Can low-density lipoprotein be too low? The safety and efficacy of achieving very low low-density lipoprotein with intensive statin therapy

被引:273
作者
Wiviott, SD [1 ]
Cannon, CP [1 ]
Morrow, DA [1 ]
Ray, KK [1 ]
Pfeffer, MA [1 ]
Braunwald, E [1 ]
机构
[1] Brigham & Womens Hosp, Div Cardiovasc, TIMI Study Grp, Boston, MA 02115 USA
关键词
D O I
10.1016/j.jacc.2005.04.064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This study sought to evaluate the safety and efficacy of achieving very low calculated low-density lipoprotein (LDL) levels with intensive statin therapy. BACKGROUND Intensive statin therapy reduces clinical events occurring after acute coronary syndrome (ACS) and may result in LDL levels markedly lower than guideline levels. Prior epidemiologic and preclinical studies raise concerns about the safety of very low cholesterol levels. METHODS The Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis In Myocardial Infarction 22 (PROVE IT-TIMI 22) study compared intensive therapy (atorvastatin, 80 mg) and moderate therapy (pravastatin, 40 mg) in patients after ACS. Patients treated with atorvastatin were divided by four-month LDL values into groups: > 100, > 80 to 100 (reference-range-meeting guidelines), > 60 to 80, > 40 to 60, and < 40 mg/dl. Baseline, clinical, and safety data were compared among groups achieving guideline recommendation levels or lower. RESULTS Among 1,825 patients with four-month LDL, 91% were at goal (< 100 mg/dl). The distribution was > 80 to 100 mg/dl (14%), > 60 to 80 mg/dl (31%), > 40 to 60 mg/dl (34%), and < 40 mg/dl (11%). Those with lower LDL levels were more often male, older, and diabetic, and had lower baseline LDL levels. They had prior statin therapy and fewer prior myocardial infarctions (MI). There were no significant differences in safety parameters, including muscle, liver, or retinal abnormalities, intracranial hemorrhage, or death, in the very low LDL groups. The < 40 mg/dl and 40 to 60 mg/dl groups had fewer major cardiac events (death, MI, stroke, recurrent ischemia, revascularization). CONCLUSIONS Compared with patients treated with an accepted LDL goal (80 to 100 mg/dl), there was no adverse effect on safety with lower achieved LDL levels, and apparent improved clinical efficacy. These data identify no intrinsic safety concern of achieving low LDL and, therefore, a strategy of intensive treatment need not be altered in patients achieving very low LDL levels.
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页码:1411 / 1416
页数:6
相关论文
共 28 条
[11]  
Grundy SM, 2001, AM J CARDIOL, V88, p23J
[12]   SERUM TOTAL CHOLESTEROL AND MORTALITY IN JAPANESE POPULATION [J].
ISO, H ;
NAITO, Y ;
KITAMURA, A ;
SATO, S ;
KIYAMA, M ;
TAKAYAMA, Y ;
IIDA, M ;
SHIMAMOTO, T ;
SANKAI, T ;
KOMACHI, Y .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1994, 47 (09) :961-969
[13]   Intensive lipid lowering with atorvastatin in patients with stable coronary disease [J].
LaRosa, JC ;
Grundy, SM ;
Waters, DD ;
Shear, C ;
Barter, P ;
Fruchart, J ;
Gotto, AM ;
Greten, H ;
Kastelein, JJP ;
Shepherd, J ;
Wenger, NK .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (14) :1425-1435
[14]   SERUM-CHOLESTEROL LEVEL AND MORTALITY FINDINGS FOR MEN SCREENED IN THE MULTIPLE RISK FACTOR INTERVENTION TRIAL [J].
NEATON, JD ;
BLACKBURN, H ;
JACOBS, D ;
KULLER, L ;
LEE, DJ ;
SHERWIN, R ;
SHIH, J ;
STAMLER, J ;
WENTWORTH, D .
ARCHIVES OF INTERNAL MEDICINE, 1992, 152 (07) :1490-1500
[15]   Safety of atorvastatin derived from analysis of 44 completed trials in 9,416 patients [J].
Newman, CB ;
Palmer, G ;
Silbershatz, H ;
Szarek, M .
AMERICAN JOURNAL OF CARDIOLOGY, 2003, 92 (06) :670-676
[16]   Optimal low-density lipoprotein is 50 to 70 mg/dl - Lower is better and physiologically normal [J].
O'Keefe, JH ;
Cordain, L ;
Harris, WH ;
Moe, RM ;
Vogel, R .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (11) :2142-2146
[17]  
Packard CJ, 1998, CIRCULATION, V97, P1440
[18]   ACC/AHA/NHLBI clinical advisory on the use and safety of statins [J].
Pasternak, RC ;
Smith, SC ;
Merz, CNB ;
Grundy, SM ;
Cleeman, JI ;
Lenfant, C .
STROKE, 2002, 33 (09) :2337-2341
[19]  
PEDERSEN TR, 1994, LANCET, V344, P1383
[20]   Safety and tolerability of pravastatin in long-term clinical trials - Prospective pravastatin pooling (PPP) project [J].
Pfeffer, MA ;
Keech, A ;
Sacks, FM ;
Cobbe, SM ;
Tonkin, A ;
Byington, RP ;
Davis, BR ;
Friedman, CP ;
Braunwald, E .
CIRCULATION, 2002, 105 (20) :2341-2346