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胎儿血红蛋白的药理学调控:使用羟基脲和重组人促红细胞生成素的试验

The pharmacological manipulation of fetal haemoglobin: trials using hydroxyurea and recombinant human erythropoietin.

作者信息

el-Hazmi M A, al-Momen A, Warsy A S, Kandaswamy S, Huraib S, Harakati M, al-Mohareb F

机构信息

College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Acta Haematol. 1995;93(2-4):57-61. doi: 10.1159/000204112.

Abstract

Hydroxyurea (HU) and recombinant human erythropoietin (rHuEpo) have been used in several studies to elevate Hb F level in sickle cell disease (SCD) patients and hence to ameliorate the clinical presentations of the disease. The treatment protocol and doses have varied in the different studies. We studied the effects of HU+rHuEpo combination therapy in sickle cell anaemia (SCA patients) to investigate the Hb F manipulation and hence treatment of SCA. Six patients with severe SCA were selected for treatment with HU (20-25 mg/kg body weight) and rHuEpo (400-800 U/kg body weight) combination therapy for 4 weeks followed by HU (20-25 mg/kg body weight) maintenance therapy for 6 months to 1 year. Iron and folic acid were administered during HU+rHuEpo treatment. Signs, symptoms and complications were recorded to obtain the severity index. Only patients with a severity index > or = 6 were included in the study. Haematological and biochemical parameter values, Hb A2, Hb F, Hb F distribution, Hb F cells, bilirubin level and reticulocyte count were assessed at least on 2-3 occasions prior to initiation of the therapy protocol to establish baseline values. During the treatment period, the clinical presentations were monitored and the estimation of the laboratory parameters was carried out every 4-8 weeks. The results of these parameters during HU and rHuEpo combination therapy and HU maintenance therapy were compared with baseline values using paired t test. The elevation in the level of Hb F, Hb F cells, total haemoglobin, red cell count and MCV were significant (p < 0.005), while reticulocyte count and total bilirubin were significantly decreased (p < 0.05). Each patient showed an individual pattern of Hb F elevation. The increase in Hb F level was correlated with the haematological and biochemical parameters using the General Linear Model Programme of Statistical Analysis System. In general, the clinical presentation improved as Hb F level increased in each patient. In addition, the positive correlation with the haematological parameters and negative correlation with reticulocytes and total bilirubin confirmed the beneficial effect of elevated Hb F level on reducing red cell haemolysis. No correlation could be demonstrated between the pretreatment Hb F level and the increase in Hb F during the treatment period. Daily doses of HU with a single intravenous rHuEpo and iron supplementation elevate Hb F and Hb F cells in SCA patients. The Hb F level can be maintained high on HU therapy alone.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在多项研究中,已使用羟基脲(HU)和重组人促红细胞生成素(rHuEpo)来提高镰状细胞病(SCD)患者的Hb F水平,从而改善该病的临床表现。不同研究中的治疗方案和剂量各不相同。我们研究了HU+rHuEpo联合疗法对镰状细胞贫血(SCA患者)的影响,以探究对Hb F的调控作用,进而治疗SCA。选取6例重度SCA患者,采用HU(20 - 25mg/kg体重)和rHuEpo(400 - 800U/kg体重)联合疗法治疗4周,随后采用HU(20 - 25mg/kg体重)维持治疗6个月至1年。在HU+rHuEpo治疗期间给予铁剂和叶酸。记录体征、症状和并发症以获得严重程度指数。仅将严重程度指数≥6的患者纳入研究。在开始治疗方案前至少2 - 3次评估血液学和生化参数值、Hb A2、Hb F、Hb F分布、Hb F细胞、胆红素水平和网织红细胞计数,以确定基线值。治疗期间,监测临床表现,并每4 - 8周进行一次实验室参数评估。使用配对t检验将HU和rHuEpo联合治疗及HU维持治疗期间这些参数的结果与基线值进行比较。Hb F水平、Hb F细胞、总血红蛋白、红细胞计数和平均红细胞体积升高显著(p < 0.005),而网织红细胞计数和总胆红素显著降低(p < 0.05)。每位患者的Hb F升高呈现个体模式。使用统计分析系统的通用线性模型程序将Hb F水平的升高与血液学和生化参数相关联。总体而言,随着每位患者Hb F水平升高,临床表现有所改善。此外,与血液学参数的正相关以及与网织红细胞和总胆红素的负相关证实了升高的Hb F水平对减少红细胞溶血的有益作用。治疗前Hb F水平与治疗期间Hb F升高之间未显示出相关性。每日给予HU、单次静脉注射rHuEpo和补充铁剂可提高SCA患者的Hb F和Hb F细胞水平。仅使用HU治疗就能维持较高的Hb F水平。(摘要截取自400字)

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