a marker of intracranial atherosclerosis. In fact, as previously demonstrated , the highest MFV was not associated with the side of the stroke, and this observation supports the hypothesis that increased MFV reflects a generalized process providing evidence that there is a strong independent association between MCA MFV and the risk of stroke (in particular the ischemic one).
The association between altered cerebrovascular reactivity and the degree of coronary atherosclerosis has been found  and it was confirmed also in patients without carotid stenosis , so the link between CAD and cerebrovascular functional impairment has been supported.
This study has several limitations. First of all, Authors have not yet provided a follow up assessment for the subjects (it could be useful to detect any damage progression within 1 or more years from the baseline results, as assessed for what concerns CIMT in previous report ). Moreover, it has not been tested the effects of acute smoking in non-smokers, as other Authors have analysed in order to speculate about the acute smoking-induce hemodynamic alterations in the common carotid artery , this choice for ethical reasons. Nevertheless, it is a matter of fact that cigarette smoking has a specific fibrogenic effect which causes intimal thickening, as previously demonstrated [42, 43].
We have discussed about this topic in a recent study .
In that study we aimed to assess whether cigarette smoking-induced oxidative stress affects lipoprotein associated phospholipase A2 (Lp-PLA2) expression in peripheral blood mononuclear cells (PBMC) and hence Lp-PLA2 and lysoPC plasma concentrations, as well as the relationship between lysoPC and CIMT in healthy smokers. The correlation between lysoPC and CIMT together with the finding that lysoPC up-regulates proteoglycan synthesis suggests that lysoPC may be a link between smoking and intimal thickening.
On the basis of these results, it is reasonable to consider that smoking has a “physical” effect on CIMT, it is not only a physiologic adaptation.
It is to mention that BHI is considered the most practical, inexpensive, best-tolerated and easy to perform alternative to the previous methods, as previously explained . Nevertheless, to reach this goal, almost all studies report that subjects, even young, must be instructed before the recordings [13, 44]. This process allows good compliance and reliable results. Also in the present study, subjects were preliminary instructed on how to perform BHI and they test the procedure before starting the recordings.
Even so, older subjects may be unable to complete the test, as previously described .
Further studies are needed to test the same “ABCD” also in patients with different cardiovascular risk factors and ages, nevertheless, our results seems to underline the importance of the assessment of B and C, that, though in the normal range, present significant differences between young healthy smokers and non-smokers. These results could drive the screening between smokers in age-related manner.
The “ABCD” examination could represent a valid and quick (8 min) method to detect and then monitor smokers’ vascular damage, and could be the systematic approach to be considered also for older smokers. Finally, this approach should be contemplated in the wider context of possible not-invasive and practical screening and follow-up modalities. This would be designed to implement preventive strategies and tools aimed at discouraging tobacco addiction and monitoring cardiovascular risk patients.
Accurate assessment of cardiovascular risk is an essential goal to be achieved, and many attempts to collect reliable vascular biomarkers have been made, as recently reviewed , for primary and secondary prevention.
Although the “ABCD” examination is now far to be used as a screening tool, it could be considered a further attempt in this area.
AAA, abdominal aortic aneurysm; ABI, ankle-brachial index; BHI, breath-holding index; BMI, body mass index; CAD, coronary artery disease; CIMT, carotid intima media thickness; DBP, diastolic blood pressure; HR, heart rate; MCA, middle cerebral artery; MFV, mean flow velocity; PAD, peripheral artery disease; SBP, systolic blood pressure; TCCD, trans-cranial colour Doppler
CM, AC, GR, LC designed the study, CM performed the examinations, CM, AC, GR, LC wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The study was conducted in accordance with the ethical standards laid down in the Helsinki Declaration of 1975 and its late amendments. Healthy volunteers were recruited among the students of Verona University School of Medicine and among the Internal Medicine certification board students of the same institution. All participants provided written consent prior to commencing the study and the local ethical committee (University of Verona.- Azienda Ospedaliera Universitaria Integrata Verona) approved the study.
