Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan; Division of Hematology and Oncology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Division of Hematology and Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Kaohsiung J Med Sci. 2017 Aug;33(8):405-410. doi: 10.1016/j.kjms.2017.05.011. Epub 2017 Jul 2.
Paroxysmal nocturnal hemoglobinuria (PNH) is an extremely rare acquired disorder. The aim of this study was to investigate the demographics, clinical manifestations, and outcomes of PNH patients in southern Taiwan. Data on PNH patients diagnosed over a 30-year period (1985-2015) were retrospectively collected from four tertiary medical centers in southern Taiwan. Blood samples were collected for hematologic panel testing and flow cytometry detection of PNH clones. Radiologic studies were performed to assess the frequency of complications. Twenty-four patients were enrolled in this study. The median duration of disease in the study participants was 10.8 years. The median granulocyte PNH clone size was 92.5% (range, 1.3%-99.8%), and the median lactate dehydrogenase (LDH) level was 2920.2 ± 1462.0 IU/L. The incidence of thromboembolism and impaired renal function was 16.7% and 29.2%, respectively. The primary treatment strategies included steroids (79.2%), androgens (42.0%), eculizumab (33.3%), immunosuppressants (16.7%), and anticoagulants (4.2%). In eight patients treated with eculizumab, there was a marked reduction in the LDH levels of 14.89-fold-1.63-fold that of the upper limit of normal; seven patients exhibited decreased transfusion requirements. Twenty-one patients were alive with regular follow-up at the time of publication. Our study demonstrates that PNH patients in southern Taiwan may exhibit different clinical characteristics and outcomes relative to patients in other countries. There was a trend toward a greater PNH granulocyte clone size, which may lead to more hemolysis. In our study, the percentage of patients with impaired renal function, but not the percentage of patients with thrombotic events, was higher than values reported worldwide and in the observational cross-sectional International PNH Registry. More large-scale studies with comprehensive data on the clinical response to different treatments are needed.
阵发性睡眠性血红蛋白尿症(PNH)是一种极为罕见的获得性疾病。本研究旨在探讨台湾南部 PNH 患者的人口统计学、临床表现和结局。从台湾南部的四家三级医疗中心回顾性收集了 30 年来(1985-2015 年)诊断的 PNH 患者的数据。采集血样进行血液学检测和 PNH 克隆的流式细胞术检测。进行放射学研究以评估并发症的频率。本研究共纳入 24 例患者。研究参与者的疾病中位持续时间为 10.8 年。粒细胞 PNH 克隆的中位大小为 92.5%(范围 1.3%-99.8%),中位乳酸脱氢酶(LDH)水平为 2920.2±1462.0 IU/L。血栓栓塞和肾功能不全的发生率分别为 16.7%和 29.2%。主要治疗策略包括类固醇(79.2%)、雄激素(42.0%)、依库珠单抗(33.3%)、免疫抑制剂(16.7%)和抗凝剂(4.2%)。在接受依库珠单抗治疗的 8 例患者中,LDH 水平显著降低,正常上限的 14.89 倍至 1.63 倍;7 例患者减少了输血需求。在发表时,有 21 例患者在定期随访中存活。本研究表明,台湾南部的 PNH 患者可能表现出与其他国家患者不同的临床特征和结局。PNH 粒细胞克隆大小较大的趋势可能导致更多的溶血。在本研究中,肾功能不全的患者比例较高,而血栓事件的患者比例与全球和观察性横断面国际 PNH 登记处报告的结果相比并无不同。需要进行更多的大型研究,以提供关于不同治疗方法的临床反应的综合数据。