Nephrology Grand Rounds. Vasishta Tatapudi, MD January 24 th, 2013

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1 Nephrology Grand Rounds Vasishta Tatapudi, MD January 24 th, 2013

2 Case Summary Chief complaint: A twenty-six year old African American female veteran presented to ER with left flank pain for two days. History of present illness: The patient complained of mild aching pain for several weeks. It worsened acutely two days prior to presentation. The patient had several episodes of similar pain in the past that resolved with bed rest. She did not report frequency, dysuria, hematuria, fever, change in bowel habits or any recent injuries.

3 Medical history: Hypertension, kidney disease, allergic rhinitis, recurrent urinary tract infections, PTSD. Surgical history: none. Medications: Lisinopril 10mg daily, loratidine 10mg daily, trimethoprim 100mg daily, citalopram 40mg daily. Allergies: Iodinated radio contrast.

4 Family history: Grandmother with ESRD, father with kidney disease. Social history: occasional alcohol use, no smoking or drug use.

5 Physical exam Vital signs: 99 F, HR 98, RR 20, BP 132/66 General: young female patient in acute distress. HEENT: normal. RS: normal vesicular breath sounds. CVS: S1, S2 normal, no added sounds. Abdomen: normal bowel sounds, no bruit, no palpable organomegaly, non tender, no guarding or rebound tenderness, no CVA tenderness. CNS: no focal deficits. Extremities: no edema, well perfused.

6 Laboratory data Hemoglobin 13.6 Sodium 141 Protein 7.9 Hematoctrit 39.1 Potassium 4.0 Albumin 4.6 MCV 83.1 Chloride 108 ALT 22 White count 5.3 Bicarbonate 24 AST 20 Platelets 374 Blood urea 24 ALP 58 Creatinine 0.6 Total Bilirubin 0.5 Glucose 107 Direct Bilirubin 0.2 Calcium 9.9 Amylase 51 AG 9.0 Lipase 24

7 Urinalysis Color Yellow Specific Gravity ph 6.5 Protein Negative Glucose Negative Bilirubin Negative Ketones Negative Blood Negative Leuk. Est. Negative EKG: normal sinus rhythm. Chest x-ray: clear lung fields. CT abdomen/pelvis w/o contrast: Innumerable bilateral renal cysts. Several are hyperdense, compatible with hemorrhagic cysts. Liver demonstrates multiple hypodense lesions compatible with cysts. Nitrite Negative RBC 0-2 WBC 0-2 Bacteria Negative

8 Polycystic kidney disease

9 Introduction Polycystic kidney disease (PKD) includes inherited diseases that cause an irreversible decline in kidney function. PKD may be inherited as an autosomal dominant or recessive trait. The autosomal dominant form (ADPKD) is the most common genetic cause of chronic kidney disease. ADPKD is caused by mutations of either PKD1 or PKD2. Patel V, et al, Curr Opin Nephrol Hypertens. 2009;18(2):99. Torres VE, Harris PC, Kidney Int. 2009;76(2):149.

10 Epidemiology Autosomal dominant PKD (ADPKD) occurs in all races. Reported prevalence is 1:400 to 1:1000. ADPKD is the underlying cause of kidney disease in approximately five percent of patients who initiate dialysis annually in the United States. It is the fourth leading cause of end-stage kidney disease in adults worldwide. Torres VE, Harris PC, Kidney Int. 2009;76(2):149

11 Epidemiology: PKD 1 vs PKD 2 PKD1 mutations are more common (approximately 85 percent) than PKD2 mutations (approximately 15 percent). The relative frequency of PKD1 and PKD2 mutations depends on the age of the population being studied. Patients with PKD2 mutations present at an older age and progress more slowly than patients with PKD1 mutations. Median age of patients who presented with renal failure is 54 and 74 years for those with PKD1 and PKD2, respectively. Rossetti S, et al, J Am Soc Nephrol. 2007;18(7):2143. Hateboer N, et al, Lancet. 1999;353(9147):103.

12 Clinical presentation Patients can present with hypertension, hematuria, proteinuria or renal insufficiency detected by routine laboratory examinations. Flank pain due to renal hemorrhage, calculi or urinary tract infection is the most common symptom reported by patients. Symptoms secondary to cysts in other organs - liver, pancreas, spleen, thyroid or epididymis. Torres VE,Lancet. 2007;369(9569):1287.

Progression of disease Chapman AB, et al, Kidney Disease (CRISP) cohort. Kidney, Int 2003;64:1035-45. Patients develop renal enlargement prior to loss of renal function.