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- Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Blaha MJ, et al. Heart Disease and Stroke Statistics 2014 Update: A Report From the American Heart Association. Circulation. 2014;129:e28–e292.View ArticlePubMedGoogle Scholar
- Yusuf S, Hawken S, Ounpuu S, Dans T, Avezum A, Lanas F, et al. INTERHEART Study Investigators. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): Case–control study. Lancet. 2004;364:937–52.View ArticlePubMedGoogle Scholar
- Boht VM, Cole JW, Sorkin JD, Wozniak MA, Malarcher AM, et al. Dose–response relationship between cigarette smoking and risk of ischemic stroke in young women. Stroke. 2008;39:2439–43.View ArticleGoogle Scholar
- Aboyans V, Criqui MH, Abraham P, Allison MA, Creager MA. Measurement and interpretation of the Ankle-brachial index. A scientific statement from the American Heart Association. Circulation. 2012;126:2890–909.View ArticlePubMedGoogle Scholar
- Winsor T. Influence of arterial disease on the systolic blood pressure gradients of the extremity. Am J Med Sci. 1950;220:117–26.View ArticlePubMedGoogle Scholar
- Fowkes FG, Murray GD, Butcher I, Heald CL, Lee RJ, et al. Ankle-brachial index combined with Framingham risk score to predict cardiovascular events and mortality: a meta-analysis. JAMA. 2008;300:197–208.View ArticlePubMedGoogle Scholar
- Baldassarre D, Castelnuovo S, Frigerio B, Amato M, Werba JP. Effects of timing and extent of smoking, type of cigarettes, and concomitant risk factors on the association between smoking and subclinical atherosclerosis. Stroke. 2009;40:1991–8.View ArticlePubMedGoogle Scholar
- Fratta Pasini A, Stranieri C, Pasini A, Vallerio P, Mozzini C, Solani E, et al. Lysophosphatidylcholine and Carotid intima-media thickness in young smokers: a role for oxidized LDL induced expression of PBMC Lipoprotein-associated Phospholipase A2? PLoS ONE. 2013;8(12), e83092.View ArticlePubMedPubMed CentralGoogle Scholar
- Aguilar-Shea AL, Gallardo-Mayo C, Garrido-Elustondio S, Calvo Manuel E, Zamorano-Gomez JL. Carotid intima-media thickness as a screening tool in cardiovascular primary prevention. Eur J Clin Invest. 2011;41:521–6.View ArticlePubMedGoogle Scholar
- Terborg C, Bramer S, Weller C, Rother J. Short-term effect of cigarette smoking on CO2 –induced vasomotor reactivity in man: a study with near-infrared spectroscopy and transcranial Doppler sonography. J Neurol Sci. 2002;205:15–20.View ArticlePubMedGoogle Scholar
- Silvestrini M, Troisi E, Matteis M, Cupini LM, Bernardi G. Effect of smoking on cerebrovascular reactivity. J Cereb Blood Flow Metab. 1996;16:746–9.View ArticlePubMedGoogle Scholar
- Bullock R, Mendelow AD, Bone I, Patterson J, Macleod WN, Allardice G. Cerebral blood flow and CO2 responsiveness as indicator of collateral reserve capacity in patients with carotid arterial disease. Br J Surg. 1985;72:348–51.View ArticlePubMedGoogle Scholar
- Markus HS, Harrison MJ. Estimation of cerebrovascular reactivity using transcranial Doppler, including the use of breath-holding index as the vasodilatory stimulus. Stroke. 1992;23:668–73.View ArticlePubMedGoogle Scholar
- Rucka D, Marek J, Rucklova A, Lubanda JC, Havranek S, Skvaril J, et al. Arterial stiffening contributes to impairment of cerebrovascular reactivity in patients with coronary artery disease without carotid stenosis. Physiol Res. 2015;64:335–43.PubMedGoogle Scholar
