Abstract
Background
Arterial stiffness is an important predictor of cardiovascular risk in adult life. Increased arterial stiffness can also be present in children and may be associated with several other cardiovascular risk factors. Until now, however, we know little about measuring arterial stiffness in preschool children. In this study, we assessed the feasibility of measuring arterial stiffness in preschool children and explored possible determinants related to arterial stiffness at this age.
Methods
We studied 168 healthy children, aged 3.3–4.1 years, who were recruited from a prospective birth cohort. We measured arterial stiffness, expressed in aortic pulse wave velocity and augmentation index, using a non-invasive oscillometric device (Arteriograph). We measured anthropometry and recorded other determinants using a questionnaire.
Results
In 100 children (59.5%) at least one valid arterial stiffness measurement was obtained. Of these infants, 89 had at least two valid measurements and 73 infants had at least three valid measurements. The mean aortic pulse wave velocity was 5.56 m/s (SD 0.77), and the mean augmentation index of the aorta was 19.7 m/s (SD 7.0). The augmentation index was significantly inversely associated with body height, with a regression coefficient of –0.78 (m/s)/cm (95% confidence interval –1.13 to –0.42). The augmentation index was not significantly associated with age, sex or (birth) weight.
Conclusion
The feasibility of measuring arterial stiffness in preschool children using the Arteriograph is moderate. We identified height as the most important determinant of the augmentation index in preschool children.
Keywords: Vascular stiffness, children, pulse wave analysis, cardiovascular disease
Introduction
Arterial stiffness is an important marker for the risk of developing cardiovascular diseases in adult life. Arterial stiffness, which describes the loss of capability of an artery to react on pressure changes due to loss of elasticity, is influenced by several parameters. In adulthood, male sex, older age, increased weight and a lower height are shown to be the most important determinants of increased arterial stiffness.1,2 In childhood, low birth weight (small for gestational age),3 higher gestational age3 and breastfeeding in the first year of life are associated with a higher arterial stiffness.4–8 Furthermore, several studies have demonstrated that chronic inflammation increases arterial stiffness.9–12
Arterial stiffness is expressed in several parameters, such as carotid-femoral pulse wave velocity (PWVao) and the augmentation index (AIX) of the aorta (AIXao) and the brachial artery (AIXbr). While PWVao is used as a direct marker for arterial stiffness, the AIX is used as a direct marker for wave reflection and an indirect marker for arterial stiffness.13–15 In addition, central systolic blood pressure (SBP) is an important parameter describing arterial stiffness, and shows a strong correlation with an increased arterial stiffness when increased.15 PWVao and AIX increase with the ageing process and both markers provide information about the status of the arterial system.14
Atherosclerosis, the leading cause of cardiovascular disease, starts to develop in early life; however, this does not directly cause symptoms in childhood.4,16–18 Increasing evidence suggests that cardiovascular risk factors are in childhood associated with increased arterial stiffness and other cardiovascular risk factors.4,5,18 These studies mainly focused on children over 5 years of age. Little is known about measurements of arterial stiffness in preschool children.
Arterial stiffness can be measured with many different devices. However, many of them are not validated in childhood and are not suitable to measure preschool children. With this study, we aim to assess the feasibility of measurements of arterial stiffness in preschool children, using the Arteriograph, a non-invasive oscillometric device. Secondly, we aim to explore possible determinants for arterial stiffness in preschool children.
Methods
Study population
We performed arterial stiffness measurements in 3-year-old healthy children, recruited from the Wheezing Illnesses Study Leidsche Rijn (WHISTLER), a population-based birth cohort study in Utrecht, the Netherlands.19 The study design was described in detail earlier.19 In short, healthy children born in Leidsche Rijn, Utrecht, the Netherlands, were invited to participate. Children were excluded when gestational age was under 36 weeks, when they were born with congenital abnormalities or when they suffered from respiratory diseases. From December 2011 to April 2013 participants were invited for a follow-up visit at the age of 3 years. At this visit, the investigated subjects each underwent a physical examination, a lung resistance measurement using a MicroRint device (MicroMedical; VIASYS Healthcare, Kent, UK)20 a transthoracic echocardiography and arterial stiffness measurements. The paediatric medical ethics committee of the University Medical Centrum Utrecht, the Netherlands, approved the study. Written informed consent was obtained from the parents.
