ALLHAT RENAL DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED INTO 4 GROUPS BY BASELINE GLOMERULAR FILTRATION RATE (GFR)

Similar documents
ALLHAT. Major Outcomes in High Risk Hypertensive Patients Randomized to Angiotensin-Converting Enzyme Inhibitor or Calcium Channel Blocker vs Diuretic

HYPERTENSION GUIDELINES WHERE ARE WE IN 2014

ALLHAT. ALLHAT Antihypertensive Trial Results by Baseline Diabetic & Fasting Glucose Status

Caring for Australians with Renal Impairment. BP lowering and CVD

DISCLOSURE PHARMACIST OBJECTIVES 9/30/2014 JNC 8: A REVIEW OF THE LONG-AWAITED/MUCH-ANTICIPATED HYPERTENSION GUIDELINES. I have nothing to disclose.

Treating Hypertension in Individuals with Diabetes

University of Groningen. Evaluation of renal end points in nephrology trials Weldegiorgis, Misghina Tekeste

Aggressive blood pressure reduction and renin angiotensin system blockade in chronic kidney disease: time for re-evaluation?

Antihypertensive Trial Design ALLHAT

The CARI Guidelines Caring for Australasians with Renal Impairment. ACE Inhibitor and Angiotensin II Antagonist Combination Treatment GUIDELINES

Guest Speaker Evaluations Viewer Call-In Thanks to our Sponsors: Phone: Fax: Public Health Live T 2 B 2

Reducing proteinuria

Prevention And Treatment of Diabetic Nephropathy. MOH Clinical Practice Guidelines 3/2006 Dr Stephen Chew Tec Huan

Optimal blood pressure targets in chronic kidney disease

Combination Therapy for Hypertension

The CARI Guidelines Caring for Australasians with Renal Impairment. Blood Pressure Control role of specific antihypertensives

CKD and risk management : NICE guideline

Lessons learned from AASK (African-American Study of Kidney Disease and Hypertension)

Keywords albuminuria, hypertension, nephropathy, proteinuria

Seung Hyeok Han, MD, PhD Department of Internal Medicine Yonsei University College of Medicine

SLOWING PROGRESSION OF KIDNEY DISEASE. Mark Rosenberg MD University of Minnesota

Managing Hypertension in Diabetes Sean Stewart, PharmD, BCPS, BCACP, CLS Internal Medicine Park Nicollet Clinic St Louis Park.

Outline. Outline CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW 7/23/2013. Question 1: Which of these patients has CKD?

Management of Hypertensive Chronic Kidney Disease: Role of Calcium Channel Blockers. Robert D. Toto, MD

MANAGEMENT CALL TO DISCUSS LONGER-TERM IMPROVEMENTS IN KIDNEY FUNCTION WITH BARDOXOLONE

Randomized Design of ALLHAT BP Trial

Outline. Outline 10/14/2014 CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW. Question 1: Which of these patients has CKD?

The CARI Guidelines Caring for Australians with Renal Impairment. Specific effects of calcium channel blockers in diabetic nephropathy GUIDELINES

Interventions to reduce progression of CKD what is the evidence? John Feehally

Prevalence of anemia and cardiovascular diseases in chronic kidney disease patients: a single tertiary care centre study

Systolic Blood Pressure Intervention Trial (SPRINT)

HYPERTENSION IN CKD. LEENA ONGAJYOOTH, M.D., Dr.med RENAL UNIT SIRIRAJ HOSPITAL

Blood Pressure Monitoring in Chronic Kidney Disease

Clinical Review & Education. Special Communication

Outline. Outline. Introduction CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW 8/11/2011

RENAAL, IRMA-2 and IDNT. Three featured trials linking a disease spectrum IDNT RENAAL. Death IRMA 2

The Latest Generation of Clinical

Outline. Outline CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW. Question 1: Which of these patients has CKD?

