Arcasoy A, Cavdar A, Cin S, Erten J, Babacan E, Gözdasoglu S, Akar N
Am J Hematol. 1987 Feb;24(2):127-36. doi: 10.1002/ajh.2830240203.
Linear growth was evaluated in 32 patients with beta-thalassemia major. At the beginning of the study of 40.6% of the patients were below the 10th percentile with biochemical evidence of zinc deficiency. Effects of zinc supplementation on growth velocity (height) were assessed in a controlled manner. Twenty-one children received oral zinc sulphate for a period of 1 to 7 years (15 early- and 6 late-supplemented cases), while the remaining 11 thalassemics were maintained only on conventional transfusion therapy. The mean height velocity of early-zinc supplemented children was significantly greater than that of normal children (P less than 0.01). An increase in height was also observed in the patients who received delayed zinc retardation. The present study demonstrated that zinc deficiency is one of the factors responsible for retarded linear growth in beta-thalassemia major. Only the patients who received zinc supplementation showed an acceleration of growth in height. Administration of zinc could, therefore, be considered as an effective adjuvant therapy in homozygous beta-thalassemia.
对32例重型β地中海贫血患者的线性生长情况进行了评估。在研究开始时,40.6%的患者低于第10百分位数,并有锌缺乏的生化证据。以对照方式评估了补锌对生长速度(身高)的影响。21名儿童接受口服硫酸锌1至7年(15例早期补锌和6例晚期补锌病例),而其余11名地中海贫血患者仅接受传统输血治疗。早期补锌儿童的平均身高增长速度显著高于正常儿童(P<0.01)。在接受延迟补锌的患者中也观察到身高增加。本研究表明,锌缺乏是导致重型β地中海贫血线性生长迟缓的因素之一。只有接受补锌的患者身高增长加速。因此,补锌可被视为纯合子β地中海贫血的一种有效辅助治疗方法。