Plasma glial fibrillary acidic protein levels in children with sickle cell disease

To determine if glial fibrillary acidic protein (GFAP) is associated with brain injury in children with sickle cell disease (SCD), we measured plasma GFAP among cross-sectional groups of unselected children with SCD, subsets of children with SCD and normal brain MRI or MRI evidence of cerebral infar...

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Veröffentlicht in:American journal of hematology 2011-05, Vol.86 (5), p.427-429
Hauptverfasser: Savage, William J., Barron‐Casella, Emily, Fu, Zongming, Dulloor, Pratima, Williams, Lisa, Crain, Barbara J., White, Desiree A., Jennings, Jacky M., Van Eyk, Jennifer E., Debaun, Michael R., Everett, Allen, Casella, James F.
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container_end_page 429
container_issue 5
container_start_page 427
container_title American journal of hematology
container_volume 86
creator Savage, William J.
Barron‐Casella, Emily
Fu, Zongming
Dulloor, Pratima
Williams, Lisa
Crain, Barbara J.
White, Desiree A.
Jennings, Jacky M.
Van Eyk, Jennifer E.
Debaun, Michael R.
Everett, Allen
Casella, James F.
description To determine if glial fibrillary acidic protein (GFAP) is associated with brain injury in children with sickle cell disease (SCD), we measured plasma GFAP among cross-sectional groups of unselected children with SCD, subsets of children with SCD and normal brain MRI or MRI evidence of cerebral infarct, healthy pediatric controls, and adults with brain injury. Children with SCD had higher plasma GFAP than healthy pediatric controls (mean concentrations 0.14 ± 0.37 vs. 0.07 ± 0.08 ng/mL; P 5 0.003); also, 16.0% (16/100) of children with SCD and cerebral infarct had GFAP elevations above the 95th percentile of healthy pediatric controls (P 5 0.04). Although not statistically significant, children with SCD and cerebral infarct had more elevated GFAP levels than with SCD and no infarct (16/100, 16.0% vs. 14/168, 8.3%; P 5 0.07). Children with SCD and acute brain ischemia had a higher proportion of elevated GFAP than SCD children with normal MRI (3/6, 50% vs.8.3%; P 5 0.01). GFAP was associated with elevated systolic blood pressure in the preceding year and correlated positively with white blood cell count and negatively with age and performance IQ. Plasma GFAP is elevated among children with SCD and may be associated with subclinical brain injury.
doi_str_mv 10.1002/ajh.21995
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Children with SCD had higher plasma GFAP than healthy pediatric controls (mean concentrations 0.14 ± 0.37 vs. 0.07 ± 0.08 ng/mL; P 5 0.003); also, 16.0% (16/100) of children with SCD and cerebral infarct had GFAP elevations above the 95th percentile of healthy pediatric controls (P 5 0.04). Although not statistically significant, children with SCD and cerebral infarct had more elevated GFAP levels than with SCD and no infarct (16/100, 16.0% vs. 14/168, 8.3%; P 5 0.07). Children with SCD and acute brain ischemia had a higher proportion of elevated GFAP than SCD children with normal MRI (3/6, 50% vs.8.3%; P 5 0.01). GFAP was associated with elevated systolic blood pressure in the preceding year and correlated positively with white blood cell count and negatively with age and performance IQ. 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Children with SCD had higher plasma GFAP than healthy pediatric controls (mean concentrations 0.14 ± 0.37 vs. 0.07 ± 0.08 ng/mL; P 5 0.003); also, 16.0% (16/100) of children with SCD and cerebral infarct had GFAP elevations above the 95th percentile of healthy pediatric controls (P 5 0.04). Although not statistically significant, children with SCD and cerebral infarct had more elevated GFAP levels than with SCD and no infarct (16/100, 16.0% vs. 14/168, 8.3%; P 5 0.07). Children with SCD and acute brain ischemia had a higher proportion of elevated GFAP than SCD children with normal MRI (3/6, 50% vs.8.3%; P 5 0.01). GFAP was associated with elevated systolic blood pressure in the preceding year and correlated positively with white blood cell count and negatively with age and performance IQ. 