Department of Surgery, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Department of Gastroenterology and Hepatology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Br J Surg. 2021 Apr 5;108(3):326-333. doi: 10.1093/bjs/znaa066.
Anastomotic leakage in patients undergoing colorectal surgery is associated with morbidity and mortality. Although multiple risk factors have been identified, the underlying mechanisms are mainly unknown. The aim of this study was to perform a transcriptome analysis of genes underlying the development of anastomotic leakage.
A set of human samples from the anastomotic site collected during stapled colorectal anastomosis were used in the study. Transcriptomic profiles were generated for patients who developing anastomotic leakage and case-matched controls with normal anastomotic healing to identify genes and biological processes associated with the development of anastomotic leakage.
The analysis included 22 patients with and 69 without anastomotic leakage. Differential expression analysis showed that 44 genes had adjusted P < 0.050, consisting of two upregulated and 42 downregulated genes. Co-functionality analysis of the 150 most upregulated and 150 most downregulated genes using the GenetICA framework showed formation of clusters of genes with different enrichment for biological pathways. The enriched pathways for the downregulated genes are involved in immune response, angiogenesis, protein metabolism, and collagen cross-linking. The enriched pathways for upregulated genes are involved in cell division.
These data indicate that patients who develop anastomotic leakage start the healing process with an error at the level of gene regulation at the time of surgery. Despite normal macroscopic appearance during surgery, the transcriptome data identified several differences in gene expression between patients who developed anastomotic leakage and those who did not. The expressed genes and enriched processes are involved in the different stages of wound healing. These provide therapeutic and diagnostic targets for patients at risk of anastomotic leakage.
结直肠手术后吻合口漏与发病率和死亡率有关。尽管已经确定了多个危险因素,但潜在机制主要未知。本研究旨在对导致吻合口漏的基因进行转录组分析。
本研究使用了一组在吻合钉结直肠吻合术中收集的吻合口部位的人类样本。对发生吻合口漏的患者和吻合口愈合正常的病例匹配对照进行转录组谱分析,以确定与吻合口漏发展相关的基因和生物学过程。
该分析包括 22 例吻合口漏患者和 69 例无吻合口漏患者。差异表达分析显示,有 44 个基因的调整 P < 0.050,包括 2 个上调基因和 42 个下调基因。使用 GenetICA 框架对 150 个上调基因和 150 个下调基因进行共功能分析显示,基因簇的形成具有不同的生物学途径富集。下调基因富集的途径涉及免疫反应、血管生成、蛋白质代谢和胶原蛋白交联。上调基因富集的途径涉及细胞分裂。
这些数据表明,发生吻合口漏的患者在手术时的基因调控水平上开始愈合过程出现错误。尽管手术时宏观外观正常,但转录组数据在发生吻合口漏和未发生吻合口漏的患者之间识别出了几个基因表达的差异。表达的基因和富集的过程涉及伤口愈合的不同阶段。这些为有吻合口漏风险的患者提供了治疗和诊断靶点。