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Review: Opportunities and barriers for omics-based biomarker discovery in steatotic liver diseases

组学 生物标志物发现 生物标志物 计算生物学 医学 数据科学 生物信息学 生物 计算机科学 蛋白质组学 遗传学 基因
作者
Maja Thiele,Ida Villesen,Lili Niu,Stine Liv Johansen,Karolina Sulek,Suguru Nishijima,Lore Van Espen,Marisa Isabell Keller,Mads Israelsen,Tommi Suvitaival,Andressa de Zawadzki,Helene Bæk Juel,Maximilian Joseph Brol,Sara Stinson,Yuancheng Huang,M Silva,Michael Kuhn,Ema Anastasiadou,Diana Julie Leeming,Morten A. Karsdal,Jelle Matthijnssens,Manimozhiyan Arumugam,Louise Torp Dalgaard,Cristina Legido‐Quigley,Mathias Mann,Jonel Trebicka,Peer Bork,Lars Juhl Jensen,Torben Hansen,Aleksander Krag,Aleksander Krag,Peer Bork,Torben Hansen,Manimozhiyan Arumugam,Jonel Trebicka,Morten A. Karsdal,Ema Anastasiadou,Hans Israelsen,Hans Olav Melberg,Cristina Legido‐Quigley,Maja Thiele,Torben Hansen,Matthias Mann,Jelle Matthijnssens,Aleksander Krag
出处
期刊:Journal of Hepatology [Elsevier]
标识
DOI:10.1016/j.jhep.2024.03.035
摘要

Summary

The rising prevalence of liver diseases related to obesity and excessive use of alcohol is fuelling an increasing demand for accurate biomarkers aimed at community screening, diagnosis of steatohepatitis and significant fibrosis, monitoring, prognosis and prediction of treatment efficacy. Breakthroughs in omics methodologies and the power of bioinformatics have created an excellent opportunity to combine clinical needs with technological advancements. Omics technologies allow for advanced investigations into biological processes from the genes to transcription and regulation, to circulating protein, metabolite and lipid levels, as well as the microbiome including bacteria, viruses and fungi. We consequently find ourselves in a period of rapid progress in technology and bioinformatics that may allow for development of precision biomarkers for personalised medicine. However, there are important barriers to consider in omics biomarker discovery and validation, including the use of semi-quantitative measurements from untargeted platforms, which may exhibit high analytical, inter- and intra-individual variance. Standardising methods and the need to validate across diverse populations, presents a challenge, partly due to disease complexity and the dynamic nature of biomarker expression in different disease stages. Lack of validity causes lost opportunities when studies fail to provide the knowledge needed for regulatory approvals, all of which contributes to a delayed translation of these discoveries into clinical practice. While no omics-based biomarkers have matured to clinical implementation, the extent of data generated through omics-technologies holds the power of hypothesis-free discovery of a plethora of candidate biomarkers to be further validated. To explore the many opportunities of omics technologies, hepatologists need detailed knowledge of commonalities and differences between the various omics layers, and both the barriers to and advantages of these approaches.
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