Author:
Hsu Te-Yao,Cheng Hsin-Hsin,Lan Kuo-Chung,Hung Hsuan-Ning,Lai Yun-Ju,Tsai Chih-Chang,Fan Wen-Lang,Li Sung-Chou
Abstract
AbstractNeonates who are born preterm (PT) are usually characterized by immature physiological development, and preterm birth (PTB) is the leading cause of neonatal morbidity and mortality if intensive medical care is not available to PTB neonates. Early prediction of a PTB enables medical personnel to make preparations in advance, protecting the neonate from the subsequent health risks. Therefore, many studies have worked on identifying invasive or noninvasive PT biomarkers. In this study, we collected amniocentesis-derived (at the second trimester of gestation) amniotic fluid (AF) samples. At delivery, AF samples were classified into PTB or full-term birth (FTB). We first applied protein mass spectrometry technology to globally screen AF proteins, followed by specific protein validation with ELISA. We identified four protein biomarkers of PTB, including lactotransferrin (LTF), glutathione-disulfide reductase (GSR), myeloperoxidase (MPO) and superoxide dismutase 2 (SOD2). Further analyses demonstrated that their abundances were negatively correlated with neonatal weight and gestational age. In addition, by mimicking survival rate analysis widely used in tumor biology, we found that LTF and SOD2 were prognostic factors of gestational age, with higher levels denoting shorter gestational age. Finally, using the abundances of the four protein biomarkers, we developed a prediction model of PTB with an auROC value of 0.935 (sensitivity = 0.94, specificity = 0.89, p value = 0.0001). This study demonstrated that the abundances of specific proteins in amniotic fluid were not only the prognostic factors of gestational age but also the predictive biomarkers of PTB. These four AF proteins enable identification of PTB early in the second trimester of gestation, facilitating medical intervention to be applied in advance.
Funder
Kaohsiung Chang Gung Memorial Hospital
Publisher
Springer Science and Business Media LLC
Reference38 articles.
1. Arman, B. M., Binder, N. K., de Alwis, N., Kaitu’u-Lino, T. J. & Hannan, N. J. Repurposing existing drugs as a therapeutic approach for the prevention of preterm birth. Reproduction 165(1), R9–R23 (2023).
2. Sharma, D., Padmavathi, I. V., Tabatabaii, S. A. & Farahbakhsh, N. Late preterm: A new high risk group in neonatology. J Matern Fetal Neonatal Med 34(16), 2717–2730 (2021).
3. Steer, P. The epidemiology of preterm labour. BJOG Int. J. Obstet. Gynaecol. 112(1), s1-3 (2005).
4. Taiwan HBndi: Taiwan https://www.hpagovtw/Pages/Detailaspx?nodeid=649&pid=13646 2010.
5. Smith, R., Mesiano, S., Chan, E. C., Brown, S. & Jaffe, R. B. Corticotropin-releasing hormone directly and preferentially stimulates dehydroepiandrosterone sulfate secretion by human fetal adrenal cortical cells. J. Clin. Endocrinol. Metab. 83(8), 2916–2920 (1998).
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献