DISCLOSURES OUTLINE OUTLINE 9/29/2014 ANTI-HYPERTENSIVE MANAGEMENT OF CHRONIC KIDNEY DISEASE

JNC Evidence-Based Guidelines for the Management of High Blood Pressure in Adults

Supplementary Online Content

Hypertension Management: A Moving Target

CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW MICHAEL G. SHLIPAK, MD, MPH

THE IMPACT OF CCB AND RAS INHIBITOR COMBINATION THERAPY TO PREVENT CKD INCIDENCE IN HYPERTENSION AND ADVANCED ATHEROSCLEROSIS

CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW

Chronic Kidney Disease Management for Primary Care Physicians. Dr. Allen Liu Consultant Nephrologist KTPH 21 November 2015

Hypertension Update Clinical Controversies Regarding Age and Race

Cedars Sinai Diabetes. Michael A. Weber

THE PROGNOSIS OF PATIENTS WITH CHRONIC KIDNEY DISEASE AND DIABETES MELLITUS

Hypertension and the SPRINT Trial: Is Lower Better

Managing Chronic Kidney Disease: Reducing Risk for CKD Progression

Concept and General Objectives of the Conference: Prognosis Matters. Andrew S. Levey, MD Tufts Medical Center Boston, MA

2 Furthermore, quantitative coronary angiography

Outline. Introduction. Outline CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW 6/26/2012

ADVANCES IN MANAGEMENT OF HYPERTENSION

QUICK REFERENCE FOR HEALTHCARE PROVIDERS

The Seventh Report of the Joint National Commission

Management of High Blood Pressure in Adults

KDIGO conference on high CV risk associated with CKD. The role of BP in CKD stage 1-4

Kidney Disease, Hypertension and Cardiovascular Risk

신장환자의혈압조절 나기영. Factors involved in the regulation of blood pressure

Dialysis Initiation and Optimal Vascular Access: Outcomes and Mortality

2014 HYPERTENSION GUIDELINES

Prof. Armando Torres Nephrology Section Hospital Universitario de Canarias University of La Laguna Tenerife, Canary Islands, Spain.

Launch Meeting 3 rd April 2014, Lucas House, Birmingham

The CARI Guidelines Caring for Australasians with Renal Impairment. Protein Restriction to prevent the progression of diabetic nephropathy GUIDELINES

CARDIO-RENAL SYNDROME

Reframe the Paradigm of Hypertension treatment Focus on Diabetes

SUPPLEMENTARY DATA. Supplementary Figure S1. Cohort definition flow chart.

An acute fall in estimated glomerular filtration rate during treatment with losartan predicts a slower decrease in long-term renal function

Jackson T. Wright, Jr. MD, PhD

Hypertension in Geriatrics. Dr. Allen Liu Consultant Nephrologist 10 September 2016

1. Albuminuria an early sign of glomerular damage and renal disease. albuminuria

Hypertension Update 2009

What should you do next? Presenter Disclosure Information. Learning Objectives. Case: George

Screening for chronic kidney disease racial implications. Not everybody that pees has healthy kidneys!

New Antihypertensive Strategies to Improve Blood Pressure Control

SpringerLink Header: Hypertension (WB White and AJ Peixoto, Section

Acknowledgements. National Kidney Foundation of Connecticut Mark Perazella. Co-PI Slowing the progression of chronic kidney disease to ESRD

Clinical Pearls in Renal Medicine

Uric acid and CKD. Sunil Badve Conjoint Associate Professor, UNSW Staff Specialist, St George

Hypertension. Does it Matter What Medications We Use? Nishant K. Sekaran, M.D. M.Sc. Intermountain Heart Institute

Hypertension is an important global public

ADVANCES IN MANAGEMENT OF HYPERTENSION

Predicting and changing the future for people with CKD

Pre-ALLHAT Drug Use. Diuretics. ß-Blockers. ACE Inhibitors. CCBs. Year. % of Treated Patients on Medication. CCBs. Beta Blockers.

Jared Moore, MD, FACP

Diabetes and kidney disease.

New Lipid Guidelines. PREVENTION OF CARDIOVASCULAR DISEASE IN WOMEN: Implications of the New Guidelines for Hypertension and Lipids.