Questionnaire
We used questionnaires completed at the first neonatal visit, at approximately 4 weeks of age, to assess characteristics, including gender, age at visit, gestational age, birth weight and height, socioeconomic status based on maternal education and exposure to environmental factors, such as tobacco smoke exposure during pregnancy. Information about the duration of breastfeeding was obtained from monthly taken questionnaires in the first year of life. Prior to the visit at the age of 3 years, the parents completed a new questionnaire containing information about current risk factors, current smoke exposure and health status of both the child and the relatives.
Anthropometric measurement
During the visit, the body weight of the children was measured wearing light clothing, using a standard electronic scale. Body height was measured without shoes, using an infant stadiometer. Body mass index (BMI) was calculated according to the World Health Organization (WHO) BMI-for-age growth standards. We measured the distance between the jugulum and the upper edge of the symphysis, measuring from the sternal notch to the pubic bone, to be able to calculate the aortic PWVao.
Arterial stiffness measurement
The children were measured with the Arteriograph (Tensiomed, Budapest, Hungary), a non-invasive oscillometric device, which has been validated earlier in adults,13–15,21 but not yet in (preschool) children.15,22 Measurements were taken in a supine position after 30 minutes of rest. The Arteriograph measures several parameters of arterial stiffness, such as blood pressure, PWVao and AIX.
Measuring the arterial stiffness is based on the physiological process of pulse waves. This pulse wave is measured in the brachial artery, with a brachial cuff.23 As the cuff is pressurised, approximately 35–40 mmHg above the SBP, the brachial artery is completely occluded, so that oscillations can be recorded and pressure peaks can be detected. There are two systolic peaks that can be distinguished. First, there is the ‘early’ systolic pulse pressure wave (P1), which is formed by the left ventricle ejecting blood into the aorta. The ‘late’ systolic peak (P2) is due to the first pressure wave travelling along the aorta, being reflected at the site of the aortic bifurcation.2,23,24 The return time of the systolic pressure wave, from the aortic root to the iliac bifurcation and back, is equal to the time lapses between the peaks of P1 and P2. PWVao can be calculated by halving this time and measuring the distance between the jugulum and the symphysis, which is comparable with the aortic length.23 AIX can be abstracted from the measured pulse pressure, and expresses the effect of the reflected wave.25 The Arteriograph software gives an overall value of arterial stiffness, if all consecutive pulse waves can be analysed. As pulse waves in early childhood are small and movement can distort the shape of a pulse wave, which could make evaluation of pulse waves impossible, we analysed each cardiac cycle one by one using the automatic Arteriograph software. A measurement was considered valid after a visual check and if the software was able to calculate a reliable value from the pressure wave curves. For every individual subject, we used the median of at least three valid curves.
Of randomly selected children, we also measured the blood pressure with the Dinamap oscillometric device (Dinamap 1846 SX/P; GE Healthcare, Waukesha, WI, USA).26
Statistical analysis
The subjects’ characteristics are presented in percentages, mean (standard deviation; SD) or median. All variables were checked for normality of distribution. An intraclass correlation coefficient (ICC) was used to determine the intrameasurement variability of average AIXbr, AIXao and PWVao based on one to three or more valid curve measurements. The correlation between the blood pressure measured with the Dinamap and the pressure measured with the Arteriograph was analysed calculating Pearson’s correlation coefficient.27 Differences in characteristics of children with and without a valid measurement were tested using independent samples t-test for continuous variables or χ2 for categorical variables. Univariable linear regression analysis was used to assess the associations of determinants based on the previous literature, with the arterial stiffness parameters as dependent variables.
Statistical analysis was performed using SPSS Inc. version 21.0 for Windows (IBM, 2012, Chicago, IL, USA). A statistical significance was considered reached at a P value of less than 0.05.
Results
We studied 168 healthy children, ranging in age between 3.29 and 4.11 years (mean age 3.72 years). An overview of the study population, showing the baseline characteristics including anthropometry, constitutional and environmental factors, is shown in Table 1.28 Of the 168 children, 34 children were also measured with the Dinamap device.
Table 1.
