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Diabetic Nephropathy

Diabetic Nephropathy. Diabetic Nephropathy A clinical syndrome. DM + Persistent albuminuria, Worsening proteinuria, Hypertension & progressive renal failure. Diabetic nephropathy (DN) is a major cause of ESRD, and the incidence of diabetes mellitus is rising rapidly. Objectives.

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Diabetic Nephropathy

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  1. Diabetic Nephropathy

  2. Diabetic NephropathyA clinical syndrome DM + Persistent albuminuria, Worsening proteinuria, Hypertension & progressive renal failure

  3. Diabetic nephropathy (DN) is a major cause of ESRD, and the incidence of diabetes mellitus is rising rapidly.

  4. Objectives • Prevalence of diabetic kidney disease • Pathogenesis of diabetic nephropathy • Clinical course of diabetic nephropathy • Slowing the progression of nephropathy • Screening for early nephropathy

  5. Causes of End Stage Renal Disease USRDS 1993 Annual Data Report

  6. Diabetic Nephropathy • The most common cause of ESRD in USA. • However one needs to keep in mind all diabetic patients with ESRD do not have DN as underlying cause of ESRD.

  7. Diabetic Nephropathy • Mortality of ESRD patients with Diabetes Mellitus is higher than in ESRD patients without Diabetes. • This higher mortality is due to increase in Cardiovascular, cerebro-vascular, peripheral vascular and infection related morbidity.

  8. Patient Survival on Dialysis by Cause of Renal Failure From UpToDate v 6.2; Data from USRDS 1995 Annual Report

  9. Diabetic Nephropathy • DN occurs in 35-40% of patients with type I diabetes (IDDM) whereas it occurs only in 15-20% of patients with type II diabetes (NIDDM). • Definition or Criteria for diagnosis of DN • Presence of persistent proteinuria in sterile urine of diabetic patients with concomitant diabetic retinopathy and hypertension.

  10. D.N.- Pathogenesis • Familial - Genetic • Only 35-40% patients with IDDM develop DN. • There is an increased risk of DN in a patient with family member having DN.

  11. D.N.- Pathogenesis • Glycemic Control-in both expt & human • DN does not occur in euglycemic patients. • Confirmed role of hyperglycemia in pathogenesis of DN. • Renal transplant with early DN showed structural recovery in euglycemicreceipient. (Abouna)

  12. Strict Glycemic Control PreventsMicroalbuminuria in Type 1 Diabetes mellitus From UpToDate v 6.2; Data from the DCCT Research Group, NEJM(1993) 329:977.

  13. D.N.- Pathogenesis • GlomerularHyperfiltration • GlomerularHypertension • GlomerularHypertrophy • GBM thickening • Mesangial Expansion

  14. D.N.- Pathogenesis • Renal lesions mainly related to extracellular matrix accumulation - Occurs in glomerular & tubular basement membrane - Principal cause of mesangial expansion

  15. D.N.- Pathogenesis • Extracellular matrix accumulation - Imbalance between synthesis & degradation of ECM components - Linkage between glucose concentration & ECM accumulation - Transforming growth factor-Beta associated with increased production of ECM molecules

  16. D.N.- Pathogenesis • Extracellular matrix accumulation - TGF-B can down regulate synthesis of ECM degrading enzymes & upregulate inhibitors of these enzymes - Angiotensin II can stimulate ECM synthesis through TGF-B activity - Hyperglycemia activates protein kinase C, stimulating ECM production through cyclic AMP Pathway

  17. Diffuse and Nodular Glomerulosclerosis in Diabetic Nephropathy

  18. Diabetic Nephropathy

  19. Advanced Diabetic Glomerulosclerosis

  20. Diabetic Nephropathy

  21. Diabetic NephropathyGlomerular Basement Membrane Thickening From: UpToDate v 6.2 Courtesy H. Rennke, M.D.

  22. Natural Course of D.N. • Stage 1: Renal hypertrophy - hyperfunction • Stage 2 : Presence of detectable glomerular lesion with normal albumin excretion rate & normal blood pressure • Stage 3 : Microalbuminuria • Stage 4 : Dipstick positive proteinuria • Stage 5 : End stage renal disease

  23. Natural History of IDDM Clinical type 1 diabetes Functional changes* Structural changes† Microalbuminuria Proteinuria Rising blood pressure Proteinuria Rising serum creatinine levels End-stage renal disease CV events 2 5 10 20 30 Onset of diabetes Years * Kidney size ­, GFR ­. † GBM thickening ­, mesangial expansion ­

  24. Natural History of NIDDM Clinical type 2 diabetes Functional changes* Structural changes† Rising blood pressure Microalbuminuria Proteinuria Rising serum creatinine levels End-stage renal disease Cardiovascular death Onset of diabetes 2 5 10 20 30 Years * Kidney size ­, GFR ­. † GBM thickening ­, mesangial expansion ­

  25. D.N.- Pathogenesis • Hypertension - in both expt & human • Hypertension follows 8-10 years of hyperglycemia in IDDM patients but it is frequently present at the diagnosis of NIDDM. • Many experimental & human studies have shown HTN accelerating progressive renal injury in DN.

