Association between C-reactive protein and QTc interval in middle-aged men and women

被引:26
作者
Kim, Eunhee
Joo, SoonJae
Kim, Jinyoung
Ahn, JeongCheon
Kim, JeHyeong
Kimm, Kuchan
Shin, Chol
机构
[1] Korea Univ, Ansan Hosp, Dept Internal Med, Div Pulm & Crit Care Med, Ansan 425707, Gyeonggi Do, South Korea
[2] Natl Inst Toxicol Res, Dept Biostat, Seoul, South Korea
[3] Korea Univ, Coll Med, Inst Human Genomic Study, Seoul 136701, South Korea
[4] Korea Univ, Ansan Hosp, Dept Internal Med, Div Cardiol, Gyeonggi Do, South Korea
[5] Korea Natl Inst Hlth, Ctr Genome Sci, Seoul, South Korea
关键词
C-reactive protein; epidemiology; QT interval;
D O I
10.1007/s10654-006-9034-9
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Both of prolonged QT interval and elevated C-reactive protein (CRP) levels are known to be risk factors of cardiovascular disease. To our knowledge, few studies have reported the direct relationship between CRP levels and the QT interval in middle-aged population. The objective of the present study was to examine the association of CRP level with QT interval. Methods and results: A total of 2471 men and 2287 women from the Korea n Health and Genome study underwent physical examination and completed a questionnaire. A 12-lead electrocardiogram (ECG) recording was obtained from each subject. Subjects who were taking statins, non-steroidal anti-inflammatory drugs (NSAID) and postmenopausal hormone replacement therapy, which are known to have an effect on CRP levels, were excluded. Geometric means of CRP levels were compared among three groups, which were classified by heart rate-corrected QT (QTc) interval: prolonged (>= 440 msec in men and >= 450 msec in women), borderline (420-439 msec in men and 430-449 msec in women) and normal (< 420 msec in men and < 430 msec in women) groups. The means of CRP level in women, though over normal range, increased significantly as QTc interval was longer, independent of confounding factors, while those of men were on the borderline of significance. However, compared to normal range of QTc interval, prolonged QTc interval was associated with elevated CRP level, defined as more than 95 percentile of CRP, in men and women, respectively. Conclusions: Prolonged QTc interval in middle-aged men and women is associated with the elevated CRP, independent of confounding factors.
引用
收藏
页码:653 / 659
页数:7
相关论文
共 51 条
[1]   INFLUENCE OF HEART-RATE AND INHIBITION OF AUTONOMIC TONE ON THE QT INTERVAL [J].
AHNVE, S ;
VALLIN, H .
CIRCULATION, 1982, 65 (03) :435-439
[2]   Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[3]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[4]  
2-S
[5]   Interleukin-6 levels are inversely correlated with heart rate variability in patients with decompensated heart failure [J].
Aronson, D ;
Mittleman, MA ;
Burger, AJ .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2001, 12 (03) :294-300
[6]  
Bazett HC, 1920, HEART-J STUD CIRC, V7, P353
[7]  
BELLAVERE F, 1988, BRIT HEART J, V59, P379
[8]   Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin [J].
Borovikova, LV ;
Ivanova, S ;
Zhang, MH ;
Yang, H ;
Botchkina, GI ;
Watkins, LR ;
Wang, HC ;
Abumrad, N ;
Eaton, JW ;
Tracey, KJ .
NATURE, 2000, 405 (6785) :458-462
[9]   Impaired fasting glucose, diabetes mellitus, and cardiovascular disease risk factors are associated with prolonged QTc duration. Results from the Third National Health and Nutrition Examination Survey [J].
Brown, DW ;
Giles, WH ;
Greenlund, KJ ;
Valdez, R ;
Croft, JB .
JOURNAL OF CARDIOVASCULAR RISK, 2001, 8 (04) :227-233
[10]   QT interval is linked to 2 long-QT syndrome loci in normal subjects [J].
Busjahn, A ;
Knoblauch, H ;
Faulhaber, HD ;
Boeckel, T ;
Rosenthal, M ;
Uhlmann, R ;
Hoehe, M ;
Schuster, H ;
Luft, FC .
CIRCULATION, 1999, 99 (24) :3161-3164