Mula-Abed Waad-Allah, Al Hashmi Huda, Al Muslahi Muhanna, Al Muslahi Hilal, Al Lamki Mohammad
Oman Med J. 2008 Oct;23(4):257-62.
Beta-thalassaemia major is a common medical problem worldwide. There is little data dealing with the nature and prevalence of different endocrine disorders in this disease in the Sultanate of Oman.
To establish the prevalence and times of occurrence of endocrine disorders in patients with beta-thalassaemia major.
This cross-sectional study was conducted during Jan-Jul 2008 and dealt with 30 Omani patients with transfusion-dependent homozygous beta-thalassaemia major who were consulting Thalassaemia Clinic, Royal Hospital. They included 15 males and 15 females, aged 16 to 32 years with median of 21 years and mean ± SD of 21.23 ± 3.42 years. The medical records of these patients were reviewed and their endocrine functions were assessed. This assessment included pituitary and gonadal function, thyroid function, bone profile (including Parathyroid Hormone), morning cortisol and fasting glucose. These profiles were reviewed to exclude hypogonadism, hypothyroidism, hypoparathyroidism, hypoadrenalism or diabetes mellitus.
Hypogonadism was reported in 22 (73.3%) patients (13 female, 9 male). Low levels of Follicle-Stimulating Hormone (FSH) and low Luteinizing Hormone (LH) with low estradiol (in females) or testosterone (in males) was noted in 15 (50.0%) patients (7 female, 8 male). Normal (but inappropriately low) levels of FSH and LH with low estradiol (in females) or testosterone (in males) was noted in 7 (23.3%) patients (6 female, 1 male). Primary hypothyroidism was present in only 1 (3.3%) patient (female) who Hypoparathyroidism was found in 3 (10.0%) patients (2 female, 1 male). Diabetes mellitus with high fasting glucose was noted in 8 (26.7%) patients (2 female, 6 male). Morning cortisol levels for all patients were within the reference range with no suspicion of hypoadrenal cortical function. Eight (26.7%) patients had no endocrine disorder, 12 (40.0%) patients had one disorder, 8 (26.7%) patients had 2 disorders, and 2 (6.7%) patients had 3 endocrine disorders. There was no significant difference (p>0.050) in mean serum ferritin in thalassaemics with or without endocrinopathy, regardless of the number of endocrinopathy.
There is high prevalence of endocrine disorders among Omani beta-thalassaemic adult patients. This signifies the importance of awareness for their development and monitoring for early detection and replacement therapy. No relationship between serum ferritin and development of endocrinopathy was noted.
重型β地中海贫血是全球常见的医学问题。在阿曼苏丹国,关于该疾病中不同内分泌疾病的性质和患病率的数据很少。
确定重型β地中海贫血患者内分泌疾病的患病率和发病时间。
这项横断面研究于2008年1月至7月进行,研究对象为30名阿曼输血依赖型纯合重型β地中海贫血患者,他们在皇家医院地中海贫血诊所就诊。其中包括15名男性和15名女性,年龄在16至32岁之间,中位数为21岁,平均±标准差为21.23±3.42岁。回顾了这些患者的病历并评估了他们的内分泌功能。该评估包括垂体和性腺功能、甲状腺功能、骨代谢指标(包括甲状旁腺激素)、晨皮质醇和空腹血糖。对这些指标进行审查以排除性腺功能减退、甲状腺功能减退、甲状旁腺功能减退、肾上腺皮质功能减退或糖尿病。
22名(73.3%)患者报告有性腺功能减退(13名女性,9名男性)。15名(50.0%)患者(7名女性,8名男性)出现促卵泡生成素(FSH)水平低、黄体生成素(LH)水平低且雌二醇(女性)或睾酮(男性)水平低的情况。7名(23.3%)患者(6名女性,1名男性)出现FSH和LH水平正常(但异常低)且雌二醇(女性)或睾酮(男性)水平低的情况。仅1名(3.3%)患者(女性)患有原发性甲状腺功能减退。3名(10.0%)患者(2名女性,1名男性)患有甲状旁腺功能减退。8名(26.7%)患者(2名女性,6名男性)空腹血糖高,患有糖尿病。所有患者的晨皮质醇水平均在参考范围内,无肾上腺皮质功能减退的嫌疑。8名(26.7%)患者没有内分泌疾病,12名(40.0%)患者有一种疾病,8名(26.7%)患者有两种疾病,2名(6.7%)患者有三种内分泌疾病。无论内分泌疾病的数量如何,有或没有内分泌病变的地中海贫血患者的平均血清铁蛋白水平均无显著差异(p>0.050)。
阿曼成年β地中海贫血患者中内分泌疾病的患病率很高。这表明认识到其发展并进行监测以早期发现和替代治疗的重要性。未发现血清铁蛋白与内分泌病变的发展之间存在关联。