ORIGINAL RESEARCH article
Association between Carotid Intima Media Thickness and Heart Rate Variability in Adults at Increased Cardiovascular Risk
- 1Center of Innovation, Technology and Education at Anhembi Morumbi University—Laureate International Universities, Sao Jose dos Campos, Brazil
- 2Heart Institute of Santa Casa Charity (IACOR), Fernandopolis, Brazil
- 3Faculty of Medical Sciences, Brasil University, Fernandópolis, Brasil
- 4Division of Nephrology and Hypertension, University Hospitals, Cleveland, Ohio
- 5Medicine Institute, Cleveland Clinic, Cleveland, Ohio
Background: Atherosclerotic carotid intima-media thickness (IMT) may be associated with alterations in the sensitivity of carotid baroreceptors. The aim of this study was to investigate the association between carotid IMT and the autonomic modulation of heart rate variability (HRV).
Methods: A total of 101 subjects were enrolled in this prospective observational study. The carotid IMT was determined by duplex ultrasonography. The cardiac autonomic function was determined through HRV measures during the Deep Breathing Test. Linear regression models, adjusted for demographics, comorbidities, body mass index, waist-hip-ratio, and left ventricular ejection fraction were used to evaluate the association between HRV parameters and carotid IMT.
Results: Participants had a mean age of 60.4 ± 13.4 years and an estimated 10-year atherosclerotic cardiovascular disease (ASCVD) risk score (using the Pooled Cohort Equations) of 16.4 ± 17. The mean carotid media thickness was highest (0.90 ± 0.19 mm) in the first quartile of the standard deviation of all RR intervals (SDNN) (19.7 ± 5.1 ms) and progressively declined in each subsequent quartile to 0.82 ± 0.21 mm, 0.81 ± 0.16 mm, and 0.68 ± 0.19 in quartiles 2 (36.5 ± 5.9 ms), 3 (57.7 ± 6.2 ms) and 4 (100.9 ± 22.2 ms), respectively. In multivariable adjusted models, there was a statistical significant association between SDNN and carotid IMT (OR −0.002; 95%CI −0.003 to −0.001, p = 0.005). The same significant association was found between carotid IMT and other measures of HRV, including coefficient of variation of RR intervals (CV) and dispersion of points along the line of identity (SD2).
Conclusions: In a cohort of individuals at increased cardiovascular risk, carotid IMT as a marker of subclinical atherosclerosis was associated with alterations of HRV indicating an impaired cardiac autonomic control, independently of other cardiovascular risk factors.
Carotid atherosclerosis is characterized by increased intima-media thickness (IMT) and presence of atheromatous plaques in the arterial wall (Stein et al., 2008). The carotid IMT is a surrogate marker for systemic atherosclerosis and is associated with an increased risk of stroke and myocardial infarction (Bots et al., 1996, 1997). Increased carotid IMT is a risk factor for coronary and cerebrovascular events in patients without clinical cardiovascular disease (Arnold et al., 2005; Kuller et al., 2006). Duplex ultrasonography, a non-invasive method of measuring carotid IMT can be used to diagnose carotid artery atherosclerosis. However, current guidelines do not recommend using it for the routine screening of asymptomatic patients without clinical signs of or risk factors for atherosclerosis (Brott et al., 2011). Although routine screening for carotid artery stenosis is not recommended, the noninvasive carotid artery duplex ultrasonography in conjunction with other risk stratification markers may improve early diagnosis and prevention (Jonas et al., 2014; LeFevre and U. S. Preventive Services Task Force, 2014; Weyer and Davis, 2015).
