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SERUM THROMBOPOIETIN LEVELS AND ITS RELATIONSHIP WITH THROMBOCYTOPENIA IN PATIENTS WITH CIRRHOSIS

机译:肝硬化患者的血清血小板生成素水平及其与血小板减少症的关系

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Background: 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/mm3) than in healthy subjects (240000±51000/mm3, P2). Significant difference was determined for spleen size and spleen index among child A, B and C stages (Child A vs. Child B P3 (n=16, plt-count: 41000±8300/mm3, TPO levels: 73±7 pg/mL) and above 50.000/mm3 (n=76, plt-count: 105000±9500/mm3, TPO levels: 65±10 pg/mL) (PConclusions: 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.
机译:背景:肝硬化患者通常具有离散水平的血小板减少症。血小板减少症的机制被认为是脾脏螯合和破坏血小板,骨髓生成受损和肝血小板生成素合成减少的目的。 :通过简单的随机抽样,对在Eskisehir-Turkey进行的本病例对照研究的患者和对照组,纳入了92名肝硬化患者和45名健康对照者,这些患者没有病史或可能影响血小板生成素水平的病理发现。用固相酶联免疫吸附测定法测定血清样品中的血小板生成素。结果:肝硬化患者的血小板计数(97000±8000 / mm 3 )低于健康人(240000±51000 / mm 3 < / SUP>,P2 )。确定儿童A,B和C阶段的脾脏大小和脾脏指数有显着差异(儿童A与儿童B P3 (n = 16,出诊数:41000±8300 / mm 3 ,TPO含量:73±7 pg / mL)和50.000 / mm 3 (n = 76,计数:105000±9500 / mm 3 ,TPO以上浓度:65±10 pg / mL)(PConclusions:我们的结果表明,即使在疾病晚期,肝硬化也不会导致血小板生成素产生受损。血小板生成素对肝硬化中血小板减少症的发生没有任何贡献;脾脏隔离似乎是主要因素。

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