Department of Epidemiology, Tulane School of Public Health and Tropical Medicine, 1440 Canal Street, New Orleans, LA, 70112, USA.
Department of Nutrition, Nutrition Research Institute, University of North Carolina at Chapel Hill, 500 Laureate Way, Kannapolis, NC, 28081, USA.
Metabolomics. 2019 Sep 10;15(9):124. doi: 10.1007/s11306-019-1587-1.
Most known risk factors for preterm birth, a leading cause of infant morbidity and mortality, are not modifiable. Advanced molecular techniques are increasingly being applied to identify biomarkers and pathways important in disease development and progression.
We review the state of the literature and assess it from an epidemiologic perspective.
PubMed, Embase, CINAHL, and Cochrane Central were searched on January 31, 2019 for original articles published after 1998 that utilized an untargeted metabolomic approach to identify markers of preterm birth. Eligible manuscripts were peer-reviewed and included original data from untargeted metabolomics analyses of maternal tissue derived from human studies designed to determine mechanisms and predictors of preterm birth.
Of 2823 results, 14 articles met the inclusion requirements. There was little consistency in study design, outcome definition, type of biospecimen, or the inclusion of covariates and confounding factors, and few consistent associations with metabolites were identified in this review.
Studies to date on metabolomic predictors of preterm birth are highly heterogeneous in both methodology and resulting metabolite identification. There is an urgent need for larger studies in well-defined populations, to determine biomarkers predictive of preterm birth, and to reveal mechanisms and targets for development of intervention strategies.
早产是婴儿发病率和死亡率的主要原因,大多数已知的早产风险因素是不可改变的。先进的分子技术越来越多地被应用于识别生物标志物和疾病发展及进展过程中的重要途径。
我们回顾了文献现状,并从流行病学角度对其进行了评估。
2019 年 1 月 31 日,我们在 PubMed、Embase、CINAHL 和 Cochrane Central 上搜索了 1998 年后发表的利用非靶向代谢组学方法识别早产标志物的原始文章。合格的文献经过同行评审,包括来自人类研究的非靶向代谢组学分析的原始数据,这些研究旨在确定早产的机制和预测因素。
在 2823 项研究结果中,有 14 篇文章符合纳入标准。研究设计、结局定义、生物样本类型以及协变量和混杂因素的纳入方面差异很大,在本综述中很少有与代谢物一致的关联。
迄今为止,关于早产代谢标志物的研究在方法学和鉴定出的代谢物方面存在很大的异质性。迫切需要在明确界定的人群中开展更大规模的研究,以确定预测早产的生物标志物,并揭示干预策略的发展机制和目标。