Effect of LDL cholesterol and treatment with losartan on end-stage renal disease in the RENAAL study

被引:10
|
作者
Tershakovec, Andrew M. [1 ]
Keane, William F. [1 ]
Zhang, Zhongxin [1 ]
Lyle, Paulette A. [1 ]
Appel, Gerald B. [2 ]
McGill, Janet B. [3 ]
Parving, Hans-Henrik [4 ]
Cooper, Mark E. [5 ]
Shahinfar, Shahnaz [1 ]
Brenner, Barry M. [6 ]
机构
[1] Merck & Co Inc, Merck Res Labs, N Wales, PA 19454 USA
[2] Columbia Univ, Dept Clin Nephrol, New York, NY USA
[3] Washington Univ, Div Endocrinol Metab & Lipid Res, St Louis, MO USA
[4] Univ Copenhagen Hosp, Dept Med Endocrinol, DK-2100 Copenhagen, Denmark
[5] Baker Heart Res Inst, Melbourne, Vic, Australia
[6] Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
关键词
D O I
10.2337/dc07-0196
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Renal pathology and dyslipidemia commonly coexist. Treatments that lower albuminuria/ proteinuria may lower lipids, but it is not known whether lipid lowering independent of lessening albuminuria/proteinuria slows progression of kidney disease. We examined the association between LDL cholesterol levels and treatment with losartan on end-stage renal disease (ESRD). Lipid levels and albuminuria measurements were obtained at baseline and at year I in a post hoc analysis from the Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan (RENAAL) study, which compared the effects of losartan-versus placebo-based antihypertensive therapy in patients with type 2 diabetes and nephropathy. LDL cholesterol lowering was associated with a lower risk of ESRD; however, this seemed to be largely an association with the reduction in albuminuria.
引用
收藏
页码:445 / 447
页数:3
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