Reduction of proteinuria; combined effects of receptor blockade and low dose angiotensin-converting enzyme inhibition

被引:40
作者
Berger, ED [1 ]
Bader, BD [1 ]
Ebert, C [1 ]
Risler, T [1 ]
Erley, CM [1 ]
机构
[1] Univ Tubingen, Dept Med 3, Sect Nephrol & Hypertens, Dept Internal Med, D-72076 Tubingen, Germany
关键词
angiotensin-converting enzyme inhibitor; angiotensin receptor antagonist; candesartan; glomerulonephritis; hypertension; IgA-nephritis; proteinuria; renal hemodynamics; renoprotection;
D O I
10.1097/00004872-200204000-00033
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective Angiotensin-converting enzyme inhibitors (ACEI) show an antiproteinuric and thus nephroprotective effect in patients suffering from glomerulonephritis. Angiotensin II-receptor-antagonists (AT(1)RA) are also efficacious in reducing proteinuria. The study was performed to investigate the antiproteinuric effect of AT(1)RA candesartan in patients diagnosed with chronic glomerulonephritis by biopsy, and who were already being treated with an ACEI. Methods A total of 12 patients with a persistent proteinuria of at least 1 g/day who were already being treated with an ACEI for more than 3 months were included. The study was performed using a double-blind, placebo-controlled and randomized method with two treatment periods of 8 weeks (placebo or candesartan 8 mg/day) and a wash-out period of 4 weeks in between. Glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) were measured by inulin- and PAH-clearances at the beginning and the end of each treatment period. Results Proteinuria significantly decreased from 2 +/- 0.4 g/day to 1.3 +/- 0.3 g/day (P < 0.05) with the addition of candesartan treatment whereas it remained unchanged (from 1.8 +/- 0.3 g/day to 1.9 +/- 0.3 g/day) under placebo. GFR (candesartan: from 66 +/- 13 to 58 +/- 11 ml/ min per 1.73 m(2), placebo: from 64 +/- 11 to 62 +/- 13 ml/min per 1.73 m(2)) and ERPF (candesartan: from 329 +/- 44 to 304 +/- 37 ml/min per 1.73 m(2), placebo: from 362 h 48 to 315 +/- 46 ml/min per 1.73 m(2)) did not alter significantly after 8 weeks of treatment. The addition of candesartan treatment significantly reduced systolic blood pressure (from 129 +/- 3 to 123 2 mmHg, P < 0.05) and diastolic blood pressure (from 79 2 to 76 2 mmHg, P < 0.05) compared with placebo (systolic: 128 +/- 3 to 127 +/- 3 mmHg, diastolic: 79 +/- 2 to 79 +/- 2 mmHg). onclusion Candesartan promotes a complementary antiproteinuric and a small anti hypertensive effect after a treatment period of 8 weeks in patients with chronic glomerulonephritis when given in conjunction with an ACEI. Renal hemodynamics did not vary significantly. J Hypertens 20:739-743 (C) 2002 Lippincott Williams Wilkins.
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收藏
页码:739 / 743
页数:5
相关论文
共 24 条
[1]  
Arakawa K, 1996, J HYPERTENS, V14, pS3
[2]   ADDITIVE EFFECTS OF COMBINED ANGIOTENSIN-CONVERTING ENZYME-INHIBITION AND ANGIOTENSIN-II ANTAGONISM ON BLOOD-PRESSURE AND RENIN RELEASE IN SODIUM-DEPLETED NORMOTENSIVES [J].
AZIZI, M ;
CHATELLIER, G ;
GUYENE, TT ;
MURIETAGEOFFROY, D ;
MENARD, J .
CIRCULATION, 1995, 92 (04) :825-834
[3]   ANTIHYPERTENSIVE THERAPY WITH MK-421 - ANGIOTENSIN-II-RENIN RELATIONSHIPS TO EVALUATE EFFICACY OF CONVERTING ENZYME BLOCKADE [J].