Atherosclerosis of the carotid and aortic baroreceptors may be associated with cardiac autonomic dysfunction due to a decreased baroreflex sensitivity. Carotid atherosclerosis may induce these effects through both structural and biochemical mechanisms. Carotid atherosclerotic plaques are commonly found in the carotid sinus (Milei et al., 2009). Vlachakis et al. (1976) first suggested a role of atherosclerosis in diminishing baroreceptor sensitivity (Vlachakis et al., 1976). Several preclinical studies led to the hypothesis that structural and functional mechanisms in large arteries contribute to decreased baroreflex sensitivity and baroreceptor resetting in hypertension, atherosclerosis, and aging (Chapleau et al., 1995). Structural mechanisms that may contribute to the atherogenesis-induced reduction in baroreflex sensitivity include structural changes in the vessel wall, such as fibrosis with increased vascular stiffness and distensibility (Bonyhay et al., 1996). In the atherosclerotic carotid sinus, fibrotic autonomic ganglia and damaged nerve endings have been observed in both complicated and noncomplicated plaques (Milei et al., 2009). Since baroreceptors are located in the carotid bulb adventitia, decreased stretch caused by the presence of atherosclerotic plaques in this location may reduce the baroreflex sensitivity. Functional mechanisms may be paracrine through factors released by the vascular endothelium such as prostacyclin, nitric oxide and endothelin (Chapleau and Abboud, 1994) or involve the accumulation of oxygen-derived free radicals (Li et al., 1996). Therefore, carotid sinus baroreceptor dysfunction may occur, leading to alterations in the cardiac autonomic function.
Gianaros et al. associated intima–media thickness in the carotid bulb with reduced baroreflex sensitivity in patients enrolled in the REActivity and Cardiovascular risk Trial (REACT) to study preclinical atherosclerosis (Gianaros et al., 2002). Baroreflex sensitivity was found to be impaired in patients with bilateral carotid atherosclerosis (Nasr et al., 2005) or with echogenic plaques (Tsekouras et al., 2011).
Heart rate variability (HRV) analysis is a commonly used noninvasive method to measure alterations in baroreflex and autonomic tone (Campos et al., 2013; Costa et al., 2015; Miyabara et al., 2017). HRV measures are sensitive to age, gender, and cardiovascular diseases, such as diabetes, hypertension, obesity, dyslipidemia, and atherosclerosis (Campos et al., 2013; Jelinek et al., 2013). We hypothesized that indices of HRV analysis are independently associated with carotid atherosclerotic IMT in cohort with at least one cardiovascular disease risk factor. Since cardiovascular risk conditions and demographic factors could potentially affect HRV outcome variables (Campos et al., 2013), estimates for the association between HRV and carotid IMT were determined using linear multivariable modeling adjusting for these potential confounders.
Study Design and Setting
This was a prospective cross-sectional observational study. We enrolled 101 consecutive subjects who presented to the Cardiology outpatient clinic for a routine visit and agreed to have a noninvasive carotid artery duplex ultrasonography at Heart Institute of Santa Casa Charity (IACOR), Fernandopolis, Brazil, from June 2015 to February 2016. The study was approved by the Ethics Committee of Camilo Castelo Branco University in accordance with resolution 466/2012 and 340/2004 of the National Health Council (Ministry of Health) for research on human subjects (CAAE: 01328712.0.0000.5244, permit no. 18326). Written informed consent was obtained from all subjects.
Inclusion and Exclusion Criteria
Asymptomatic patients aged 18 years and older with at least one cardiovascular risk factor, including hypertension, diabetes, obesity, smoking, hypercholesterolemia, without a history of transient ischemic attack, stroke, or other neurologic signs or symptoms were selected to participate in the study. Patients with symptomatic carotid artery stenosis were excluded if the patient had transient or permanent focal neurologic symptoms corresponding to the ipsilateral retina or the cerebral hemisphere (Lanzino et al., 2009). Also, patients with heart rhythm disorders, pacemaker, heart failure, ejection fraction less than 0.45, chronic renal failure on hemodialysis, severe liver failure, myocardial infarction, endarterectomy, carotid angioplasty, carotid dissection, and carotid occlusion were excluded. Drugs known to interfere with autonomic function, such as beta-blockers, calcium channel blockers, angiotensin-converting enzyme inhibitors, vasodilators, statins, neuroleptics and nasal vasoconstrictors, were discontinued for at least 24 h before the tests.
Clinical characteristics such as diabetes mellitus, hypertension, obesity, smoking, were documented together with the lipid profile (total cholesterol, triglycerides, LDL and HDL).
