Zhou Yingying, Wang Xinyi, Zhang Yuanyuan, Zhao Tong, Shan Zhongyan, Teng Weiping
Department of Endocrinology and Metabolism, Institute of Endocrinology, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Affiliated Hospital of China Medical University, Heping Distinct, Shenyang, Liaoning, China.
Division of Endocrinology, Department of Internal Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Front Endocrinol (Lausanne). 2018 Apr 6;9:128. doi: 10.3389/fendo.2018.00128. eCollection 2018.
An increasing number of studies suggest that subclinical hypothyroidism (SCH) is associated with complications of gestation, including spontaneous abortion (SA). However, the underlying mechanism is not clear. MicroRNA (miRNA) has been demonstrated to be closely related to gynecological reproductive diseases. We determined miRNA expression in patients with SCH, SCH with SA (SCH + SA), and in those with SA as well as healthy controls (HCs), and analyzed whether dysregulation in several miRNAs was specific to these cohorts. An Agilent Human miRNA array was used to explore miRNA levels in pooled serum samples as a pilot study, followed by a validation of selected miRNAs by real-time polymerase chain reaction in SCH ( = 24), SA ( = 19), SCH + SA ( = 21), and HC cohorts ( = 18). The relative expression of miR-940 was elevated in the SCH + SA group compared with SCH, SA, and HC groups. In addition, miR-486-5p was upregulated in the SCH + SA group compared with SA and HC groups, without a difference noted between SCH + SA and SCH groups. Further analysis suggested that miR-940 or miR-486-5p may be potential predictive biomarkers for the early diagnosis of SA in patients with SCH.
越来越多的研究表明,亚临床甲状腺功能减退(SCH)与妊娠并发症有关,包括自然流产(SA)。然而,其潜在机制尚不清楚。微小RNA(miRNA)已被证明与妇科生殖疾病密切相关。我们测定了SCH患者、合并SA的SCH患者(SCH+SA)、SA患者以及健康对照者(HC)的miRNA表达,并分析了几种miRNA的失调是否对这些队列具有特异性。作为一项初步研究,使用安捷伦人类miRNA芯片检测混合血清样本中的miRNA水平,随后通过实时聚合酶链反应对SCH组(n=24)、SA组(n=19)、SCH+SA组(n=21)和HC组(n=18)中选定的miRNA进行验证。与SCH组、SA组和HC组相比,miR-940在SCH+SA组中的相对表达升高。此外,与SA组和HC组相比,miR-486-5p在SCH+SA组中上调,而SCH+SA组和SCH组之间未观察到差异。进一步分析表明,miR-940或miR-486-5p可能是SCH患者SA早期诊断的潜在预测生物标志物。