Baseline characteristics (n = 168).
| Subject characteristics | Mean | SD | |
|---|---|---|---|
| Female sex (n, %) | 93 | 55.4 | |
| Age at visit (years) | 3.72 | 0.17 | |
| Gestational age (weeks) | 39.2 | 1.4 | |
| Birth Weight (kg) | 3.60 | 0.49 | |
| Birth Length (cm) | 50.9 | 2.1 | |
| Length at visit (cm) | 102.4 | 4.4 | |
| Weight at visit (kg) | 17.2 | 2.0 | |
| BMI at visit (kg/m2) | 14.9 | 1.4 | |
| Thoracic circumference (cm) | 54.0 | 2.7 | |
| Waist circumference (cm) | 52.9 | 3.5 | |
| Hip circumference (cm) | 51.3 | 3.5 | |
| Family history | |||
| Parental BMI at visit (kg/m2) | Maternal BMI | 24.4 | 4.1 |
| Paternal BMI | 25.3 | 3.5 | |
| Criteria of metabolic syndrome in at least one parent (n, %)a | Obesity | 40 | 23.8 |
| Hypertension | 12 | 7.1 | |
| Hypercholesterolaemia | 8 | 4.8 | |
| Diabetes mellitus | 0 | 0 | |
| Coronary or peripheral artery disease in at least one relative (n, %)b | First-degree | 4 | 2.4 |
| Second-degree | 34 | 20.2 | |
| Environmental factors | |||
| Smoke exposure during pregnancy (n, %) | No | 150 | 90.4 |
| Yes | 16 | 9.6 | |
| Current smoke exposure (n, %) | No | 164 | 98.8 |
| Yes | 2 | 1.2 | |
| Breastfeeding (n, %) | None | 30 | 17.9 |
| 0–3 months | 74 | 44.0 | |
| 3–6 months | 43 | 35.6 | |
| >6 months | 21 | 12.5 | |
| Maternal education level (n, %) | Low/moderate | 36 | 25.2 |
| Highc | 107 | 74.8 | |
Data are means and standard deviations (SD) unless otherwise indicated.
BMI: body mass index.
As defined according to the National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATP III) definition.28 Parental waist circumference was not measured.
First-degree relatives are parents, second-degree relatives are grandparents. Considered positive if coronary or peripheral artery disease was present before the age of 60 years.
Higher vocational or university education.
Blood pressure measurements with the Arteriograph succeeded in 136 subjects (81.0%). Of all children with no blood pressure measurement, 13 children refused to participate and 14 measurements could not be performed due to restlessness. We were not able to measure three children due to technical errors as a consequence of low battery, and during the visit of two children measurements were prematurely stopped due to illness of the child.
At least one valid arterial stiffness measurement could be obtained in 100 subjects (59.5%), 89 of whom had at least two valid measurements, and 73 had at least three. Table 2 shows an overview of the arterial stiffness measurements. Briefly, our study showed a mean AIXao of 19.7 m/s (SD 7.0) for respectively three or more valid pulse waves. Aortic PWV showed a mean value of 5.56 m/s (SD 0.77) in one valid pulse wave curve, with decreasing mean when more valid pulse wave curves could be obtained. For every individual, we calculated the ICC to determine the intrameasurement variability. The ICCs for three or more occlusions were 0.87 for PWVao and 0.72 for AIXao.
Table 2.
Arterial stiffness parameters.
| Mean | SD | |
|---|---|---|
| Arteriograph (n = 73) | ||
| AIXbr (m/s) | –35.3 | 13.3 |
| AIXao (m/s) | 19.7 | 7.0 |
| PWVao (m/s) | 5.6 | 0.8 |
| SBPao (mmHg) | 86.7 | 6.9 |
| PPao (mmHg) | 36.2 | 4.3 |
| MAP (mmHg) | 65 | 5 |
| Systolic blood pressure (mmHg) | 94 | 7 |
| Diastolic blood pressure (mmHg) | 50 | 5 |
| ED (ms) | 275.8 | 17.7 |
| RT (ms) | 131.8 | 14.9 |
| Heart rate (1/min) | 94 | 11 |
| Dinamap (n = 34) | ||
| Systolic blood pressure (mmHg) | 97 | 6 |
| Diastolic blood pressure (mmHg) | 57 | 5 |
| Heart rate (1/min) | 95 | 9 |
AIXbr: augmentation index of the brachial artery; AIXao: augmentation index of the aorta; PWVao: aortic pulse wave velocity; SBPao: systolic blood pressure of the aorta; PPao: aortic pulse pressure; MAP: mean arterial pressure; ED: ejection duration; RT: return time.
