» Articles » PMID: 24786143

The Incidence of Kidney Injury for Patients Treated with a High-potency Versus Moderate-potency Statin Regimen After an Acute Coronary Syndrome

Overview
Date 2014 May 3
PMID 24786143
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Observational studies have raised concerns that high-potency statins increase the risk of acute kidney injury. We therefore examined the incidence of kidney injury across 2 randomized trials of statin therapy.

Methods And Results: PROVE IT-TIMI 22 enrolled 4162 subjects after an acute coronary syndrome (ACS) and randomized them to atorvastatin 80 mg/day versus pravastatin 40 mg/day. A-to-Z enrolled 4497 subjects after ACS and randomized them to a high-potency (simvastatin 40 mg/day × 1 months, then simvastatin 80 mg/day) versus a delayed moderate-potency statin strategy (placebo × 4 months, then simvastatin 20 mg/day). Serum creatinine was assessed centrally at serial time points. Adverse events (AEs) relating to kidney injury were identified through database review. Across both trials, mean serum creatinine was similar between treatment arms at baseline and throughout follow-up. In A-to-Z, the incidence of a 1.5-fold or ≥ 0.3 mg/dL rise in serum creatinine was 11.4% for subjects randomized to a high-potency statin regimen versus 12.4% for those on a delayed moderate-potency regimen (odds ratio [OR], 0.91; 95% confidence interval [CI], 0.76 to 1.10; P=0.33). In PROVE IT-TIMI 22, the incidence was 9.4% for subjects randomized to atorvastatin 80 mg/day and 10.6% for subjects randomized to pravastatin 40 mg/day (OR, 0.88; 95% CI, 0.71 to 1.09; P=0.25). Consistent results were observed for different kidney injury thresholds and in individuals with diabetes mellitus or with moderate renal dysfunction. The incidence of kidney injury-related adverse events (AEs) was not statistically different for patients on a high-potency versus moderate-potency statin regimen (OR, 1.06; 95% CI, 0.68 to 1.67; P=0.78).

Conclusions: For patients enrolled in 2 large randomized trials of statin therapy after ACS, the use of a high-potency statin regimen did not increase the risk of kidney injury.

Citing Articles

Role of Bempedoic Acid in Clinical Practice.

Ballantyne C, Bays H, Catapano A, Goldberg A, Ray K, Saseen J Cardiovasc Drugs Ther. 2021; 35(4):853-864.

PMID: 33818688 PMC: 8266788. DOI: 10.1007/s10557-021-07147-5.


Incidence, determinants and impact of acute kidney injury in patients with diabetes mellitus and multivessel disease undergoing coronary revascularization: Results from the FREEDOM trial.

Arbel Y, Fuster V, Baber U, Hamza T, Siami F, Farkouh M Int J Cardiol. 2019; 293:197-202.

PMID: 31230933 PMC: 6710128. DOI: 10.1016/j.ijcard.2019.05.064.


Statin use and the risk of acute kidney injury in older adults.

Tonelli M, Lloyd A, Bello A, James M, Klarenbach S, McAlister F BMC Nephrol. 2019; 20(1):103.

PMID: 30909872 PMC: 6434639. DOI: 10.1186/s12882-019-1280-7.

References
1.
de Lemos J, Blazing M, Wiviott S, Lewis E, Fox K, White H . Early intensive vs a delayed conservative simvastatin strategy in patients with acute coronary syndromes: phase Z of the A to Z trial. JAMA. 2004; 292(11):1307-16. DOI: 10.1001/jama.292.11.1307. View

2.
Davignon J . Beneficial cardiovascular pleiotropic effects of statins. Circulation. 2004; 109(23 Suppl 1):III39-43. DOI: 10.1161/01.CIR.0000131517.20177.5a. View

3.
Patti G, Ricottini E, Nusca A, Colonna G, Pasceri V, DAmbrosio A . Short-term, high-dose Atorvastatin pretreatment to prevent contrast-induced nephropathy in patients with acute coronary syndromes undergoing percutaneous coronary intervention (from the ARMYDA-CIN [atorvastatin for reduction of myocardial damage.... Am J Cardiol. 2011; 108(1):1-7. DOI: 10.1016/j.amjcard.2011.03.001. View

4.
Schwartz G, Olsson A, Ezekowitz M, Ganz P, Oliver M, Waters D . Effects of atorvastatin on early recurrent ischemic events in acute coronary syndromes: the MIRACL study: a randomized controlled trial. JAMA. 2001; 285(13):1711-8. DOI: 10.1001/jama.285.13.1711. View

5.
Ichiki T, Takeda K, Tokunou T, Iino N, Egashira K, Shimokawa H . Downregulation of angiotensin II type 1 receptor by hydrophobic 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors in vascular smooth muscle cells. Arterioscler Thromb Vasc Biol. 2001; 21(12):1896-901. DOI: 10.1161/hq1201.099430. View