Literature DB >> 20949593

High reticulocyte count is an independent risk factor for cerebrovascular disease in children with sickle cell anemia.

Célia Maria Silva1, Poliana Giovani, Marcos Borato Viana.   

Abstract

BACKGROUND: Transcranial Doppler ultrasonography (TCD) is an important way of detecting risk of ischemic stroke in children with sickle cell anemia. PROCEDURE: A random sample of 262 FS-hemoglobin children from a newborn screening inception cohort in Brazil (1998-2005) was followed up to May 2009. Pulsed TCD followed STOP protocol. Children with mean blood flow velocity < 170 cm/sec in cerebral arteries were classified as low risk; between 170 and 184, low conditional risk; between 185 and 199, high conditional risk; and ≥ 200, high risk.
RESULTS: Median age, 6.2 years (2-11.2 years); 147 female; 13 children (5%) had ischemic stroke prior to TCD; 186/249 (74.7%) were classified as low risk; 19 (7.6%) as low conditional; 7 (2.8%) as high conditional; and 8 (3.2%) as high risk; inadequate tests, 11.6%. The probability of ischemic stroke at 10 years was 8.3% (SEM 2.3%); of stroke or high-risk TCD 15.6% (3.5%). Children with stroke or altered TCD (conditional and high risk) were compared to children with normal examinations. They were younger (P = 0.03), with lower hemoglobin (P = 0.003), higher leukocytosis (P = 0.015), and higher reticulocytosis (P < 0.001). Episodes per year of acute chest syndrome were also higher in that group, but not significantly (P = 0.09). Reticulocytosis remained the only significant variable upon multivariate analysis (P = 0.004). Basilar and middle cerebral artery velocities were significantly correlated (R = 0.55; P < 0.001).
CONCLUSIONS: Probability of stroke was similar to international reports; of belonging to high-risk group, lower. High-reticulocyte count was the most important factor associated with cerebrovascular disease. Basilar artery velocity > 130 cm/sec seems to be an indirect sign of an underlying cerebrovascular disease.
Copyright © 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20949593     DOI: 10.1002/pbc.22680

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  11 in total

Review 1.  Not all red cells sickle the same: Contributions of the reticulocyte to disease pathology in sickle cell anemia.

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Journal:  Stroke       Date:  2014-10-28       Impact factor: 7.914

3.  Reticulocytosis and anemia are associated with an increased risk of death and stroke in the newborn cohort of the Cooperative Study of Sickle Cell Disease.

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5.  Increased reticulocytosis during infancy is associated with increased hospitalizations in sickle cell anemia patients during the first three years of life.

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Review 7.  Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease.

Authors:  André Rolim Belisário; Célia Maria Silva; Cibele Velloso-Rodrigues; Marcos Borato Viana
Journal:  Hematol Transfus Cell Ther       Date:  2017-11-26

8.  Examination of Reticulocytosis among Chronically Transfused Children with Sickle Cell Anemia.

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9.  Nocturnal oxyhemoglobin desaturation and arteriopathy in a pediatric sickle cell disease cohort.

Authors:  Nomazulu Dlamini; Dawn E Saunders; Michael Bynevelt; Sara Trompeter; Timothy C Cox; Romola S Bucks; Fenella J Kirkham
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10.  Low hemoglobin increases risk for cerebrovascular disease, kidney disease, pulmonary vasculopathy, and mortality in sickle cell disease: A systematic literature review and meta-analysis.

Authors:  Kenneth I Ataga; Victor R Gordeuk; Irene Agodoa; Jennifer A Colby; Kimberly Gittings; Isabel E Allen
Journal:  PLoS One       Date:  2020-04-03       Impact factor: 3.240

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