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Hemoglobinopathies</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Brain Injuries - blood</topic><topic>Brain Ischemia - diagnosis</topic><topic>Brain Ischemia - etiology</topic><topic>Cerebral Infarction - diagnosis</topic><topic>Cerebral Infarction - etiology</topic><topic>Cerebrovascular Disorders - diagnosis</topic><topic>Cerebrovascular Disorders - etiology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diseases of red blood cells</topic><topic>Early Diagnosis</topic><topic>Female</topic><topic>Glial Fibrillary Acidic Protein - blood</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematology</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nerve Tissue Proteins - blood</topic><topic>Severity of Illness Index</topic><topic>Stroke - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Savage, William J.</creatorcontrib><creatorcontrib>Barron‐Casella, Emily</creatorcontrib><creatorcontrib>Fu, Zongming</creatorcontrib><creatorcontrib>Dulloor, Pratima</creatorcontrib><creatorcontrib>Williams, Lisa</creatorcontrib><creatorcontrib>Crain, Barbara J.</creatorcontrib><creatorcontrib>White, Desiree A.</creatorcontrib><creatorcontrib>Jennings, Jacky M.</creatorcontrib><creatorcontrib>Van Eyk, Jennifer E.</creatorcontrib><creatorcontrib>Debaun, Michael R.</creatorcontrib><creatorcontrib>Everett, Allen</creatorcontrib><creatorcontrib>Casella, James F.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Savage, William J.</au><au>Barron‐Casella, Emily</au><au>Fu, Zongming</au><au>Dulloor, Pratima</au><au>Williams, Lisa</au><au>Crain, Barbara J.</au><au>White, Desiree A.</au><au>Jennings, Jacky M.</au><au>Van Eyk, Jennifer E.</au><au>Debaun, Michael R.</au><au>Everett, Allen</au><au>Casella, James F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma glial fibrillary acidic protein levels in children with sickle cell disease</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>2011-05</date><risdate>2011</risdate><volume>86</volume><issue>5</issue><spage>427</spage><epage>429</epage><pages>427-429</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>To determine if glial fibrillary acidic protein (GFAP) is associated with brain injury in children with sickle cell disease (SCD), we measured plasma GFAP among cross-sectional groups of unselected children with SCD, subsets of children with SCD and normal brain MRI or MRI evidence of cerebral infarct, healthy pediatric controls, and adults with brain injury. Children with SCD had higher plasma GFAP than healthy pediatric controls (mean concentrations 0.14 ± 0.37 vs. 0.07 ± 0.08 ng/mL; P 5 0.003); also, 16.0% (16/100) of children with SCD and cerebral infarct had GFAP elevations above the 95th percentile of healthy pediatric controls (P 5 0.04). Although not statistically significant, children with SCD and cerebral infarct had more elevated GFAP levels than with SCD and no infarct (16/100, 16.0% vs. 14/168, 8.3%; P 5 0.07). Children with SCD and acute brain ischemia had a higher proportion of elevated GFAP than SCD children with normal MRI (3/6, 50% vs.8.3%; P 5 0.01). GFAP was associated with elevated systolic blood pressure in the preceding year and correlated positively with white blood cell count and negatively with age and performance IQ. Plasma GFAP is elevated among children with SCD and may be associated with subclinical brain injury.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21523806</pmid><doi>10.1002/ajh.21995</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Anemia, Sickle Cell - blood
Anemia, Sickle Cell - physiopathology
Anemias. Hemoglobinopathies
Biological and medical sciences
Biomarkers - blood
Brain Injuries - blood
Brain Ischemia - diagnosis
Brain Ischemia - etiology
Cerebral Infarction - diagnosis
Cerebral Infarction - etiology
Cerebrovascular Disorders - diagnosis
Cerebrovascular Disorders - etiology
Child
Child, Preschool
Diseases of red blood cells
Early Diagnosis
Female
Glial Fibrillary Acidic Protein - blood
Hematologic and hematopoietic diseases
Hematology
Humans
Magnetic Resonance Imaging
Male
Medical sciences
Nerve Tissue Proteins - blood
Severity of Illness Index
Stroke - blood
title Plasma glial fibrillary acidic protein levels in children with sickle cell disease
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