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DIABETIC
NEPHROPATHY
DR. RAVI PATEL
INTRODUCTION
• Global public health problem affects 300 million
people worldwide & expected to 552 million by 2030
• Global mortality is 5.1 million per year majority from
cardiovascular disease
(1 Death every 6 seconds)
• India has largest number of diabetics in the world.
25-40% of these develop End Stage Renal Disease.
• One of the most serious microvascular complication
of DM
• DN occur in T1DM, T2DM & other forms of Diabetes
DEFINITION
• Structural & Functional renal damage
manifested as clinically detected Albuminuria
in the presence of normal or abnormal GFR
• Triad:- Albuminuria
(>300mg/24h or >300mg/gm of creatinine)
HTN
Declining renal function (GFR)
RISK FACTORS
• Inadequate Glucose Control
• High blood pressure
• Dyslipidemia
• Genetic Factor
• Smoking
• Pregnancy
• Age
• Race
Natural History of Kidney
Disease In Diabetic
Nephropathy
5 STAGES
Time (yrs) 0 5 20 30
Onset of
Diabetes
Onset of
Proteinuria
End Stage
Renal
Disease
Hypertension
OVERT NEPHROPATHY
Rising S Cr,
Decreasing GFR
INCIPIENT NEPHROPATHY
Hyperfiltration,
microalbuminuria,
rising blood pressure
PRECLINICAL
NEPHROPATHY
Stage 1 (Early Diabetes)
• Hyperglycemia leads to increased kidney
filtration (Hyperfiltration)
• This is due to osmotic load and toxic effects of
high sugar levels on kidney cells
• Increased Glomerular Filtration Rate
(GFR >90ml/min) with enlarged kidneys
Stage 2 (Developing Diabetes)
• Clinically silent phase with continued hyperfiltration
and hypertrophy
• The GFR remains elevated or has returned to normal
(GFR 60-89ml/min) but glomerular damage has
progressed to significant microalbuminuria.
(30-300mg/24hr)
• Significant microalbuminuria will progress to end-
stage renal disease (ESRD).
• Therefore, all diabetes patients should be screened
for microalbuminuria on a routine basis.
Stage 3 (Overt Diabetes)
• Glomerular damage has progressed to clinical
albuminuria (>300mg/24h) with
GFR 30-59ml/min.
• Basement membrane thickening due to AGEP
(Advanced glycation end products)
• Urine is “Dipstick positive"
• Hypertension typically develops during this
stage
Stage 4 (Late-stage Diabetes)
• Glomerular damage continues with increasing
amounts of protein albumin in the urine.
• The kidneys filtering ability has begun to
decline steadily and blood urea nitrogen(BUN)
and creatinine (Cr) has begun to increase.
• The glomerular filtration rate(GFR) decreases
further more with GFR 15-29ml/min.
• Almost all patients have hypertension at this
stage.
Stage 5 (ESRD or CKD)
• GFR has fallen to <15 ml/min and renal
replacement therapy required (hemodialysis,
peritoneal dialysis, kidney transplantation)
Luis-Rodríguez D, Martínez-Castelao A, Górriz JL, Álvaro FD, Navarro-González JF. Pathophysiological role and
therapeutic implications of inflammation in diabetic nephropathy. World J Diabetes 2012; 3(1): 7-18
SCREENING METHODS
Algorithm
Urine dipstick for protein
(a) Type 1 : 5 years afterdiagnosis
or earlier in the presence of other
cardiovascular risk factos
(b) Type 2 : at the time of diagnosis
NEGATIVE POSITIVE
(urine protein >300mg/l)
on 2 separate occasions (exclude
other causes e.g. UTI, CCF etc.)
Overt nephropathy
Quantify excretion rate
e.g. 24-hr urine protein
POSITIVE
Screen for microalbuminuria
on early morning spot urine
Retest twice in 3 –6 months (exclude
other causes e.g. UTI, CCF etc.)
