Absolute change in fasting plasma glucose over 12 months is associated with 2-year and 5-year major adverse cardiovascular events in patients with drug-eluting stent implants

被引:7
作者
Kang, Dong Oh [1 ]
Seo, Hong Seog [1 ]
Choi, Byung Geol [1 ]
Lee, Eunmi [2 ]
Kim, Ji Park [1 ]
Lee, Sun Ki [1 ]
Im, Sung [1 ]
Na, Jin Oh [1 ]
Choi, Cheol Ung [1 ]
Lim, Hong Euy [1 ]
Kim, Jin Won [1 ]
Kim, Eung Ju [1 ]
Rha, Seung-Woon [1 ]
Park, Chang Gyu [1 ]
Oh, Dong Joo [1 ]
机构
[1] Korea Univ, Ctr Cardiothorac, Guro Hosp, Div Cardiol,Dept Internal Med,Coll Med, Seoul 152703, South Korea
[2] Wonkwang Univ, Coll Med, Sanbon Hosp, Dept Cardiol, Gunpo, South Korea
关键词
Blood glucose; Statins; Diabetes mellitus; Major adverse cardiac event; CORONARY-HEART-DISEASE; 14; RANDOMIZED-TRIALS; STATIN THERAPY; REDUCTASE INHIBITORS; LOWERING TREATMENT; RISK-FACTOR; ALL-CAUSE; MORTALITY; STEROIDOGENESIS; GLYCEMIA;
D O I
10.1016/j.ijcard.2014.10.164
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Major adverse cardiovascular events (MACEs) in patients with or without cardiovascular disease (CVD) are greatly affected by various factors associated with metabolism and inflammation. Objective: To determine which clinical parameters at treatment are associated with the development of 2-year and 5-year MACEs in high-risk patients with CVD who have undergone drug-eluting stent (DES) implantation. Method: The present study involved a total of 432 patients who underwent percutaneous coronary intervention with DES. Variables representing the average and absolute amount of change in clinical parameters over the 12-month follow-up were assessed for association with 2-year and 5-year development of MACE. The study population was divided into quartiles for the variable showing the highest correlation to MACE development. Estimated incidence of 2-year and 5-year MACEs for each of the quartiles was determined by survival curve analysis, and subgroup analysis was performed for patients with diabetes and statin users. Results: Absolute change in fasting plasma glucose (FPG) over 12 months showed the highest correlation with 2-year and 5-year MACE development. The estimated incidence of MACE increased with increasing quartiles for absolute change in FPG. The association between absolute change in FPG and MACE development exhibited a stronger relationship for the specific subgroups of patients with diabetes and statin users. Increases and decreases in FPG had a comparable contribution to MACE development. Conclusion: A greater absolute change in FPG over 12 months post-PCI is an independent risk factor for 2-year and 5-year MACE development in DES-implanted patients, especially in the diabetes and statin users. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:146 / 152
页数:7
相关论文
共 36 条
[1]   Random fasting hyperglycemia as cardiovascular risk factor in the elderly: A 6-year longitudinal study [J].
Antonicelli, R ;
Gesuita, R ;
Boemi, M ;
Paciaroni, E .
CLINICAL CARDIOLOGY, 2001, 24 (04) :341-344
[2]   The safety of statins in clinical practice [J].
Armitage, Jane .
LANCET, 2007, 370 (9601) :1781-1790
[3]   Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins [J].
Baigent, C ;
Keech, A ;
Kearney, PM ;
Blackwell, L ;
Buck, G ;
Pollicino, C ;
Kirby, A ;
Sourjina, T ;
Peto, R ;
Collins, R ;
Simes, J .
LANCET, 2005, 366 (9493) :1267-1278
[4]  
Böhm M, 2004, Z KARDIOL, V93, P43, DOI 10.1007/s00392-004-1003-2
[5]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[6]   Beneficial cardiovascular pleiotropic effects of statins [J].
Davignon, J .
CIRCULATION, 2004, 109 (23) :39-43
[7]   LONG-TERM ENDOCRINE FUNCTION IN HYPERCHOLESTEROLEMIC PATIENTS TREATED WITH PRAVASTATIN, A NEW 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE INHIBITOR [J].
DOBS, AS ;
SARMA, PS ;
SCHTEINGART, D .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1993, 42 (09) :1146-1152
[8]   Effects of high-dose simvastatin on adrenal and gonadal steroidogenesis in men with hypercholesterolemia [J].
Dobs, AS ;
Schrott, H ;
Davidson, MH ;
Bays, H ;
Stein, EA ;
Kush, D ;
Wu, M ;
Mitchel, Y ;
Illingworth, RD .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (09) :1234-1238
[9]  
Gerstein HC, 2008, NEW ENGL J MED, V358, P2545, DOI 10.1056/NEJMoa0802743
[10]   Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel III guidelines [J].
Grundy, SM ;
Cleeman, JI ;
Merz, CNB ;
Brewer, HB ;
Clark, LT ;
Hunninghake, DB ;
Pasternak, RC ;
Smith, SC ;
Stone, NJ .
CIRCULATION, 2004, 110 (02) :227-239