Management of Hypertension. M Misra MD MRCP (UK) Division of Nephrology University of Missouri School of Medicine

Diabetic Nephropathy Larry Lehrner, Ph.D.,M.D.

Hypertension and Cardiovascular Disease

Does renin angiotensin system blockade deserve preferred status over other anti-hypertensive medications for the treatment of people with diabetes?

OCTOBER 7-10 PHILADELPHIA, PENNSYLVANIA

ABSTRACT. Special Communication February 5, 2014

Disclosures. Outline. Outline 7/27/2017 CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW

Managing patients with renal disease

Disclosures. Outline. Outline 5/23/17 CHRONIC KIDNEY DISEASE UPDATE: WHAT THE GENERALIST NEEDS TO KNOW

Update on HIV-Related Kidney Diseases. Agenda

A New Approach for Evaluating Renal Function and Predicting Risk. William McClellan, MD, MPH Emory University Atlanta

Transcription:

1 RENAL DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED INTO 4 GROUPS BY BASELINE GLOMERULAR FILTRATION RATE (GFR) 6 / 5 / 1006-1

2 Introduction Hypertension is the second most common cause of end-stage renal disease (ESRD) in the US Hypertension is a key factor contributing to progression of chronic kidney disease Successful treatment of hypertension is important in slowing down progression of renal disease 6 / 5 / 1006-2

3 Background In diabetic (DM) and nondiabetic (NDM) hypertensive patients with established chronic renal insufficiency and proteinuria, inhibition of the renin angiotensin axis is suggested to be superior to conventional therapy in slowing decline in renal function Few studies directly compared effects of different classes of antihypertensive drug therapy on decline in renal function in hypertensive patients with mild reduction in glomerular filtration rate (GFR). 6 / 5 / 1006-3

4 Overall Results Renal Outcomes In the study population as a whole, no difference was noted in the risk of ESRD with chlorthalidone compared to amlodipine and lisinopril Estimated GFR was higher at the end of the study in patients randomized to amlodipine compared to chlorthalidone. 6 / 5 / 1006-4

5 Objective Post-hoc analysis of the study to determine whether treatment with a calcium channel blocker or an ACE inhibitor, each versus a diuretic, lowers incidence of renal outcomes in high risk hypertensive patients stratified by baseline GFR. 6 / 5 / 1006-5

6 Baseline Characteristics Stratified By Estimated GFR* Normal GFR ( 90) Mild GFR (60-89) Moderate GFR (30-59) Severe GFR (<30) N 8,126 18,109 5,480 182 Mean age, y 63.3 67.3** 70.7** 70.3** Black non-hisp, % 43.1 27.7** 24.9** 42.9 Women, % 46.6 44.5** 52.1** 58.8** Mean SBP 145.9 146.3 146.6** 150.0** Mean DBP 84.9 82.5** 84.1** 83.7 Type 2 diabetes, % 45.2 32.8** 33.1** 41.8 History of CHD***, % 21.2 26.3** 30.6** 28.0** *Estimated (egfr) (ml/min/1.73 m 2 ) calculated by simplified MDRD equation (Levey et al., J Am Soc Nephrol 11, A 0828. 2000.) ** p<.05 compared with normal GFR ***p<0.022, amlodipine (28%) vs. chlorthalidone (31%) in participants with GFR 30-59. 6 / 5 / 1006-6

7 egfr during the course of the study (Baseline egfr 90) 110 100 90 80 * * * * * 70 Baseline (n=8126) 1 Year (n=5282) 2 Year (n=5188) 4 Year (n=4409) Chlorthalidone 102.5 93.4 91.9 86.9 Amlodipine 102.7 98.6 97.7 93.3 Lisinopril 102.7 94.5 93.4 88.3 * p<0.05 vs. Chlorthalidone Estimated GFR (egfr) calculated from the simplified MDRD equation 6 / 5 / 1006-7

