醛固酮
螺内酯
医学
内科学
内分泌学
糖尿病肾病
肾病
血管紧张素转换酶抑制剂
排泄
血压
糖尿病
盐皮质激素
泌尿科
血管紧张素转换酶
作者
Atsuhisa Sato,Kôichi Hayashi,Mitsuhide Naruse,Takao Saruta
出处
期刊:Hypertension
[Lippincott Williams & Wilkins]
日期:2003-01-01
卷期号:41 (1): 64-68
被引量:465
标识
DOI:10.1161/01.hyp.0000044937.95080.e9
摘要
It has been reported that continuous ACE inhibitor therapy does not necessarily produce a maintained decrease in plasma aldosterone levels, which may remain high or increase eventually during long-term use (aldosterone escape). We have examined the role of aldosterone escape in 45 patients with type 2 diabetes and early nephropathy treated with an ACE inhibitor for 40 weeks. With treatment, there was a 40% reduction in average urinary albumin excretion, although urinary albumin excretion in patients with aldosterone escape (18 patients) was significantly higher than that in patients without escape (27 patients). In the 18 patients with escape, spironolactone (25 mg/d) was added to ACE inhibitor treatment in 13. After a 24-week study period, urinary albumin excretion and left ventricular mass index were significantly reduced without blood pressure change. In conclusion, the present study demonstrates that aldosterone escape is observed in 40% of patients with type 2 diabetes with early nephropathy despite the use of ACE inhibitors. Our study suggests the possibility that aldosterone blockade may represent optimal therapy for patients with early diabetic nephropathy who show aldosterone escape during ACE inhibitor treatment and who no longer show maximal antiproteinuric effects of ACE inhibition. Additional, larger, prospectively randomized, double-blind studies will be needed before adaptation of this strategy.
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