Carotid Atherosclerosis Imaging
Carotid arteriosclerotic disease was evaluated through measuring the IMT. The subclinical vascular disease scanning protocol for evaluation of common carotid IMT and detection of carotid plaques was done according to the standardized protocol of the American Society of Echocardiography (Stein et al., 2008). Bilateral common carotid and internal carotid artery were evaluated using a high resolution ultrasound system (Philips, HD 11 XE, Andover MA, USA) equipped with 3–12 MHz linear transducer, SonoCT and XRES imaging technologies and QLAB quantification software. The images were documented through the media Digital Imaging and Communication in Medicine (DICOM). Ultrasound measurements were taken with the subjects in supine position. Carotid stenosis was investigated with an IMT automated measurement on the right and left common carotid arteries (Secil et al., 2005). The mean IMT value of the right and left common carotid arteries was calculated. Carotid IMT was measured on the posterior wall of the common carotid arteries 1–2 cm proximal to the carotid bifurcation and the proximal portion of the internal carotid (bulb) at a depth of 4 cm, by two-dimensional ultrasound (B-mode). Carotid IMT measurements were considered in longitudinal section, on the front or rear wall of the artery, the distance between two echogenic lines represented by the lumen-intima interface and media-adventitia of the arterial wall. The common mean of IMT measurements between the right and left sides (IMTm) was used. The regions containing plaques were excluded from the IMT measurements. Carotid plaque was considered at the bifurcation and proximal portion of the internal carotid artery and was defined as an IMT measurement greater than or equal to 1.5 mm. After the acquisition of the IMT values of each carotid artery, these were compared with the existing reference values, according to the normative table of the Multi-Ethnic Study of Atherosclerosis (MESA), used for both sexes, of White, black, Chinese or Hispanic ethnicity. In addition, left ventricular ejection fraction (LVEF) was measured with cardiac ultrasonography.
Quantitative Autonomic Testing
Quantitative testing of the cardiac autonomic function was performed during deep breathing test (Low et al., 2013; Zeki Al Hazzouri et al., 2014). The HRV deep breathing test was measured in real-time and online with Faros wireless ECG monitor and HRV-scanner software (Mega Electronics, Finland) that uses a respiration pacer while measuring and analyzing the variability in the heart rate in response to deep breathing. The subjects were instructed to follow the respiration pacer bar, and to breathe as deeply as possible. The tests were performed with subjects in sitting position over six respiratory cycles and a respiratory rate of six breaths per minute. Cardiac autonomic function was evaluated measuring the linear and nonlinear HRV parameters: linear (standard deviation (SD) of normal R-R wave intervals [SDNN], square root of the mean of the sum of the squares of differences between adjacent normal R wave intervals [RMSSD], coefficient of variation [CV = SDNN/mean HR], the proportion derived by dividing NN50 by the total number of RR intervals [pNN50]), where NN50 represents the number of pairs of successive RRs that differ by more than 50 ms. and nonlinear Poincaré analysis (SD of the points perpendicular to the line-of-identity [SD1, ms]; SD along the line-of-identity [SD2, ms]).
All data processing was performed while blinded to the level of deep breathing testing and analysis. The characteristics of study participants were depicted using standard descriptive statistics, overall and stratified by quartiles of SDNN. Chi-square (χ2) test of independence for categorical (nominal) variables and Analysis of variance (ANOVA) test for continuous variables were used to analyze the covariates of interest and their association with SDNN and other measures of HRV (RMSSD, CV, PNN50, SD1, and SD2).
Multivariable linear regression models were used to assess the association between heart rate variability parameters from the deep breathing test and mean carotid IMT.
The goodness of curve fit was assessed with the F-test.
The models were adjusted for relevant confounding variables, including demographics (age, sex, race/ethnicity), traditional CVD risk factors (hypertension, diabetes, smoking, total cholesterol, and high density lipoprotein) grouped into atherosclerotic cardiovascular disease (ASCVD) risk score, body mass index (BMI), waist-hip-ratio (WHR), and left ventricular ejection fraction (LVEF). Sequential multivariable models for each outcome were created based on our assessment of the covariates likelihood of being a confounder in the relationship between heart rate variability and subclinical carotid disease. Residual plots were used to confirm model assumptions.
All statistical tests were 2 sided, and P < 0.05 was considered significant. IBM Corp (2013) SPSS Statistics for Windows, Version 22.0, Armonk, NY was used for analyses.
A total of 101 study participants met the eligibility criteria and performed the deep breathing test. The mean age was 60.4 ± 13.4(SD) years, and 46% were men. Characteristics of study participants distributed according to quartiles of one of the HRV parameters (standard deviation of all RR intervals (SDNN) from the deep breathing test) are summarized in Table 1. Patients in the lowest vs. highest quartile of SDNN (reduced vs. high heart rate variability) were older (70.6 ± 10.9 vs. 49.9 ± 13.2 years), had higher supine systolic blood pressure (145.7 ± 18.8 vs. 129.0 ± 15.1 mmHg), and ASCVD risk score (27.3 ± 17.2 vs. 8.2 ± 10.7), respectively.
