Dr Jannatul Ferdousi, Department of Paediatrics, Mymensingh Medical College Hospital, Mymensingh, Bangladesh; E-mail:
Mymensingh Med J. 2024 Oct;33(4):965-972.
Most of the thalassemic children of Bangladesh are receiving repeated blood transfusion. But they do not receive chelation therapy due to financial constraints. As a result, iron overload occurs in various organs of these children. Extra iron that is loaded in thyroid gland causes thyroid dysfunction. This study was undertaken to evaluate thyroid status in children with transfusion dependent Thalassemia patient. This cross-sectional analytical study was conducted in the Department of Pediatrics, Mymensingh Medical College Hospital, Bangladesh from September 2016 to April 2018. Children having thalassemia diagnosed by Hb electrophoresis, aged 3-12 years of both sexes were included as study group. Children of same age and sex admitted in indoor of Mymensingh Medical College Hospital with minor illness and without thalassemia were taken as comparison group. Purposive Sampling technique was applied. Serum FT₄, TSH and ferritin level were estimated in all children. Data analysis was done with Statistical Package for Social Science (SPSS) version 21.0. A total of 60 patients were enrolled as study group and another 60 patients were compared as comparison group. Mean ages of study group was 7.88±2.55 years and comparison group were 7.22±2.48 years. The mean pre-transfusion hemoglobin, serum ferritin, serum FT₄ and serum TSH level were found 6.23±0.60 gm/dl, 2658.33±879.39 ng/ml, 15.14±4.40 fmol/mL, 4.29±4.60 μIU/mL respectively in study group. The mean serum FT₄ was found significantly lower and mean serum TSH was significantly higher in thalassemic children in comparison to non-thalassemic children (p= <0.05). Frequency of subclinical hypothyroidism was found significantly higher in study group (25.0%) compared to comparison group (3.3%) (p=0.001). Mean serum ferritin level was found significantly higher in hypothyroid cases. Mean FT₄ level was significantly lower and mean TSH level was significantly higher in hypothyroid thalassemic patients (p= <0.001). Significant positive correlation between serum ferritin level and serum TSH level was found. Higher serum ferritin level was found significantly associated with the development of hypothyroidism in thalassemic patients.
大多数孟加拉国的地中海贫血儿童需要接受多次输血。但由于经济拮据,他们没有接受螯合治疗。因此,这些儿童的各种器官都会出现铁过载。过多的铁会在甲状腺中蓄积,导致甲状腺功能障碍。本研究旨在评估依赖输血的地中海贫血患儿的甲状腺功能状态。这是一项在孟加拉国 Mymensingh 医学院医院儿科进行的横断面分析研究,时间为 2016 年 9 月至 2018 年 4 月。研究组纳入了通过血红蛋白电泳诊断为地中海贫血的 3-12 岁男女儿童。选择同年龄和性别、在 Mymensingh 医学院医院住院的患有轻微疾病且无地中海贫血的儿童作为对照组。采用目的抽样技术。所有儿童均检测血清游离甲状腺素(FT₄)、促甲状腺激素(TSH)和铁蛋白水平。数据采用统计软件包(SPSS)版本 21.0 进行分析。共纳入 60 例患儿作为研究组,另选 60 例患儿作为对照组。研究组的平均年龄为 7.88±2.55 岁,对照组为 7.22±2.48 岁。研究组患儿的平均输血前血红蛋白、血清铁蛋白、血清 FT₄ 和血清 TSH 水平分别为 6.23±0.60 gm/dl、2658.33±879.39 ng/ml、15.14±4.40 fmol/mL 和 4.29±4.60 μIU/mL。与非地中海贫血患儿相比,地中海贫血患儿的血清 FT₄ 明显降低,TSH 明显升高(p<0.05)。研究组亚临床甲状腺功能减退症的发生率明显高于对照组(25.0%比 3.3%)(p=0.001)。甲状腺功能减退症患儿的血清铁蛋白水平明显升高。甲状腺功能减退症地中海贫血患儿的 FT₄ 水平明显降低,TSH 水平明显升高(p<0.001)。血清铁蛋白水平与 TSH 水平呈显著正相关。血清铁蛋白水平升高与地中海贫血患儿发生甲状腺功能减退症显著相关。