Preeclampsia and fetal growth restriction: does novel proteomics reveal immunological possible candidate biomarkers?

IF 3.8 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Current opinion in lipidology Pub Date : 2025-02-01 Epub Date: 2024-11-28 DOI:10.1097/MOL.0000000000000965
Marie Winther, Morten Hanefeld Dziegiel, Steffen Ullitz Thorsen
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Abstract

Purpose of review: The aim of this review is to explore a possible link between immunological candidate proteins, identified through modern proteomic techniques, and preeclampsia (PE) and fetal growth restriction (FGR).

Recent findings: Proteomics has become a promising tool in the search for disease pathways, drug targets, and biomarkers. PE and FGR are adverse pregnancy complications with supposed immunological involvement in their pathogenesis, but no circulating immunological biomarkers are currently established for diagnosis and risk stratification. Several proteomic studies have aimed to identify PE and FGR biomarkers - often with varying results across studies. However, proteomics has revealed altered expression of human leukocyte antigen-I in PE cases, which is supported in Genome-wide association study (GWAS) studies. Proteomic results support the heterogeneous nature of PE by identification of molecular subgroups - including subgroups characterized by immune-related proteins e.g. CXCL10. No specific immunological markers are found on FGR, but differences in overall plasma proteomic signature have been suggested.

Summary: Proteomics certainly holds great potential. The immunological component in PE and FGR are still unclarified, but improvements in proteomic technologies may provide both definition of disease subgroups and subsequent discovery of biomarkers and targeted analysis within each subgroup.

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子痫前期和胎儿生长受限:新的蛋白质组学是否揭示了可能的免疫候选生物标志物?
综述目的:本综述的目的是探讨通过现代蛋白质组学技术鉴定的免疫候选蛋白与子痫前期(PE)和胎儿生长受限(FGR)之间的可能联系。最近发现:蛋白质组学已经成为寻找疾病途径、药物靶点和生物标志物的一种很有前途的工具。PE和FGR是不良妊娠并发症,其发病机制可能与免疫有关,但目前还没有建立循环免疫生物标志物用于诊断和风险分层。一些蛋白质组学研究旨在鉴定PE和FGR生物标志物——通常在不同的研究中得到不同的结果。然而,蛋白质组学揭示了PE病例中人类白细胞抗原- 1的表达改变,这在全基因组关联研究(GWAS)研究中得到了支持。通过鉴定分子亚群(包括以免疫相关蛋白为特征的亚群,如CXCL10),蛋白质组学结果支持PE的异质性。在FGR中没有发现特异性免疫标记,但总体血浆蛋白质组学特征存在差异。摘要:蛋白质组学无疑具有巨大的潜力。PE和FGR的免疫学成分尚不清楚,但蛋白质组学技术的改进可能提供疾病亚群的定义,以及随后发现的生物标志物和每个亚群内的靶向分析。
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来源期刊
Current opinion in lipidology
Current opinion in lipidology 医学-内分泌学与代谢
CiteScore
6.70
自引率
4.50%
发文量
64
审稿时长
6-12 weeks
期刊介绍: With its easy-to-digest reviews on important advances in world literature, Current Opinion in Lipidology offers expert evaluation on a wide range of topics from six key disciplines including nutrition and metabolism, genetics and molecular biology, and hyperlipidaemia and cardiovascular disease. Published bimonthly, each issue covers in detail the most pertinent advances in these fields from the previous year. This is supplemented by a section of Bimonthly Updates, which deliver an insight into new developments at the cutting edge of the disciplines covered in the journal.
期刊最新文献
Prevention of cardiometabolic diseases through dietary modifications. Recent advances in applying metabolomics to uncover dietary impact on cardiometabolic health. Preeclampsia and fetal growth restriction: does novel proteomics reveal immunological possible candidate biomarkers? Atherogenic low-density lipoprotein and cardiovascular risk. The potential of circulating nonesterified fatty acids and sphingolipids in the biological understanding of cognitive decline and dementia.
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