Ma Shuo, Chen Yaya, Gu Zhexi, Wang Jiwei, Zhao Fengfeng, Yao Yuming, Abudushalamu Gulinaizhaer, Cai Shijie, Fan Xiaobo, Miao Miao, Gao Xun, Zhang Chen, Wu Guoqiu
Center of Clinical Laboratory Medicine, Zhongda Hospital, Medical School of Southeast University, Nanjing, China.
Department of Laboratory Medicine, Medical School of Southeast University, Nanjing, China.
Diabetes Metab J. 2025 May;49(3):462-474. doi: 10.4093/dmj.2024.0205. Epub 2025 Feb 21.
Gestational diabetes mellitus (GDM) is a metabolic disorder posing significant risks to maternal and infant health, with a lack of effective early screening markers. Therefore, identifying early screening biomarkers for GDM with higher sensitivity and specificity is urgently needed.
High-throughput sequencing was employed to screen for key circular RNAs (circRNAs), which were then evaluated using reverse transcription quantitative polymerase chain reaction. Logistic regression analysis was conducted to examine the relationship between clinical characteristics, circRNA expression, and adverse pregnancy outcomes. The diagnostic accuracy of circRNAs for early and mid-pregnancy GDM was assessed using receiver operating characteristic curves. Pearson correlation analysis was utilized to explore the relationship between circRNA levels and oral glucose tolerance test results. A predictive model for early GDM was established using logistic regression.
Significant alterations in circRNA expression profiles were detected in GDM patients, with hsa_circ_0031560 and hsa_ circ_0000793 notably upregulated during the first and second trimesters. These circRNAs were associated with adverse pregnancy outcomes and effectively differentiated GDM patients, with second trimester cohorts achieving an area under the curve (AUC) of 0.836. In first trimester cohorts, these circRNAs identified potential GDM patients with AUCs of 0.832 and 0.765, respectively. The early GDM prediction model achieved an AUC of 0.904, validated in two independent cohorts.
Hsa_circ_0031560, hsa_circ_0000793, and the developed model serve as biomarkers for early prediction or midterm diagnosis of GDM, offering clinical tools for early GDM screening.
妊娠期糖尿病(GDM)是一种对母婴健康构成重大风险的代谢紊乱疾病,缺乏有效的早期筛查标志物。因此,迫切需要鉴定出具有更高敏感性和特异性的GDM早期筛查生物标志物。
采用高通量测序筛选关键环状RNA(circRNA),然后使用逆转录定量聚合酶链反应进行评估。进行逻辑回归分析以检验临床特征、circRNA表达与不良妊娠结局之间的关系。使用受试者工作特征曲线评估circRNA对妊娠早期和中期GDM的诊断准确性。利用Pearson相关分析探讨circRNA水平与口服葡萄糖耐量试验结果之间的关系。使用逻辑回归建立早期GDM的预测模型。
在GDM患者中检测到circRNA表达谱有显著变化,hsa_circ_0031560和hsa_circ_0000793在孕早期和孕中期明显上调。这些circRNA与不良妊娠结局相关,并能有效区分GDM患者,孕中期队列的曲线下面积(AUC)为0.836。在孕早期队列中,这些circRNA分别以0.832和0.765的AUC识别出潜在的GDM患者。早期GDM预测模型的AUC为0.904,并在两个独立队列中得到验证。
Hsa_circ_0031560、hsa_circ_0000793以及所建立的模型可作为GDM早期预测或中期诊断的生物标志物,为早期GDM筛查提供临床工具。