  26. Glomerulus Bowman’s Capsule Afferent arteriole Efferent arteriole • Glomerular pressure • (¯ GFR) Effect of Angiotensin Blockade Proteinuria Angiotensin II A II blockade:

  27. ACE-I Is More Renoprotective Than Conventional Therapy in Type 1 Diabetes 100 75 50 25 0 Baseline creatinine >1.5 mg/dL % with doubling of baseline creatinine Placebo n=202 P<.001 Captopril n=207 0 1 2 3 4 Years of follow-up Lewis EJ, et al. N Engl J Med. 1993;329(20):1456-1462.

  28. Losartan could delay ESRD by 1.5-2 years. Brenner BM et al.N Engl J Med 345:861-869, 2001

  29. Irbesartan in patients with type 2 diabetes & microalbuminuria study • 590 NIDDM patients with HTN and microalbuminuria with nearly normal GFR. • Randomly assigned to placebo, 150 mg or 300 mg of irbesartan for 2 years. • Primary outcome was time to the onset of diabetic nephropathy (urinary albumin excretion rate >200 mcg/min and at least 30% greater albuminuria) • 14.9% patients on placebo group, 9.7% of irbesartan 150mg group and 5.2% of irbesartan 300 mg group reached the primary point. • (Parving et al, NEJM, 2001)

  30. ARBs in NIDDM,HTN & microalbuminuria-Parving 2001

  31. Lewis et al NEJM 2001

  32. ACE-I + Verapamil: Additive Reduction of Proteinuria in Type 2 Diabetes at 1 Year Trandolapril (2.9 mg/d) + Verapamil (219 mg/d) Trandolapril (5.5 mg/d) Verapamil (315 mg/d) n=12 n=11 n=14 -27% -33% Percent reduction -62% * *p <0.001 combination vs either monotherapy Bakris GL, et al. Kidney Int. 1998;54:1283-1289. Reprinted by permission, Blackwell Science, Inc.

  33. D.N.-Management • ACEI or AII RB- in both expt & human • Reduce glomerular hypertension • Reduce proteinuria independent of hemodynamic effects • Reduce glomerular hypertrophy • well tolerated apart from hyperkalemia & worsening of anemia in severe CRF • Cautious use in presence of severe renovascular disease

  34. DN: ADA Position Statement Screening: Perform an annual test for the presence of microalbuminuria in • type 1 diabetic patients who have had diabetes > 5 years and • all type 2 diabetics patients starting at diagnosis. Treatment: • In the treatment of albuminuria/nephropathy both ACE inhibitors and ARBs can be used: • In hypertensive and nonhypertensive type 1 diabetic patients with microalbuminuria or clinical albuminuria, ACE inhibitors are the initial agents of choice • In hypertensive type 2 diabetic patients with microalbuminuria or clinical albuminuria, ARBs are the initial agents of choice. • If one class is not tolerated, the other should be substituted American Diabetes Association: Position Statement Diabetes Care 25:S85-S89, 2002

  35. Better blood pressure control reduces… Strokes by > one third Serious deterioration of vision by > one third Death related to diabetes by one third Better glucose control reduces… Early kidney damage by one third Major diabetic eye disease by one fourth UK Prospective Diabetes Study (UKPDS) Major Results: Powerful Risk Reductions Turner RC, et al. BMJ. 1998;317:703-713.

  36. National Kidney Foundation Recommendations on Treatment of HTN and Diabetes • Blood pressure goal: 130/80 mmHg • Target blood pressure: 125/75 for patients with >1 gram/day proteinuria • Blood pressure lowering medications should reduce both blood pressure + proteinuria • Therapies that reduce both blood pressure and proteinuria have been known to reduce renal disease progression and incidence of ischemic heart disease Bakris GL, et al. Am J Kidney Dis. 2000;36(3):646-661.

  37. Cholesterol Lowering Therapy and Diabetic Nephropathy

  38. Management of ESRD due to DN • Early planning of Vascular Access • Both HD & PD could be appropriate modalities. • Early initiation of Dialysis at GFR 18-20 mls/min. • Renal Transplantation • Combined Renal & Pancreatic Transplantation for IDDM.

  39. Hypertension BP < 130/80 mmHg Hypercholesterolemia LDL < 100 mg/dL Hyperglycemia Hgb A1C < 7.0 % Treatment Objectives to Prevent Macrovascular Disease in Diabetic Patients American Diabetes Association Clinical Practice Recommendations. Diabetes Care. 2001;24(suppl1):S1-S133.

  40. Management of HTN and Chronic Renal Disease (CRD) in Diabetics • Reduce BP to <130/80 mmHg • Use multiple antihypertensive drugs (ACEI, ARB, diuretic, CCB, beta-blocker) • Maximal reduction of proteinuria • Treat hyperlipidemia (LDL <100 mg/dL) • Control Hgb A1C to <7% • Low salt diet (<2 gm NaCl/day) • Stop cigarette smoking

  41. Metformin

  42. Hyperuricemia ?? Allopurinol ??

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