线粒体相关基因在亚临床甲状腺功能减退孕妇中的表达,以及miRNA在母体和脐血中的表达。

IF 1.9 Q3 ENDOCRINOLOGY & METABOLISM Thyroid Research Pub Date : 2023-09-18 DOI:10.1186/s13044-023-00180-6
Julie Kristine Guldberg Stryhn, Jacob Larsen, Palle Lyngsie Pedersen, Peter Haulund Gæde
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引用次数: 0

摘要

背景:妊娠期亚临床甲状腺功能减退症和促甲状腺激素(TSH)上限的定义存在争议。由于线粒体受到甲状腺激素的影响,本研究的目的是测量甲状腺功能正常和亚临床甲状腺功能减退孕妇线粒体相关基因的表达,以了解母体亚临床甲状腺机能减退的潜在代谢后果。此外,我们希望测试应用TSH截断是否显著改变了我们表达基因水平的结果。此外,我们旨在确定亚临床甲状腺功能减退症的潜在微小RNA生物标志物,这些标志物也可以追溯到后代。方法:从计划剖宫产的足月孕妇队列中,77名妇女的线粒体相关基因过氧化物酶体增殖因子激活受体-γ共激活因子-1β(PGC-1β)、线粒体转录因子a(TFAM)、,通过qPCR从分娩前采集的血液中测定超氧化物歧化酶2(SOD2)和核呼吸因子2(NRF-2)。定义亚临床甲状腺功能减退症的两个TSH临界水平(> 3.0和 > 3.7mIU/L)用于结果处理,生成同一队列的两个数据分析。在22个成对的母体脐带样本中(亚临床甲状腺功能减退/甲状腺功能正常率0.5,TSH临界值 > 3.0mIU/L)、微小RNA表达(miRNA)。结果:亚临床甲状腺功能减退组的所有基因表达均较低,无论TSH阈值如何,但除PGC-1β外,其他基因表达均不显著 > 3.0 mIU/L。两种miRNA(hsa-let-7d-3p和hsa-miR-345-5p)在患有亚临床甲状腺功能减退症的妇女和后代(脐带血)的血液中上调。结论:亚临床甲状腺功能减退症患者线粒体基因表达呈下降趋势。miRNA hsa-let-7d-3p和hsa-miR-345-5p可能是母体亚临床甲状腺功能减退的潜在标志物。然而,还需要更大规模的研究来验证这些发现。
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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Expressions of mitochondria-related genes in pregnant women with subclinical hypothyroidism, and expressions of miRNAs in maternal and cord blood.

Background: Subclinical hypothyroidism in pregnancy and definition by upper thyrotropin (TSH) cutoff are controversial. As mitochondria are influenced by thyroid hormones, the purpose in this study was to measure expression of mitochondria-related genes in euthyroid and subclinical hypothyroid pregnant women to obtain more knowledge of potential metabolic consequences of maternal subclinical hypothyroidism. In addition, we wished to test if applied TSH-cutoff significantly changed our results of expressed gene-levels. Moreover, we aimed to identify potential microRNA-biomarkers for subclinical hypothyroidism - markers that could be traced to offspring as well.

Methods: From a cohort of at-term pregnant women undergoing planned cesarean section, 77 women had expression levels of the mitochondria-related genes Peroxisome Proliferator-activated Receptor-γ coactivator-1β (PGC-1β), mitochondrial Transcription Factor A (TFAM), Superoxide Dismutase 2 (SOD2) and Nuclear Respiratory Factor 2 (NRF-2) determined by qPCR from blood sampled in prior to delivery. Two TSH-cutoff levels defining subclinical hypothyroidism (> 3.0 and > 3.7 mIU/L) were applied for the procession of results, generating two data analyses of the same cohort. In 22 pairwise maternal-cord samples (subclinical hypothyroid/euthyroid-rate 0.5, TSH-cutoff > 3.0 mIU/L), microRNA-expressions (miRNA) were analyzed.

Results: All gene expressions were lower in the subclinical hypothyroid group regardless of applied TSH-cutoff, but insignificant except for PGC-1β at TSH cutoff > 3.0 mIU/L. Two miRNAs (hsa-let-7d-3p and hsa-miR-345-5p) were upregulated in blood from women and offspring (cord blood) with subclinical hypothyroidism.

Conclusions: A trend towards decreased mitochondrial gene expressions in subclinical hypothyroidism were demonstrated. The miRNAs hsa-let-7d-3p and hsa-miR-345-5p might be potential markers of maternal subclinical hypothyroidism. However, larger studies are needed to verify the findings.

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来源期刊
Thyroid Research
Thyroid Research Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
3.10
自引率
4.50%
发文量
21
审稿时长
8 weeks
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