Clustering of Metabolic Syndrome Components Attenuates Coronary Plaque Regression During Intensive Statin Therapy in Patients With Acute Coronary Syndrome - The JAPAN-ACS Subanalysis Study

被引:9
作者
Takashima, Hiroaki [1 ]
Ozaki, Yukio [2 ]
Morimoto, Takeshi [3 ]
Kimura, Takeshi [4 ]
Hiro, Takafumi [5 ]
Miyauchi, Katsumi [6 ]
Nakagawa, Yoshihisa [7 ]
Yamagishi, Masakazu [8 ]
Daida, Hiroyuki [6 ]
Mizuno, Tomofumi [1 ]
Asai, Kenji [1 ]
Kuroda, Yasuo [1 ]
Kosaka, Takashi [1 ]
Kuhara, Yasushi [1 ]
Kurita, Akiyoshi [1 ]
Maeda, Kazuyuki [1 ]
Amano, Tetsuya [1 ]
Matsuzaki, Masunori [9 ]
机构
[1] Aichi Med Univ, Dept Cardiol, Nagakute, Aichi 4801195, Japan
[2] Fujita Hlth Univ, Dept Cardiol, Toyoake, Aichi, Japan
[3] Kinki Univ, Sch Med, Ctr Gen Internal Med & Emergency Care, Osaka 589, Japan
[4] Kyoto Univ, Div Cardiol, Dept Cardiovasc Med, Grad Sch Med, Kyoto, Japan
[5] Nihon Univ, Sch Med, Div Cardiol, Dept Med, Tokyo, Japan
[6] Juntendo Univ, Sch Med, Dept Cardiol, Tokyo 113, Japan
[7] Tenri Hosp, Dept Cardiol, Tenri, Nara 632, Japan
[8] Kanazawa Univ, Div Cardiovasc Med, Grad Sch Med, Kanazawa, Ishikawa, Japan
[9] Yamaguchi Univ, Div Cardiol, Dept Med & Clin Sci, Grad Sch Med, Ube, Yamaguchi 755, Japan
关键词
Acute coronary syndrome; Intravascular ultrasound; Metabolic syndrome components; Plaque; Statins; SERIAL INTRAVASCULAR ULTRASOUND; CARDIOVASCULAR-DISEASE; CLINICAL-OUTCOMES; IMPACT; PITAVASTATIN; ATORVASTATIN; PROGRESSION; PRAVASTATIN; RISK; ATHEROSCLEROSIS;
D O I
10.1253/circj.CJ-11-1495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The JAPAN-ACS (Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome) trial showed that intensive statin therapy could induce significant coronary plaque regression in acute coronary syndrome (ACS). We evaluated the impact of metabolic syndrome (MetS) and its components on coronary plaque regression in the JAPAN-ACS patients. Methods and Results: Serial intravascular ultrasound measurements over 8-12 months were performed in 242 ACS patients receiving pitavastatin or atorvastatin. Patients were divided into groups according to the presence of MetS or the number of MetS components. Although the percent change in plaque volume (%PV) was not significantly different between the MetS (n=119) and non-MetS (n=123) groups (P=0.50), it was significantly associated with an increasing number of MetS components (component 0: -24.0%, n=7; components 1: -20.8%, n=31; components 2: -16.1%, n=69; components 3: -18.7%, n=83; components 4: -13.5%, n=52; P=0.037 for trend). The percent change in body mass index (%BMI) significantly correlated with %PV (r=0.15, P=0.021), especially in the MetS components 4 group (r=0.35, P=0.017). In addition, %BMI was an independent predictor of plaque regression after adjustment for the changes of low- and high-density lipoprotein cholesterol, triglycerides and HbA1c. Conclusions: The clustering of MetS components, but not the presence of MetS itself, could attenuate coronary plaque regression during intensive statin therapy in ACS patients. Therefore, to achieve a greater degree of plaque regression, it is necessary to treat to each MetS component and use lifestyle modification. (Circ J 2012; 76: 2840-2847)
引用
收藏
页码:2840 / 2847
页数:8
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