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Thyroid Dysfunction in Chinese Children and Adolescents with Down Syndrome

机译:中国儿童唐氏综合症的甲状腺功能异常

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Objective: To document the occurrence of thyroid dysfunction in Chinese children and adolescents with Down syndrome. Method: Four hundred and sixteen Chinese children and adolescents with Down syndrome were studied retrospectively for thyroid dysfunction. Hospital records from seven regional hospitals were reviewed. Records could not be traced in 65 of them. Among the 351 subjects, 200 were boys while 151 were girls. The age ranged from 0 to 18.99 years. Results: Thyroid function was normal in 250 patients (71.2%). Seven patients had congenital hypothyroidism (2.0%), seven had acquired hypothyroidism (2.0%) and seventy-nine had subclinical hypothyroidism (22.5%). Hyperthyroidism was found in 8 of them (2.3%). Serum thyroid stimulating hormone (TSH) or free thyroxine (fT4) level could be traced in 200 of them. There was no significant difference in mean fT4 levels between the normal group (118 patients) and the group with subclinical hypothyroidism (70 patients). Patients with subclinical hypothyroidism were subdivided into two groups: G1 (n=61) with TSH=5-10 mIU/L and G2 (n=9) with TSH>10 mIU/L. There was no significant difference in fT4 levels between the two groups. Sixty-seven patients had been screened for auto-antibodies. Anti-thyroglobulin antibodies and/or anti-thyroid microsomal antibodies were found in 25 patients. All 8 patients with hyperthyroidism were positive in either one or both autoantibodies. Two out of 6 patients with acquired hypothyroidism and 10 out of 29 with subclinical hypothyroidism had positive autoantibodies while thyroid autoantibodies were present in 5 out of 20 patients with normal thyroid function. Conclusion: Thyroid dysfunction is very common in patients with Down syndrome. Regular blood test for thyroid function is recommended. The fT4 levels of subclinical hypothyroidism did not differ significantly from the normal group. Further study is required to support the need for treatment in these patients. The presence of thyroid autoantibodies in all patients with hyperthyroidism highly suggests an autoimmune origin.
机译:目的:记录中国唐氏综合症儿童和青少年甲状腺功能障碍的发生情况。方法:回顾性研究416例中国唐氏综合症儿童和青少年的甲状腺功能障碍。审查了七家地区医院的医院记录。其中有65条记录无法追踪。在351名受试者中,有200名是男孩,而151名是女孩。年龄范围是0到18.99岁。结果:250例患者的甲状腺功能正常(71.2%)。先天性甲状腺功能减退症7例(2.0%),先天性甲状腺功能减退症7例(2.0%),亚临床甲状腺功能减退症79例(22.5%)。其中8例(2.3%)发现甲状腺功能亢进。可以在其中200例中发现血清甲状腺刺激激素(TSH)或游离甲状腺素(fT4)水平。正常组(118例患者)与亚临床甲状腺功能减退组(70例)之间的平均fT4水平无显着差异。亚临床甲状腺功能减退症患者分为两组:TS1 = 5-10 mIU / L的G1(n = 61)和TSH> 10 mIU / L的G2(n = 9)。两组之间的fT4水平无显着差异。已筛查了67位患者的自身抗体。在25例患者中发现了抗甲状腺球蛋白抗体和/或抗甲状腺微粒体抗体。所有8例甲亢患者的一种或两种自身抗体均为阳性。甲状腺功能正常的6名获得性甲状腺功能减退患者中有2名,亚临床甲状腺功能减退的29名患者中有10名具有阳性抗体,而甲状腺功能正常的20名患者中有5名存在甲状腺自身抗体。结论:唐氏综合征患者甲状腺功能异常很常见。建议定期对甲状腺功能进行血液检查。亚临床甲状腺功能减退症的fT4水平与正常组无显着差异。需要进一步的研究来支持这些患者的治疗需求。所有甲状腺功能亢进症患者中甲状腺自身抗体的存在都强烈提示自身免疫起源。

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