13 Progression of disease Chapman AB, et al, Kidney Disease (CRISP) cohort. Kidney, Int 2003;64: Patients develop renal enlargement prior to loss of renal function. Renal architecture is lost early. May account for the lack of successful interventional trials designed to slow the progression. It is necessary to identify reliable markers of disease progression other than renal function.

14 Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease. Multicenter cohort study of 241 patients. Ages between 15 and 45(32.4±8.9). ecrcl >70ml/min(107±28). MR measurement of total renal volume, cyst volume and their relation to GFR measured by iothalamate clearance.

15 Chapman AB, et al, Kidney Int. 2003;64(3):1035. Standardization studies

16 Chapman AB, et al, Kidney Int. 2003;64(3):1035. Volume vs GFR

17 3 year multicenter cohort study of 241 patients. Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease. Ages between 15 and 45(32.4±8.9). ecrcl >70ml/min(107±28). MR measurement of total renal volume, cyst volume and their relation to GFR measured by iothalamate clearance. Rate of growth in PKD1 vs PKD 2 patients.

18 Grantham, N Engl J Med. 2006;354(20):2122. Volume vs age

19 Log transformed volume vs time Grantham, N Engl J Med. 2006;354(20):2122.

20 The mean (±SD) total kidney volume was 1060±642 ml at baseline and increased by a mean of 204±246 ml over a three-year period. 5.27±3.92%per year. Total cyst volume increased by 218±263 ml (P<0.001) during the same period.

21 Grantham, N Engl J Med. 2006;354(20):2122. Volume vs volume

22 Baseline volume vs slope of volume and GFR Grantham, N Engl J Med. 2006;354(20):2122.

23 Grantham, N Engl J Med. 2006;354(20):2122. PKD1 vs PKD 2

24 Discussion Patients with the largest kidneys at a given age should have the fastest rates of renal enlargement and decline in renal function. Total kidney volume is a marker of progression of disease. This supposition has practical value in judging the prognosis in individual patients. Study has implications for the design of clinical trials in ADPKD.

25 Other risk factors for progressive disease Genetic factors (PKD1 versus PKD2). Hypertension. Early onset of symptoms including proteinuria and hematuria. Male gender. Dipstick detectable proteinuria. Low birth weight. Decreased renal blood flow. Copeptin.

26 Genetic factors Careful attention to family history may allow the prediction of the mutation. Shown in a study of 484 patients from 90 families with well-characterized ADPKD mutations. The presence of at least one family member who developed ESRD before age 55 predicted a PKD1 mutation with a positive predictive value of 100 % and a sensitivity of 72 %. The presence of at least one family member who reached 70 years of age without ESRD predicted a PKD2 mutation with a positive predictive value of 100 % and a sensitivity of 74 %. Barua, J Am Soc Nephrol. 2009;20(8):1833.

27 Approach to treatment No specific treatment has been proven to prevent or delay progression of ADPKD. Promising therapies include: Vasopressin receptor antagonists, increased water intake, maximal inhibition of the renin-angiotensin-aldosterone system, use of mtor inhibitors and rigorous blood pressure control. Non-specific measures: dietary protein restriction, a low salt diet, and statins. Supportive therapy: pain control, bed rest during gross hematuria, and treatment of infection.

28 V2R antagonists In vitro evidence suggests that increased intracellular cyclic AMP (camp) plays a role in cystogenesis. camp plays a role in cyst epithelial cell proliferation and cyst fluid secretion in patients with PKD. Vasopressin leads to increased levels of camp in distal tubular epithelial cells. The vasopressin V2 receptor antagonists OPC and tolvaptan(opc-41061) decrease camp levels, inhibit cystogenesis and prevent renal enlargement and dysfunction in three different murine models. Calvet JP, Clin J Am Soc Nephrol. 2008;3(4):1205 Torres VE, Nat Med. 2004;10(4):363.

29 Torres VE, Nat Med. 2004;10(4):363. Torres VE, Nat Med. 2004;10(4):363.

30 Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes (TEMPO) 3:4 trial

31 Methods 3-year, multicenter, double-blind, placebo-controlled, trial involving 1445 patients. Inclusion criteria: Patients 18 to 50 years of age, who had ADPKD with kidney volume of 750 ml or more and an estimated creatinine clearance of 60 ml per minute or more. Received tolvaptan at the highest of three twice-daily dose regimens or placebo.

