Advancing omics technologies in acute respiratory distress syndrome: paving the way for personalized medicine.

IF 2.8 Q2 CRITICAL CARE MEDICINE
Lou'i Al-Husinat, Mohammad Araydah, Sarah Al Sharie, Saif Azzam, Denise Battaglini, Arqam Alrababah, Rana Haddad, Khaled Al-Asad, Claudia C Dos Santos, Marcus J Schultz, Fernanda F Cruz, Pedro L Silva, Patricia R M Rocco
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Abstract

Despite advances in critical care, acute respiratory distress syndrome (ARDS) remains a potentially life-threatening condition with high mortality. The heterogeneous nature of ARDS, caused by diverse etiologies, poses considerable challenges to accurate diagnosis, treatment, and prognosis. Conventional methods often fail to elucidate the pathophysiology of ARDS, thus limiting therapeutic efficacy. However, recent advances in omics technologies, including genomics, transcriptomics, proteomics, metabolomics, lipidomics, and epigenomics, have provided deeper insights into ARDS mechanisms. Genomic studies have identified genetic variants associated with ARDS susceptibility, such as polymorphisms in genes encoding angiotensin-converting enzyme, surfactant proteins, toll-like receptor 4, interleukin-6, Fas/FasL, and vascular endothelial growth factor, offering potential therapeutic targets. Transcriptomic and proteomic reveal distinct biomarker profiles associated with ARDS pathogenesis, including dysregulated inflammatory signaling, epithelial and endothelial barrier dysfunction, and compromised immune responses. Metabolomics has highlighted biomarkers, such as phenylalanine and choline, aiding in severity assessment, subphenotype stratification, and treatment response prediction. Lipidomics has uncovered disruptions in lipid metabolism, including altered phospholipids, sphingolipids, and eicosanoids, with key lipid species such as lysophosphatidylcholine and ceramide emerging as biomarkers for severity and outcomes. Epigenomics explores DNA methylation, histone modifications, and non-coding RNAs, revealing their role in regulating inflammation, immune responses, and tissue repair in ARDS. These epigenetic changes hold promise for biomarker discovery and personalized therapy. Integrating these omics technologies advances our understanding of ARDS pathophysiology, enabling precision medicine approaches. This review examines the latest advancements in omics research related to ARDS, emphasizing its role in developing personalized diagnostics and therapeutic strategies to improve disease monitoring, prognosis, and treatment outcomes.

Abstract Image

推进急性呼吸窘迫综合征组学技术:为个性化医疗铺平道路。
尽管在重症监护方面取得了进展,急性呼吸窘迫综合征(ARDS)仍然是一种潜在的危及生命的疾病,死亡率很高。ARDS由多种病因引起的异质性给准确的诊断、治疗和预后带来了相当大的挑战。传统的方法往往不能阐明ARDS的病理生理,从而限制了治疗效果。然而,组学技术的最新进展,包括基因组学、转录组学、蛋白质组学、代谢组学、脂质组学和表观基因组学,为ARDS机制提供了更深入的见解。基因组研究已经确定了与ARDS易感性相关的遗传变异,如编码血管紧张素转换酶、表面活性剂蛋白、toll样受体4、白细胞介素-6、Fas/FasL和血管内皮生长因子的基因多态性,为潜在的治疗靶点提供了可能。转录组学和蛋白质组学揭示了与ARDS发病机制相关的不同生物标志物,包括炎症信号失调、上皮和内皮屏障功能障碍以及免疫反应受损。代谢组学强调了生物标志物,如苯丙氨酸和胆碱,有助于严重程度评估,亚表型分层和治疗反应预测。脂质组学已经发现了脂质代谢的紊乱,包括磷脂、鞘脂和类二十烷类物质的改变,而溶血磷脂酰胆碱和神经酰胺等关键脂质物种正成为严重程度和结果的生物标志物。表观基因组学研究DNA甲基化、组蛋白修饰和非编码rna,揭示它们在ARDS中调节炎症、免疫反应和组织修复中的作用。这些表观遗传变化为生物标志物的发现和个性化治疗带来了希望。整合这些组学技术促进了我们对ARDS病理生理学的理解,使精准医学方法成为可能。本文综述了与ARDS相关的组学研究的最新进展,强调了其在制定个性化诊断和治疗策略以改善疾病监测、预后和治疗结果方面的作用。
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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来源期刊
Intensive Care Medicine Experimental
Intensive Care Medicine Experimental CRITICAL CARE MEDICINE-
CiteScore
5.10
自引率
2.90%
发文量
48
审稿时长
13 weeks
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