Data are means and standard deviations (SD).
The mean value of SBP measured by the Dinamap device was 95 mmHg (SD 6), whereas diastolic blood pressure (DBP) measured showed a mean value of 58 mmHg (SD 6). In the same 34 children, SBP measured by the Arteriograph showed a mean value of 94 mmHg (SD 7), with a DBP mean value of 50 mmHg (SD 5). Pearson’s correlation coefficients of blood pressures measured using the Arteriograph and the Dinamap were 0.56 for SBP and 0.69 for DBP.
The non-significant differences in child characteristics between individuals with and without a valid measurement (three or more valid pulse wave analyses) are shown in Table 3.
Table 3.
Differences in characteristics of children with and without a valid measurement.
| Not valid |
Valid |
|||||
|---|---|---|---|---|---|---|
| Subject characteristics | Mean | SD | Mean | SD | P value | |
| Female sex (n, %) | 56.0 | 58.9 | 37 | 50.7 | 0.29 | |
| Age at visit (years) | 3.69 | 0.17 | 3.74 | 0.16 | 0.22 | |
| Length at visit (cm) | 101.9 | 4.8 | 102.6 | 4.1 | 0.34 | |
| Weight at visit (kg) | 17.1 | 2.6 | 17.3 | 1.8 | 0.50 | |
| BMI at visit (kg/m2) | 14.9 | 1.3 | 15.0 | 1.5 | 0.49 | |
| Parental BMI at visit (kg/m2) | Maternal BMI | 24.8 | 4.5 | 24.2 | 3.8 | 0.24 |
| Paternal BMI | 25.7 | 4.0 | 25.0 | 3.0 | 0.33 | |
| Smoke exposure during pregnancy (n, %) | No | 83 | 87.4 | 67 | 94.4 | 0.13 |
| Yes | 12 | 12.6 | 4 | 5.6 | ||
| Breastfeeding (n, %) | None | 17 | 17.9 | 13 | 17.8 | 0.67 |
| 0–3 months | 44 | 46.3 | 30 | 41.1 | ||
| 3–6 months | 21 | 22.1 | 22 | 30.1 | ||
| >6 months | 13 | 13.7 | 8 | 11.0 | ||
| Maternal education level (n, %) | Low/moderate | 21 | 25.0 | 15 | 25.4 | 0.95 |
| Higha | 63 | 75.0 | 44 | 74.6 | ||
Data are means and standard deviations (SD).
BMI: body mass index.
P value <0.05 is considered significant.
Higher vocational or university education.
Table 4 shows the influence of several subject characteristics on the AIXao and PWVao. Although the direction of the regression coefficients was confirmed in earlier findings,2 none of the selected characteristics were significantly associated with PWVao. Measurement of the AIXao showed a significant inverse association with body height, with a regression coefficient of –0.78 (m/s)/cm (95% confidence interval –1.13 to –0.42). Age, sex, birth weight and current weight showed no significant association with the AIX.
Table 4.
Association between arterial stiffness and child characteristics in early life.
| AIXao (n = 73) |
PWVao (n = 73) |
|||||
|---|---|---|---|---|---|---|
| Linear regression coefficient | 95% CI | P value | Linear regression coefficient | 95% CI | P value | |
| Female sex | 0.60 | –2.68–3.87 | 0.72 | 0.25 | –0.11–0.61 | 0.17 |
| Age (years) | –5.73 | –15.77–4.31 | 0.26 | 0.06 | –1.07–1.18 | 0.92 |
| Weight at visit (kg) | –0.75 | –1.64–0.15 | 0.10 | 0.03 | –0.07–0.13 | 0.57 |
| Height at visit (cm) | –0.78 | –1.13–0.42 | <0.01 | 0.01 | –0.03–0.06 | 0.53 |
| Birth weight (kg) | 1.53 | –2.24–5.30 | 0.42 | 0.13 | –0.29–0.55 | 0.53 |
AIXao: augmentation index of the aorta; PWVao: aortic pulse wave velocity; CI: confidence interval.
P value <0.05 is considered significant.
Discussion
This is the first study that has assessed the feasibility of measuring arterial stiffness using the Arteriograph in a large group of preschool children. We were able to measure arterial stiffness (with at least three valid curve waves) in almost half of our study population, which indicates that the feasibility is moderate.
