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Evaluation of the 5mg-g liver iron concentration threshold and its association with morbidity in patients with β-thalassemia intermedia

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dc.contributor.author Musallam K.M.
dc.contributor.author Cappellini M.D.
dc.contributor.author Taher A.T.
dc.contributor.editor
dc.date Jun-2013
dc.date.accessioned 2017-10-05T15:38:18Z
dc.date.available 2017-10-05T15:38:18Z
dc.date.issued 2013
dc.identifier 10.1016/j.bcmd.2013.01.015
dc.identifier.isbn
dc.identifier.issn 10799796
dc.identifier.uri http://hdl.handle.net/10938/16265
dc.description.abstract Iron overload may still occur in transfusion-independent patients with β-thalassemia intermedia due to increased intestinal iron absorption. In this study, we evaluated the association between iron overload, using a liver iron concentration threshold of therapeutic significance (≥. 5. mg-g), and morbidity in 168 chelation naive patients with β-thalassemia intermedia. We demonstrated that patients with a liver iron concentration ≥. 5. mg-g have a significantly higher prevalence of several serious vascular and endocrine-bone morbidities than do patients with . 5. mg-g, and we established absolute morbidity risk values differentiating both groups. We also demonstrated that the association between iron overload and morbidity in such patients is independent of the effects of advancing age and disease severity. These findings suggest that treating iron burden in β-thalassemia intermedia may be associated with reduction in serious morbidity risk. © 2013 Elsevier Inc.
dc.format.extent
dc.format.extent Pages: (35-38)
dc.language English
dc.publisher SAN DIEGO
dc.relation.ispartof Publication Name: Blood Cells, Molecules, and Diseases; Publication Year: 2013; Volume: 51; no. 1; Pages: (35-38);
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Evaluation of the 5mg-g liver iron concentration threshold and its association with morbidity in patients with β-thalassemia intermedia
dc.type Article
dc.contributor.affiliation Musallam, K.M., Department of Medicine and Medical Specialties, IRCCS Ca' Granda Foundation Maggiore Policlinico Hospital, University of Milan, Milan, Italy, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Cappellini, M.D., Department of Medicine and Medical Specialties, IRCCS Ca' Granda Foundation Maggiore Policlinico Hospital, University of Milan, Milan, Italy
dc.contributor.affiliation Taher, A.T., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon, Chronic Care Center, Hazmieh, Lebanon
dc.contributor.authorAddress Taher, A.T.; Department of Internal Medicine, American University of Beirut Medical Center, P.O. Box: 11-0236, Riad El-Solh 1107 2020, Beirut, Lebanon; email: ataher@aub.edu.lb
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Internal Medicine;
dc.contributor.authorDepartment Internal Medicine
dc.contributor.authorDivision
dc.contributor.authorEmail ataher@aub.edu.lb
dc.contributor.faculty Faculty of Medicine
dc.contributor.authorInitials Musallam, KM
dc.contributor.authorInitials Cappellini, MD
dc.contributor.authorInitials Taher, AT
