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Diabetic type 2 patients compared to nondiabetic patients exhibit an increased risk of developing diabetic kidney disease (DKD), the leading cause of end-stage renal disease. Hyperglycemia, hypertension, oxidative stress (OS), and genetic background are some of the mechanisms and pathways implicated in DKD pathogenesis. However, data on OS pathway susceptibility genes show limited success and conflicting or inconclusive results. Our study is aimed at exploring OS pathway genes and variants which could be associated with DKD. We recruited 121 diabetes mellitus type 2 (DM2) patients with DKD (cases) and 220 DM2, non-DKD patients (control) of Greek origin and performed a case-control association study using genome-wide association data. PLINK and EIGENSOFT were used to analyze the data. Our results indicate 43 single nucleotide polymorphisms with their 21 corresponding genes on the OS pathway possibly contributing or protecting from DKD: SPP1, TPO, TTN, SGO2, NOS3, PDLIM1, CLU, CCS, GPX4, TXNRD2, EPHX2, MTL5, EPX, GPX3, ALOX12, IPCEF1, GSTA, OXR1, GPX6, AOX1, and PRNP. Therefore, a genetic OS background might underlie the complex pathogenesis of DKD in DM2 patients.
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Athanasios Roumeliotis
Aristotle University of Thessaloniki
Stefanos Roumeliotis
Aristotle University of Thessaloniki
Fotis Tsetsos
Democritus University of Thrace
Oxidative Medicine and Cellular Longevity
SHILAP Revista de lepidopterología
Purdue University West Lafayette
Indiana University – Purdue University Indianapolis
Aristotle University of Thessaloniki
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Roumeliotis et al. (Fri,) studied this question.
synapsesocial.com/papers/69daa46b2d871caad68359c5 — DOI: https://doi.org/10.1155/2021/2531062
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