Meyer Nuala J
Pulmonary, Allergy, and Critical Care Medicine, University of Pennsylvania, Perelman School of Medicine, 3600 Spruce Street, 5039 Maloney Building, Philadelphia, PA 19104, USA.
Clin Chest Med. 2014 Dec;35(4):673-84. doi: 10.1016/j.ccm.2014.08.006. Epub 2014 Sep 23.
This article summarizes the contributions of high-throughput genomic, proteomic, metabolomic, and gene expression investigations to the understanding of inherited or acquired risk for acute respiratory distress syndrome (ARDS). Although not yet widely applied to a complex trait like ARDS, these techniques are now routinely used to study a variety of disease states. Omic applications hold great promise for identifying novel factors that may contribute to ARDS pathophysiology or may be appropriate for further development as biomarkers or surrogates in clinical studies. Opportunities and challenges of different techniques are discussed, and examples of successful applications in non-ARDS fields are used to illustrate the potential use of each technique.
本文总结了高通量基因组学、蛋白质组学、代谢组学和基因表达研究对理解急性呼吸窘迫综合征(ARDS)的遗传或获得性风险所做的贡献。尽管这些技术尚未广泛应用于像ARDS这样的复杂性状,但它们现在已常规用于研究多种疾病状态。组学应用在识别可能有助于ARDS病理生理学或可能适合在临床研究中进一步开发为生物标志物或替代指标的新因素方面具有巨大潜力。文中讨论了不同技术的机遇与挑战,并列举了在非ARDS领域成功应用的实例来说明每种技术的潜在用途。