8 egfr During the Course of the Study (Baseline egfr 60-89) 80.0 75.0 * * * 70.0 65.0 Baseline (n=18109) 1 Year (n=12264) 2 Year (n=12011) 4 Year (n=10262) Chlorthalidone 75.1 72.8 72.2 68.9 Amlodipine 75.2 76.7 75.9 73.0 Lisinopril 75.1 73.2 72.5 69.1 * p<0.05 vs. Chlorthalidone Estimated GFR (egfr) calculated from the simplified MDRD equation 6 / 5 / 1006-8

9 egfr During the Course of the Study (Baseline egfr 30-59) 60.0 55.0 50.0 * * * 45.0 Baseline (n=5480) 1 Year (n=3498) 2 Year (n=3350) 4 Year (n=2679) Chlorthalidone 51.0 51.3 50.7 48.5 Amlodipine 51.5 55.3 54.9 51.9 Lisinopril 51.0 51.7 51.2 48.6 * p<0.05 vs. Chlorthalidone Estimated GFR (egfr) calculated from the simplified MDRD equation 6 / 5 / 1006-9

10 egfr During the Course of the Study (Baseline egfr <30) 40.0 30.0 20.0 10.0 0.0 Baseline (n=182) 1 Year (n=85) 2 Year (n=71) 4 Year (n=39) Chlorthalidone 23.7 26.0 26.4 24.4 Amlodipine 23.8 26.2 26.3 22.9 Lisinopril 24.4 29.3 26.6 25.3 Estimated GFR (egfr) calculated from the simplified MDRD equation 6 / 5 / 1006-10

Evaluating Treatment Effects by Subgroup Significant treatment difference within 1 or more subgroups? Significant Test for Treatment x Subgroup Interaction? Yes No Yes Interaction No interaction No Interaction No interaction Interaction Use subgroup estimates of treatment effects No interaction Use estimate of treatment effect in total population

12 End Stage Renal Disease by Baseline Diabetes & Treatment Amlodipine vs Chlorthalidone Diabetic participants Nondiabetic participants 6-year rates per 100 (se) & total events / N Chlorthalidone 2.7 (0.3) 109 / 5,528 1.3 (0.2) 84 / 9,727 Total 1.8 (0.1) 193 / 15,255 Amlodipine 3.6 (0.4) 86 / 3,323 1.0 (0.1) 43 / 5,725 2.1 (0.2) 129 / 9,048 Relative Risk (A/C) (95% CI) p value 1.30 (0.98 1.73) p = 0.07 0.86 (0.60 1.25) p = 0.43 1.12 (0.89 1.40) P = 0.33 Differences among treatment group effects by baseline history of diabetes are not statistically significant. 6 / 5 / 2006-12

13 End Stage Renal Disease by Baseline GFR & Treatment Amlodipine vs Chlorthalidone 6-year rates per 100 (se) & total events / N Chlorthalidone GFR 90 0.27 (0.10) 11 / 3648 Amlodipine 0.60 (0.22) 9 / 2274 Relative Risk (A/C) (95% CI) p value 1.31 (0.54 3.17) p = 0.54 GFR 60-89 0.84 (0.14) 47 / 8360 GFR 30-59 4.93 (0.56) 91 / 2530 GFR <30 48.82 (7.15) 33 / 83 1.24 (0.21) 41 / 4850 4.87 (0.74) 52 / 1471 33.49 (7.68) 13 / 45 1.47 (0.97 2.23) p = 0.07 1.00 (0.71 1.41) p = 0.99 0.67 (0.35 1.28) p = 0.23 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-13

14 End Stage Renal Disease by Baseline GFR & Treatment Amlodipine vs Chlorthalidone Diabetic Participants 6-year rates per 100 (se) & total events / N Chlorthalidone GFR 90 0.54 (0.21) 8 / 1,667 GFR 60-89 1.38 (0.30) 26 / 2,755 GFR 30-59 7.89 (1.18) 49 / 848 GFR <30 65.64 (9.76) 19 / 33 Amlodipine 0.76 (0.39) 5 / 1,026 2.62 (0.54) 27 / 1,626 10.38 (1.83) 37 / 486 38.49 (11.44) 7 / 20 Relative Risk (A/C) (95% CI) p value 1.03 (0.34 3.16) p = 0.95 1.72 (1.01 2.95) p = 0.05 1.32 (0.86 2.03) p = 0.20 0.44 (0.19 1.05) p = 0.06 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-14

