Cited by 302Lipoproteins and Cardiovascular HealthChronic Kidney Disease and DiabetesBlood Pressure and Hypertension Studies

Intensive Lipid Lowering With Atorvastatin in Patients With Coronary Heart Disease and Chronic Kidney Disease

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Shepherd, James, Kastelein, John J.P., Bittner, Vera, Deedwania, Prakash, Breazna, Andrei, Dobson, Stephen, Wilson, Daniel J., Zuckerman, Andrea +1 more·2008·Journal of the American College of Cardiology

Abstract

Objectives This subanalysis of the TNT (Treating to New Targets) study investigates the effects of intensive lipid lowering with atorvastatin in patients with coronary heart disease (CHD) with and without pre-existing chronic kidney disease (CKD).Background Cardiovascular disease is a major cause of morbidity and mortality in patients with CKD.Methods A total of 10,001 patients with CHD were randomized to double-blind therapy with atorvastatin 80 mg/day or 10 mg/day. Patients with CKD were identified at baseline on the basis of an estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 m(2) using the Modification of Diet in Renal Disease equation. The primary efficacy outcome was time to first major cardiovascular event.Results Of 9,656 patients with complete renal data, 3,107 had CKD at baseline and demonstrated greater cardiovascular comorbidity than those with normal eGFR (n = 6,549). After a median follow-up of 5.0 years, 351 patients with CKD (11.3%) experienced a major cardiovascular event, compared with 561 patients with normal eGFR (8.6%) (hazard ratio [HR] = 1.35; 95% confidence interval [CI] 1.18 to 1.54; p < 0.0001). Compared with atorvastatin 10 mg, atorvastatin 80 mg reduced the relative risk of major cardiovascular events by 32% in patients with CKD (HR = 0.68; 95% CI 0.55 to 0.84; p = 0.0003) and 15% in patients with normal eGFR (HR = 0.85; 95% CI 0.72 to 1.00; p = 0.049). Both doses of atorvastatin were well tolerated in patients with CKD.Conclusions Aggressive lipid lowering with atorvastatin 80 mg was both safe and effective in reducing the excess of cardiovascular events in a high-risk population with CKD and CHD.

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Crossref · 10.1016/j.jacc.2007.11.072

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References 21 · Cited by 302

Authors
Shepherd, J., Kastelein, J. J. P., Bittner, V., Deedwania, P., Breazna, A., Dobson, S., Wilson, D. J., Zuckerman, A., & Wenger, N. K.
Affiliations
  • University of Glasgow (GB)
  • Amsterdam UMC Location University of Amsterdam (NL)
  • University of Alabama at Birmingham (US)
  • University of California, San Francisco (US)
  • Pfizer (United States) (US)
  • Emory University (US)
Corresponding author
Shepherd, James
Venue
Journal of the American College of Cardiology
Publisher
Elsevier BV
Published
2008-04
Volume
51
Issue
15
Pages
1448-1454
ISSN
0735-1097 (ISSN-L)
OpenAlex
W1483531931
Cited by
302
References
21
Citations by year
2026: 1 · 2025: 4 · 2024: 8 · 2023: 7 · 2022: 8 · 2021: 5 · 2020: 12 · 2019: 12 · 2018: 16 · 2017: 15 · 2016: 18 · 2015: 22 · 2014: 34 · 2013: 21 · 2012: 21
FWCI
34.42
Type
journal article
Language
en
Open access
Locations
  • Journal of the American College of Cardiology (publishedVersion)
  • PubMed (publishedVersion)
  • Pure Amsterdam UMC (publishedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
Funders
Pfizer
Topics
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
  • Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
Keywords
atorvastatin, intensive lipid lowering, coronary artery disease, chronic kidney disease, major adverse cardiovascular events, statin dose comparison, estimated glomerular filtration rate, TNT trial
MeSH terms
Atorvastatin, Adult, Aged, Anticholesteremic Agents, Coronary Artery Disease, Double-Blind Method, Female, Glomerular Filtration Rate, Heptanoic Acids, Humans, Kidney Failure, Chronic, Lipids, Cholesterol, LDL, Male, Middle Aged, Pyrroles, Risk, Triglycerides, Hydroxymethylglutaryl-CoA Reductase Inhibitors

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