Transitions in Metabolic Risk and Long‐Term Cardiovascular Health: Coronary Artery Risk Development in Young Adults (CARDIA) Study

Background Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life, missing early transitions in metabolic risk that may represent opportunities for averting the development of cardiovascular disease...

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Published inJournal of the American Heart Association Vol. 5; no. 10
Main Authors Murthy, Venkatesh L., Abbasi, Siddique A., Siddique, Juned, Colangelo, Laura A., Reis, Jared, Venkatesh, Bharath A., Carr, J. Jeffrey, Terry, James G., Camhi, Sarah M., Jerosch‐Herold, Michael, Ferranti, Sarah, Das, Saumya, Freedman, Jane, Carnethon, Mercedes R., Lewis, Cora E., Lima, Joao A. C., Shah, Ravi V.
Format Journal Article
LanguageEnglish
Published England John Wiley and Sons Inc 01.10.2016
Wiley
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Abstract Background Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life, missing early transitions in metabolic risk that may represent opportunities for averting the development of cardiovascular disease. Methods and Results In 4420 young adults in the Coronary Artery Risk Development in Young Adults (CARDIA) study, we defined a “metabolic” risk score based on components of the Third Report of the Adult Treatment Panel's definition of metabolic syndrome. Using latent class trajectory analysis adjusted for sex, race, and time‐dependent body mass index, we identified 6 distinct metabolic trajectories over time, specified by initial and final risk: low‐stable, low‐worsening, high‐stable, intermediate‐worsening, intermediate‐stable, and high‐worsening. Overall, individuals gained weight over time in CARDIA with statistically but not clinically different body mass index trend over time. Dysglycemia and dyslipidemia over time were highest in initially high or worsening trajectory groups. Divergence in metabolic trajectories occurred in early adulthood (before age 40), with 2 of 3 individuals experiencing an increase in metabolic risk over time. Membership in a higher‐risk trajectory (defined as initially high or worsening over time) was associated with greater prevalence and extent of coronary artery calcification, left ventricular mass, and decreased left ventricular strain at year 25. Importantly, despite similar rise in body mass index across trajectories over 25 years, coronary artery calcification and left ventricular structure and function more closely tracked risk factor trajectories. Conclusions Transitions in metabolic risk occur early in life. Obesity‐related metabolic dysfunction is related to subclinical cardiovascular phenotypes independent of evolution in body mass index, including coronary artery calcification and myocardial hypertrophy and dysfunction.
AbstractList Background Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life, missing early transitions in metabolic risk that may represent opportunities for averting the development of cardiovascular disease. Methods and Results In 4420 young adults in the Coronary Artery Risk Development in Young Adults (CARDIA) study, we defined a “metabolic” risk score based on components of the Third Report of the Adult Treatment Panel's definition of metabolic syndrome. Using latent class trajectory analysis adjusted for sex, race, and time‐dependent body mass index, we identified 6 distinct metabolic trajectories over time, specified by initial and final risk: low‐stable, low‐worsening, high‐stable, intermediate‐worsening, intermediate‐stable, and high‐worsening. Overall, individuals gained weight over time in CARDIA with statistically but not clinically different body mass index trend over time. Dysglycemia and dyslipidemia over time were highest in initially high or worsening trajectory groups. Divergence in metabolic trajectories occurred in early adulthood (before age 40), with 2 of 3 individuals experiencing an increase in metabolic risk over time. Membership in a higher‐risk trajectory (defined as initially high or worsening over time) was associated with greater prevalence and extent of coronary artery calcification, left ventricular mass, and decreased left ventricular strain at year 25. Importantly, despite similar rise in body mass index across trajectories over 25 years, coronary artery calcification and left ventricular structure and function more closely tracked risk factor trajectories. Conclusions Transitions in metabolic risk occur early in life. Obesity‐related metabolic dysfunction is related to subclinical cardiovascular phenotypes independent of evolution in body mass index, including coronary artery calcification and myocardial hypertrophy and dysfunction.
Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life, missing early transitions in metabolic risk that may represent opportunities for averting the development of cardiovascular disease. In 4420 young adults in the Coronary Artery Risk Development in Young Adults (CARDIA) study, we defined a "metabolic" risk score based on components of the Third Report of the Adult Treatment Panel's definition of metabolic syndrome. Using latent class trajectory analysis adjusted for sex, race, and time-dependent body mass index, we identified 6 distinct metabolic trajectories over time, specified by initial and final risk: low-stable, low-worsening, high-stable, intermediate-worsening, intermediate-stable, and high-worsening. Overall, individuals gained weight over time in CARDIA with statistically but not clinically different body mass index trend over time. Dysglycemia and dyslipidemia over time were highest in initially high or worsening trajectory groups. Divergence in metabolic trajectories occurred in early adulthood (before age 40), with 2 of 3 individuals experiencing an increase in metabolic risk over time. Membership in a higher-risk trajectory (defined as initially high or worsening over time) was associated with greater prevalence and extent of coronary artery calcification, left ventricular mass, and decreased left ventricular strain at year 25. Importantly, despite similar rise in body mass index across trajectories over 25 years, coronary artery calcification and left ventricular structure and function more closely tracked risk factor trajectories. Transitions in metabolic risk occur early in life. Obesity-related metabolic dysfunction is related to subclinical cardiovascular phenotypes independent of evolution in body mass index, including coronary artery calcification and myocardial hypertrophy and dysfunction.