15 End Stage Renal Disease by Baseline Diabetes & Treatment Lisinopril vs Chlorthalidone Diabetic participants Nondiabetic participants 6-year rates per 100 (se) & total events / N Chlorthalidone 2.7 (0.3) 109 / 5,528 1.3 (0.2) 84 / 9,727 Total 1.8 (0.1) 193 / 15,255 Lisinopril 3.3 (0.4) 73 / 3,212 1.3 (0.2) 53 / 5,842 2.0 (0.2) 126 / 9,054 Relative Risk (95% CI) p value 1.17 (0.87 1.57) p = 0.31 1.05 (0.74 1.48) p = 0.78 1.11 (0.88 1.38) P = 0.38 Differences among treatment group effects by baseline history of diabetes are not statistically significant. 6 / 5 / 2006-15

16 End Stage Renal Disease by Baseline GFR & Treatment Lisinopril vs Chlorthalidone 6-year rates per 100 (se) & total events / N Chlorthalidone GFR 90 0.27 (0.10) 11 / 3,648 GFR 60-89 0.84 (0.14) 47 / 8,360 GFR 30-59 4.93 (0.56) 91 / 2,530 GFR <30 48.82 (7.15) 33 / 83 Lisinopril 0.40 (0.15) 7 / 2,204 1.06 (0.18) 37 / 4,899 5.03 (0.73) 55 / 1,479 34.45 (7.59) 15 / 54 Relative Risk (95% CI) p value 1.08 (0.42 2.78) p = 0.88 1.34 (0.87 2.06) p = 0.18 1.05 (0.75 1.47) p = 0.78 0.69 (0.37 1.26) p = 0.23 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-16

17 End Stage Renal Disease by Baseline GFR & Treatment Lisinopril vs Chlorthalidone Diabetic Participants 6-year rates per 100 (se) & total events / N Chlorthalidone GFR 90 0.54 (0.21) 8 / 1,667 GFR 60-89 1.38 (0.30) 26 / 2,755 GFR 30-59 7.89 (1.18) 49 / 848 GFR <30 65.64 (9.76) 19 / 33 Lisinopril 0.27 (0.19) 2 / 981 2.35 (0.49) 25 / 1,563 9.74 (1.76) 33 / 478 37.66 (10.61) 8 / 23 Relative Risk (95% CI) p value 0.43 (0.09 2.04) p = 0.29 1.74 (1.00 3.01) p = 0.05 1.21 (0.78 1.88) p = 0.40 0.54 (0.23 1.23) p = 0.14 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-17

18 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline Diabetes & Treatment Amlodipine vs Chlorthalidone Diabetic participants Events per 100 & total events / N Chlorthalidone 5.0 279 / 5,528 Amlodipine 4.9 164 / 3,323 Relative Risk (A/C) p value 0.98 p = 0.82 Nondiabetic participants 2.2 214 / 9,727 1.6 92 / 5,725 0.73 p = 0.01 Total 3.2 493 / 15,255 2.8 256 / 9,048 0.87 p = 0.08 Differences among treatment group effects by baseline history of diabetes are not statistically significant. 6 / 5 / 2006-18

19 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline GFR & Treatment Amlodipine vs Chlorthalidone Events per 100 (se) & total events / N Chlorthalidone GFR 90 3.1% 112 / 3,648 GFR 60-89 2.3% 190 / 8,360 GFR 30-59 5.7% 143 / 2,530 GFR <30 44.6% 37 / 83 Amlodipine 2.0% 46 / 2,274 2.2% 106 / 4,850 5.2% 77 / 1,471 28.9% 13 / 45 Relative Risk (A/C) p value 0.65 p = 0.02 0.96 p = 0.74 0.92 p = 0.58 0.51 p = 0.08 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-19

