Original Article

Journal of Cerebral Blood Flow & Metabolism (2009) 29, 803–810; doi:10.1038/jcbfm.2009.6; published online 11 February 2009

Hemodynamic etiology of elevated flow velocity and stroke in sickle-cell disease

Isak Prohovnik1, Anne Hurlet-Jensen2, Robert Adams3, Darryl De Vivo4 and Steven G Pavlakis2,5

  1. 1Department of Psychiatry and Radiology, Mount Sinai School of Medicine, New York, New York, USA
  2. 2Mount Sinai School of Medicine, New York, New York, USA
  3. 3Medical University of South Carolina, Charleston, South Carolina, USA
  4. 4Columbia University, New York, New York, USA
  5. 5Maimonides Infants and Children's Hospital, Brooklyn, New York, USA

Correspondence: Professor Isak Prohovnik, Department of Psychiatry and Radiology, Mount Sinai School of Medicine, One Gustave Levy Place, Box 1230, New York, NY 10029, USA. E-mail: Isak.Prohovnik@mssm.edu

Received 21 October 2008; Revised 5 December 2008; Accepted 4 January 2009; Published online 11 February 2009.

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Abstract

Elevation of blood flow velocity in the large cerebral vessels is known to be of substantial pathophysiologic and prognostic significance in sickle-cell disease (SCD). Its precise cause is not established, but the two obvious proximal mechanisms are obstructive vascular stenosis and hemodynamic dilatation. Here we revisit this distinction by analyzing cerebrovascular reserve capacity. Forty-two patients with SCD underwent measurements of global cerebral blood flow in grey matter by the 133Xe inhalation method during normocapnia and hypercapnia to quantify cerebrovascular reactivity. Cerebral blood flow was significantly higher in SCD patients (120plusminus31 ml/100 g/min) than in controls (76plusminus20 ml/100 g/min). Reactivity was significantly lower in SCD patients (1.06plusminus1.92 versus 2.16plusminus1.15%/mm Hg). Stepwise multiple regressions within the SCD sample determined that normocapnic cerebral blood flow was largely predicted by hematocrit (r=-0.59; P<0.0001), whereas hypercapnic reactivity was only predicted by normocapnic flow across all subjects (r=-0.52; P<0.0001). None of the controls, but 24% of the SCD patients showed 'steal' (negative reactivity, chi2=6.05; P<0.02). This impairment of vasodilatory capacity, occurring at perfusion levels above 150 ml/100 g/min, may reflect intrinsic limitations of the human cerebrovascular system and can explain both the elevated blood flow velocities and the high risk of stroke observed in such patients.

Keywords:

cerebral blood flow, cerebrovascular reserve capacity, hypercapnic dilatation, sickle-cell disease

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