Table 1. Characteristics of study participants by quartile of heart rate variability (SDNN) from the Deep Breathing Test.
The participants had a carotid intima media thickness mean 0.80 ± 0.20 mm with a median [IQR] 0.80 [0.65–0.93] mm. The characteristics of HRV parameters are depicted in Table 2.
Association between Heart Rate Variability and Intima Media Thickness
Scatterplot distribution of IMT by SDNN from the deep breathing test is shown in Figure 1. Similar distribution was observed for IMT by CV and SD2 (data not shown). The Pearson correlation between carotid IMT and HRV parameters from the deep breathing test showed a significant negative correlation: −0.44 [95%CI: −0.58 to −0.26], −0.47 [95%CI: −0.61 to −0.3], and −0.44 [95%CI: −0.59 to −0.27] for SDNN, CV and SD2, respectively (Figure 2).
Figure 2. Pearson correlation between carotid intima media thickness (IMT) and deep breathing test (DBT) heart rate variability (HRV) parameters: SDNN, standard deviation of all RR intervals, CV, coefficient of variation of RR intervals, RMSSD, root-mean square of differences between adjacent normal RR intervals, SD1, dispersion of points perpendicular to the axis of line-of-identity, SD2, dispersion of points along the line of identity. Values are Pearson r and 95% CI, *p < 0.005, #p < 0.0001.
The median carotid media thickness was highest (0.90 ± 0.19 mm) in the first quartile of SDNN (19.7 ± 5.1 ms) and progressively declined in each subsequent quartile to 0.82 ± 0.21 mm, 0.81 ± 0.16 mm, and 0.68 ± 0.19 in quartiles 2 (36.5 ± 5.9 ms), 3 (57.7 ± 6.2 ms) and 4 (100.9 ± 22.2 ms), respectively (p = 0.001 between groups). In multivariable adjusted models, there was a statistical significant association between SDNN and carotid IMT. Each 1 ms increase in SDNN is associated with a reduction by 2 μm in carotid IMT (OR −0.002; 95%CI −0.003 to −0.001, p = 0.005). The same significant association was found between carotid IMT and other measures of HRV: coefficient of variation (CV) of RR intervals (OR −0.016; 95%CI −0.026 to −0.006, p = 0.002), root-mean square of differences between adjacent normal RR intervals (RMSSD) (OR −0.002; 95%CI −0.003 to −0.000, p = 0.03), dispersion of points perpendicular to the axis of line-of-identity (SD1) (OR −0.002; 95%CI −0.005 to −0.000, p = 0.03), and dispersion of points along the line of identity (SD2) (OR −0.001; 95%CI −0.002 to −0.000, p = 0.004) (Table 3).
Table 3. Association between Heart Rate Variability (HRV) Parameters from the Deep Breathing Test and mean Carotid Artery Intimal-Media Thickness (CIMT).
In this cohort of individuals with subclinical carotid atherosclerosis and at increased cardiovascular risk, carotid IMT as a marker of subclinical atherosclerosis was associated with alterations of HRV indicating an impaired cardiac autonomic control. This association was found to be independent of atherosclerotic cardiovascular disease (ASCVD) risk score (to include age, gender, race, HDL, and total cholesterol, diabetes, systolic blood pressure, hypertension treatment and smoking), body mass index (BMI), waist-hip-ratio (WHR), left ventricular ejection fraction (LVEF). By demonstrating a significant inverse relationship between carotid IMT and HRV, our results are in line with the hypothesis that carotid atherosclerotic lesions are associated with impaired ANS function.