20 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline GFR & Treatment Diabetic Participants Amlodipine vs Chlorthalidone Events per 100 (se) & total events / N Chlorthalidone GFR 90 4.6% 77 / 1,667 GFR 60-89 3.6% 99 / 2,755 GFR 30-59 9.1% 77 / 848 GFR <30 57.6% 19 / 33 Amlodipine 2.9% 30 / 1,026 4.2% 68 / 1,626 10.1% 49 / 486 35.0% 7 / 20 Relative Risk (A/C) p value 0.62 p=0.03 1.17 p=0.33 1.12 p=0.55 0.40 p=0.11 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-20

21 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline Diabetes & Treatment Lisinopril vs Chlorthalidone Diabetic participants Events per 100 & total events / N Chlorthalidone 5.0 279 / 5,528 Lisinopril 5.2 168 / 3,212 Relative Risk (L/C) p value 1.04 p = 0.71 Nondiabetic participants 2.2 214 / 9,727 Total 3.2 493 / 15,255 2.3 132 / 5,842 3.3 300 / 9,054 1.03 p = 0.81 1.03 P = 0.65 Differences among treatment group effects by baseline history of diabetes are not statistically significant. 6 / 5 / 2006-21

22 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline GFR & Treatment Lisinopril vs Chlorthalidone Events per 100 (se) & total events / N Chlorthalidone GFR 90 3.1% 112 / 3,648 Lisinopril 2.6% 57 / 2,204 Relative Risk (L/C) p value 0.84 p = 0.28 GFR 60-89 2.3% 190 / 8,360 GFR 30-59 5.7% 143 / 2,530 GFR <30 44.6% 37 / 83 2.6% 125 / 4,899 6.1% 90 / 1,479 29.6% 16 / 54 1.13 p = 0.31 1.08 p = 0.57 0.52 p = 0.08 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-22

23 End Stage Renal Disease or 50% or Greater Decline in GFR by Baseline GFR & Treatment Diabetic Participants Lisinopril vs Chlorthalidone Events per 100 (se) & total events / N Chlorthalidone GFR 90 4.6% 77 / 1,667 Lisinopril 3.6% 35 / 981 Relative Risk (L/C) p value 0.76 p=0.20 GFR 60-89 3.6% 99 / 2,755 GFR 30-59 9.1% 77 / 848 GFR <30 57.6% 19 / 33 4.3% 67 / 1,563 11.1% 53 / 478 34.8% 8 / 23 1.20 p=0.26 1.25 p=0.24 0.39 p=0.09 Differences among treatment group effects by baseline GFR group are not statistically significant. 6 / 5 / 1006-23

24 Summary The overall study results of no difference in ESRD and the composite (ESRD/50% decline in GFR) for the lisinopril vs. chlorthalidone and amlodipine vs. chlorthalidone comparisons was consistent across diabetes, GFR, and diabetes-gfr subgroups. 6 / 5 / 2006-24

25 Discussion # events Six year event rate /100 Combined CVD Events ESRD events 8887 448 30.9-33.3 1.8-2.1 High risk hypertensive patients are at higher risk for CVD than ESRD Risk of ESRD is higher in diabetic participants, and those with reduced GFR at baseline Since risk of CVD is much higher than risk for ESRD in CKD patients, choices of therapy need to be guided by effects on CVD outcomes 6 / 5 / 2006-25

26 Strengths & Limitations Strength - The number of patients with moderate reduction in GFR, and the number of patients developing ESRD are higher in compared to any other renal study, including AASK, RENAAL and IDNT Limitation Proteinuria is an independent predictor of decline in renal function. Information about proteinuria was not available in participants. 6 / 5 / 2006-26

27 Conclusion In high risk hypertensive patients with reduced GFR, amlodipine and lisinopril are not superior to chlorthalidone in reducing the rate of development of ESRD and significant decrements in GFR 6 / 5 / 2006-27