TY - CHAP M1 - Book, Section TI - Genomics and Acute Care Surgery A1 - Brakenridge, Scott C. A1 - Efron, Philip A. A1 - Moldawer, Lyle L. A2 - Feliciano, David V. A2 - Mattox, Kenneth L. A2 - Moore, Ernest E. PY - 2020 T2 - Trauma, 9e AB - KEY POINTSVariability in clinical phenotypes results from the following: differences in DNA sequence (genomics), RNA transcription (transcriptomics), and protein translation and structure (posttranscriptional regulation and posttranslational modification).It is estimated that only 2% of total DNA includes the code for the approximately 20,000 protein-coding genes of the human genome.Exons are the regions of DNA that are transcribed to mRNA and then translated into the amino acid structure of proteins.Histone proteins play a key role in the functional regulation of the genome.The most common type of DNA sequence variations are single base substitutions termed single nucleotide polymorphisms (SNPs).SNPs relevant to acute care surgery are found within the promotor regions of genes for Toll-like receptor 1 and tumor necrosis factor-α, both associated with increased mortality after trauma and sepsis.MicroRNAs are short single-stranded RNA fragments that downregulate gene expression when bound to messenger RNA.Postinjury systemic inflammatory response syndrome–induced early multiple organ failure is related to a “genomic storm” at the level of circulating leukocyte gene transcription and occurs simultaneously with a compensatory anti-inflammatory and immunosuppressive response.Chronic critical illness is characterized by an underlying pathophysiology of persistent inflammation, immunosuppression, and catabolism.A 63-gene transcriptomic metric score within 24 hours after injury has been shown to be associated with subsequent adverse outcomes including multiple organ dysfunction, length of mechanical ventilation and hospital stay, and infection rates. SN - PB - McGraw Hill CY - New York, NY Y2 - 2024/04/17 UR - accesssurgery.mhmedical.com/content.aspx?aid=1175130719 ER -