Optimal dose of angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker for renoprotection

被引:6
|
作者
Hou, Fan Fan [1 ]
Zhou, Qiu Gen [1 ]
机构
[1] So Med Univ, Nanfang Hosp, Div Nephrol, Key Lab Organ Failure Res,Minist Educ, Guangzhou 510515, Guangdong, Peoples R China
关键词
angiotensin receptor blocker; angiotensin-converting enzyme inhibitor; chronic kidney disease; proteinuria; TYPE-2; DIABETIC-NEPHROPATHY; RENAL-DISEASE; CONTROLLED-TRIAL; ALBUMINURIA; PROTEINURIA; LOSARTAN; TELMISARTAN; LISINOPRIL; THERAPY; SYSTEM;
D O I
10.1111/j.1440-1797.2010.01315.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II type 1 receptor blockers (ARB) have become the cornerstone in the treatment of chronic kidney disease (CKD), as numerous lines of evidence have shown that these agents have a blood pressure lowing independent anti-proteinuric effect. However, despite the benefits of ACEI or ARB therapy, a substantial proportion of patients still experience renal morbidity and mortality. Considering the prognostic impact of proteinuria reduction, it is currently assumed that titration of ACEI or ARB for optimal anti-proteinuric effect would be a logical step towards improvement of renoprotection. Recent published studies, performed with higher than recommended doses of either ACEI or particularly ARB, suggest that the approach is associated with a further decrement in urinary protein excretion and probably improved renal outcome. Although most patients achieve their maximum benefit at standard doses, there is a residual group of patients who may do so at higher doses of renin-angiotensin system inhibitors. Because patients who would benefit from higher doses are not identifiable a priori, a titration process might be cogent in order to provide more robust anti-proteinuric benefit to such patients.
引用
收藏
页码:57 / 60
页数:4
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