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Colorectal anastomotic leak: transcriptomic profile analysis.
van Praagh, J B; de Wit, J G; Olinga, P; de Haan, J J; Nagengast, W B; Fehrmann, R S N; Havenga, K.
Affiliation
  • van Praagh JB; Department of Surgery, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • de Wit JG; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • Olinga P; Pharmaceutical Technology and Biopharmacy, Department of Pharmacy, University of Groningen, Groningen, the Netherlands.
  • de Haan JJ; Department of Medical Oncology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • Nagengast WB; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • Fehrmann RSN; Department of Medical Oncology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • Havenga K; Department of Surgery, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Br J Surg ; 108(3): 326-333, 2021 04 05.
Article de En | MEDLINE | ID: mdl-33793728
ABSTRACT

BACKGROUND:

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.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Analyse de profil d&apos;expression de gènes / Désunion anastomotique / Transcriptome Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Br J Surg Année: 2021 Type de document: Article Pays d'affiliation: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Analyse de profil d&apos;expression de gènes / Désunion anastomotique / Transcriptome Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Br J Surg Année: 2021 Type de document: Article Pays d'affiliation: Pays-Bas