Abstract
Background: Passive smoking (PS) is associated with increased risk for cerebrovascular and cardiovascular events, however, there has been little focus on cerebrovascular function. The purpose of this study is to assess cerebrovascular flow velocities and regulation in PS children. Methods: Noninvasive ultrasonographic measurements were made in 51 children (age:9 ± 4years) who have been exposed to tobacco smoking since intrauterine life and 35 age-matched children without PS. Using transcranial color Doppler sonography, peak systolic (PSV), end-diastolic (EDV), and average peak flow (APV) velocities of middle cerebral artery were measured during supine rest and 3 minutes-upright posture. Pulsatile index as a parameter of vascular resistance was calculated. Pulsatile index was defined as (PSV-EDV)/APV. Quantitative B-mode ultrasound scans were used to measure intima-media thickness and diameters of the common carotid artery. Urine cotinine concentrations were assessed. Results: Flow velocities and pulsatile index were not significantly different between controls and PS children (p > 0.05). In controls and PS children with urine cotinine concentrations <5ng/ml (n = 26), pulsatile index did not change during upright position (p > 0.05). However, in PS children with urine cotinine concentrations ≥ 5ng/ml (n = 25), there was a significant increase in pulsatile index during upright position (0.93 ± 0.14 vs. 0.87 ± 0.12, p < 0.01), because APV and EDV were significantly lower (69 ± 16 vs. 76 ±17 cm/sec and 44 ± 9 vs. 50 ± 11 cm/sec, p <0.05, respectively), although PSV was not significantly different. The percent change in pulsatile index during an upright position correlated significantly with urine cotinine level (r =0.57, p < 0.01). Intima-media thickness at carotid artery and stiffness did not correlate with cerebral blood flow velocities. Conclusions: The present study indicates that passive smoking can adversely affect cerebral blood flow and regulation in the cerebrovascular bed in childhood. Passive smoking not only is a risk factor for later cardiovascular disease, but also is associated with significant impairment of cerebral flow dynamics.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.