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Classification of CKD with diabetes. DKD diabetic kidney disease, NDKD non-DKD, ORG obesity-related glomerulopathy, ADPKD autosomal dominant polycystic kidney disease

Classification of CKD with diabetes. DKD diabetic kidney disease, NDKD non-DKD, ORG obesity-related glomerulopathy, ADPKD autosomal dominant polycystic kidney disease

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The natural history of typical and classical “diabetic nephropathy” has been described as high levels of albuminuria and subsequent renal function decline. However, recent decades, the cases, who show the reduced glomerular filtration rate (GFR) without the progression of albuminuria, has been increased. “Diabetic kidney disease (DKD)” is a concept...

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... The natural history of typical and classical "diabetic nephropathy" has been described as high levels of albuminuria and subsequent declined renal function. However, in recent decades, the diabetic cases, who show the reduced estimated glomerular filtration rate (eGFR) without the progression of albuminuria, have been increased [1], which may be explained by that diabetic kidney disease (DKD) includes hypertensive nephrosclerosis, aging, obesity, and atherosclerosis-related renal diseases, in addition to classical diabetic nephropathy. According to the American Diabetes Association (ADA) and Kidney Disease Improving Global Outcomes (KDIGO) guidelines, sodium-glucose co-transporter 2 inhibitors (SGLT2is) are now recommended the first-line agents for patients with type 2 diabetes, chronic kidney disease (CKD), and eGFR ≥ 20 mL/min/1.73 ...
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Diabetic kidney disease (DKD) includes hypertensive nephrosclerosis, aging, obesity, and atherosclerosis-related renal diseases, in addition to classical diabetic nephropathy. Sodium-glucose co-transporter 2 inhibitors (SGLT2is) have been approved for diabetic and non-diabetic patients at risk of chronic kidney disease progression. As the main mechanism for SGLT2i-mediated improvement of renal function, the normalization of tubulo-glomerular feedback (TGF) has been proposed. Enhanced TGF and resulting glomerular hypertension are observed in diabetic patients, and SGLT2is normalize TGF, reducing the intraglomerular pressure, which may reduce albuminuria and improve renal function. A type 2 diabetic patient with DKD complicated with hypertensive nephrosclerosis, whose renal function was deteriorated by SGLT2i and improved by glucagon-like peptide-1 receptor agonists (GLP-1RAs), was presented. In patients with hypertensive nephrosclerosis such as this case, the normalization of TGF by SGLT2i may further reduce afferent arteriolar blood flow which may worsen glomerular ischemia, resulting in deterioration of renal function. GLP-1RAs have no effect on TGF and have multiple effects to improve vascular endothelial function, which may be associated with an improvement in renal function in this patient.
... 4 However, previous studies often define patients with DM with CKD as diabetic nephropathy or simply CKD, leading to underexplored medical perspectives on diabetes with other CKD subtypes. 5 Furthermore, it has been reported that up to one-third of patients with newly diagnosed diabetes already had kidney damage, implying that the effect of hyperglycemia on the occurrence of CKD may initiate before glucose levels reach the diagnostic threshold. 6 7 Nevertheless, the effect of non-diabetic hyperglycemia, namely prediabetes, remains largely unclear. ...
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Introduction Cohort evidence of the association of diabetes mellitus (DM) with chronic kidney disease (CKD) is limited. Previous studies often describe patients with kidney disease and diabetes as diabetic kidney disease (DKD) or CKD, ignoring other subtypes. The present study aimed to assess the prospective association of diabetes status (no diabetes, pre-diabetes, screened diabetes, previously diagnosed controlled/uncontrolled diabetes with/without antidiabetic treatment) and random plasma glucose (RPG) with CKD risk (including CKD subtypes) among Chinese adults. Research design and methods The present study included 472 545 participants from the China Kadoorie Biobank, using baseline information on diabetes and RPG. The incident CKD and its subtypes were collected through linkage with the national health insurance system during follow-up. Cox regression models were used to calculate the HR and 95% CI. Results During 11.8 years of mean follow-up, 5417 adults developed CKD. Screened plus previously diagnosed diabetes was positively associated with CKD (HR=4.52, 95% CI 4.23 to 4.83), DKD (HR=33.85, 95% CI 29.56 to 38.76), and glomerulonephritis (HR=1.66, 95% CI 1.40 to 1.97). In those with previously diagnosed diabetes, participants with uncontrolled diabetes represented higher risks of CKD, DKD, and glomerulonephritis compared with those with controlled RPG. The risk of DKD was found to rise in participants with pre-diabetes and increased with the elevated RPG level, even in those without diabetes. Conclusions Among Chinese adults, diabetes was positively associated with CKD, DKD, and glomerulonephritis. Screen-detected and uncontrolled DM had a high risk of CKD, and pre-diabetes was associated with a greater risk of DKD, highlighting the significance of lifelong glycemic management.
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