Longitudinal Change in Fasting Blood Glucose and Myocardial Infarction Risk in a Population Without Diabetes

被引:156
|
作者
Jin, Cheng [1 ,2 ]
Chen, Shuohua [1 ]
Vaidya, Anand [3 ,4 ]
Wu, Yuntao [1 ]
Wu, Zhijun [5 ]
Hu, Frank B. [6 ]
Kris-Etherton, Penny [2 ]
Wu, Shouling [1 ]
Gao, Xiang [2 ]
机构
[1] Kailuan Gen Hosp, Dept Cardiol, Tangshan, Peoples R China
[2] Penn State Univ, Dept Nutr Sci, State Coll, PA 16804 USA
[3] Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, 75 Francis St, Boston, MA 02115 USA
[4] Harvard Med Sch, Boston, MA USA
[5] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Cardiol, Sch Med, Shanghai, Peoples R China
[6] Harvard TH Chan Sch Publ Hlth, Dept Nutr & Epidemiol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
ALL-CAUSE MORTALITY; FOLLOW-UP; CARDIOVASCULAR MORTALITY; METABOLIC SYNDROME; SAS PROCEDURE; LIFE-STYLE; MELLITUS; DISEASE; TOLERANCE; METAANALYSIS;
D O I
10.2337/dc17-0610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To examine the change in fasting blood glucose (FBG) during repeated assessments over time and its potential impact on the risk of developing myocardial infarction (MI). RESEARCH DESIGN AND METHODS This prospective cohort study included 68,297 participants without diabetes (mean age 49 years) who were free of MI, stroke, and cancer prior to or in 2010 (baseline of the current analysis). FBG concentrations were measured in 2006, 2008, and 2010. The FBG trajectories during 2006-2010, the primary exposure of the current study, were identified by latent mixture modeling. Incident MI cases were confirmed via review of medical records by cardiologists. RESULTS We identified five discrete FBG trajectories according to FBG range and changing pattern over time: elevated-stable (n = 3,877), elevated-decreasing (n = 7,060), moderate-increasing (n = 10,298), moderate-stable (n = 40,352), and low-stable (n = 6,710). During 4 years of follow-up, we documented 283 incident MI cases. Relative to the moderate-stable pattern (FBG ranged from 4.9 to 5.1 mmol/L), adjusted hazard ratios (HRs) were 1.53 (95% CI 1.04, 2.26) for the elevated-stable pattern (FBG ranged from 6.1 to 6.3 mmol/L) and HR 0.61 (95% CI 0.38, 0.98) for the elevated-decreasing pattern (FBG decreased from 6.0 to 5.4 mmol/L), after adjustment for potential confounders such as age, sex, lifestyle factors, obesity, medical history, blood pressure, blood lipids, and C-reactive protein. Consistently, cumulative average and increasing rate of FBG during 2006-2010, but not a single baseline FBG, predicted future risk of MI. CONCLUSIONS We found that discrete FBG trajectories were significantly associated with subsequent risk of MI in individuals without diabetes. These observations suggest that long-term trajectories of FBG may be important for risk prediction of MI and possibly other macrovascular diseases.
引用
收藏
页码:1565 / 1572
页数:8
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