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dc.contributor.authorNasifov, Muharrem
dc.contributor.authorGenc, Sema
dc.contributor.authorEkinci, Iskender
dc.contributor.authorToprak, Aybala Erek
dc.contributor.authorÇETİN, GÜVEN
dc.contributor.authorCikrikcioglu, Mehmet Ali
dc.contributor.authorCelik, Kenan
dc.date.accessioned2021-03-03T19:24:09Z
dc.date.available2021-03-03T19:24:09Z
dc.date.issued2017
dc.identifier.citationCikrikcioglu M. A. , Celik K., Ekinci I., Nasifov M., Toprak A. E. , ÇETİN G., Genc S., "Mean Platelet Volume in Heterrozygous Beta Thallassaermia", ACTA HAEMATOLOGICA, cilt.137, sa.2, ss.100-105, 2017
dc.identifier.issn0001-5792
dc.identifier.otherav_544be7ad-5ce0-4c80-bd76-a474097a0582
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/59702
dc.identifier.urihttps://doi.org/10.1159/000455813
dc.description.abstractBackground/Aim: It is not known why cerebrovascular and cardiovascular ischaemic events are less frequently observed in heterozygous beta thalassaemia (HBT) patients than in the general population. However, we previously reported that serum levels of some platelet function markers, i.e. soluble CD40 ligand and soluble P-selectin, are lower in patients with HBT than in controls. A high mean platelet volume (MPV) is an indicator of in vivo platelet activation and may indicate a tendency to thrombosis. We investigated whether MPV is lower in HBT patients than in controls. Methods: Forty-eight patients with HBT were compared with 51 controls matched for gender, age, and BMI for MPV in a cross-sectional study. Results: The MPV was within the normal range and higher in the HBT group (9.64 +/- 1.20 vs. 9.07 +/- 082 fL, p = 0.006). The 2 groups were similar in terms of atherosclerosis risk factors and medications. After linear regression analysis, the MPV was correlated with HBT, sensitive CRP, and BMI. Conclusion: The higher MPV in patients with HBT could indicate platelet activation, and this may repre-sent a dilemma. Higher MPV in the HBT group might have resulted from higher sympathetic nervous system activity, mild ineffective erythropoiesis, and haemolysis. (C) 2017 S. Karger AG, Basel
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectHEMATOLOJİ
dc.titleMean Platelet Volume in Heterrozygous Beta Thallassaermia
dc.typeMakale
dc.relation.journalACTA HAEMATOLOGICA
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , ,
dc.identifier.volume137
dc.identifier.issue2
dc.identifier.startpage100
dc.identifier.endpage105
dc.contributor.firstauthorID239118


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