NEGATIVE
If 2 of 3 tests are positive, diagnosis
of microalbuminuria is established
3-6 monthly follow-up of
microalbuminuria
Optimise glycaemic control
Strict BP control
ACEI/ARB
Stop smoking
Lifestyle modification
Treat hyperlipidaemia
Avoid excessive protein
intake
Monitor renal function
Monitor for other diabetic
endorgan damage
Yearly test
Albumin Excretion
SPECIMEN COLLECTED
24hr collection
(mg/24h)
Timed collection
(μg/min)
First voided morning specimen
UrineAlbumin
concentration
(mg/l)
Urine ACR
Albumin:Creatinine
ratio* (mg/gm)
Normoalbuminuria <30 <20 <20 <30
Microalbuminuria 30-300 20-200 20-200 30-300
Overt proteinuria >300 >200 >200 >300
Microalbuminuria
• 1st sign of nephropathy
• 30-300mg/24hr Urine sample
• Powerful predictor of CVD and mortality
• Earlier 80% pts progress to clinical
albuminuria but due to multifactorial
intervention this has reduced to 20%.
Clinical Albuminuria
• Sensitive marker of CKD & CVD
• 1st indicator of DN
• >300mg/24hr Urine sample
• Increase transglomerular pressure gradient
Loss of negative charged in GBM
Increase GBM pore size
• Majority pts progress to ESRD
Increases AER Decreases AER
 Strenuous exercise
 Poorly controlled DM
 Heart failure
 UTI
 Acute febrile illness
 Uncontrolled HTN
 Haematuria
 Menstruation
 Pregnancy
 NSAIDs
 ACE inhibitors
 ARBs
Factors affecting urinary albumin excretion
Other Markers
• Cystatin C
• Transferrin
• Type IV collagen
• Ceruloplasmin
• Fibronectin
• NGAL(Neutrophil gelatinase associated lipocalin)
• KIM
• Liver fatty acid binding protein
• B-microglobulin
• A-1 macroglobulin
MANAGEMENT
• Glycemic control
• Blood pressure control
• Blood lipid modifiers
• Dietary protein & salt restriction
• Smoking cessation
• Management of anemia
• Fluid management
• Cardiovascular disease screening
• No Nephrotoxics (NSAIDS, Contrast,Aminoglycosides)
• Drug dose adjustment
• Options of renal replacement
• Treat infections properly
• Vaccination
• Early referral to Nephrologist
Diabetes Mellitus
• Drugs contraindicated: Metformin
• Preferably not used: Glibenclamide
• Can be used: Glimiperide, Glipizide,
Repaglinide, Pioglitazone,
• Preferable: Insulin, SGLT 2 inhibitors, DPP4
inhibitors, GLP1 analogues
Target : HbA1c <7 %, FBS: <100 mg/dl, PPBS<140 mg/dl
Hypertension
Systemic BP reduction Intra-glomerular BP reduction
Anti-proteinuric effect
Blood pressure control
Beta blockers
Alpha -blockers
Vasodilators
ARB
ACEi
Preservation of other target organs Preservation of kidneys
Target BP <130/80 mmHg
Recommendations
• Nonpregnant patient with micro- or macroalbuminuria either ACE inhibitors
or ARBs should be used (A)
• In patients with type 1 diabetes, hypertension, and any degree of
albuminuria, ACE inhibitors have been shown to delay progression of
nephropathy (A)
• In patients with type 2 diabetes, hypertension, and
microalbuminuria, Both ACE inhibitors and ARBs have been
shown to delay progression to macroalbuminuria (A)
• Reduction of protein intake may improve measures of renal function (urine
albumin excretion rate, GFR)
• When ACE inhibitors, ARBs, or Diuretics are used, monitor serum creatinine,
potassium levels for development of acute kidney disease, hyperkalemia.
Anemia
• May occur when GFR < 50 % & almost always
present when GFR < 30 %
• Correct deficiencies
Iron, Folic acid, Vit B12, Pyridoxine
• Erythropoietin 75 - 150 IU/kg SC
– With Iron supplements
– Expensive therapy Rs. 8 - 10, 000 / month
– Hb % maintained at 11 – 12
– > 13 in pts with CAD
Vaccination
• Hepatitis B
• Pneumococcal vaccine
• Influenza vaccine
Fluid management
Many diabetics have nephrotic state and severe
edema and need salt & fluid restriction
600 - 800 ml / day
equal to UOP
• Severe edema
• Mild to moderate
• No edema UOP + insensible
losses
Renal Replacement Therapy
• Hemodialysis
• Peritoneal dialysis
• Renal transplantation
Peritoneal dialysis
Advantages
• Slow, gentle
• Round the clock clearance
• Greater salt, fluid and
dietary freedom
• Mobility
• No need for vascular
access
Disadvantages
• Metabolic problems and some
mechanical problems
• Peritonitis
Diabetic nephropathy
Diabetic nephropathy

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Diabetic nephropathy

  • 3. • Global public health problem affects 300 million people worldwide & expected to 552 million by 2030 • Global mortality is 5.1 million per year majority from cardiovascular disease (1 Death every 6 seconds) • India has largest number of diabetics in the world. 25-40% of these develop End Stage Renal Disease. • One of the most serious microvascular complication of DM • DN occur in T1DM, T2DM & other forms of Diabetes
  • 5. • Structural & Functional renal damage manifested as clinically detected Albuminuria in the presence of normal or abnormal GFR • Triad:- Albuminuria (>300mg/24h or >300mg/gm of creatinine) HTN Declining renal function (GFR)
  • 7. • Inadequate Glucose Control • High blood pressure • Dyslipidemia • Genetic Factor • Smoking • Pregnancy • Age • Race
  • 8. Natural History of Kidney Disease In Diabetic Nephropathy 5 STAGES
  • 9. Time (yrs) 0 5 20 30 Onset of Diabetes Onset of Proteinuria End Stage Renal Disease Hypertension OVERT NEPHROPATHY Rising S Cr, Decreasing GFR INCIPIENT NEPHROPATHY Hyperfiltration, microalbuminuria, rising blood pressure PRECLINICAL NEPHROPATHY
  • 10.
  • 11. Stage 1 (Early Diabetes) • Hyperglycemia leads to increased kidney filtration (Hyperfiltration) • This is due to osmotic load and toxic effects of high sugar levels on kidney cells • Increased Glomerular Filtration Rate (GFR >90ml/min) with enlarged kidneys
  • 12. Stage 2 (Developing Diabetes) • Clinically silent phase with continued hyperfiltration and hypertrophy • The GFR remains elevated or has returned to normal (GFR 60-89ml/min) but glomerular damage has progressed to significant microalbuminuria. (30-300mg/24hr) • Significant microalbuminuria will progress to end- stage renal disease (ESRD). • Therefore, all diabetes patients should be screened for microalbuminuria on a routine basis.
  • 13. Stage 3 (Overt Diabetes) • Glomerular damage has progressed to clinical albuminuria (>300mg/24h) with GFR 30-59ml/min. • Basement membrane thickening due to AGEP (Advanced glycation end products) • Urine is “Dipstick positive" • Hypertension typically develops during this stage
  • 14. Stage 4 (Late-stage Diabetes) • Glomerular damage continues with increasing amounts of protein albumin in the urine. • The kidneys filtering ability has begun to decline steadily and blood urea nitrogen(BUN) and creatinine (Cr) has begun to increase. • The glomerular filtration rate(GFR) decreases further more with GFR 15-29ml/min. • Almost all patients have hypertension at this stage.
  • 15. Stage 5 (ESRD or CKD) • GFR has fallen to <15 ml/min and renal replacement therapy required (hemodialysis, peritoneal dialysis, kidney transplantation)
  • 16. Luis-Rodríguez D, Martínez-Castelao A, Górriz JL, Álvaro FD, Navarro-González JF. Pathophysiological role and therapeutic implications of inflammation in diabetic nephropathy. World J Diabetes 2012; 3(1): 7-18
  • 18. Algorithm Urine dipstick for protein (a) Type 1 : 5 years afterdiagnosis or earlier in the presence of other cardiovascular risk factos (b) Type 2 : at the time of diagnosis NEGATIVE POSITIVE (urine protein >300mg/l) on 2 separate occasions (exclude other causes e.g. UTI, CCF etc.) Overt nephropathy Quantify excretion rate e.g. 24-hr urine protein POSITIVE Screen for microalbuminuria on early morning spot urine Retest twice in 3 –6 months (exclude other causes e.g. UTI, CCF etc.) NEGATIVE If 2 of 3 tests are positive, diagnosis of microalbuminuria is established 3-6 monthly follow-up of microalbuminuria Optimise glycaemic control Strict BP control ACEI/ARB Stop smoking Lifestyle modification Treat hyperlipidaemia Avoid excessive protein intake Monitor renal function Monitor for other diabetic endorgan damage Yearly test
  • 19. Albumin Excretion SPECIMEN COLLECTED 24hr collection (mg/24h) Timed collection (μg/min) First voided morning specimen UrineAlbumin concentration (mg/l) Urine ACR Albumin:Creatinine ratio* (mg/gm) Normoalbuminuria <30 <20 <20 <30 Microalbuminuria 30-300 20-200 20-200 30-300 Overt proteinuria >300 >200 >200 >300
  • 20. Microalbuminuria • 1st sign of nephropathy • 30-300mg/24hr Urine sample • Powerful predictor of CVD and mortality • Earlier 80% pts progress to clinical albuminuria but due to multifactorial intervention this has reduced to 20%.
  • 21. Clinical Albuminuria • Sensitive marker of CKD & CVD • 1st indicator of DN • >300mg/24hr Urine sample • Increase transglomerular pressure gradient Loss of negative charged in GBM Increase GBM pore size • Majority pts progress to ESRD
  • 22. Increases AER Decreases AER  Strenuous exercise  Poorly controlled DM  Heart failure  UTI  Acute febrile illness  Uncontrolled HTN  Haematuria  Menstruation  Pregnancy  NSAIDs  ACE inhibitors  ARBs Factors affecting urinary albumin excretion
  • 23. Other Markers • Cystatin C • Transferrin • Type IV collagen • Ceruloplasmin • Fibronectin • NGAL(Neutrophil gelatinase associated lipocalin) • KIM • Liver fatty acid binding protein • B-microglobulin • A-1 macroglobulin
  • 25. • Glycemic control • Blood pressure control • Blood lipid modifiers • Dietary protein & salt restriction • Smoking cessation • Management of anemia • Fluid management • Cardiovascular disease screening • No Nephrotoxics (NSAIDS, Contrast,Aminoglycosides) • Drug dose adjustment • Options of renal replacement • Treat infections properly • Vaccination • Early referral to Nephrologist
  • 26.
  • 27. Diabetes Mellitus • Drugs contraindicated: Metformin • Preferably not used: Glibenclamide • Can be used: Glimiperide, Glipizide, Repaglinide, Pioglitazone, • Preferable: Insulin, SGLT 2 inhibitors, DPP4 inhibitors, GLP1 analogues Target : HbA1c <7 %, FBS: <100 mg/dl, PPBS<140 mg/dl
  • 28. Hypertension Systemic BP reduction Intra-glomerular BP reduction Anti-proteinuric effect Blood pressure control Beta blockers Alpha -blockers Vasodilators ARB ACEi Preservation of other target organs Preservation of kidneys Target BP <130/80 mmHg
  • 29. Recommendations • Nonpregnant patient with micro- or macroalbuminuria either ACE inhibitors or ARBs should be used (A) • In patients with type 1 diabetes, hypertension, and any degree of albuminuria, ACE inhibitors have been shown to delay progression of nephropathy (A) • In patients with type 2 diabetes, hypertension, and microalbuminuria, Both ACE inhibitors and ARBs have been shown to delay progression to macroalbuminuria (A) • Reduction of protein intake may improve measures of renal function (urine albumin excretion rate, GFR) • When ACE inhibitors, ARBs, or Diuretics are used, monitor serum creatinine, potassium levels for development of acute kidney disease, hyperkalemia.
  • 30. Anemia • May occur when GFR < 50 % & almost always present when GFR < 30 % • Correct deficiencies Iron, Folic acid, Vit B12, Pyridoxine • Erythropoietin 75 - 150 IU/kg SC – With Iron supplements – Expensive therapy Rs. 8 - 10, 000 / month – Hb % maintained at 11 – 12 – > 13 in pts with CAD
  • 31. Vaccination • Hepatitis B • Pneumococcal vaccine • Influenza vaccine
  • 32. Fluid management Many diabetics have nephrotic state and severe edema and need salt & fluid restriction 600 - 800 ml / day equal to UOP • Severe edema • Mild to moderate • No edema UOP + insensible losses
  • 33. Renal Replacement Therapy • Hemodialysis • Peritoneal dialysis • Renal transplantation
  • 34. Peritoneal dialysis Advantages • Slow, gentle • Round the clock clearance • Greater salt, fluid and dietary freedom • Mobility • No need for vascular access Disadvantages • Metabolic problems and some mechanical problems • Peritonitis