BACKGROUNDDespite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life, missing early transitions in metabolic risk that may represent opportunities for averting the development of cardiovascular disease.METHODS AND RESULTSIn 4420 young adults in the Coronary Artery Risk Development in Young Adults (CARDIA) study, we defined a "metabolic" risk score based on components of the Third Report of the Adult Treatment Panel's definition of metabolic syndrome. Using latent class trajectory analysis adjusted for sex, race, and time-dependent body mass index, we identified 6 distinct metabolic trajectories over time, specified by initial and final risk: low-stable, low-worsening, high-stable, intermediate-worsening, intermediate-stable, and high-worsening. Overall, individuals gained weight over time in CARDIA with statistically but not clinically different body mass index trend over time. Dysglycemia and dyslipidemia over time were highest in initially high or worsening trajectory groups. Divergence in metabolic trajectories occurred in early adulthood (before age 40), with 2 of 3 individuals experiencing an increase in metabolic risk over time. Membership in a higher-risk trajectory (defined as initially high or worsening over time) was associated with greater prevalence and extent of coronary artery calcification, left ventricular mass, and decreased left ventricular strain at year 25. Importantly, despite similar rise in body mass index across trajectories over 25 years, coronary artery calcification and left ventricular structure and function more closely tracked risk factor trajectories.CONCLUSIONSTransitions in metabolic risk occur early in life. Obesity-related metabolic dysfunction is related to subclinical cardiovascular phenotypes independent of evolution in body mass index, including coronary artery calcification and myocardial hypertrophy and dysfunction.
Author Ferranti, Sarah
Venkatesh, Bharath A.
Das, Saumya
Lima, Joao A. C.
Shah, Ravi V.
Reis, Jared
Camhi, Sarah M.
Carnethon, Mercedes R.
Carr, J. Jeffrey
Terry, James G.
Murthy, Venkatesh L.
Abbasi, Siddique A.
Colangelo, Laura A.
Freedman, Jane
Siddique, Juned
Jerosch‐Herold, Michael
Lewis, Cora E.
AuthorAffiliation 11 Preventative Cardiology Boston Children's Hospital Boston MA
2 Nuclear Medicine Division Department of Radiology University of Michigan Ann Arbor MI
1 Cardiovascular Medicine Division Department of Medicine University of Michigan Ann Arbor MI
13 Department of Medicine University of Massachusetts at Worcester MA
8 Vanderbilt University Nashville TN
10 Noninvasive Cardiovascular Imaging Section Cardiovascular Division Department of Medicine and Department of Radiology Brigham and Women's Hospital Boston MA
3 Providence VA Medical Center and Cardiovascular Institute Alpert Medical School of Brown University Providence RI
4 Department of Preventive Medicine Feinberg School of Medicine Northwestern University Chicago IL
7 Department of Medicine Division of Cardiology Johns Hopkins Medical Institute Johns Hopkins University Baltimore MD
15 Department of Medicine Massachusetts General Hospital Boston MA
6 Division of Cardiovascular Sciences National Heart, Lung, and Blood Institute Bethesda MD
9 Exer
AuthorAffiliation_xml – name: 3 Providence VA Medical Center and Cardiovascular Institute Alpert Medical School of Brown University Providence RI
– name: 1 Cardiovascular Medicine Division Department of Medicine University of Michigan Ann Arbor MI
– name: 6 Division of Cardiovascular Sciences National Heart, Lung, and Blood Institute Bethesda MD
– name: 8 Vanderbilt University Nashville TN
– name: 7 Department of Medicine Division of Cardiology Johns Hopkins Medical Institute Johns Hopkins University Baltimore MD
– name: 13 Department of Medicine University of Massachusetts at Worcester MA
– name: 2 Nuclear Medicine Division Department of Radiology University of Michigan Ann Arbor MI
– name: 12 Cardiovascular Division Department of Medicine Beth Israel Deaconess Medical Center Boston MA
– name: 5 Department of Preventative Medicine Feinberg School of Medicine Northwestern University Chicago IL
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– name: 9 Exercise and Health Sciences Department College of Nursing and Health Sciences University of Massachusetts, Boston MA
– name: 4 Department of Preventive Medicine Feinberg School of Medicine Northwestern University Chicago IL
– name: 10 Noninvasive Cardiovascular Imaging Section Cardiovascular Division Department of Medicine and Department of Radiology Brigham and Women's Hospital Boston MA
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Issue 10
Keywords metabolic syndrome
epidemiology
risk factor
obesity
Language English
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2016 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell.
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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Dr Murthy and Dr Shah contributed equally to this work.
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Snippet Background Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later...
Despite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later in life,...
BACKGROUNDDespite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later...
BackgroundDespite evidence suggesting that early metabolic dysfunction impacts cardiovascular disease risk, current guidelines focus on risk assessments later...
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wiley
SourceType Open Website
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Index Database
Publisher
SubjectTerms Adolescent
Adult
Blood Glucose - metabolism
Blood Pressure
Body Mass Index
Cardiovascular Diseases - diagnostic imaging
Cardiovascular Diseases - epidemiology
Cholesterol, HDL - blood
Cohort Studies
Coronary Artery Disease - diagnostic imaging
Coronary Artery Disease - epidemiology
Diabetes Mellitus - epidemiology
Diabetes Mellitus - metabolism
Disease Progression
Echocardiography
epidemiology
Female
Follow-Up Studies
Heart Ventricles - diagnostic imaging
Heart Ventricles - pathology
Humans
Hypertension - epidemiology
Logistic Models
Longitudinal Studies
Male
metabolic syndrome
Metabolic Syndrome - blood
Metabolic Syndrome - epidemiology
obesity
Organ Size
Original Research
risk factor
Risk Factors
Tomography, X-Ray Computed
Triglycerides - blood
United States - epidemiology
Vascular Calcification - diagnostic imaging
Vascular Calcification - epidemiology
Waist Circumference
Young Adult
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Title Transitions in Metabolic Risk and Long‐Term Cardiovascular Health: Coronary Artery Risk Development in Young Adults (CARDIA) Study
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