Motta Irene, Delbini Paola, Scaramellini Natalia, Ghiandai Viola, Duca Lorena, Nava Isabella, Nascimbeni Fabio, Lugari Simonetta, Consonni Dario, Trombetta Elena, Di Stefano Valeria, Migone De Amicis Margherita, Cassinerio Elena, Carubbi Francesca, Cappellini Maria Domenica
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, SC Medicina ad Indirizzo Metabolico, Via Francesco Sforza 35, Milan, 20122, Italy.
Ann Hematol. 2024 Dec;103(12):5113-5121. doi: 10.1007/s00277-024-05918-2. Epub 2024 Oct 7.
Anemia and hyperferritinemia are frequent findings at diagnosis of Gaucher disease (GD). Macrophage-independent dyserythropoiesis and abnormal iron metabolism have been shown. We evaluated hematological and iron status at diagnosis (T0) and the effect of enzyme replacement therapy (ERT) on erythropoiesis and iron utilization over 5-year follow-up in type 1 GD patients and in an ex vivo model of erythropoiesis from CD34 + peripheral blood cells. At T0, 41% of patients had anemia and 51% hyperferritinemia. Hemoglobin increased from 12.6 (T0) to 13.9 g/dL (T6), GFD15, a marker of ineffective erythropoiesis, decreased from 5401 to 710 pg/ml, and serum ferritin decreased from 614 to 140 mcg/L (p < 0.001). In parallel, transferrin saturation (TSAT) increased. Hepcidin, although in the normal range, decreased from T0 to T6. Ex vivo studies showed that ERT restores the erythroid cells derived from CD34 + impaired ability to differentiate. During ERT, an increase in TFRC expression, consistent with the ability of erythroid precursors to uptake iron, and a reduction in HAMP and concomitant increase in SLC40A1 were observed. This is the largest study with a longitudinal follow-up evaluating erythropoiesis and iron metabolism, combining clinical and ex vivo data in GD. Iron dysregulation likely contributes to anemia, and ERT, by improving iron distribution, improves erythropoiesis.
贫血和高铁蛋白血症是戈谢病(GD)诊断时的常见表现。已证实存在非巨噬细胞依赖性红细胞生成异常和铁代谢异常。我们评估了1型GD患者诊断时(T0)的血液学和铁状态,以及在5年随访期间酶替代疗法(ERT)对红细胞生成和铁利用的影响,并在来自CD34 +外周血细胞的红细胞生成体外模型中进行了评估。在T0时,41%的患者有贫血,51%有高铁蛋白血症。血红蛋白从12.6(T0)增加到13.9 g/dL(T6),无效红细胞生成标志物GFD15从5401降至710 pg/ml,血清铁蛋白从614降至140 mcg/L(p < 0.001)。同时,转铁蛋白饱和度(TSAT)增加。铁调素虽然在正常范围内,但从T0到T6有所下降。体外研究表明,ERT可恢复源自CD34 +的受损红细胞分化能力。在ERT期间,观察到TFRC表达增加,这与红系前体细胞摄取铁的能力一致,同时HAMP减少,SLC40A1增加。这是一项结合GD临床和体外数据进行红细胞生成和铁代谢纵向随访评估的最大规模研究。铁调节异常可能导致贫血,而ERT通过改善铁分布来改善红细胞生成。