Tracking of High-Sensitivity C-Reactive Protein after an Initially Elevated Concentration: The JUPITER Study

被引:77
作者
Glynn, Robert J. [1 ,2 ]
MacFadyen, Jean G. [1 ,2 ]
Ridker, Paul M. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Prevent Med, Boston, MA 02215 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Cardiovasc Dis Prevent, Boston, MA 02215 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc Med, Boston, MA 02215 USA
关键词
CORONARY-HEART-DISEASE; DENSITY-LIPOPROTEIN CHOLESTEROL; PRIMARY PREVENTION; BLOOD-PRESSURE; PLASMA-CONCENTRATION; STATIN THERAPY; FOLLOW-UP; RISK; INFLAMMATION; EVENTS;
D O I
10.1373/clinchem.2008.120642
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: The JUPITER (justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin) trial suggests that increased high-sensitivity C-reactive protein (hsCRP) concentrations may be useful in decisions about the initiation of statin therapy for primary prevention of vascular disease. Although studies of specific populations have suggested that hsCRP is a reliable longitudinal marker, it is unclear how strongly hsCRP tracks in individuals after a single increased concentration. METHODS: We evaluated tracking of hsCRP in 8901 individuals randomized to placebo in the JUPITER trial. These individuals had screening LDL cholesterol concentrations <130 mg/dL (<3.37 mmol/L) and hsCRP concentrations >= 2 mg/L, with subsequent hsCRP measurements made before randomization; at 13 weeks; 1, 2, 3, and 4 years later; and at trial termination. Longitudinal trends and associations were evaluated nonparametrically with box plots and Spearman correlations. After data transformation to achieve normality, repeated-measures regression models estimated the intraclass correlation of hsCRP, with and without controlling for known demographic, lifestyle, and medical determinants of hsCRP concentration. For comparison, we evaluated tracking of systolic and diastolic blood pressure; total, LDL, and HDL cholesterol; and fasting triglycerides. RESULTS: The median hsCRP concentration in these untreated individuals showed modest regression to the mean over time, declining from 3.8 mg/L at randomization to 3.4 mg/L at 4 years. Tracking correlations for hsCRP over time were comparable to those for blood pressure and LDL cholesterol, but lower than those for HDL, fasting triglycerides, and total cholesterol. The intraclass correlation for repeated hsCRP measure-adjustment and 0.50 (95% CI, 0.49-0.51) after adjustment for demographic, lifestyle, and comorbidity determinants. CONCLUSIONS: Concentrations of hsCRP show strong tracking, even after selection of individuals with initially high values. Without statin therapy, increased concentrations of hsCRP generally remain high over time. (C) 2008 American Association for Clinical Chemistry
引用
收藏
页码:305 / 312
页数:8
相关论文
共 29 条
[1]   C-reactive protein levels among women of various ethnic groups living in the United States - (from the Women's Health Study) [J].
Albert, MA ;
Glynn, RJ ;
Buring, J ;
Ridker, PM .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (10) :1238-1242
[2]   Effect of physical activity on serum C-reactive protein [J].
Albert, MA ;
Glynn, RJ ;
Ridker, PM .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (02) :221-225
[3]   Alcohol consumption and plasma concentration of C-reactive protein [J].
Albert, MA ;
Glynn, RJ ;
Ridker, PM .
CIRCULATION, 2003, 107 (03) :443-447
[4]   Lipoprotein-associated phospholipase A2, high-sensitivity C-reactive protein, and risk for incident coronary heart disease in middle-aged men and women in the Atherosclerosis Risk in Communities (ARIC) study [J].
Ballantyne, CM ;
Hoogeveen, RC ;
Bang, H ;
Coresh, J ;
Folsom, AR ;
Heiss, G ;
Sharrett, AR .
CIRCULATION, 2004, 109 (07) :837-842
[5]  
Bishop M.M., 1975, DISCRETE MULTIVARIAT
[6]   AN ANALYSIS OF TRANSFORMATIONS [J].
BOX, GEP ;
COX, DR .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1964, 26 (02) :211-252
[7]   C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease [J].
Danesh, J ;
Wheeler, JG ;
Hirschfield, GM ;
Eda, S ;
Eiriksdottir, G ;
Rumley, A ;
Lowe, GDO ;
Pepys, MB ;
Gudnason, V .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (14) :1387-1397
[8]   MODIFICATION OF INCREASING SYSTOLIC BLOOD-PRESSURE IN THE ELDERLY DURING THE 1980S [J].
GLYNN, RJ ;
FIELD, TS ;
SATTERFIELD, S ;
HEBERT, PR ;
BURING, JE ;
TAYLOR, JO ;
HENNEKENS, CH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 138 (06) :365-379
[9]   Expanding the Orbit of Primary Prevention - Moving beyond JUPITER. [J].
Hlatky, Mark A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (21) :2280-2282
[10]   UNBALANCED REPEATED-MEASURES MODELS WITH STRUCTURED COVARIANCE MATRICES [J].
JENNRICH, RI ;
SCHLUCHTER, MD .
BIOMETRICS, 1986, 42 (04) :805-820