AUTHOR=Schimunek Lukas , Namas Rami A. , Yin Jinling , Barclay Derek , Liu Dongmei , el-Dehaibi Fayten , Abboud Andrew , Cohen Maria , Zamora Ruben , Billiar Timothy R. , Vodovotz Yoram TITLE=MPPED2 Polymorphism Is Associated With Altered Systemic Inflammation and Adverse Trauma Outcomes JOURNAL=Frontiers in Genetics VOLUME=10 YEAR=2019 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2019.01115 DOI=10.3389/fgene.2019.01115 ISSN=1664-8021 ABSTRACT=
Trauma is a leading cause of morbidity and mortality. It is unclear why some trauma victims follow a complicated clinical course and die, while others, with apparently similar injury characteristics, do not. Interpatient genomic differences, in the form of single nucleotide polymorphisms (SNPs), have been associated previously with adverse outcomes after trauma. Recently, we identified seven novel SNPs associated with mortality following trauma. The aim of the present study was to determine if one or more of these SNPs was also associated with worse clinical outcomes and altered inflammatory trajectories in trauma survivors. Accordingly, of 413 trauma survivors, DNA samples, full blood samples, and clinical data were collected at multiple time points in the first 24 h and then daily over 7 days following hospital admission. Subsequently, single-SNP groups were created and outcomes, such as hospital length of stay (LOS), ICU LOS, and requirement for mechanical ventilation, were compared. Across a broad range of Injury Severity Scores (ISS), patients carrying the rs2065418 TT SNP in the metallophosphoesterase domain-containing 2 (