Circulating microparticles and the risk of thromboembolic events in Egyptian beta thalassemia patients

dc.contributor.authorYoussry, Ilham
dc.contributor.authorSoliman, Nohair
dc.contributor.authorEl-Ghamrawy, Mona Kamal
dc.contributor.authorSamy, Rania Mohamed
dc.contributor.authorNasr, Amal Soliman
dc.contributor.authorAbdel Mohsen, Mohamed
dc.contributor.authorElShahaat, Mohamed
dc.contributor.authorBou-Fakhredin, Rayan
dc.contributor.authorTaher, Ali T.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:51:27Z
dc.date.available2025-01-24T11:51:27Z
dc.date.issued2017
dc.description.abstractThe presence of elevated numbers of circulating microparticles (MPs) has been hypothesized to be responsible for the occurrence of thromboembolic events (TEEs) in thalassemic patients. Our aim is to evaluate the presence and the thrombotic risk of circulating MPs in thalassemia patients and to determine the difference in MPs between β-thalassemia major (β-TM) and thalassemia intermedia (TI). The percentage of the annexin-labeled MPs, platelet-derived MPs (PMPs), erythrocyte-derived MPs (RMPs), and endothelial-derived MPs (EMPs) was measured by flow cytometry, in 87 thalassemia patients (39 β-TM and 48 TI). By multiple regression analysis, we then assessed the various independent risk factors for the occurrence of TEE. The thalassemic patients who experienced TEE had a significantly higher platelet count, higher percentage of annexin-labeled MPs, and higher percentage of PMPs (p value = 0.014, 0.003, and 0.014, respectively). There was no significant difference between β-TM and TI patients at the level of any of the studied MPs. The predictive risk factors for TEE in thalassemic patients were splenectomy, total and direct bilirubin, the RMPs, and the EMPs (OR = 10.07 (CI = 3.7–27.1), 4.3 (CI = 2.1–8.7), 1.4 (CI = 1.5–6.2), 1.6 (CI = 1.1–2.2), 3.0 (CI = 1.9–4.9), respectively). In conclusion, the elevated numbers of circulating MPs is a risk factor for the TEE in thalassemia patients. © 2017, Springer-Verlag Berlin Heidelberg.
dc.identifier.doihttps://doi.org/10.1007/s00277-017-2925-x
dc.identifier.eid2-s2.0-85011681253
dc.identifier.pmid28168351
dc.identifier.urihttp://hdl.handle.net/10938/31005
dc.language.isoen
dc.publisherSpringer Verlag
dc.relation.ispartofAnnals of Hematology
dc.sourceScopus
dc.subjectHypercoagulable state
dc.subjectMicroparticles
dc.subjectThalassemia intermedia
dc.subjectThalassemia major
dc.subjectAdolescent
dc.subjectAdult
dc.subjectBeta-thalassemia
dc.subjectCell-derived microparticles
dc.subjectChild
dc.subjectChild, preschool
dc.subjectCross-sectional studies
dc.subjectEgypt
dc.subjectFemale
dc.subjectHumans
dc.subjectInfant
dc.subjectMale
dc.subjectRandom allocation
dc.subjectRisk factors
dc.subjectThromboembolism
dc.subjectYoung adult
dc.subjectAnnexin
dc.subjectBilirubin glucuronide
dc.subjectArticle
dc.subjectAvascular necrosis
dc.subjectBasal ganglion
dc.subjectBeta thalassemia
dc.subjectBilirubin blood level
dc.subjectBrain infarction
dc.subjectControlled study
dc.subjectCross-sectional study
dc.subjectDeep vein thrombosis
dc.subjectEgyptian
dc.subjectEndothelium
dc.subjectErythrocyte
dc.subjectFlow cytometry
dc.subjectHuman
dc.subjectMajor clinical study
dc.subjectMembrane microparticle
dc.subjectPlatelet microparticle
dc.subjectPortal vein thrombosis
dc.subjectPriority journal
dc.subjectRisk factor
dc.subjectSchool child
dc.subjectSplenectomy
dc.subjectSuperficial thrombophlebitis
dc.subjectThrombocyte count
dc.subjectBlood
dc.subjectMetabolism
dc.subjectPreschool child
dc.subjectRandomization
dc.titleCirculating microparticles and the risk of thromboembolic events in Egyptian beta thalassemia patients
dc.typeArticle

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