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Hemodynamic variability and cerebrovascular control after transient cerebral ischemia.
Allan, Philip D; Faulkner, James; O'Donnell, Terrence; Lanford, Jeremy; Wong, Lai-Kin; Saleem, Saqib; Woolley, Brandon; Lambrick, Danielle; Stoner, Lee; Tzeng, Yu-Chieh.
Afiliación
  • Allan PD; Centre for Translational Physiology, University of Otago, Wellington, New Zealand Department of Surgery and Anaesthesia, University of Otago, Wellington, New Zealand.
  • Faulkner J; Department of Sport and Exercise, University of Winchester, Winchester, UK.
  • O'Donnell T; Centre for Translational Physiology, University of Otago, Wellington, New Zealand Department of Surgery and Anaesthesia, University of Otago, Wellington, New Zealand.
  • Lanford J; Department of Neurology, Wellington Hospital, Wellington, New Zealand.
  • Wong LK; Department of Neurology, Wellington Hospital, Wellington, New Zealand.
  • Saleem S; Centre for Translational Physiology, University of Otago, Wellington, New Zealand School of Engineering and Computer Science, Victoria University of Wellington, Wellington, New Zealand.
  • Woolley B; School of Sport and Exercise, Massey University, Wellington, New Zealand.
  • Lambrick D; Faculty of Health Science, University of Southampton, Southampton, UK.
  • Stoner L; School of Sport and Exercise, Massey University, Wellington, New Zealand.
  • Tzeng YC; Centre for Translational Physiology, University of Otago, Wellington, New Zealand Department of Surgery and Anaesthesia, University of Otago, Wellington, New Zealand shieak.tzeng@otago.ac.nz.
Physiol Rep ; 3(11)2015 Nov.
Article en En | MEDLINE | ID: mdl-26537345
ABSTRACT
We investigated if hemodynamic variability, cerebral blood flow (CBF) regulation, and their interrelationships differ between patients with transient ischemic attack (TIA) and controls. We recorded blood pressure (BP) and bilateral middle cerebral artery flow velocity (MCAv) in a cohort of TIA patients (n = 17), and age-matched controls (n = 15). Spontaneous fluctuations in BP and MCAv were characterized by spectral power analysis, and CBF regulation was assessed by wavelet phase synchronization analysis in the very low- (0.02-0.07 Hz), low- (0.07-0.20 Hz), and high-frequency (0.20-0.40 Hz) ranges. Furthermore, cerebrovascular CO2 reactivity was assessed as a second metric of CBF regulation by inducing hypercapnia with 8% CO2 inhalation followed by hyperventilation driven hypocapnia. We found that TIA was associated with higher BP power (group effect, P < 0.05), but not MCAv power (P = 0.11). CBF regulation (assessed by wavelet phase synchronization and CO2 reactivity) was intact in patients (all P ≥ 0.075) across both hemispheres (all P ≥ 0.51). Pooled data (controls and affected hemisphere of patients) showed that BP and MCAv power were positively correlated at all frequency ranges (R(2) = 0.20-0.80, all P < 0.01). Furthermore, LF phase synchronization index was a significant determinant of MCAv power (P < 0.05), while VLF and HF phase synchronization index, and TIA were not (all P ≥ 0.50). These results indicate that CBF stability and control is maintained in TIA patients, but BPV is markedly elevated. BPV attenuation may be an important therapeutic strategy for enhancing secondary stroke prevention in patients who suffer a TIA.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Physiol Rep Año: 2015 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Physiol Rep Año: 2015 Tipo del documento: Article País de afiliación: Nueva Zelanda