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

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). This prospective cohort study included 68,297 participants without diabetes (mean age 49 years) who were free of MI, stroke, and c...

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Veröffentlicht in:Diabetes care 2017-11, Vol.40 (11), p.1565-1572
Hauptverfasser: Jin, Cheng, Chen, Shuohua, Vaidya, Anand, Wu, Yuntao, Wu, Zhijun, Hu, Frank B, Kris-Etherton, Penny, Wu, Shouling, Gao, Xiang
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container_end_page 1572
container_issue 11
container_start_page 1565
container_title Diabetes care
container_volume 40
creator Jin, Cheng
Chen, Shuohua
Vaidya, Anand
Wu, Yuntao
Wu, Zhijun
Hu, Frank B
Kris-Etherton, Penny
Wu, Shouling
Gao, Xiang
description 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). 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. We identified five discrete FBG trajectories according to FBG range and changing pattern over time: elevated-stable ( = 3,877), elevated-decreasing ( = 7,060), moderate-increasing ( = 10,298), moderate-stable ( = 40,352), and low-stable ( = 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. 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.
doi_str_mv 10.2337/dc17-0610
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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. We identified five discrete FBG trajectories according to FBG range and changing pattern over time: elevated-stable ( = 3,877), elevated-decreasing ( = 7,060), moderate-increasing ( = 10,298), moderate-stable ( = 40,352), and low-stable ( = 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. We found that discrete FBG trajectories were significantly associated with subsequent risk of MI in individuals without diabetes. 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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. We identified five discrete FBG trajectories according to FBG range and changing pattern over time: elevated-stable ( = 3,877), elevated-decreasing ( = 7,060), moderate-increasing ( = 10,298), moderate-stable ( = 40,352), and low-stable ( = 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. We found that discrete FBG trajectories were significantly associated with subsequent risk of MI in individuals without diabetes. 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, Cheng</au><au>Chen, Shuohua</au><au>Vaidya, Anand</au><au>Wu, Yuntao</au><au>Wu, Zhijun</au><au>Hu, Frank B</au><au>Kris-Etherton, Penny</au><au>Wu, Shouling</au><au>Gao, Xiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal Change in Fasting Blood Glucose and Myocardial Infarction Risk in a Population Without Diabetes</atitle><jtitle>Diabetes care</jtitle><addtitle>Diabetes Care</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>40</volume><issue>11</issue><spage>1565</spage><epage>1572</epage><pages>1565-1572</pages><issn>0149-5992</issn><eissn>1935-5548</eissn><abstract>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). 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. We identified five discrete FBG trajectories according to FBG range and changing pattern over time: elevated-stable ( = 3,877), elevated-decreasing ( = 7,060), moderate-increasing ( = 10,298), moderate-stable ( = 40,352), and low-stable ( = 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. 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.</abstract><cop>United States</cop><pub>American Diabetes Association</pub><pmid>28887409</pmid><doi>10.2337/dc17-0610</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2617-6509</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Blood Glucose - metabolism
Blood pressure
C-reactive protein
C-Reactive Protein - metabolism
Cancer
Cardiovascular and Metabolic Risk
Cerebral infarction
Cholesterol - blood
Diabetes
Diabetes mellitus
Diabetes Mellitus - blood
Diabetes Mellitus - diagnosis
Fasting
Female
Follow-Up Studies
Glucose
Health risks
Heart attacks
Humans
Incidence
Laboratory testing
Life Style
Lipids
Male
Medical records
Middle Aged
Myocardial infarction
Myocardial Infarction - blood
Myocardial Infarction - epidemiology
Obesity - blood
Predictions
Prospective Studies
Research design
Risk Factors
Stroke - blood
Stroke - epidemiology
Trajectories
Triglycerides - blood
Young Adult
title Longitudinal Change in Fasting Blood Glucose and Myocardial Infarction Risk in a Population Without Diabetes
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