Main results and strengths
In our study, height was the only determinant that was significantly associated with the AIXao. The influence of body height on arterial stiffness, in particular the AIXao, had been investigated before. This study showed that the influence of body height changes over time, probably due to a changing aorta growth rate.29 Other studies in childhood, using different devices, also found evidence for age and weight as determinants of arterial stiffness.1,2,4 Although these two determinants were not significantly associated with the PWVao or the AIXao in our study, the trends of the regression coefficients were comparable to these previous findings. The age range of our study population was small, which might explain these differences in statistical significance. We found comparable arterial stiffness in boys and girls, while previous studies found evidence for increased arterial stiffness in boys.1,2 As previous studies were performed in older age groups, these sex differences probably develop at an older age. These differences might be influenced by hormonal puberty-related changes.4,16,30
To determine the intra-measurement variability we calculated the ICC. This showed a good correlation, with an ICC of 0.87 for PWVao and 0.72 for AIXao for three or more occlusions per child. Regarding blood pressure measurements, we calculated the correlation between the measurements by the Arteriograph and the Dinamap device, using a Pearson correlation coefficient. In our homogeneous study population with a low variability in age, weight and height, the values of these correlation coefficients can be considered strong.
We were able to determine the feasibility of the Arteriograph device in a relatively large group of healthy 3-year-old children, which we consider moderate. In addition, we were able to investigate the characteristics of arterial stiffness measurement in this age group. One previous study determined reference values in the preschool age group, but they only studied a small group of preschool children (n = 44).2 This previous study only stratified for sex and age and did not study the associations between child characteristics and arterial stiffness. The measured PWVao and AIXao in our 3-year-olds are in accordance with the results of the previously performed study.2
In preschool children many devices are not suitable to measure arterial stiffness. The feasibility of measuring arterial stiffness using the Arteriograph had not previously been assessed in this group. Measurement of arterial stiffness using the Arteriograph was relatively quick (a few minutes), and children experienced only a little discomfort, comparable with the amount of discomfort experienced during a blood pressure measurement. However, we must note that recent studies have demonstrated the feasibility of measuring arterial stiffness with different devices, although this mainly applies to older subjects.31–34
Limitations
Our study has several limitations. First, we measured the arterial stiffness in children during a study visit after other measurements: the children first underwent a physical examination (length and weight), a lung function measurement and a transthoracic echocardiography. However, performing multiple consecutive tests reflects current practice. Also, children were allowed to rest for at least 10 minutes before the measurements were taken, according to the Arteriograph’s manual.
A second limitation is that there is a reasonable chance of dropout of the children because the children were tired or restless, even though these measurements are all completely non-invasive. In our study, we were able to obtain one valid measurement in a relatively high percentage of subjects, while we were able to obtain at least three valid measurements per child in only almost half of the study group. The number of valid measurements will probably increase in a study without performing other tests.
Future directions
Although the Arteriograph has been validated in adults and adolescents before, the Arteriograph should be further validated in young children.15 Given the fact that atherosclerosis starts early and increasing evidence suggests that early life adverse exposures could lead to structural changes in the vascular system, it is of the utmost importance to gain more knowledge about the vascular system in early childhood. In our study, we only measured the arterial stiffness at the 3-year visit. We recommend measuring arterial stiffness during follow-up later in life, in order to track possible alterations in risk factors and arterial stiffness parameters.
In conclusion, in our study, we were able to determine the feasibility of measuring arterial stiffness in preschool children using the Arteriograph, which is considered moderate. We consider height as the most important determinant of the AIX.
Acknowledgements
The authors gratefully acknowledge all parents and children who participated, and Eltje Bloemen for her contribution of analysing the pulse waves and Myriam Olling-de Kok for secretarial support.
Author contribution
All authors contributed to the conception and design of the work and to the analysis and interpretation of data. MMV and JBE contributed to acquisition of data. MMV drafted the manuscript. CSPMU, CKvdE and JBE critically revised the manuscript. All authors gave final approval and agreed to be accountable for all aspects of work ensuring integrity and accuracy.
Declaration of conflicting interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: the Wheezing Illnesses STudy LEidsche Rijn received grant 2100.0095 from The Netherlands Organisation for Health Research and Development (ZonMw). An unrestricted grant was received from Glaxo Smith Kline.