We previously investigated the relationship between carotid IMT and cardiovagal dysfunction assessed through frequency (Pereira et al., 2013) and time-domain (Pereira et al., 2015) HRV measures of 20-min office ECG measurement in patients with subclinical carotid atherosclerosis. Time-domain indices of HRV had the strongest inverse correlation with carotid IMT. Other groups have found a significant correlation between carotid IMT and baroreflex in hypertensives possibly due to aging (Labrova et al., 2005). Also, an increased carotid IMT was associated with a significant decrease in baroreflex sensitivity in prehypertensives and hypertensives (Celovska et al., 2017). In type 2 diabetic patients, cardiovascular autonomic neuropathy was associated with carotid atherosclerosis (Meyer et al., 2004; Gottsater et al., 2005). Moreover, decreased heart rate variability as a measure of cardiac autonomic neuropathy may predict the progression of carotid atherosclerosis in type 2 diabetes (Gottsater et al., 2006; Miyamoto et al., 2010). In subjects with preclinical atherosclerosis, a higher task-induced cardiac autonomic reactivity was associated with lower carotid IMT even after adjusting for cardiovascular risk factors (Heponiemi et al., 2007; Chumaeva et al., 2009). The Hyogo Sleep Cardio-Autonomic Atherosclerosis (HSCAA) Study identified HRV parameters associated significantly with carotid plaque, independent of sleep condition (Kadoya et al., 2015).
Our study indicates that carotid IMT as marker of subclinical atherosclerosis is associated with impaired cardiac autonomic control as represented by a decrease in HRV indices. Moreover, the relationship between deep breathing HRV and subclinical carotid disease was maintained after adjustment for relevant confounding variables, including traditional CVD risk factors (age, sex, race, hypertension, diabetes, smoking, total cholesterol, and high density lipoprotein) grouped into the atherosclerotic cardiovascular disease (ASCVD) risk score, body mass index (BMI), waist-hip-ratio (WHR), and left ventricular ejection fraction.
HRV has been studied in conjunction with clinical autonomic tests, of which the most used are the Valsalva maneuver, head-up tilt, and deep breathing tests (1996; Novak, 2011; Freeman and Chapleau, 2013). Of these, we selected the autonomic deep breath testing, which has been used as a sensitive and reliable clinical test for the early detection of cardiac autonomic dysfunction in various diseases (Olney, 1998; Hilz and Dutsch, 2006; Shields, 2009). Deep breathing test appears to have the greatest specificity (~80%) (Tesfaye et al., 2010). This test is based on the observation first noted by Karl Ludwig in 1847 that heart rate increases with inspiration and decreases with expiration (Melcher, 1976; Shields, 2009). In our study, we employed user-friendly portable equipment for HRV deep breathing test that could be used both in the office and under ambulatory conditions. The test has good sensitivity, specificity and reproducibility (it has reproducibility required for use in clinical studies), is noninvasive, safe, well standardized and easy to perform. In this study, we observed that time-domain measures of the HRV deep breathing test had again a strong negative correlation with the carotid IMT.
This study has several strengths, including concurrent assessment of bilateral common carotid and internal carotid artery media thickness, in conjunction with several indices related to cardiac autonomic function during deep breathing test, including SDNN, RMSSD, CV, pNN50, SD1, and SD2, and along with several cardiovascular risk factors. In the present study, multivariable regression analysis revealed a significant inverse association between carotid IMT and HRV that is independent of several cardiovascular risk factors. The cross-sectional design of our study was also appropriate to examine several cardiovascular risk factors related with HRV. To quantify autonomic dysfunction, we utilized comprehensive, portable and easy to use heart rate variability analyzing system that can be easily carried out in any patient setting. HRV deep breathing test is a fast and convenient method to quantify autonomic dysfunction. HRV measures have been suggested for initial screening of cardiovascular risk as it is noninvasive, economical and easy to use in clinical practice (Jelinek et al., 2013). We suggest further investigation of this association of HRV measures of deep breathing test to carotid IMT in larger cohort, case-control and longitudinal studies in order to certify HRV measures of deep breathing test as initial screening tool for adults with subclinical carotid disease and at increased cardiovascular risk.
This study has several limitations. First, this is a cross-sectional analysis and causality cannot be inferred. Second limitation relates to selection bias, given the nature of high risk patients referred directly from the Cardiology clinic. Furthermore, the results are only applicable to adults with at least one cardiovascular risk factor. Finally, these analyses are based on a sample of patients referred for single measurement of carotid IMT; whether changes in IMT over time add incremental predictive value to the development of cardiac autonomic dysfunction will need further study.
In summary, our study indicates that subclinical carotid atherosclerosis is associated with impairment in the cardiac autonomic control in individuals with at least one cardiovascular disease risk factor, regardless of the confounding effects of cardiovascular risk factors.
