Chirico Valeria, Rigoli Luciana, Lacquaniti Antonio, Salpietro Vincenzo, Piraino Basilia, Amorini Maria, Salpietro Carmelo, Arrigo Teresa
Department of Pediatric Sciences, University of Messina, Messina, Italy.
Eur J Haematol. 2015 May;94(5):404-12. doi: 10.1111/ejh.12444. Epub 2014 Oct 18.
Endocrinopathies and metabolic disorders-characterized β thalassemic (βT) patients and the prevention and treatment of these comorbidities are important targets to be achieved. The aim of the study was to analyze the diagnostic and prognostic role of ferritin for endocrinopathies and metabolic disorders in βT patients. The ability of iron chelators to treat iron overload and to prevent or reverse metabolic disorders and endocrinopathies was also evaluated.
Seventy-two βT patients were treated with different chelation strategies during the study. Receiver operating characteristics analysis was employed to calculate the area under the curve for serum ferritin to find the best cutoff values capable of identifying endocrine dysfunction in thalassemic patients. Kaplan-Meier curves were generated to assess the incidence of endocrinopathy. Adjusted risk estimates for endocrinopathy were calculated using univariate followed by multivariate Cox proportional hazard regression analysis.
High ferritin levels were observed in patients with hypothyroidism [1500 (872.5-2336.5) μg/L], hypogonadism [878 (334-2010) μg/L], and in patients with hypoparathyroidism or osteoporosis [834 (367-1857) μg/L]. A strict correlation between ferritin and T2* magnetic resonance imaging of heart (r = -0.64; P:0.0006) and liver (r = -0.40; P:0.03) values was observed. Patients with ferritin values above 1800 μg/L experienced a significantly faster evolution to hypothyroidism [log-rank (χ(2) ):7.7; P = 0.005], hypogonadism [log-rank (χ(2) ):10.7; P = 0.001], and multiple endocrinopathies [log-rank (χ(2) ):5.72; P = 0.02]. Ferritin predicted high risk of endocrine dysfunction independently of confounding factors (HR:1.23; P < 0.0001). The intensification of chelation therapy led to an amelioration of hypothyroidism.
Ferritin represents a prognostic marker for βT patients and a predictive factor for progression to endocrine dysfunctions. Intensive chelation therapy allows the reversibility of hypothyroidism.
内分泌疾病和代谢紊乱是β地中海贫血(βT)患者的特征,对这些合并症的预防和治疗是需要实现的重要目标。本研究的目的是分析铁蛋白对βT患者内分泌疾病和代谢紊乱的诊断及预后作用。同时评估了铁螯合剂治疗铁过载以及预防或逆转代谢紊乱和内分泌疾病的能力。
在研究期间,72例βT患者采用了不同的螯合策略进行治疗。采用受试者工作特征分析来计算血清铁蛋白的曲线下面积,以找出能够识别地中海贫血患者内分泌功能障碍的最佳临界值。绘制Kaplan-Meier曲线以评估内分泌疾病的发生率。使用单因素分析,随后进行多因素Cox比例风险回归分析来计算内分泌疾病的校正风险估计值。
甲状腺功能减退患者[1500(872.5 - 2336.5)μg/L]、性腺功能减退患者[878(334 - 2010)μg/L]以及甲状旁腺功能减退或骨质疏松患者[834(367 - 1857)μg/L]中观察到高铁蛋白水平。观察到铁蛋白与心脏的T2磁共振成像(r = -0.64;P:0.0006)和肝脏的T2磁共振成像(r = -0.40;P:0.03)值之间存在严格相关性。铁蛋白值高于1800μg/L的患者发展为甲状腺功能减退[对数秩(χ(2)):7.7;P = 0.005]、性腺功能减退[对数秩(χ(2)):10.7;P = 0.001]和多种内分泌疾病[对数秩(χ(2)):5.72;P = 0.02]的速度明显更快。铁蛋白可独立于混杂因素预测内分泌功能障碍的高风险(HR:1.23;P < 0.0001)。螯合治疗的强化导致甲状腺功能减退有所改善。
铁蛋白是βT患者的预后标志物,也是进展为内分泌功能障碍的预测因素。强化螯合治疗可使甲状腺功能减退可逆。