References
- 1.Jatoi NA, Mahmud A, Bennett K, et al. Assessment of arterial stiffness in hypertension: comparison of oscillometric (Arteriograph), piezoelectronic (Complior) and tonometric (SphygmoCor) techniques. J Hypertens 2009; 27: 2186–2191. [DOI] [PubMed] [Google Scholar]
- 2.Hidvégi EV, Illyés M, Benczúr B, et al. Reference values of aortic pulse wave velocity in a large healthy population aged between 3 and 18 years. J Hypertens 2012; 30: 2314–2321. [DOI] [PubMed] [Google Scholar]
- 3.Atsuko T, Mori A, Kondo A, et al. Non-invasive assessment of arterial stiffness in appropriate-for-gestational age newborn infants. Early Hum Dev 2008; 84: 403–408. [DOI] [PubMed] [Google Scholar]
- 4.Schack-Nielsen L, Mølgaard C, Larsen D, et al. Arterial stiffness in 10-year-old children: current and early determinants. Br J Nutr 2005; 94: 1004–1004. [DOI] [PubMed] [Google Scholar]
- 5.Skilton MR, Nakhla S, Ayer JG, et al. Telomere length in early childhood: early life risk factors and association with carotid intima-media thickness in later childhood. Eur J Prev Cardiol 2016; 23: 1086–1092. [DOI] [PubMed] [Google Scholar]
- 6.Batista MS, Mill JG, Pereira TSS, et al. Factors associated with arterial stiffness in children aged 9–10 years. Rev Saude Publica 2015; 49: 23–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Silveira PP, Portella AK, Goldani MZ, et al. Developmental origins of health and disease (DOHaD). J Pediatr (Rio J) 2007; 83: 494–504. [DOI] [PubMed] [Google Scholar]
- 8.Evelein AM, Visseren FL, van der Ent CK, et al. Allergies are associated with arterial changes in young children. Eur J Prev Cardiol 2015; 22: 1480–1487. [DOI] [PubMed] [Google Scholar]
- 9.Picarelli MM, Danzmann LC, Grun LK, et al. Arterial stiffness by oscillometric device and telomere lenght in juvenile idiopathic artrhitis with no cardiovascular risk factors: a cross-sectional study. Pediatr Rheumatol 2017; 15: 34–34. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Buehler T, Steinmann M, Singer F, et al. Increased arterial stiffness in children with cystic fibrosis. Eur Respir J 2012; 39: 1536–1537. [DOI] [PubMed] [Google Scholar]
- 11.Lurz E, Aeschbacher E, Carman N, et al. Pulse wave velocity measurement as a marker of arterial stiffness in pediatric inflammatory bowel disease: a pilot study. Eur J Pediatr 2017; 176: 983–987. [DOI] [PubMed] [Google Scholar]
- 12.Steinmann M, Abbas C, Singer F, et al. Arterial stiffness is increased in asthmatic children. Eur J Pediatr 2015; 174: 519–523. [DOI] [PubMed] [Google Scholar]
- 13.Nemcsik J, Egresits J, El Hadj Othmane T, et al. Validation of arteriograph – a new oscillometric device to measure arterial stiffness in patients on maintenance hemodialysis. Kidney Blood Press Res 2009; 32: 223–229. [DOI] [PubMed] [Google Scholar]
- 14.Baulmann J, Schillings U, Rickert S, et al. A new oscillometric method for assessment of arterial stiffness: comparison with tonometric and piezo-electronic methods. J Hypertens 2008; 26: 523–528. [DOI] [PubMed] [Google Scholar]
- 15.Horváth IG, Németh A, Lenkey Z, et al. Invasive validation of a new oscillometric device (Arteriograph) for measuring augmentation index, central blood pressure and aortic pulse wave velocity. J Hypertens 2010; 28: 2068–2075. [DOI] [PubMed] [Google Scholar]
- 16.Morrison KM, Dyal L, Conner W, et al. Cardiovascular risk factors and non-invasive assessment of subclinical atherosclerosis in youth. Atherosclerosis 2010; 208: 501–505. [DOI] [PubMed] [Google Scholar]
