Chronic Kidney Disease of Uncertain Aetiology - Clinical Features. Dr. Tilak Abeysekera Consultant Nephrologist

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Chronic Kidney Disease of Uncertain Aetiology - Clinical Features Dr. Tilak Abeysekera Consultant Nephrologist

Geographical Distribution

Dry Zone

Factors Considered for the Diagnosis of CKDu >5 years stay in the endemic region Dipstick proteinuria + and above No known identifiable cause for CKD No H/O of diabetes / long standing uncontrolled hypertension 4

Prevalence of Non Communicable Diseases Community-based apparently healthy Sinhala males Age 20-70 yrs living in endemic area for at least 10 yrs 43% of the apparently healthy population >140/90 mmhg n=154 proteinuria and/or glysosuria n=24 HbA1c >6.5% n=17 SCr >1.2 mg/dl and/or A1M>15.5 mg/l n=23 Blood Pressure n= 504 Dipstick test for proteinuria and glycosuria n=350 HbA1c n=326 Controls n=286 SCr and A1M n=309 5

GLOMERULAR SCLEROSIS 9% MINIMAL CHANGE 0% REFLUX 2% IgA 5% SLE 2% NORMAL 2% MCGN 3% CHRONIC PYELONEPHRITIS 9% FSGS 7% CHRONIC INTESTITIAL FIBROSIS 7% ESRD 3% ESRF/CHRONIC TUBULOINTESTITIAL DISEASE 8% CHRONIC TUBULOINTESTIAL NEPHRITIS 38% DIFFERENTIAL DIAGNOSIS IN RENAL HISTOLOGY TEACHING HOSPITAL ANURADHAPURA FROM JULY2006 TO 2008 Jan (n=268 ) 6

Differential Diagnosis of Renal Biopsy in Giradurukotte 2006 (n=41) 7

Occupation Farmers

Characteristics of CKDu Majority were males Between 40-70yrs Insidious onset Presented during late stages

Clinical Features Insidious onset Slowly progressive Asymptomatic until advanced stage Some present with backache, joint pains, abdominal ( flank ) pain, febrile feeling towards the end of the day, dysuria and feeling unwell.

Family History 14% have similarly affected first-degree relatives.

Genetic Susceptibility- Familial Clustering in CKDu Dr Surendra Ramachandran Oration- SLMA- July 2013

SLC13A3- Sodium dicarboxylate cotransporter 3 Location- basolateral membrane of human renal proximal tubules, liver, brain, and placenta Diabetic nephropathy- one of the most likely genes to affect the renal function Bento et al. (2008) Genomics 92(4): 226-234. Hypertension- suggestive association with blood pressure Simino et al. (2011) Am J Hypertens 24(11): 1227 1233. Renal fibrosis- potentially useful molecular predictor of CKD progression Ju et al. (2009) Am J Pathol 174(6): 2073 2085.

KCNA10- human voltage-gated K channel located in the heart, renal vasculature, and proximal tubular cells. Thus, it may have a role in regulation of blood pressure LAMB2- known to be associated with congenital nephrotic and nephritic syndromes SLC39A8- known to be involved in damage to the kidney tissue

Oedema Oedema occour at late stage of the disease

Hypertension In early stages of disease hypertension is usually mild and labile. In advanced disease hypertension is frequent.

Anaemia Not different from anaemia of CKD Usually normocytic normochromic Mild in early disease Severity increases with progression of disease

Characteristics of CKDu ctd. No uroepithelial tumours as seen in Balkan Nephropathy No specific features seen in CVS, RS, CNS,GIT and skin to suggest an aetiology

Urine Analysis Minor and intermittent proteinuria Urinary sediment is normal

kd Marker 1 2 3 4 5 6 250 150 100 75 50 95 67 albumin 53.7 45 37 32 a 1 microglobulin 25 15 10? 24 Retinol binding Protein? 16.6 Protein 1?

Smooth outline Bilateral small kidneys Loss of corticomedullary demarcation Echogenic Ultrasonography

Pathological Changes Interstitial inflammation with tibulitis Periglomerular fibrosis Perivascular fibrosis Focal interstitial hypocelleular fibrosis Tubular atrophy Glomerular sclerosis

Interstitial Inflammation with Tubulitis, Tubular Atrophy, Interstitial Fibrosis 57

Periglomerular Fibrosis

Perivascular Fibrosis

Focus of Tubular Atrophy

Sclerosed Glomeruli and Fibrosis

Dental Fluorosis

Skeletal Fluorosis

> 100,000 people are currently affected Number of deaths secondary to CKD in the affected region currently approximates 5000/year

How We Screened Standard Dipstick - ve + ve Urine Full Report Recheck at periodic health evaluation Diagnostic Evaluation Serum Creatinin Creatinin Clearence Serum Protein, Calcium, Phosphate Full Blood Count Ultra Sound Scan K.U.B Treatment Consultation

10-11 February 2006 32

10-11 February 2006 33

Future Microalbuminuria Alpha 1 Microglobulin Beta 2 Microglobulin Serum Creatinine/ Cystatin C A combination of tests?

Prevention of Further Progression Control of hypertension Restriction of dietary proteins Attention on drinking water Fluoride filters Abstinence from smoking & alcohol Not to use drugs that can harm kidneys Early referral to nephrologist Regular medical attention Reduction of protienurea

Management of ESRD Dialysis Kidney transplantation