共 50 条
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
来源:
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
相关论文