- 17.Ceponiene I, Klumbiene J, Tamuleviciute-Prasciene E, et al. Associations between risk factors in childhood (12–13 years) and adulthood (48–49 years) and subclinical atherosclerosis: the Kaunas Cardiovascular Risk Cohort Study. BMC Cardiovasc Disord 2015; 15: 80–89. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Chu C, Dai Y, Mu J, et al. Associations of risk factors in childhood with arterial stiffness 26 years later: the Hanzhong adolescent hypertension cohort. J Hypertens 2017; 35: S10–S15. [DOI] [PubMed] [Google Scholar]
- 19.Katier N, Uiterwaal CSPM, de Jong BM, et al. The Wheezing Illnesses Study Leidsche Rijn (WHISTLER): rationale and design. Eur J Epidemiol 2004; 19: 895–903. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Beydon N, Davis SD, Lombardi E, et al. An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children. Am J Respir Crit Care Med 2007; 175: 1304–1345. [DOI] [PubMed] [Google Scholar]
- 21.Ring M, Eriksson MJ, Zierath JR, et al. Arterial stiffness estimation in healthy subjects: a validation of oscillometric (Arteriograph) and tonometric (SphygmoCor) techniques. Hypertens Res 2014; 37: 999–1007. [DOI] [PubMed] [Google Scholar]
- 22.Hidvégi EV, Illyés M, Benczúr B, et al. Reference values of aortic pulse wave velocity in a large healthy population aged between 3 and 18 years. J Hypertens 2012; 30: 2314–2321. [DOI] [PubMed] [Google Scholar]
- 23.Davies JM, Bailey MA, Griffin KJ, et al. Pulse wave velocity and the non-invasive methods used to assess it: Complior, SphygmoCor, Arteriograph and Vicorder. Vascular 2012; 20: 342–349. [DOI] [PubMed] [Google Scholar]
- 24.Trachet B, Reymond P, Kips J, et al. Numerical validation of a new method to assess aortic pulse wave velocity from a single recording of a brachial artery waveform with an occluding cuff. Ann Biomed Eng 2010; 38: 876–888. [DOI] [PubMed] [Google Scholar]
- 25.London GM, Pannier B. Arterial functions: how to interpret the complex physiology. Nephrol Dial Transplant 2010; 25: 3815–3823. [DOI] [PubMed] [Google Scholar]
- 26.Lim SM, Kim HC, Lee HS, et al. Association between blood pressure and carotid intima-media thickness. J Pediatr 2009; 154: 667–671. [DOI] [PubMed] [Google Scholar]
- 27.Katier N, Uiterwaal CSPM, Jong BM De, et al. Feasibility and variability of neonatal and infant lung function measurement using the single occlusion technique. Chest 2005; 128: 1822–1829. [DOI] [PubMed]
- 28.Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement. Circulation 2005; 112: 2735–2752. [DOI] [PubMed] [Google Scholar]
- 29.Hidvegi EV, Illyes M, Molnar FT, et al. Influence of body height on aortic systolic pressure augmentation and wave reflection in childhood. J Hum Hypertens 2015; 29: 495–501. [DOI] [PubMed] [Google Scholar]
- 30.Urbina EM, Williams RV, Alpert BS, et al. Noninvasive assessment of subclinical atherosclerosis in children and adolescents: recommendations for standard assessment for clinical research: a scientific statement from the American Heart Association. Hypertension 2009; 54: 919–950. [DOI] [PubMed] [Google Scholar]
- 31.Ghazi L, Dudenbostel T, Xing D, et al. Assessment of vascular function in low socioeconomic status preschool children: a pilot study. J Am Soc Hypertens 2017; 11: 101–109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Correia-Costa A, Correia-Costa L, Caldas Afonso A, et al. Determinants of carotid-femoral pulse wave velocity in prepubertal children. Int J Cardiol 2016; 218: 37–42. [DOI] [PubMed] [Google Scholar]
- 33.Cruickshank JK, Silva MJ, Molaodi OR, et al. Ethnic differences in and childhood influences on early adult pulse wave velocity: the Determinants of Adolescent, Now Young Adult, Social Wellbeing, and Health Longitudinal Study. Hypertens (Dallas, Tex 1979) 2016; 67: 1133–1141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Currie KD, Proudfoot NA, Timmons BW, et al. Noninvasive measures of vascular health are reliable in preschool-aged children. Appl Physiol Nutr Metab 2010; 35: 512–517. [DOI] [PubMed] [Google Scholar]
