Intelligence quotient in children with congenital hypothyroidism on treatment: A cross-sectional study

Q4 Medicine
Deepthi Joella Fernandes, Suman Rath
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引用次数: 0

Abstract

Introduction: Congenital hypothyroidism (CH) is the most commonly identified endocrine disorder. Early intervention can prevent intellectual deficits. Objective: To determine the intelligence quotient (IQ) and aetiology in children diagnosed with CH undergoing treatment and the associations between the IQ and the age of diagnosis. Method: A cross-sectional study was conducted in a tertiary care hospital in Bangalore, which enrolled 52 children aged 6 months to 15 years diagnosed with CH. Using a pre-designed proforma, we collected demographic data and confirmed CH aetiology. For IQ assessment, children under 3 years underwent the Vineland Social Maturity Scale (VSMS) and developmental screening test (DST), while those over 3 years were evaluated with the VSMS and Binet Kamat test of intelligence (BKT). Results: Among the 52 children with CH, dyshormonogenesis was the predominant aetiology. In the under-3-year age group (n=17), all demonstrated average to above-average intelligence. Among those over 3 years (n=35), 10.9% (95% CI: 6.5% to 17.2%) exhibited low average and borderline intelligence with the VSMS, and 5.7% (95% CI: 2.3% to 12.5%) had extremely low IQ (IQ <70). The BKT scale showed 20% (95% CI: 12.8% to 29.7%) with low average and borderline intelligence, and 2.9% (95% CI: 0.7% to 8.3%) with extremely low IQ (IQ <70). Children diagnosed at a mean age of 4.2 and 4.4 years exhibited intellectual disability on the VSMS and BKT scales, respectively. Conversely, those diagnosed at a mean age of 1.2 and 1.8 years showed average and above-average intelligence on the VSMS (p-value 0.02) and BKT scale (p-value 0.001), respectively. Conclusions: Children diagnosed with CH at mean ages of 4.2 and 4.4 years exhibited intellectual disability on the VSMS and BKT scales, respectively. Conversely, those diagnosed with CH at mean ages of 1.2 and 1.8 years showed average and above-average intelligence on the VSMS (p = 0.02) and BKT scale (p = 0.001), respectively.
接受治疗的先天性甲状腺功能减退症患儿的智商:横断面研究
导言先天性甲状腺功能减退症(CH)是最常见的内分泌疾病。早期干预可预防智力缺陷。研究目的确定被诊断患有先天性甲状腺功能减退症并正在接受治疗的儿童的智商(IQ)和病因,以及智商与诊断年龄之间的关联。研究方法:采用横断面研究方法:在班加罗尔的一家三级甲等医院进行了一项横断面研究,共招募了52名被诊断为CH的6个月至15岁儿童。我们使用预先设计的表格收集了人口统计学数据,并确认了 CH 的病因。在智商评估方面,3岁以下的儿童接受了文兰社会成熟度量表(VSMS)和发育筛查测试(DST),而3岁以上的儿童则接受了文兰社会成熟度量表和比奈-卡马特智力测验(BKT)。研究结果在52名CH患儿中,主要病因是胚胎发育不良。在3岁以下年龄组(17人)中,所有患儿的智力均达到平均水平或高于平均水平。在3岁以上的儿童中(人数=35),10.9%(95% CI:6.5%至17.2%)的儿童在VSMS中表现出低水平和边缘智力,5.7%(95% CI:2.3%至12.5%)的儿童智商极低(智商<70)。BKT 量表显示,20% 的儿童(95% CI:12.8% 至 29.7%)智力处于平均和边缘水平,2.9% 的儿童(95% CI:0.7% 至 8.3%)智商极低(智商小于 70)。平均年龄分别为 4.2 岁和 4.4 岁的儿童在 VSMS 和 BKT 量表上表现出智力障碍。相反,在平均年龄为 1.2 岁和 1.8 岁时确诊的儿童,在 VSMS 量表(p 值为 0.02)和 BKT 量表(p 值为 0.001)上分别表现出平均和高于平均水平的智力。结论平均年龄分别为 4.2 岁和 4.4 岁时被诊断为 CH 的儿童在 VSMS 和 BKT 量表上表现出智力缺陷。相反,平均年龄分别为 1.2 岁和 1.8 岁的儿童在 VSMS 量表(p = 0.02)和 BKT 量表(p = 0.001)上分别表现出平均智力水平和高于平均智力水平。
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来源期刊
Sri Lanka Journal of Child Health
Sri Lanka Journal of Child Health Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
101
审稿时长
24 weeks
期刊介绍: This is the only journal of child health in Sri Lanka. It is designed to publish original research articles and scholarly articles by recognized authorities on paediatric subjects. It is distributed widely in Sri Lanka and bears the ISSN number 1391-5452 for the print issues and e-ISSN 2386-110x for the electronic version in the internet. The journal is published quarterly and the articles are reviewed by both local and foreign peers. The Journal is the primary organ of Continuing Paediatric Medical Education in Sri Lanka.
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