Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorTemel, Tuncer
dc.contributor.authorCansu, Dondu Üsküdar
dc.contributor.authorTemel, Halide Edip
dc.contributor.authorÖzakyol, Ayşegül Harmancı
dc.date.accessioned2019-10-19T14:03:07Z
dc.date.available2019-10-19T14:03:07Z
dc.date.issued2014
dc.identifier.issn1735-143X
dc.identifier.issn1735-3408
dc.identifier.urihttps://dx.doi.org/10.5812/hepatmon.18556
dc.identifier.urihttps://hdl.handle.net/11421/12504
dc.descriptionWOS: 000344637300011en_US
dc.descriptionPubMed ID: 24976834en_US
dc.description.abstractBackground: Patients with cirrhosis usually have thrombocytopenia in discrete levels. The mechanism of thrombocytopenia is thought as splenic sequestration and destruction of platelets, impaired bone marrow generation and diminished hepatic thrombopoietin synthesis. Objectives: The aim of this study was to evaluate serum thrombopoietin levels and its relationship with thrombocytopenia at patients with cirrhosis. Patients and Methods: Ninety-two cirrhotic patients and 45 healthy controls without history or findings of pathologies that can effect thrombopoietin levels were enrolled by simple random sampling to patient and control groups of this case control study performed at Eskisehir-Turkey. Thrombopoietin was measured in serum samples with a solid phase enzyme-linked immune absorbent assay. Additionally, spleen size and volume index were determined. Results: Platelet counts were lower in patients with cirrhosis (97000 +/- 8000/mm(3)) than in healthy subjects (240000 +/- 51000/mm(3), P < 0.001). Significant difference was determined for platelet counts among child A, B and C stages (Child A vs. Child B P < 0.05 Child A vs. Child C P < 0.001-Child B vs. Child C P < 0.05). Serum TPO concentration was higher (69 +/- 12 pg/mL) in cirrhotic group than healthy controls (49 +/- 9 pg/ml) (P < 0.05). No significant difference in TPO levels were found among the Child A, B and C stages (64 +/- 11 pg/mL, 75 +/- 13 pg/mL and 68 +/- 10 pg/mL, respectively). Spleen size and SVI was significantly higher in the cirrhotic patients than healthy controls (148 +/- 14 mm vs. 98 +/- 11 mm, P < 0.001-9167 +/- 287 cm(2) vs. 4118 +/- 123 cm(2)). Significant difference was determined for spleen size and spleen index among child A, B and C stages (Child A vs. Child B P < 0.05 Child A vs. Child C P < 0.001-Child B vs. Child C P < 0.05). TPO levels were significantly different between cirrhotic patients with platelet levels below 50.000/mm(3) (n = 16, plt-count: 41000 +/- 8300/mm(3), TPO levels: 73 +/- 7 pg/mL) and above 50.000/mm(3) (n = 76, plt-count: 105000 +/- 9500/mm(3), TPO levels: 65 +/- 10 pg/mL) (P < 0.01). In correlation analysis, there was a strong negative correlation between platelet count-spleen size (P < 0.001, r = -0.74) and platelet count-serum TPO levels (P < 0.001, r = -0.71). Conclusions: Our results suggest that liver cirrhosis does not cause impaired thrombopoietin production even in the late stage of disease. Thrombopoietin has no contribution for the occurrence of thrombocytopenia in cirrhosis; splenic sequestration seems to be the main factor.en_US
dc.description.sponsorshipEskisehir Ic Hastaliklari Dernegi (Foundation of Eskisehir Internal Medicine)en_US
dc.description.sponsorshipFinancial support of the study was carried out by Eskisehir Ic Hastaliklari Dernegi (Foundation of Eskisehir Internal Medicine).en_US
dc.language.isoengen_US
dc.publisherKowsar Publen_US
dc.relation.isversionof10.5812/hepatmon.18556en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectLiver Cirrhosisen_US
dc.subjectThrombocytopeniaen_US
dc.subjectThrombopoietinen_US
dc.titleSerum Thrombopoietin Levels and Its Relationship With Thrombocytopenia in Patients With Cirrhosisen_US
dc.typearticleen_US
dc.relation.journalHepatitis Monthlyen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Biyokimya Anabilim Dalıen_US
dc.identifier.volume14en_US
dc.identifier.issue5en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorTemel, Halide Edip


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster