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AETIOPATHOGENESIS
OF CKD
Group 09
DEFINITION
Diminished GFR that is persistently less
than 60ml/min/1.73m2 for at least 3
months from any cause and/or
persistent albuminuria.
. "CKD is defined as abnormalities of kidney structure or
function, present for >3 months, with implications for health,"
and requires one of two criteria documented or inferred for >3
months: either GFR <60 ml/min/1.73 m2 or markers of kidney
damage, including albuminuria.
Causes of CKD(better to refer kumar & clerk)
Congenital and inherited disease
Polycystic kidney disease (adult and infantile forms)
Medullary cystic disease
Tuberous sclerosis
Oxalosis
Cystinosis
Congenital obstructive uropathy
Glomerular disease
Primary glomerulonephritides including focal
glomerulosclerosis
Secondary glomerular disease (systemic lupus,
polyangiitis, Wegenerā€™s granulomatosis, amyloidosis,
diabetic glomerulosclerosis, accelerated hypertension,
haemolytic uraemic syndrome, thrombotic
thrombocytopenic purpura, systemic sclerosis, sickle
cell disease)
Vascular disease
Hypertensive nephrosclerosis (common in black Africans)
Renovascular disease
Small and medium-sized vessel vasculitis
Tubulointerstitial disease
Tubulointerstitial nephritis ā€“ idiopathic, due to drugs
(especially nephrotoxic analgesics), immunologically
mediated
Reflux nephropathy
Tuberculosis
Schistosomiasis
Nephrocalcinosis
Multiple myeloma (myeloma kidney)
Balkan nephropathy
Renal papillary necrosis (diabetes, sickle cell disease and
trait, analgesic nephropathy)
Chinese herb nephropathy
Urinary tract obstruction
Calculus disease
Prostatic disease
Pelvic tumours
Retroperitoneal fibrosis
Schistosomiasis
Aetiology of CKD
??
Glomerular diseases
ā€¢Primary
glomerulopathies
ā€¢Systemic
glomerulopathies
ā€¢Hereditary causes
Tubulointerstitial
pathologies
ā€¢Vascular causes
ā€¢Infectious causes
ā€¢Toxic causes
ā€¢Obstructive causes
Primary glomerulopathies
1. Acute diffuse proliferative
glomerulonephritis (post
streptococcal and non post
streptococcal)
2. Rapidly progressive
glomerulonephritis
3. Minimal change glomerular
nephropathies
4. Membranous nephropathies
5. IgA nephropathy
6. Focal proliferative glomerulonephritis
7. Chronic glomerulonephritis
Systemic
glomerulopathies
1. Systemic lupus
erythromatosis
2. Serum sickness nepritis
3. Diabetic nephropathy
4. Good pastureā€™s syndrome
5. Polyarteritis nodosa
6. Wegernerā€™s granulomatosis
7. Henoch- schonlein purpura
8. Bacterial endocarditis
Hereditary causes
1. Alportā€™s syndrome
2. Fabry disease
3. Dent disease
4. Nephronophthisis
5. Atypical haemolytic ureamic
syndrome
Vascular diseases
1. Hypertensive nephrosclerosis
2. Renal artery stenosis
3. Atheroemboli
4. Renal vein thrombosis
5. C-ANCA positive vasculitides
6. P-ANCA positive vasculitides
7. ANCA negative vasculitides
Infectious diseases
ā€¢ Chronic pyelonephritis
Toxic causes
ā€¢ Chronic analgesic nephritis (Phenacetin , Aspirin ,
Acetaminophen)
ā€¢ Prolonged exposure to lead , cadmium and uranium
Obstructive causes
ā€¢ Chronic obstruction of urinary tract due to stones , blood clots ,
tumors , strictures and enlarged prostate
Prevalence of aetiological factors of CKD
Underlying nephropathy
Reduction in nephron number
Many nephrons have failed and scared so burden
of filtration falls to fewer functioning nephrons
Remaining functional nephrons experience
increased flow and pressure per nephron
Pathogenesis of Chronic Kidney Disease
Adapt with glomerular hypertrophy and decreased arterioles resistance
Hyperfiltration
Increased glomerular permeability Increased RAAS
Increased filtration of protein
and macromolecules
Proteinurea Nephrotoxic inflammation Hypertension
and remodeling
Tubulointerstitial fibrosis and focal segment glomerular sclerosis
Reduced GFR Reduced urine output Systemic complications
Chronic Kidney Disease of
Unknown etiology
(CKDu)
What is CKDu?
ā€¢ A new form of CKD seen in epidemic proportions which is
NOT attributed to Diabetes Mellitus, Hypertension,
Glomerulonephritis or any other conventional risk factors.
ā€¢ Currently CKDu occurs chiefly in Sri Lanka (Mainly North
Central province), El Salvador, Nicaragua, India and parts of
Central America.
ā€¢ All affected countries are located close to the equator and
have agriculture-based economies that engage in Chena
and Paddy cultivation.
Distribution
North Central
North Western
Uva
Eastern
Central
Sabaragamuwa
Southern
Western
Northern
Disease Profile
ā€¢ Male preponderance
ā€¢ Farmers (Male 85%,
Female 71.1%)
ā€¢ Age 30 ā€“ 60 years
ā€¢ Asymptomatic in early
stages
ā€¢ Slowly progressive
How CKDu differs from common
CKD?
In CKDu,
ā€¢ Working age males are mainly
affected
ā€¢ No previous history of
glomerulonephritis, DM and
Hypertension or other conventional
risk factors.
ā€¢ Proteins in urine- Low
Contributive factors
ā€¢It is hypothesized from the distribution and epidemiology
that the condition is linked to the environment and is likely
to be related to human activities in particular agriculture.
ā€¢Environmental Factors
Excessive Cadmium or Arsenic
High Fluoride in ground water
Cyanobacterial toxins in water
Bio accumulation of pesticides residues
Aluminium utensils + Flouride water
Naturally occurring hard water
ā€¢Lifestyle Factors
Locally brewed liquor
Ayurveic medicinal concoctions
ā€¢Genetic Predisposition
Thank you!

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Presentation CKD 11.pptx

  • 2. DEFINITION Diminished GFR that is persistently less than 60ml/min/1.73m2 for at least 3 months from any cause and/or persistent albuminuria. . "CKD is defined as abnormalities of kidney structure or function, present for >3 months, with implications for health," and requires one of two criteria documented or inferred for >3 months: either GFR <60 ml/min/1.73 m2 or markers of kidney damage, including albuminuria.
  • 3. Causes of CKD(better to refer kumar & clerk) Congenital and inherited disease Polycystic kidney disease (adult and infantile forms) Medullary cystic disease Tuberous sclerosis Oxalosis Cystinosis Congenital obstructive uropathy Glomerular disease Primary glomerulonephritides including focal glomerulosclerosis Secondary glomerular disease (systemic lupus, polyangiitis, Wegenerā€™s granulomatosis, amyloidosis, diabetic glomerulosclerosis, accelerated hypertension, haemolytic uraemic syndrome, thrombotic thrombocytopenic purpura, systemic sclerosis, sickle cell disease) Vascular disease Hypertensive nephrosclerosis (common in black Africans) Renovascular disease Small and medium-sized vessel vasculitis Tubulointerstitial disease Tubulointerstitial nephritis ā€“ idiopathic, due to drugs (especially nephrotoxic analgesics), immunologically mediated Reflux nephropathy Tuberculosis Schistosomiasis Nephrocalcinosis Multiple myeloma (myeloma kidney) Balkan nephropathy Renal papillary necrosis (diabetes, sickle cell disease and trait, analgesic nephropathy) Chinese herb nephropathy Urinary tract obstruction Calculus disease Prostatic disease Pelvic tumours Retroperitoneal fibrosis Schistosomiasis
  • 4. Aetiology of CKD ?? Glomerular diseases ā€¢Primary glomerulopathies ā€¢Systemic glomerulopathies ā€¢Hereditary causes Tubulointerstitial pathologies ā€¢Vascular causes ā€¢Infectious causes ā€¢Toxic causes ā€¢Obstructive causes
  • 5. Primary glomerulopathies 1. Acute diffuse proliferative glomerulonephritis (post streptococcal and non post streptococcal) 2. Rapidly progressive glomerulonephritis 3. Minimal change glomerular nephropathies 4. Membranous nephropathies 5. IgA nephropathy 6. Focal proliferative glomerulonephritis 7. Chronic glomerulonephritis Systemic glomerulopathies 1. Systemic lupus erythromatosis 2. Serum sickness nepritis 3. Diabetic nephropathy 4. Good pastureā€™s syndrome 5. Polyarteritis nodosa 6. Wegernerā€™s granulomatosis 7. Henoch- schonlein purpura 8. Bacterial endocarditis
  • 6. Hereditary causes 1. Alportā€™s syndrome 2. Fabry disease 3. Dent disease 4. Nephronophthisis 5. Atypical haemolytic ureamic syndrome Vascular diseases 1. Hypertensive nephrosclerosis 2. Renal artery stenosis 3. Atheroemboli 4. Renal vein thrombosis 5. C-ANCA positive vasculitides 6. P-ANCA positive vasculitides 7. ANCA negative vasculitides
  • 7. Infectious diseases ā€¢ Chronic pyelonephritis Toxic causes ā€¢ Chronic analgesic nephritis (Phenacetin , Aspirin , Acetaminophen) ā€¢ Prolonged exposure to lead , cadmium and uranium Obstructive causes ā€¢ Chronic obstruction of urinary tract due to stones , blood clots , tumors , strictures and enlarged prostate
  • 8. Prevalence of aetiological factors of CKD
  • 9. Underlying nephropathy Reduction in nephron number Many nephrons have failed and scared so burden of filtration falls to fewer functioning nephrons Remaining functional nephrons experience increased flow and pressure per nephron Pathogenesis of Chronic Kidney Disease
  • 10. Adapt with glomerular hypertrophy and decreased arterioles resistance Hyperfiltration Increased glomerular permeability Increased RAAS Increased filtration of protein and macromolecules Proteinurea Nephrotoxic inflammation Hypertension and remodeling Tubulointerstitial fibrosis and focal segment glomerular sclerosis Reduced GFR Reduced urine output Systemic complications
  • 11. Chronic Kidney Disease of Unknown etiology (CKDu)
  • 12. What is CKDu? ā€¢ A new form of CKD seen in epidemic proportions which is NOT attributed to Diabetes Mellitus, Hypertension, Glomerulonephritis or any other conventional risk factors. ā€¢ Currently CKDu occurs chiefly in Sri Lanka (Mainly North Central province), El Salvador, Nicaragua, India and parts of Central America. ā€¢ All affected countries are located close to the equator and have agriculture-based economies that engage in Chena and Paddy cultivation.
  • 14. Disease Profile ā€¢ Male preponderance ā€¢ Farmers (Male 85%, Female 71.1%) ā€¢ Age 30 ā€“ 60 years ā€¢ Asymptomatic in early stages ā€¢ Slowly progressive How CKDu differs from common CKD? In CKDu, ā€¢ Working age males are mainly affected ā€¢ No previous history of glomerulonephritis, DM and Hypertension or other conventional risk factors. ā€¢ Proteins in urine- Low
  • 15. Contributive factors ā€¢It is hypothesized from the distribution and epidemiology that the condition is linked to the environment and is likely to be related to human activities in particular agriculture. ā€¢Environmental Factors Excessive Cadmium or Arsenic High Fluoride in ground water Cyanobacterial toxins in water Bio accumulation of pesticides residues Aluminium utensils + Flouride water Naturally occurring hard water
  • 16. ā€¢Lifestyle Factors Locally brewed liquor Ayurveic medicinal concoctions ā€¢Genetic Predisposition