J Clin Endocrinol Metab
December 2023
Context: Younger onset of type 2 diabetes (T2D) was associated with higher risks of vascular complications and mortality.
Objective: To prospectively assess risk profiles for incident T2D stratified by age at onset.
Methods: A total of 471 269 participants free of T2D at baseline were included from the UK Biobank.
Background: Long non-coding RNAs (lncRNAs) have been reported to play vital roles in diabetic nephropathy (DN). The aim of this study was to explore the function of mechanism of lncRNA KCNQ1 opposite strand/antisense transcript 1 (KCNQ1OT1) in DN.
Methods: DN cell models were established using high glucose (HG) treatment in human glomerular mesangial cells (HGMC) and human renal glomerular endothelial cells (HRGEC).
Diabetic nephropathy (DN), a frequent diabetes complication, has complex pathogenesis. Circular RNAs (circRNAs) circ_0000712 has been reported to be upregulated in kidney tissues and high glucose (HG)-inducted Mesangial cells (MCs). This study is designed to explore the role and mechanism of circ_0000712 in the HG-inducted MCs injury in DN.
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