- Vardulaki KA, Walker NM, Day NE. Quantifying the risks of hypertension, age, sex and smoking in patients with abdominal aortic aneurysm. Br J Surg. 2000;87:195–200.View ArticlePubMedGoogle Scholar
- Shreibati JB, Baker LC, Hlatky MA. Impact of the Screening Abdominal Aortic Aneurysm very efficiently (SAAVE). Act on abdominal ultrasonography use among Medicare beneficiaries. Arch Intern Med. 2012;172:1456–60.View ArticlePubMedGoogle Scholar
- Isaac PF, Rand MJ. Cigarette smoking and plasma levels of nicotine. Nature. 1972;236:308–10.View ArticlePubMedGoogle Scholar
- Alexandrov AV, Sloan MA, Wong LKS, Douville C, Rzumovsky AY, Koroshetz WJ, et al. For the American Society of Neuroimaging Practice Guidelines Committee. Practice standards for transcranial Doppler ultrasound: part I, test performance. J Neuroimaging. 2007;17:11–8.View ArticlePubMedGoogle Scholar
- Nicoletto HA, Boland S. Transcranial Doppler series part V: speciality applications. Am J Electroneurodiagnostic Technol. 2011;51:31–41.PubMedGoogle Scholar
- Touboul PJ, Hennerici MG, Meairs S, Adams H, Amarenco P. An Update on behalf of the Advisory Board of the 3rd and 4th Watching the Risk Symposium 13th and 15th European Stroke Conferences, Mannheim, Germany, 2004, and Brussels, Belgium, 2006. Cerebrovasc Dis. 2007;23:75–80.View ArticlePubMedGoogle Scholar
- Bianchini E, Bozec E, Gemignani V, Faita F, Laurent S. Assessment of carotid stiffness and intima-media thickness from ultrasound data: comparison between two methods. J Ultrasound Med. 2010;29:1169–75.PubMedGoogle Scholar
- Mancia G, Groppelli A, Di Rienzo M, Castiglioni P, Parati G. Smoking impairs baroreflex sensitivity in humans. Am J Physiol. 1997;273:H1555–60.PubMedGoogle Scholar
- Koo HS, Gil TY, Lee HW, Lee K, Hong YM. Effects of smoking on the pulse wave velocity and ankle-brachial index in adolescents. Korean Circulation J. 2007;37:414–8.View ArticleGoogle Scholar
- Syvanen K, Aarnio P, Jaatinen P. Korhonen P Effects of age, sex and smoking on ankle-brachial index in a Finnish population at risk for cardiovascular disease. Int J Angiol. 2007;16(4):128–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Silvestrini M, Troisi E, Matteis M, Cupini LM, Caltagirone C. Transcranial Doppler assessment of cerebrovascular reactivity in symptomatic and asymptomatic severe carotid stenosis. Stroke. 1996;27:1970–3.View ArticlePubMedGoogle Scholar
- Boms N, Yonai Y, Molnar S, Rosengarten B, Bornstein NM, Csiba L, et al. Effect of smoking cessation on visually evoked cerebral blood flow response in healthy volunteers. J Vasc Res. 2010;47:214–20.View ArticlePubMedGoogle Scholar
- Zavoreo I, Demarin V. Breath holding index in the evaluation of cerebral vasoreactivity. Acta Clin Croat. 2004;43:15–9.Google Scholar
- Arnolds BJ, von Reutern GM. Transcranial Doppler sonography. Examination techniques and normal reference values. Ultrasound Med Biol. 1986;12:115–23.View ArticlePubMedGoogle Scholar
- Matteis M, Troisi E, Bruno C, Caltagirone C, Silvestrini M. Age and sex differences in cerebral hemodynamics: a transcranial Dopller study. Stroke. 1998;29:963–7.View ArticlePubMedGoogle Scholar
- Howard G, Wagenknecht LE, Burke GL, Diez-Roux A, Evans GW, et al. Cigarette smoking and progression of atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) Study. JAMA. 1998;279:119–24.View ArticlePubMedGoogle Scholar
- Johnson HM, Piper ME, Jorenby DE, Fiore MC, Baker TB, et al. Risk factors for subclinical carotid atherosclerosis among current smokers. Prev Cardiol. 2010;13:166–71.View ArticlePubMedPubMed CentralGoogle Scholar
