Effect of intensive lipid lowering with atorvastatin on renal function in patients with coronary heart disease: The treating to new targets (TNT) study

被引:240
作者
Shepherd, James
Kastelein, John J. P.
Bittner, Vera
Deedwania, Prakash
Breazna, Andrei
Dobson, Stephen
Wilson, Daniel J.
Zuckerman, Andrea
Wenger, Nanette K.
机构
[1] Univ Glasgow, Dept Vasc Biochem, Glasgow, Lanark, Scotland
[2] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Alabama Birmingham, Div Cardiovasc Dis, Birmingham, AL USA
[4] VA Cent Calif Healthcare Syst, Fresno, CA USA
[5] UCSF, Sch Med, Fresno, CA USA
[6] Pfizer Inc, Global Res & Dev, New York, NY USA
[7] Pfizer Inc, Pfizer Global Pharmaceut, New York, NY USA
[8] Envision Pharma Ltd, Sci Solut, Horsham, W Sussex, England
[9] Emory Univ, Sch Med, Div Cardiol, Atlanta, GA 30322 USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2007年 / 2卷 / 06期
关键词
D O I
10.2215/CJN.04371206
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
Background and objectives: Data suggest that atorvastatin may be nephroprotective. This subanalysis of the Treating to New Targets study investigated how intensive lipid lowering with 80 mg of atorvastatin affects renal function when compared with 10 mg in patients with coronary heart disease. Design, setting, participants, & measurements: A total of 10,001 patients with coronary heart disease and LDL cholesterol levels of <130 mg/dl were randomly assigned to double-blind therapy with 10 or 80 mg/d atorvastatin. Estimated GFR using the Modification of Diet in Renal Disease equation was compared at baseline and at the end of follow-up in 9656 participants with complete renal data. Results: Mean estimated GFR at baseline was 65.6 +/- 11.4 ml/min per 1.73 m(2) in the 10-mg group and 65.0 +/- 11.2 ml/min per 1.73 m(2) in the 80-mg group. At the end of follow-up (median time to final creatinine measurement 59.5 months), mean change in estimated GFR showed an increase of 3.5 +/- 0.14 ml/min per 1.73 m(2) with 10 mg and 5.2 +/- 0.14 ml/min per 1.73 m(2) with 80 mg (P < 0.0001 for treatment difference). In the 80-mg arm, estimated GFR improved to 2:60 ml/min per 1.73 m(2) in significantly more patients and declined to <60 ml/min per 1.73 m(2) in significantly fewer patients than in the 10-mg arm. Conclusions: The expected 5-yr decline in renal function was not observed. Estimated GFR improved in both treatment groups but was significantly greater with 80 mg than with 10 mg, suggesting this benefit may be dosage related.
引用
收藏
页码:1131 / 1139
页数:9
相关论文
共 46 条
  • [41] Rosuvastatin-induced arrest in progression of renal disease
    Vidt, DG
    Cressman, MD
    Harris, S
    Pears, JS
    Hutchinson, HG
    [J]. CARDIOLOGY, 2004, 102 (01) : 52 - 60
  • [42] Treating to New Targets (TNT) study: Does lowering low-density lipoprotein cholesterol levels below currently recommended guidelines yield incremental clinical benefit?
    Waters, DD
    Guyton, JR
    Herrington, DM
    McGowan, MP
    Wenger, NK
    Shear, C
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (02) : 154 - 158
  • [43] Acute myocardial infarction and renal dysfunction: A high-risk combination
    Wright, RS
    Reeder, GS
    Herzog, CA
    Albright, RC
    Williams, BA
    Dvorak, DL
    Miller, WL
    Murphy, JG
    Kopecky, SL
    Jaffe, AS
    [J]. ANNALS OF INTERNAL MEDICINE, 2002, 137 (07) : 563 - 570
  • [44] A 3-hydroxy-3-methylglutaryl co-enzyme A reductase inhibitor reduces hypertensive nephrosclerosis in stroke-prone spontaneously hypertensive rats
    Yamashita, T
    Kawashima, S
    Miwa, Y
    Ozaki, M
    Namiki, M
    Hirase, T
    Inoue, N
    Hirata, K
    Yokoyama, M
    [J]. JOURNAL OF HYPERTENSION, 2002, 20 (12) : 2465 - 2473
  • [45] Effect of simvastatin on proliferative nephritis and cell-cycle protein expression
    Yoshimura, A
    Nemoto, T
    Sugenoya, Y
    Inui, K
    Watanabe, S
    Inoue, Y
    Sharif, S
    Yokota, N
    Uda, S
    Morita, H
    Ideura, T
    [J]. KIDNEY INTERNATIONAL, 1999, 56 : S84 - S87
  • [46] Atorvastatin prevents end-organ injury in salt-sensitive hypertension - Role of eNOS and oxidant stress
    Zhou, MS
    Jaimes, EA
    Raij, L
    [J]. HYPERTENSION, 2004, 44 (02) : 186 - 190