Serum glucose and triglyceride determine high-risk subgroups in non-diabetic postinfarction patients

被引:14
作者
Corsetti, JP
Zareba, W
Moss, AJ
Sparks, CE
机构
[1] Univ Rochester, Med Ctr, Dept Pathol & Lab Med, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Med, Cardiol Unit, Rochester, NY USA
关键词
metabolic syndrome; glucose; triglyceride; BMI; fibrinogen; PAI-1; postinfarction;
D O I
10.1016/j.atherosclerosis.2005.03.046
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
A strategy was developed to identify subgroups at high risk for recurrent coronary events in non-diabetic postinfarction patients as a function of metabolic, inflammatory, and thrombogenic blood markers. A graphical screening technique for presumptively identifying high-risk subgroups from outcome prevalence maps was devised that was equally sensitive for all values of risk factors in contrast to traditional approaches where risk is presumed for the highest or the lowest values. Traditional statistical analysis confirms high risk in identified Subgroups. Serum glucose and triglyceride served as bivariate search domain. Results demonstrated three high-risk subgroups. One was characterized as pre-diabetic; another as metabolic syndrorne-enriched; and the third, with unexpectedly high risk, as normoglycemic and modestly hypertriglyceridemic. Within-subgroup risk as determined by Cox proportional hazards model gave for odds ratios and 95 percentile confidence intervals: glucose, 2.49 (1.17-5.33) in pre-diabetic; PAI-I, 3.95 (1.81-8.61) in metabolic syndrorne-enriched; and BMI, 2.79 (1.17-6.63) and fibrinogen, 2.79 (1.29-6.04) in normoglycemic, modestly hypertriglyceridemic patients. We conclude that the graphical approach holds promise in screening for high-risk patient subgroups. Finding different within-subgroup predictors of risk underscores the notion of context-dependent risk, an observation that may be relevant for determining optimal use of emerging risk factors. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
相关论文
共 25 条
[1]
Progression of coronary artery disease in young male post-infarction patients is linked to disturbances of carbohydrate and lipoprotein metabolism and to impaired fibrinolytic function [J].
Bavenholm, P ;
de Faire, U ;
Landou, C ;
Efendic, S ;
Nilsson, J ;
Wiman, B ;
Hamsten, A .
EUROPEAN HEART JOURNAL, 1998, 19 (03) :402-410
[2]
Apolipoprotein B determines risk for recurrent coronary events in postinfarction patients with metabolic syndrome [J].
Corsetti, JP ;
Zareba, W ;
Moss, AJ ;
Sparks, CE .
ATHEROSCLEROSIS, 2004, 177 (02) :367-373
[3]
Metabolic syndrome best defines the multivariate distribution of blood variables in postinfarction patients [J].
Corsetti, JP ;
Zareba, W ;
Moss, AJ ;
Ridker, PM ;
Marder, VJ ;
Rainwater, DL ;
Sparks, CE .
ATHEROSCLEROSIS, 2003, 171 (02) :351-358
[4]
Inflammation in the prediabetic state is related to increased insulin resistance rather than decreased insulin secretion [J].
Festa, A ;
Hanley, AJG ;
Tracy, RP ;
D'Agostino, R ;
Haffner, SM .
CIRCULATION, 2003, 108 (15) :1822-1830
[5]
Genuth S, 2003, DIABETES CARE, V26, P3160
[6]
Insulin-resistant prediabetic subjects have more atherogenic risk factors than insulin-sensitive prediabetic subjects -: Implications for preventing coronary heart disease during the prediabetic state [J].
Haffner, SM ;
Mykkänen, L ;
Festa, A ;
Burke, JP ;
Stern, MP .
CIRCULATION, 2000, 101 (09) :975-980
[7]
Pre-diabetes, insulin resistance, inflammation and CVD risk [J].
Haffner, SM .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2003, 61 :S9-S18
[8]
Insulin resistance, inflammation, and the prediabetic state [J].
Haffner, SM .
AMERICAN JOURNAL OF CARDIOLOGY, 2003, 92 (4A) :18J-26J
[9]
HAMSTEN A, 1987, LANCET, V2, P3
[10]
Insulin resistance and the metabolic syndrome - a challenge of the new millennium [J].
Hauner, H .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2002, 56 (Suppl 1) :S25-S29