Study conception and design: OB, VP, and LC. Performed the study: VP, Sd and JF. Analyzed de data: MD, AB, and VP. Drafting of manuscript: OB, LC. Critical revision: MD, AB, VP, and CO.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors gratefully acknowledge Ana Paula do Prado Cardoso, nurse for coordination and providing support of all clinical visits. This research was supported by São Paulo Research Foundation (FAPESP 13/14724-0; FAPESP 14/10985-7). OB is supported by the National Counsel of Technological and Scientific Development (CNPq 301706/2013-1). We thank the reviewers for their constructive comments, which helped us to improve the manuscript.
Arnold, A. M., Psaty, B. M., Kuller, L. H., Burke, G. L., Manolio, T. A., Fried, L. P., et al. (2005). Incidence of cardiovascular disease in older Americans: the cardiovascular health study. J. Am. Geriatr. Soc. 53, 211–218. doi: 10.1111/j.1532-5415.2005.53105.x
Bots, M. L., Hoes, A. W., Koudstaal, P. J., Hofman, A. and Grobbee, D. E. (1997). Common carotid intima-media thickness and risk of stroke and myocardial infarction: the Rotterdam Study. Circulation 96, 1432–1437. doi: 10.1161/01.CIR.96.5.1432
Bots, M. L., Hofman, A., De Jong, P. T., and Grobbee, D. E. (1996). Common carotid intima-media thickness as an indicator of atherosclerosis at other sites of the carotid artery. The Rotterdam Study. Ann. Epidemiol. 6, 147–153. doi: 10.1016/1047-2797(96)00001-4
Brott, T. G., Halperin, J. L., Abbara, S., Bacharach, J. M., Barr, J. D., Bush, R. L., et al. (2011). 2011 ASA/ACCF/AHA/AANN/AANS/ACR/ASNR/CNS/SAIP/SCAI/SIR/SNIS/SVM/SVS guideline on the management of patients with extracranial carotid and vertebral artery disease. A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, and the American Stroke Association, American Association of Neuroscience Nurses, American Association of Neurological Surgeons, American College of Radiology, American Society of Neuroradiology, Congress of Neurological Surgeons, Society of Atherosclerosis Imaging and Prevention, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of NeuroInterventional Surgery, Society for Vascular Medicine, and Society for Vascular Surgery. Circulation 124, e54–e130. doi: 10.1161/CIR.0b013e31820d8d78
Campos, L. A., Pereira, V. L. Jr., Muralikrishna, A., Albarwani, S., Bras, S., Gouveia, S., et al. (2013). Mathematical biomarkers for the autonomic regulation of cardiovascular system. Front. Physiol. 4:279. doi: 10.3389/fphys.2013.00279
Celovska, D., Gonsorcik, J., Gaspar, L., and Stvrtinova, V. (2017). Baroreflex sensitivity and carotid intima-media thickness in risk stratification of prehypertensives and hypertensives. Int. Angiol. 36, 69–74. doi: 10.23736/S0392-9590.16.03641-5
Chapleau, M. W., Cunningham, J. T., Sullivan, M. J., Wachtel, R. E., and Abboud, F. M. (1995). Structural versus functional modulation of the arterial baroreflex. Hypertension 26, 341–347. doi: 10.1161/01.HYP.26.2.341
Chumaeva, N., Hintsanen, M., Ravaja, N., Puttonen, S., Heponiemi, T., Pulkki-Raback, L., et al. (2009). Interactive effect of long-term mental stress and cardiac stress reactivity on carotid intima-media thickness: the Cardiovascular Risk in Young Finns study. Stress 12, 283–293. doi: 10.1080/10253890802372406
Costa, A. S., Costa, P. H., de Lima, C. E., Padua, L. E., Campos, L. A., and Baltatu, O. C. (2015). ICU blood pressure variability may predict nadir of respiratory depression after coronary artery bypass surgery. Front. Neurosci. 9:506. doi: 10.3389/fnins.2015.00506
Gianaros, P. J., Jennings, J. R., Olafsson, G. B., Steptoe, A., Sutton-Tyrrell, K., Muldoon, M. F., et al. (2002). Greater intima-media thickness in the carotid bulb is associated with reduced baroreflex sensitivity. Am. J. Hypertens. 15, 486–491. doi: 10.1016/S0895-7061(02)02923-0
Gottsater, A., Ahlgren, A. R., Taimour, S., and Sundkvist, G. (2006). Decreased heart rate variability may predict the progression of carotid atherosclerosis in type 2 diabetes. Clin. Auton. Res. 16, 228–234. doi: 10.1007/s10286-006-0345-4