- Lerant B, Straesser C, Kovacs RK, Olah L, Kardos L, et al. Morphological, hemodynamic and stiffness changes in arteries of young smokers. Perspectives in Medicine. 2012;1:152–5.View ArticleGoogle Scholar
- Rundek T, Blanton SH, Bartels S, Dong C, Raval A, Demmer RT, et al. Traditional risk factors are not major contributors to the variance in Carotid Intima-Media Thickness. Stroke. 2013;44(8):2101–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Touboul PJ. Intima-Media-Thickness of carotid arteries. Front Neurol Neurosci. 2015;36:31–6.View ArticlePubMedGoogle Scholar
- Lederle FA, Nelson DB, Joseph AM. Smoker’s relative risk for aortic aneurysm compared with other smoking related disease: a systematic review. J Vasc Surg. 2003;38:329–34.View ArticlePubMedGoogle Scholar
- Mc Evoy JW, Nasir K, De Filippis AP, Lima J, Bluembke D, Hundley WG, et al. Relationship of cigarette smoking with inflammation and subclinical vascular disease. The multi-ethnic study of atherosclerosis. Arterioscler Thromb Vasc Biol. 2015;35:1002–10.View ArticleGoogle Scholar
- Vernieri F, Pasqualetti P, Passarelli F, Rossini PM, Silvestrini M. Outcome of carotid artery occlusion is predicted by cerebrovascular reactivity. Stroke. 1999;30:593–8.View ArticlePubMedGoogle Scholar
- Markus H, Cullinane M. Severely impaired cerebrovascular reactivity predicts stroke and TIA risk in patients with carotid artery stenosis and occlusion. Brain. 2001;124:457–67.View ArticlePubMedGoogle Scholar
- Silvestrini M, Vernieri F, Pasqualetti P, Matteis M, Passarelli F, Troisi E, et al. Impaired cerebral vasoreactivity and risk of stroke in patients with asymptomatic carotid artery stenosis. JAMA. 2000;283:2122–7.View ArticlePubMedGoogle Scholar
- Bos MJ, Koudstaal PJ, Hofman A, Witteman J. Breteler M Transcranial Doppler hemodynamic parameters and risk of stroke. The ROTTERDAM study. Stroke. 2007;38:2453–8.View ArticlePubMedGoogle Scholar
- Rosengarten B, Grebe M, Muller A, Voss RK, Kaps M. Severity of coronary artery disease but not degree of coronary stenosis is correlated to cerebrovascular reactivity. Cerebrovasc Dis. 2009;28:290–7.View ArticlePubMedGoogle Scholar
- Benowitz NL. Cigarette smoking and cardiovascular disease: pathophysiology and implications for treatment. Prog Cardiovasc Dis. 2003;46:91–111.View ArticlePubMedGoogle Scholar
- Csiszar A, Podlutsky A, Wolin MS, Losonczy G, Pacher P. Oxidative stress and accelerated vascular aging: implications for cigarette smoking. Front Biosci. 2009;14:3128–44.View ArticleGoogle Scholar
- Molinari F, Liboni W, Grippi G, Negri E. Relationship between oxygen supply and cerebral blood flow assessed by transcranial Doppler and near-infrared spectroscopy in healthy subjects during breath holding. J Neuroeng Rehabil. 2006;3:16–29.View ArticlePubMedPubMed CentralGoogle Scholar
- Mousavi SA, Khorvash F, Asadi B, Karkheiran F. Evaluation of vasomotor reactivity by transcranial Doppler sonography: age and sex related differences in breath holding index in Iranian population. J Res Med Sci. 2005;10(2):93–6.Google Scholar
- Vlachopoulos C, Xaplanteris P, Aboyans A, Brodmann M, Cifkova R, Cosentino F, et al. The role of vascular biomarkers for primary and secondary prevention. A position paper from the European society of Cardiology Working Group on peripheral circulation. Endorsed by the Association for Research into Arterial Structure and Physiology (ARTERY) Society. Atherosclerosis. 2015;241:507–32.View ArticlePubMedGoogle Scholar