32 Methods Primary outcome: annual rate of change in the total kidney volume (MRI at baseline and at months 12, 24, and 36). Secondary end points: composite of clinical progression. rate of kidney-function (inverse of Cr) decline. Composite outcome: Worsening kidney function(egfr by CKD EPI). Kidney pain. Hypertension. Albuminuria. Stratification: Age, gender, hypertension, GFR, total kidney volume.

33 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Enrollment and outcomes

34 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Enrollment and outcomes

35 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Baseline characteristics

36 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Baseline characteristics

37 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Baseline characteristics

38 Effect on total kidney volume Torres VE, et al, N Engl J Med. 2012;367(25):2407.

39 Effect on total kidney volume Torres VE, et al, N Engl J Med. 2012;367(25):2407.

40 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Effect on kidney function

41 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Effect on kidney function

42 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Secondary end points

43 Torres VE, et al, N Engl J Med. 2012;367(25):2407. Secondary endpoints

44 Adverse effects Torres VE, et al, N Engl J Med. 2012;367(25):2407.

45 Summary of results Over the 3-year period, total kidney volume increased by 2.8% per year (95% CI, 2.5 to 3.1) with tolvaptan versus 5.5% per year (95% CI, 5.1 to 6.0) with placebo. Slope of kidney function with a slope of 2.61 (mg per milliliter) 1 per year, as compared with 3.81 (mg per milliliter) 1 per year with placebo. Fewer ADPKD-related events with tolvaptan than with placebo (44 vs. 50 events; hazard ratio, 0.87; 95% CI, 0.78 to 0.97; P = 0.01).

46 Discussion Adverse effects and discontinuation. Long term outcome data. Tolvaptan effect on development of hypertension was not studied. Effect of water intake.

48 Methods 13 ADPKD patients and 10 healthy controls. The diagnosis of ADPKD was based on a positive family history and ultrasonographic diagnostic criteria. Inclusion criteria: older than 18 years, egfr > 60 ml/min per 1.73 m2 using the MDRD equation. Exclusion criteria: no history of syndrome of antidiuresis, vasopressin agonist or antagonist therapy, serum sodium concentrations of > 135 meq/l, PTH levels. (MRI) to assess kidney volumes. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

49 Methods The effects of acute and sustained water loading on levels of urine osmolality (Uosm) and camp in 13 subjects with ADPKD and 10 healthy controls were studied. Uosm and camp concentrations were measured before and after water loading. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

50 Acute water loading No food or drink for 12 hours before study visit to achieve maximal AVP secretion and urine concentration. No caffeine. A urine sample was obtained at the end of the thirsting period. 200 ml of bottled water every 15 minutes for 2.5 hours, for a total of 2L. A post-water loading urine sample was collected. All samples were aliquoted and frozen at 80 C within an hour of collection. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

51 Chronic water loading Participants collected a baseline 24-hour urine on their usual fluid intake. Subjects were then instructed to drink at least 3 L of water daily for 7 days. On days 6 and 7 of sustained water loading, participants collected two consecutive 24-hour urines, which were stored at 4 C. Aliquots of the 24-hour collections were frozen at 80 C until further analysis. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

52 Statistical analysis Changes in urine camp concentration were indexed to urine osmolality in the acute water loading part of the study to account for effects of dilution. In the chronic water loading phase, 24-hour total urine camp amount was indexed to 24-hour total urine creatinine. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

53 Baseline characteristics Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

54 Effect of acute water load on camp Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

55 Correlation between osmolality and camp Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

56 Effect of chronic water load on camp Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

57 Discussion Possibilities that could account for the inability to detect predictable changes in urine camp during chronic water loading: Other agonists can generate camp in the kidney, including PTH, catecholamines, caffeine, and a forskolin-like molecule Insufficient water intake to suppress AVP levels. Urine camp may not closely reflect kidney camp levels in some patients. Urine camp measurements to predict responders to water therapy. A larger longitudinal study will be needed to determine the potential of water as therapy for ADPKD using hard endpoints. Barash I, Ponda MP, Goldfarb DS, Skolnik EY, Clin J Am Soc Nephrol. 2010;5(4):693.

58 Thank you.

Autosomal Dominant Polycystic Kidney Disease. Dr. Sameena Iqbal Nephrologist CIUSSS West Island

Autosomal Dominant Polycystic Kidney Disease Dr. Sameena Iqbal Nephrologist CIUSSS West Island Disclosure Honorarium for Consulting on the Reprise trial from Otsuka Mayo clinic preceptorship for PKD with