用重组人促红细胞生成素治疗β地中海贫血患者:对输血需求和可溶性黏附分子的影响。
Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules.
作者信息
Chaidos Aristeidis, Makis Alexandros, Hatzimichael Eleftheria, Tsiara Stavroula, Gouva Maria, Tzouvara Evangelia, Bourantas Konstantinos L
机构信息
Department of Hematology, University of Ioannina Medical School, Ioannina, Greece.
出版信息
Acta Haematol. 2004;111(4):189-95. doi: 10.1159/000077551.
The most common single genetic disorder and a major public health issue in Greece and other Mediterranean countries is beta-thalassemia. Current therapeutic approaches for homozygous beta-thalassemia entail blood transfusions and iron chelation therapy with deferoxamine or deferiprone for preventing tissue hemosiderosis. Recently, much effort has focused on various inducers of fetal hemoglobin (HbF) such as recombinant human erythropoietin (rHuEPO), especially in beta-thalassemia intermedia. Ten adult patients, 5 with beta-thalassemia major and 5 with beta-thalassemia intermedia, received 150 IU/kg rHuEPO (epoetin-alpha) subcutaneously three times a week. Seven patients were transfused every 14-30 days and 3 with beta-thalassemia intermedia were only occasionally transfused. The minimum duration of treatment was 12 weeks in order to define if there was any response. Transfusion intervals were modified according to the rHuEPO response to maintain stable Hb values. Lower transfusion requirements were observed in 5 patients after rHuEPO treatment (p = 0.028). In the 3 non-transfused patients, Hb values increased, and the patients are still being treated and followed up for a period ranging from 14 weeks to 2 years. Two patients with thalassemia major discontinued treatment after 12 weeks, as they did not achieve any response regarding transfusion requirements or Hb values. Pretreatment serum transferrin receptor levels were higher than in controls (p < 0.001) and significantly increased following rHuEPO treatment (p = 0.027). Patients had higher serum endothelin-3, sICAM-1 and sE-selectin values before rHuEPO treatment compared to controls (p < 0.001, p < 0.001 and p = 0.016, respectively), but these values were not altered during treatment. HbF values presented a slight, non-significant increase. rHuEPO treatment has a beneficial effect in transfusion-dependent beta-thalassemia patients. Although a slight increase in HbF levels was observed, other possible mechanisms are probably involved. None of our patients experienced thrombotic complications and a rise in blood pressure.
β地中海贫血是希腊和其他地中海国家最常见的单基因疾病及主要的公共卫生问题。目前,纯合子β地中海贫血的治疗方法包括输血以及使用去铁胺或去铁酮进行铁螯合治疗,以预防组织含铁血黄素沉着症。最近,人们将大量精力集中在各种胎儿血红蛋白(HbF)诱导剂上,如重组人促红细胞生成素(rHuEPO),尤其是在中间型β地中海贫血中。10名成年患者,5名重型β地中海贫血患者和5名中间型β地中海贫血患者,每周皮下注射3次150 IU/kg的rHuEPO(阿法依泊汀)。7名患者每14 - 30天输血一次,3名中间型β地中海贫血患者仅偶尔输血。治疗的最短持续时间为12周,以确定是否有任何反应。根据rHuEPO反应调整输血间隔,以维持稳定的血红蛋白值。rHuEPO治疗后,5名患者的输血需求降低(p = 0.028)。在3名未输血的患者中,血红蛋白值升高,这些患者仍在接受治疗并随访14周至2年不等。2名重型地中海贫血患者在12周后停止治疗,因为他们在输血需求或血红蛋白值方面未取得任何反应。治疗前血清转铁蛋白受体水平高于对照组(p < 0.001),rHuEPO治疗后显著升高(p = 0.027)。与对照组相比,患者在rHuEPO治疗前血清内皮素-3、可溶性细胞间黏附分子-1和可溶性E选择素值更高(分别为p < 0.001、p < 0.001和p = 0.016),但这些值在治疗期间未改变。HbF值有轻微的、无统计学意义的升高。rHuEPO治疗对依赖输血的β地中海贫血患者有有益作用。尽管观察到HbF水平有轻微升高,但可能涉及其他潜在机制。我们的患者均未出现血栓并发症和血压升高。