Clinical and Genetic Characteristics of Adult Nonautoimmune Hypothyroidism: A Single-Institution Study.

Chiho Sugisawa, Erika Uehara, Kanako Tanase-Nakao, Kosuke Inoue, Tatsuya Iida, Fumiko Otsuka, Nami Suzuki, Hidemi Ohye, Miho Fukushita, Masako Matsumoto, Ai Yoshihara, Natsuko Watanabe, Kiminori Sugino, Jaeduk Yoshimura Noh, Matsuo Taniyama, Satoshi Narumi, Koichi Ito
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Abstract

Purpose: Nonautoimmune hypothyroidism is characterized by hypothyroidism with negative thyroid autoantibodies with limited knowledge of its clinical and genetic characteristics. The aim was to characterize the clinical and genetic features of nonautoimmune hypothyroidism.

Methods: This retrospective study included 1,470 treatment-naive adult hypothyroid patients (serum TSH >10 mU/L) born before 1979 and were followed up at Ito Hospital, Tokyo, Japan. Of them, 220 patients were diagnosed with idiopathic nonautoimmune hypothyroidism by thyroid autoantibody measurements. Sequencing of 13 genes associated with nonautoimmune hypothyroidism was performed of 101 of the 220 patients. Clinical characteristics, including thyroid function and morphology, were systematically evaluated.

Results: The proportion of idiopathic nonautoimmune hypothyroidism among the 1,470 patients with treatment-naive non-transient hypothyroidism was 15.0%. Idiopathic nonautoimmune hypothyroidism patients had lower serum TSH (17.0 vs. 28.3 mU/L; P<0.001), higher serum fT4 (11.5 vs. 8.9 pmol/L; P<0.001), and a smaller thyroid volume (13.4 vs. 24.9 g; P<0.001) than autoimmune hypothyroidism patients. Genetic analysis showed that 5.0% of the analyzed idiopathic nonautoimmune hypothyroidism patients had a Mendelian disorder, with PAX8 being the most commonly affected gene. An additional 19% of the analyzed patients carried monoallelic variants in hypothyroidism-associated genes, such as DUOX2, DUOXA2, SLC26A4, TG, TPO, and TSHR, that cause autosomal recessive genetic defects.

Conclusions: In patients with treatment-naive adult nonautoimmune hypothyroidism, thyroid dysfunction was milder, and thyroid volume was smaller than in patients with autoimmune hypothyroidism. Mendelian forms were rare, but the unexpectedly high frequency of monoallelic variant carriers suggests that these variants may confer genetic risk for nonautoimmune hypothyroidism.

成人非自身免疫性甲状腺功能减退症的临床和遗传特征:一项单机构研究
目的:非自身免疫性甲状腺功能减退症以甲状腺自身抗体阴性的甲状腺功能减退为特征,对其临床和遗传特征的了解有限。目的是表征非自身免疫性甲状腺功能减退症的临床和遗传特征。方法:对日本东京伊藤医院1979年以前出生的1470例未接受治疗的成人甲状腺功能减退患者(血清TSH bbb10 mU/L)进行回顾性研究。其中,220例患者通过甲状腺自身抗体检测被诊断为特发性非自身免疫性甲状腺功能减退症。对220例患者中的101例进行了与非自身免疫性甲状腺功能减退症相关的13个基因测序。临床特征,包括甲状腺功能和形态进行系统评估。结果:1470例初治非短暂性甲状腺功能减退患者中特发性非自身免疫性甲状腺功能减退的比例为15.0%。特发性非自身免疫性甲状腺功能减退患者血清TSH较低(17.0 vs 28.3 mU/L;结论:未接受治疗的成人非自身免疫性甲状腺功能减退患者的甲状腺功能障碍较自身免疫性甲状腺功能减退患者轻,甲状腺体积较小。孟德尔形式是罕见的,但单等位基因变异携带者的意外高频率表明,这些变异可能赋予非自身免疫性甲状腺功能减退的遗传风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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