BIOLLAZ, J ;
BRUNNER, HR ;
GAVRAS, I ;
WAEBER, B ;
GAVRAS, H .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1982, 4 (06) :966-972
[4]  
Cohen David S., 1996, Journal of the American Society of Nephrology, V7, P1852
[5]   Combination ACE inhibitor and angiotensin II receptor antagonist therapy in diabetic nephropathy [J].
Hebert, LA ;
Falkenhain, ME ;
Nahman, NS ;
Cosio, FG ;
O'Dorisio, TM .
AMERICAN JOURNAL OF NEPHROLOGY, 1999, 19 (01) :1-6
[6]   Impact of angiotensin II on the kidney: Does an angiotensin II receptor blocker make sense? [J].
Hollenberg, NK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (03) :S18-S23
[7]  
KOHZUKI M, 1995, J HYPERTENS, V13, P97
[8]   Effect of the angiotensin-converting-enzyme inhibitor benazepril on the progression of chronic renal insufficiency [J].
Maschio, G ;
Alberti, D ;
Janin, G ;
Locatelli, F ;
Mann, JFE ;
Motolese, M ;
Ponticelli, C ;
Ritz, E ;
Zucchelli, P ;
Marai, P ;
Marcelli, D ;
Tentori, F ;
Andriani, M ;
Drago, G ;
Meneghel, G ;
Oldrizzi, L ;
Rugiu, C ;
Salvadeo, A ;
Villa, G ;
Picardi, L ;
Borghi, M ;
Moriggi, M ;
Vendramin, G ;
Fusaroli, M ;
Esposti, ED ;
Fabbri, A ;
Koch, KM ;
Frey, U ;
Schaeffer, J ;
Mann, J ;
Schweitzer, C ;
Zuccala, A ;
Gaggi, R ;
Stahl, R ;
Blaser, C ;
Rivolta, E ;
Buccianti, G ;
Gastaldi, L ;
Baratelli, M ;
Ducret, F ;
Pointet, P ;
Sterzel, R ;
Oberdorf, E ;
Pedrini, L ;
Faranna, P ;
Cairo, G ;
Ferrari, L ;
Albertazzi, A ;
Cappelli, P ;
Cantu, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (15) :939-945
[9]   Angiotensin-converting enzyme inhibitors and kidney protection:: The AIPRI trial [J].
Maschio, G ;
Alberti, D ;
Locatelli, F ;
Mann, JFE ;
Motolese, M ;
Ponticelli, C ;
Ritz, E ;
Janin, G ;
Zucchelli, P ;
Marai, P ;
Marcelli, D ;
Tentori, F ;
Andriani, M ;
Drago, G ;
Meneghel, G ;
Oldrizzi, L ;
Rugiu, C ;
Salvadeo, A ;
Villa, G ;
Picardi, L ;
Borghi, M ;
Moriggi, M ;
Vendramin, G ;
Fusaroli, M ;
Esposti, ED ;
Fabbri, A ;
Zucchelli, P ;
Zuccali, A ;
Gaggi, R ;
Ponticelli, C ;
Rivolta, E ;
Buccianti, G ;
Gastaldi, L ;
Baratelli, M ;
Pedrini, L ;
Faranna, P ;
Cairo, G ;
Ferrari, L ;
Albertazzi, A ;
Cappelli, P ;
Canti, P ;
Limido, A ;
Mioni, G ;
Montanaro, D ;
Sasdelli, M ;
Imperiali, P ;
Cagnoli, L ;
Rigotti, A ;
Grassi, C ;
Orazi, E .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1999, 33 :S16-S20
[10]   PLASMA ANGIOTENSINS AND BLOOD-PRESSURE DURING CONVERTING ENZYME-INHIBITION [J].
MENTO, PF ;
WILKES, BM .
HYPERTENSION, 1987, 9 (06) :42-48