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Liver biopsy results in patients with sickle cell disease on chronic transfusions: Poor correlation with ferritin levels

dc.contributor.authorKaram, Lina B.en_US
dc.contributor.authorDisco, Deborahen_US
dc.contributor.authorJackson, Sherron M.en_US
dc.contributor.authorLewin, Daviden_US
dc.contributor.authorMckie, Virgilen_US
dc.contributor.authorBaker, Robert D.en_US
dc.contributor.authorBaker, Susan S.en_US
dc.contributor.authorLaver, Joseph H.en_US
dc.contributor.authorNietert, Paul J.en_US
dc.contributor.authorAbboud, Miguel R.en_US
dc.date.accessioned2007-12-04T18:36:51Z
dc.date.available2009-01-07T20:01:15Zen_US
dc.date.issued2008-01en_US
dc.identifier.citationKaram, Lina B.; Disco, Deborah; Jackson, Sherron M.; Lewin, David; Mckie, Virgil; Baker, Robert D.; Baker, Susan S.; Laver, Joseph H.; Nietert, Paul J.; Abboud, Miguel R. (2008). "Liver biopsy results in patients with sickle cell disease on chronic transfusions: Poor correlation with ferritin levels." Pediatric Blood & Cancer 50(1): 62-65. <http://hdl.handle.net/2027.42/57399>en_US
dc.identifier.issn1545-5009en_US
dc.identifier.issn1545-5017en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/57399
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=17457853&dopt=citationen_US
dc.description.abstractBackground: Chronic transfusions are effective in preventing stroke and other complications of sickle cell disease. The aim of this study was to determine whether serum ferritin levels correlated with liver iron content in sickle cell patients on chronic transfusion. Procedure: Forty-four liver biopsy specimens from 38 patients with homozygous sickle cell anemia (HbSS) and one patient with sickle thalassemia receiving chronic transfusions were studied. Five patients underwent a second liver biopsy for follow up. Three ferritin measurements were used to calculate a mean for each patient. The association between serum ferritin levels and liver iron quantitation was measured using the Spearman rank correlation, and sensitivity and specificity were determined for selected threshold values of serum ferritin. Results: Serum ferritin levels ranged from 515 to 6076 ng/ml, liver iron concentration ranged from 1.8 to 67.97 mg/g dry weight. The amount of iron per gram liver dry weight was moderately correlated with serum ferritin values ( r  = 0.46). The correlation of duration of transfusion with serum ferritin ( r  = 0.40) and with liver iron content ( r  = 0.41) also indicated moderate correlation. Liver biopsy results led to changes in the management after 29/44 (66%) of the biopsies. Serum ferritin ≥2500 ng/ml predicted high liver iron content (≥7 mg/g), with a sensitivity of 62.5% and a specificity of 77.8%. Conclusion: We found a poor correlation between serum ferritin levels and liver iron content (LIC). Despite being on chelation therapy, many patients on chronic transfusion had high levels of liver iron. Measurement of LIC is highly recommended in these patients. Pediatr Blood Cancer 2008;50:62–65. © 2007 Wiley-Liss, Inc.en_US
dc.format.extent140572 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleLiver biopsy results in patients with sickle cell disease on chronic transfusions: Poor correlation with ferritin levelsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatric Gastroenterology, University of Michigan-Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Medical University of South Carolina, Charleston, South Carolinaen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Medical University of South Carolina, Charleston, South Carolinaen_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolinaen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Medical College of Georgia, Augusta, Georgiaen_US
dc.contributor.affiliationotherChildren's Hospital of Buffalo, Digestive Diseases and Nutrition Center, Buffalo, New Yorken_US
dc.contributor.affiliationotherChildren's Hospital of Buffalo, Digestive Diseases and Nutrition Center, Buffalo, New Yorken_US
dc.contributor.affiliationotherDepartment of Pediatrics, Virginia Commonwealth University, Richmond, Virginiaen_US
dc.contributor.affiliationotherDepartment of Biostatistics, Bioinformatics, and Epidemiology, Medical University of South Carolina, Charleston, South Carolinaen_US
dc.contributor.affiliationotherChildren's Cancer Center of Lebanon, American University of Beirut-Medical Center, Beirut, Lebanon ; Professor of Pediatrics, Children's Cancer Center of Lebanon, American University of Beirut-Medical Center, P.O. Box 11-0236, Beirut, Lebanon.en_US
dc.identifier.pmid17457853en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/57399/1/21215_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/pbc.21215en_US
dc.identifier.sourcePediatric Blood & Canceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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