Gottsater, A., Szelag, B., Berglund, G., Wroblewski, M., and Sundkvist, G. (2005). Changing associations between progressive cardiovascular autonomic neuropathy and carotid atherosclerosis with increasing duration of type 2 diabetes mellitus. J. Diabetes Complications 19, 212–217. doi: 10.1016/j.jdiacomp.2005.02.001
Heponiemi, T., Elovainio, M., Pulkki, L., Puttonen, S., Raitakari, O., and Keltikangas-Jarvinen, L. (2007). Cardiac autonomic reactivity and recovery in predicting carotid atherosclerosis: the cardiovascular risk in young Finns study. Health Psychol. 26, 13–21. doi: 10.1037/0278-622.214.171.124
Jelinek, H. F., Md Imam, H., Al-Aubaidy, H., and Khandoker, A. H. (2013). Association of cardiovascular risk using non-linear heart rate variability measures with the framingham risk score in a rural population. Front. Physiol. 4:186. doi: 10.3389/fphys.2013.00186
Jonas, D. E., Feltner, C., Amick, H. R., Sheridan, S., Zheng, Z. J., Watford, D. J., et al. (2014). Screening for asymptomatic carotid artery stenosis: a systematic review and meta-analysis for the U.S. Preventive Services Task Force. Ann. Intern. Med. 161, 336–346. doi: 10.7326/M14-0530
Kadoya, M., Koyama, H., Kurajoh, M., Kanzaki, A., Kakutani-Hatayama, M., Okazaki, H., et al. (2015). Sleep, cardiac autonomic function, and carotid atherosclerosis in patients with cardiovascular risks: HSCAA study. Atherosclerosis 238, 409–414. doi: 10.1016/j.atherosclerosis.2014.12.032
Kuller, L. H., Arnold, A. M., Psaty, B. M., Robbins, J. A., O'Leary, D. H., Tracy, R. P., et al. (2006). Chaves: 10-year follow-up of subclinical cardiovascular disease and risk of coronary heart disease in the Cardiovascular Health Study. Arch. Intern. Med. 166, 71–78. doi: 10.1001/archinte.166.1.71
Labrova, R., Honzikova, N., Maderova, E., Vysocanova, P., Novakova, Z., Zavodna, E., et al. (2005). Age-dependent relationship between the carotid intima-media thickness, baroreflex sensitivity, and the inter-beat interval in normotensive and hypertensive subjects. Physiol. Res. 54, 593–600.
Lanzino, G., Rabinstein, A. A., and Brown, R. D. Jr. (2009). Treatment of carotid artery stenosis: medical therapy, surgery, or stenting? Mayo Clin. Proc. 84, 362–387; quiz 367–368. doi: 10.1016/S0025-6196(11)60546-6
LeFevre, M. L., and U. S. Preventive Services Task Force (2014). Screening for asymptomatic carotid artery stenosis: U.S. Preventive Services Task Force recommendation statement. Ann. Intern. Med. 161, 356–362. doi: 10.7326/M14-1333
Li, Z., Mao, H. Z., Abboud, F. M., and Chapleau, M. W. (1996). Oxygen-derived free radicals contribute to baroreceptor dysfunction in atherosclerotic rabbits. Circ. Res. 79, 802–811. doi: 10.1161/01.RES.79.4.802
Meyer, C., Milat, F., McGrath, B. P., Cameron, J., Kotsopoulos, D., and Teede, H. J. (2004). Vascular dysfunction and autonomic neuropathy in Type 2 diabetes. Diabet. Med. 21, 746–751. doi: 10.1111/j.1464-5491.2004.01241.x
Milei, J., Lavezzi, A. M., Bruni, B., Grana, D. R., Azzato, F., and Matturri, L. (2009). Carotid barochemoreceptor pathological findings regarding carotid plaque status and aging. Can. J. Cardiol. 25, e6–e12. doi: 10.1016/S0828-282X(09)70023-6
Miyabara, R., Berg, K., Kraemer, J. F., Baltatu, O. C., Wessel, N., and Campos, L. A. (2017). Quantifying effects of pharmacological blockers of cardiac autonomous control using variability parameters. Front. Physiol. 8:10. doi: 10.3389/fphys.2017.00010
Miyamoto, M., Kotani, K., Yagyu, H., Koibuchi, H., Fujii, Y., Konno, K., et al. (2010). The correlation between CVR-R and carotid atherosclerosis in type 2 diabetes mellitus patients with diabetic neuropathy. J. Physiol. Anthropol. 29, 149–152. doi: 10.2114/jpa2.29.149
Olney, R. K. (1998). Clinical trials for polyneuropathy: the role of nerve conduction studies, quantitative sensory testing, and autonomic function testing. J. Clin. Neurophysiol. 15, 129–137. doi: 10.1097/00004691-199803000-00005
Pereira, V. L., Franqueiro, L. F., de Godoy, M. F., Campos, L. A., and Baltatu, O. C. (2013). Extracranial artery disease is associated with an impairment of cardiac autonomic control. Hypertension 62:A483.
