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• W2100852010 abstract "Genetic variations in TGF- β and IFN- γ may interfere with proinflammatory cytokine production and, consequently, may be involved with inflammatory diseases, as acute kidney injury (AKI). We considered that genetic polymorphisms of these cytokines may have a crucial role in the outcome of critically ill patients. To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF- β , and rs2430561 (+874 T/A) from IFN- γ may be a risk factor for ICU patients to the development of AKI and/or death. In a prospective nested case-control study, were included 139 ICU patients who developed AKI, 164 ICU patients without AKI, and 244 healthy individuals. We observed a higher frequency to T/A genotype for IFN- γ (intermediate producer phenotype) and higher frequency of TT GG and TC GG genotype (high producer) for TGF- β polymorphism in overall population. However, these polymorphisms have not been shown as a predictor of risk for AKI and death. We found an increased prevalence of high and intermediate producer phenotypes from TGF- β and IFN- γ , respectively, in patients in ICU setting. However, the studied genetic polymorphism of the TGF- β and IFN- γ was not associated as a risk factor for AKI or death in our population." @default.
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• W2100852010 date "2014-01-01" @default.
• W2100852010 modified "2023-10-02" @default.
• W2100852010 title "Frequency of TGF-<b><i>β</i></b>and IFN-<b><i>γ</i></b>Genotype as Risk Factors for Acute Kidney Injury and Death in Intensive Care Unit Patients" @default.
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• W2100852010 doi "https://doi.org/10.1155/2014/904730" @default.
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