Huang Jiamin, Chen Yi, Guo Zaiwen, Yu Yanzhen, Zhang Yi, Li Pingsong, Shi Lei, Lv Guozhong, Sun Bingwei
Department of Burns and Plastic Surgery, Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou 215002, Jiangsu Province, China.
Department of Burns and Plastic Surgery, Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian 223300, Jiangsu, China.
Burns Trauma. 2023 Jan 15;11:tkac050. doi: 10.1093/burnst/tkac050. eCollection 2023.
Early detection, timely diagnosis and rapid response are essential for case management and precautions of burn-associated sepsis. However, studies on indicators for early warning and intervention have rarely been conducted. This study was performed to better understand the pathophysiological changes and targets for prevention of severe burn injuries.
We conducted a multi-center, prospective multi-omics study, including genomics, microRNAomics, proteomics and single-cell transcriptomics, in 60 patients with severe burn injuries. A mouse model of severe burn injuries was also constructed to verify the early warning ability and therapeutic effects of potential markers.
Through genomic analysis, we identified seven important susceptibility genes (DNAH11, LAMA2, ABCA2, ZFAND4, CEP290, MUC20 and ENTPD1) in patients with severe burn injuries complicated with sepsis. Through plasma miRNAomics studies, we identified four miRNAs (hsa-miR-16-5p, hsa-miR-185-5p, hsa-miR-451a and hsa-miR-423-5p) that may serve as early warning markers of burn-associated sepsis. A proteomic study indicated the changes in abundance of major proteins at different time points after severe burn injury and revealed the candidate early warning markers S100A8 and SERPINA10. In addition, the proteomic analysis indicated that neutrophils play an important role in the pathogenesis of severe burn injuries, as also supported by findings from single-cell transcriptome sequencing of neutrophils. Through further studies on severely burned mice, we determined that S100A8 is also a potential early therapeutic target for severe burn injuries, beyond being an early warning indicator.
Our multi-omics study identified seven susceptibility genes, four miRNAs and two proteins as early warning markers for severe burn-associated sepsis. In severe burn-associated sepsis, the protein S100A8 has both warning and therapeutic effects.
早期发现、及时诊断和快速反应对于烧伤相关脓毒症的病例管理和预防至关重要。然而,关于早期预警和干预指标的研究很少。本研究旨在更好地了解严重烧伤的病理生理变化及预防靶点。
我们对60例严重烧伤患者进行了一项多中心、前瞻性多组学研究,包括基因组学、微小RNA组学、蛋白质组学和单细胞转录组学。还构建了严重烧伤小鼠模型,以验证潜在标志物的早期预警能力和治疗效果。
通过基因组分析,我们在合并脓毒症的严重烧伤患者中鉴定出7个重要的易感基因(DNAH11、LAMA2、ABCA2、ZFAND4、CEP290、MUC20和ENTPD1)。通过血浆微小RNA组学研究,我们鉴定出4种微小RNA(hsa-miR-16-5p、hsa-miR-185-5p、hsa-miR-451a和hsa-miR-423-5p),它们可能作为烧伤相关脓毒症的早期预警标志物。蛋白质组学研究表明严重烧伤后不同时间点主要蛋白质丰度的变化,并揭示了候选早期预警标志物S100A8和SERPINA10。此外,蛋白质组学分析表明中性粒细胞在严重烧伤的发病机制中起重要作用,中性粒细胞单细胞转录组测序结果也支持这一点。通过对严重烧伤小鼠的进一步研究,我们确定S100A8不仅是早期预警指标,也是严重烧伤的潜在早期治疗靶点。
我们的多组学研究鉴定出7个易感基因、4种微小RNA和2种蛋白质作为严重烧伤相关脓毒症的早期预警标志物。在严重烧伤相关脓毒症中,蛋白质S100A8具有预警和治疗双重作用。