Pereira, V. L. J., dos Santos, S. G., Fuzatti, J. S., Campos, L. A., and Baltatu, O. C. (2015). PP.LB01.19: subclinical carotid atherosclerosis is associated with alterations of time-domain indices of heart rate variability. J. Hypertens. 33, e258. doi: 10.1097/01.hjh.0000468141.83380.a7
Secil, M., Altay, C., Gulcu, A., Cece, H., Goktay, A. Y., and Dicle, O. (2005). Automated measurement of intima-media thickness of carotid arteries in ultrasonography by computer software. Diagn. Interv. Radiol. 11, 105–108.
Stein, J. H., Korcarz, C. E., Hurst, R. T., Lonn, E., Kendall, C. B., Mohler, E. R. et al. (2008). Use of carotid ultrasound to identify subclinical vascular disease and evaluate cardiovascular disease risk: a consensus statement from the American Society of Echocardiography Carotid Intima-Media Thickness Task Force. Endorsed by the society for vascular medicine. J. Am. Soc. Echocardiogr. 21, 93–111; quiz 189–190. doi: 10.1016/j.echo.2007.11.011
Tesfaye, S., Boulton, A. J., Dyck, P. J., Freeman, R., Horowitz, M., Kempler, P. et al. (2010). Diabetic neuropathies: update on definitions, diagnostic criteria, estimation of severity, and treatments. Diabetes Care 33, 2285–2293. doi: 10.2337/dc10-1303
Tsekouras, N. S., Katsargyris, A., Skrapari, I., Bastounis, E. E., Georgopoulos, S., Klonaris, C., et al. (2011). The role of carotid plaque echogenicity in baroreflex sensitivity. J. Vasc. Surg. 54, 93–99. doi: 10.1016/j.jvs.2010.11.121
Vlachakis, N. D., Mendlowitz, M., DGuia, D., and DGusman, D. (1976). Diminished baroreceptor sensitivity in elderly hypertensives. Possible role of atherosclerosis. Atherosclerosis 24, 243–249. doi: 10.1016/0021-9150(76)90079-4
Zeki Al Hazzouri, A., Haan, M. N., Deng, Y., Neuhaus, J., and Yaffe, K. (2014). Reduced heart rate variability is associated with worse cognitive performance in elderly Mexican Americans. Hypertension 63, 181–187. doi: 10.1161/HYPERTENSIONAHA.113.01888
Keywords: carotid, atherosclerosis, heart rate/heart rate variability, cardiovagal, deep breathing test
Citation: Pereira VL Jr., Dobre M, dos Santos SG, Fuzatti JS, Oliveira CR, Campos LA, Brateanu A and Baltatu OC (2017) Association between Carotid Intima Media Thickness and Heart Rate Variability in Adults at Increased Cardiovascular Risk. Front. Physiol. 8:248. doi: 10.3389/fphys.2017.00248
Received: 27 January 2017; Accepted: 07 April 2017;
Published: 26 April 2017.
Edited by:Jean-Pierre Montani, University of Fribourg, Switzerland
Reviewed by:Alun Hughes, University College London, UK
Carolyn J. Barrett, University of Auckland, New Zealand
Sofia Ahmed, University of Calgary, Canada
Copyright © 2017 Pereira, Dobre, dos Santos, Fuzatti, Oliveira, Campos, Brateanu and Baltatu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ovidiu C. Baltatu, firstname.lastname@example.org