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress Taher, AT (reprint author), Amer Univ Beirut, Med Ctr, Dept Internal Med, POB 11-0236,Riad El Solh 1107, Beirut 2020, Lebanon.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited Belhoul KM, 2012, ANN HEMATOL, V91, P1107, DOI 10.1007-s00277-012-1412-7; Haidar R, 2011, BONE, V48, P425, DOI 10.1016-j.bone.2010.10.173; Kell DB, 2009, BMC MED GENOMICS, V2, DOI 10.1186-1755-8794-2-2; Musallam KM, 2011, HEMOGLOBIN, V35, P503, DOI 10.3109-03630269.2011.605499; Musallam KM, 2012, BLOOD CELL MOL DIS, V49, P136, DOI 10.1016-j.bcmd.2012.06.001; Musallam KM, 2011, HAEMATOL-HEMATOL J, V96, P1605, DOI 10.3324-haematol.2011.047852; Musallam KM, 2012, BLOOD REV, V26, pS16, DOI 10.1016-S0268-960X(12)70006-1; Musallam KM, 2012, THROMB RES, V130, P695, DOI 10.1016-j.thromres.2012.07.013; Pootrakul P, 2003, BRIT J HAEMATOL, V122, P305, DOI 10.1046-j.1365-2141.2003.04412.x; Rivella S, 2012, BLOOD REV, V26, pS12, DOI 10.1016-S0268-960X(12)70005-X; St Pierre TG, 2005, BLOOD, V105, P855, DOI 10.1182-blood-2004-01-0177; Taher A, 2008, HAEMATOL-HEMATOL J, V93, P1584, DOI 10.3324-haematol.13098; Taher AT, 2012, BLOOD, V120, P970, DOI 10.1182-blood-2012-02-412692; Taher AT, 2010, BLOOD, V115, P1886, DOI 10.1182-blood-2009-09-243154; Wood JC, 2005, BLOOD, V106, P1460, DOI 10.1182-blood-2004-10-3982
dc.description.citedCount 5
dc.description.citedTotWOSCount 10
dc.description.citedWOSCount 10
dc.format.extentCount 4
dc.identifier.articleNo
dc.identifier.coden BCMDF
dc.identifier.pubmedID 23425967
dc.identifier.scopusID 84877128415
dc.identifier.url
dc.publisher.address 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA
dc.relation.ispartofConference
dc.relation.ispartofConferenceCode
dc.relation.ispartofConferenceDate
dc.relation.ispartofConferenceHosting
dc.relation.ispartofConferenceLoc
dc.relation.ispartofConferenceSponsor
dc.relation.ispartofConferenceTitle
dc.relation.ispartofFundingAgency
dc.relation.ispartOfISOAbbr Blood Cells Mol. Dis.
dc.relation.ispartOfIssue 1
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Blood Cells, Molecules, and Diseases
dc.relation.ispartofPubTitleAbbr Blood Cells Mol. Dis.
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 51
dc.source.ID WOS:000330206500008
dc.type.publication Journal
dc.subject.otherAuthKeyword Iron overload
dc.subject.otherAuthKeyword Liver iron concentration
dc.subject.otherAuthKeyword Morbidity
dc.subject.otherAuthKeyword Thalassemia intermedia
dc.subject.otherChemCAS Iron, E1UOL152H7
dc.subject.otherIndex age
dc.subject.otherIndex aged
dc.subject.otherIndex article
dc.subject.otherIndex beta thalassemia
dc.subject.otherIndex bone disease
dc.subject.otherIndex child
dc.subject.otherIndex cross-sectional study
dc.subject.otherIndex disease severity
dc.subject.otherIndex endocrine disease
dc.subject.otherIndex human
dc.subject.otherIndex hypogonadism
dc.subject.otherIndex hypothyroidism
dc.subject.otherIndex iron chelation
dc.subject.otherIndex iron liver level
dc.subject.otherIndex iron overload
dc.subject.otherIndex liver level
dc.subject.otherIndex morbidity
dc.subject.otherIndex osteoporosis
dc.subject.otherIndex prevalence
dc.subject.otherIndex priority journal
dc.subject.otherIndex pulmonary hypertension
dc.subject.otherIndex risk reduction
dc.subject.otherIndex school child
dc.subject.otherIndex thrombosis
dc.subject.otherIndex vascular disease
dc.subject.otherIndex Adolescent
dc.subject.otherIndex Adult
dc.subject.otherIndex Aged
dc.subject.otherIndex beta-Thalassemia
dc.subject.otherIndex Child
dc.subject.otherIndex Cross-Sectional Studies
dc.subject.otherIndex Female
dc.subject.otherIndex Humans
dc.subject.otherIndex Iron
dc.subject.otherIndex Iron Overload
dc.subject.otherIndex Liver
dc.subject.otherIndex Male
dc.subject.otherIndex Middle Aged
dc.subject.otherIndex Morbidity
dc.subject.otherIndex Young Adult
dc.subject.otherKeywordPlus TRANSFUSION-DEPENDENT THALASSEMIA
dc.subject.otherKeywordPlus SERUM FERRITIN LEVELS
dc.subject.otherKeywordPlus MAGNETIC-RESONANCE
dc.subject.otherKeywordPlus CHELATION
dc.subject.otherKeywordPlus OVERLOAD
dc.subject.otherKeywordPlus R2
dc.subject.otherWOS Hematology


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