Angiotensin-converting enzyme inhibitors and progression of nondiabetic renal disease - A meta-analysis of patient-level data

被引:795
作者
Jafar, TH
Schmid, CH
Landa, M
Giatras, I
Toto, R
Remuzzi, G
Maschio, G
Brenner, BM
Kamper, A
Zucchelli, P
Becker, G
Himmelmann, A
Bannister, K
Landais, P
Shahinfar, S
de Jong, PE
de Zeeuw, D
Lau, J
Levey, AS
机构
[1] Tufts Univ New England Med Ctr, Div Nephrol, Boston, MA 02111 USA
[2] Tufts Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02111 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Texas SW, Dallas, TX USA
[5] Mario Negri Inst Pharmacol Res, I-24100 Bergamo, Italy
[6] Osped Civile, I-37126 Verona, Italy
[7] Osped M Malphigi, Bologna, Italy
[8] Univ Copenhagen, DK-1168 Copenhagen, Denmark
[9] Royal Melbourne Hosp, Melbourne, Vic, Australia
[10] Royal Adelaide Hosp, Adelaide, SA 5000, Australia
[11] Sahlgrens Univ Hosp, S-41345 Gothenburg, Sweden
[12] Hop Necker Enfants Malad, F-75730 Paris, France
[13] Merck Res Labs, West Point, PA USA
[14] Univ Groningen, NL-9700 AB Groningen, Netherlands
关键词
D O I
10.7326/0003-4819-135-2-200107170-00007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To examine the efficacy of ACE inhibitors for treatment of nondiabetic renal disease. Data Sources: 11 randomized, controlled trials comparing the efficacy of antihypertensive regimens including ACE inhibitors to the efficacy of regimens without ACE inhibitors in predominantly nondiabetic renal disease. Study Selection: studies were identified by searching the MEDLINE database for English-language studies evaluating the effects of ACE inhibitors on renal disease in humans between May 1977 (when ACE inhibitors were approved for trials in humans) and September 1997. Data Extraction: Data on 1860 nondiabetic patients were analyzed. Data Synthesis: Mean duration of follow-up was 2.2 years. Patients in the ACE inhibitor group had a greater mean decrease in systolic and diastolic blood pressure (4.5 mm Hg [95% CI, 3.0 to 6.1 mm Hg]) and 2.3 mm Hg [CI, 1.4 to 3.2 mm Hg], respectively) and urinary protein excretion (0.46 g/d [CI, 0.33 to 0.59 g/d]), After adjustment for patient and study characteristics at baseline and changes in systolic blood pressure and urinary protein excretion during follow-up, relative risks in the ACE inhibitor group were 0.69 (CI, 0.51 to 0.94) for end-stage renal disease and 0.70 (CI, 0.55 to 0.88) far the combined outcome of doubling of the baseline serum creatinine concentration or end-stage renal disease. Patients with greater urinary protein excretion at baseline benefited more from ACE inhibitor therapy (P= 0.03 and P= 0.001, respectively), but the data were inconclusive as to whether the benefit extended to patients with baseline urinary protein excretion less than 0.5 g/d. Conclusion: Antihypertensive regimens that include ACE inhibitors are more effective than regimens without ACE inhibitors in slowing the progression of nondiabetic renal disease. The beneficial effect of ACE inhibitors is mediated by factors in addition to decreasing blood pressure and urinary protein excretion and is greater in patients with proteinuria. Angiotensin-converting inhibitors are indicated for treatment of nondiabetic patients with chronic renal disease and proteinuria and, possibly, those without proteinuria.
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页码:73 / 87
页数:15
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