Literature DB >> 17895109

Evidence of cranial artery ectasia in sickle cell disease patients with ectasia of the basilar artery.

R G Steen1, W E Reddick, J O Glass, W C Wang.   

Abstract

GOAL: To determine if children with sickle cell disease (SCD) and basilar artery ectasia show evidence of general arterial ectasia.
METHODS: A novel method was used to analyze the base images normally used to reconstruct a magnetic resonance angiogram (MRA). A signal intensity threshold was set empirically to exclude pixels from subcutaneous fat, then base images for each patient were evaluated for the number and relative size of vessel profiles. Data from three SCD patients, imaged before and after transfusion, were analyzed to determine sensitivity of the method to blood flow. We then compared 11 SCD patients with basilar ectasia to 11 age-matched SCD patients with a normal basilar, after excluding patients with clinical stroke.
FINDINGS: Before transfusion, patients have an apparent blood volume 48% higher than after (P<.001). Transfusion reduces apparent blood volume because flow rate is reduced by transfusion and MRA is flow-sensitive. But apparent blood volume was not significantly lower in any individual vessel size class, suggesting that fast flow simply increases vessel conspicuity. Patients with basilar ectasia have an apparent blood volume 62% higher than normal (P<.001). Although this could be due to faster blood flow, apparent blood volume was higher specifically in vessels > or =2 mm in diameter (P<.001), suggesting that small arteries can become generally ectatic in patients with basilar ectasia.
CONCLUSIONS: Basilar ectasia is associated with an increased blood flow rate, generalized arterial ectasia, or both phenomena. This suggests that basilar volume measurements may supplement blood flow velocity measurements as an indicator of stroke risk.

Entities:  

Year:  1998        PMID: 17895109     DOI: 10.1016/s1052-3057(98)80051-7

Source DB:  PubMed          Journal:  J Stroke Cerebrovasc Dis        ISSN: 1052-3057            Impact factor:   2.136


  6 in total

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Review 2.  Hypoxic adaptation during development: relation to pattern of neurological presentation and cognitive disability.

Authors:  Fenella J Kirkham; Avijit K Datta
Journal:  Dev Sci       Date:  2006-07

Review 3.  Hypoxia and inflammation in children with sickle cell disease: implications for hippocampal functioning and episodic memory.

Authors:  Mary Iampietro; Tania Giovannetti; Reem Tarazi
Journal:  Neuropsychol Rev       Date:  2014-04-18       Impact factor: 7.444

4.  Arterial spin-labeled perfusion combined with segmentation techniques to evaluate cerebral blood flow in white and gray matter of children with sickle cell anemia.

Authors:  Kathleen J Helton; Amir Paydar; John Glass; Eric M Weirich; Jane Hankins; Chin-Shang Li; Matthew P Smeltzer; Winfred C Wang; Russell E Ware; Robert J Ogg
Journal:  Pediatr Blood Cancer       Date:  2009-01       Impact factor: 3.167

5.  Removal of Arterial Vessel Contributions in Susceptibility-Weighted Images for Quantification of Normalized Visible Venous Volume in Children with Sickle Cell Disease.

Authors:  Adam M Winchell; Ruitian Song; Ralf B Loeffler; Winfred C Wang; Jane S Hankins; Kathleen J Helton; Claudia M Hillenbrand
Journal:  J Healthc Eng       Date:  2017-08-28       Impact factor: 2.682

6.  Vascular Instability and Neurological Morbidity in Sickle Cell Disease: An Integrative Framework.

Authors:  Hanne Stotesbury; Jamie M Kawadler; Patrick W Hales; Dawn E Saunders; Christopher A Clark; Fenella J Kirkham
Journal:  Front Neurol       Date:  2019-08-13       Impact factor: 4.003

  6 in total

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