found that miR-182, miR-143, miR-145, miR-146a, miR-150, and miR-155 were dysregulated in sepsis patients, and dysregulated miRNAs have immunological associations with clinical disease in sepsis, especially, the decrease in miR-146a correlated with elevated IL-6 levels and monocyte proliferation, indicating immunological associations with clinical disease in sepsis (20, 39, 48–50). This evidence concerns the gene IL6 and Sepsis.