Literature DB >> 26676665

Improvements in the Management of Diabetic Nephropathy.

Evangelia Dounousi1, Anila Duni1, Konstantinos Leivaditis2, Vasilios Vaios2, Theodoros Eleftheriadis2, Vassilios Liakopoulos2.   

Abstract

The burden of diabetes mellitus is relentlessly increasing. Diabetic nephropathy is the most common cause of end-stage renal disease (ESRD) worldwide and a major cause of morbidity and mortality in patients with diabetes. The current standard therapy of diabetic nephropathy involves intensive treatment of hyperglycemia and strict blood pressure control, mainly via blockade of the renin-angiotensin system (RAS). Attention has been drawn to additional beneficial effects of oral hypoglycemic drugs and fibrates on other aspects of diabetic nephropathy. On the other hand, antiproteinuric effects of RAS combination therapy do not seem to enhance the prevention of renal disease progression, and it has been associated with an increased rate of serious adverse events. Novel agents, such as bardoxolone methyl, pentoxifylline, inhibitors of protein kinase C (PKC), sulodexide, pirfenidone, endothelin receptor antagonists, vitamin D supplements, and phosphate binders have been associated with controversial outcomes or significant side effects. Although new insights into the pathogenetic mechanisms have opened new horizons towards novel interventions, there is still a long way to go in the field of DN research. The aim of this review is to highlight the recent progress made in the field of diabetes management based on the existing evidence. The article also discusses novel targets of therapy, with a special focus on the major pathophysiologic mechanisms implicated in the initiation and progression of diabetic nephropathy.

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Year:  2015        PMID: 26676665      PMCID: PMC5397987          DOI: 10.1900/RDS.2015.12.119

Source DB:  PubMed          Journal:  Rev Diabet Stud        ISSN: 1613-6071


  150 in total

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Review 2.  Microalbuminuria and potential confounders. A review and some observations on variability of urinary albumin excretion.

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4.  Effects of intensive blood-pressure control in type 2 diabetes mellitus.

Authors:  William C Cushman; Gregory W Evans; Robert P Byington; David C Goff; Richard H Grimm; Jeffrey A Cutler; Denise G Simons-Morton; Jan N Basile; Marshall A Corson; Jeffrey L Probstfield; Lois Katz; Kevin A Peterson; William T Friedewald; John B Buse; J Thomas Bigger; Hertzel C Gerstein; Faramarz Ismail-Beigi
Journal:  N Engl J Med       Date:  2010-03-14       Impact factor: 91.245

5.  Rosiglitazone reduces microalbuminuria and blood pressure independently of glycemia in type 2 diabetes patients with microalbuminuria.

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Review 6.  The necessity and effectiveness of mineralocorticoid receptor antagonist in the treatment of diabetic nephropathy.

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Review 7.  Treatment and impact of dyslipidemia in diabetic nephropathy.

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8.  Addition of angiotensin receptor blockade or mineralocorticoid antagonism to maximal angiotensin-converting enzyme inhibition in diabetic nephropathy.

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9.  In patients with type 1 diabetes and new-onset microalbuminuria the development of advanced chronic kidney disease may not require progression to proteinuria.

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10.  Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes.

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Journal:  Rep Biochem Mol Biol       Date:  2021-10

3.  Assessment of angiotensin-converting enzyme inhibitor/angiotensin receptor blocker on the split renal function in the patients with primary hypertension.

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Review 4.  Diabetic nephropathy: Time to withhold development and progression - A review.

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Review 5.  Epigenetic Regulations in Diabetic Nephropathy.

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Review 6.  Oxidative Stress in Hemodialysis Patients: A Review of the Literature.

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7.  A Network Pharmacology Approach to Uncover the Mechanisms of Shen-Qi-Di-Huang Decoction against Diabetic Nephropathy.

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8.  The Effect of Vitamin D on Cellular Pathways of Diabetic Nephropathy.

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10.  LncRNA HCP5 knockdown inhibits high glucose-induced excessive proliferation, fibrosis and inflammation of human glomerular mesangial cells by regulating the miR-93-5p/HMGA2 axis.

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