Clin Endocrinol (Oxf). 1995 Jun;42(6):581-6. doi: 10.1111/j.1365-2265.1995.tb02683.x.
Thalassaemia major is a common and serious medical problem, worldwide. However, there are few data concerning the various endocrine disorders which occur in this condition. We have surveyed 25 Italian centres in order to establish the prevalences and times of onset of endocrine disorders in patients with beta-thalassaemia major. PROJECT AND PATIENTS: A questionnaire specifically designed to investigate the prevalences of endocrinopathies was sent to 25 paediatric and haematology departments. The following data were recorded in the questionnaire: sex, age, height and weight, pubertal status according to Tanner's classification, history of secondary amenorrhoea, type of endocrinopathy and hormone levels at diagnosis, associated complications, serum ferritin level, liver enzymes (ALT) and compliance with treatment.
An analysis of data from 1861 patients showed that failure of puberty was the major clinical endocrine problem and was present in 51% of boys and 47% of girls, all over the age of 15 years. Secondary amenorrhoea was recorded in 23% of patients (mean age 18.3 years), primary hypothyroidism in 6.2% (mean age 15.8 years), insulin dependent diabetes mellitus in 4.9% (mean age 18.1 years) and hypoparathyroidism in 3.6% of the patients (mean age 18.7 years). At present, the majority are in the second or third decades of life. The prevalences of hypothyroidism, insulin dependent diabetes mellitus and hypoparathyroidism differed in the various centres, whereas the frequency of pubertal disorders was very similar.
Our study has demonstrated several points. Endocrine evaluation in thalassaemic patients must be carried out regularly, especially in those patients over the age of 10 years with iron overload and poor compliance with chelation therapy. The prevalences of some complications, such as insulin dependent diabetes and hypothyroidism, were lower than previously recorded. Hence, it is to be hoped endocrine complications will be less common in the future, for patients who have started chelation therapy during the first years of life. Because of the improved survival of thalassaemic patients with insulin dependent diabetes, and the high incidence of multiple endocrine complications, it is important to carry out careful follow-up studies for the early detection of any other associated complications to facilitate correct treatment.
重型地中海贫血是全球范围内常见且严重的医学问题。然而,关于这种疾病中出现的各种内分泌紊乱的数据很少。我们调查了25个意大利中心,以确定重型β地中海贫血患者内分泌紊乱的患病率和发病时间。
向25个儿科和血液科发送了一份专门设计用于调查内分泌疾病患病率的问卷。问卷中记录了以下数据:性别、年龄、身高和体重、根据坦纳分类法的青春期状态、继发性闭经病史、内分泌疾病类型和诊断时的激素水平、相关并发症、血清铁蛋白水平、肝酶(ALT)以及治疗依从性。
对1861例患者的数据分析表明,青春期发育迟缓是主要的临床内分泌问题,在所有15岁以上的男孩和女孩中,分别有51%和47%存在该问题。23%的患者记录有继发性闭经(平均年龄18.3岁),6.2%有原发性甲状腺功能减退(平均年龄15.8岁),4.9%有胰岛素依赖型糖尿病(平均年龄18.1岁),3.6%的患者有甲状旁腺功能减退(平均年龄18.7岁)。目前,大多数患者处于二三十岁。甲状腺功能减退、胰岛素依赖型糖尿病和甲状旁腺功能减退的患病率在不同中心有所不同,而青春期疾病的发生率非常相似。
我们的研究表明了几点。地中海贫血患者必须定期进行内分泌评估,尤其是对于那些10岁以上、有铁过载且螯合治疗依从性差的患者。一些并发症,如胰岛素依赖型糖尿病和甲状腺功能减退的患病率低于先前记录。因此,对于在生命最初几年开始螯合治疗的患者,希望未来内分泌并发症会不那么常见。由于重型地中海贫血合并胰岛素依赖型糖尿病患者的生存率提高,且多内分泌并发症发生率高,因此进行仔细的随访研究以早期发现任何其他相关并发症以便进行正确治疗很重要。