TY - JOUR
T1 - The Timing and Sequence of Cardiovascular Health Decline
AU - Pool, Lindsay R.
AU - Krefman, Amy E.
AU - Labarthe, Darwin R.
AU - Greenland, Philip
AU - Juonala, Markus
AU - Kähönen, Mika
AU - Lehtimäki, Terho
AU - Day, Rena Sue
AU - Bazzano, Lydia A.
AU - Van Horn, Linda
AU - Liu, Lei
AU - Fernandez-Alonso, Camilo
AU - Webber, Larry S.
AU - Pahkala, Katja
AU - Laitinen, Tomi T.
AU - Raitakari, Olli T.
AU - Lloyd-Jones, Donald M.
AU - Allen, Norrina B.
N1 - Funding Information:
The Young Finns Study has been financially supported by the Academy of Finland: Grants 322098, 286284, 134309 (Eye), 126925, 121584, 124282, 129378 (Salve), 117787 (Gendi), and 41071 (Skidi); the Social Insurance Institution of Finland; Competitive State Research Financing of the Expert Responsibility area of Kuopio, Tampere and Turku University Hospitals (Grant X51001); Juho Vainio Foundation; Paavo Nurmi Foundation; Finnish Foundation for Cardiovascular Research; Finnish Cultural Foundation; Tampere Tuberculosis Foundation; Emil Aaltonen Foundation; Yrjö Jahnsson Foundation; Signe and Ane Gyllenberg Foundation; Diabetes Research Foundation of Finnish Diabetes Association and EU Horizon 2020 (Grant 755320 for TAXINOMISIS and Grant 848146 for TO_AITION). The Bogalusa Heart Study was supported by Grants R01HL121230 from the National Heart, Lung, and Blood Institute; ES021724 from National Institute of Environmental Health Sciences; R01AG016592 from National Institute of Aging; and P20GM109036 from the National Institute of General Medical Sciences of NIH. The Coronary Artery Risk Development in Young Adults Study is conducted and supported by the National Heart, Lung, and Blood Institute in collaboration with the University of Alabama at Birmingham (HHSN268201800005I & HHSN268201800007I), Northwestern University (HHSN268201800003I), University of Minnesota (HHSN268201800006I), and Kaiser Foundation Research Institute (HHSN268201800004I). This manuscript has been reviewed by Coronary Artery Risk Development in Young Adults for the scientific content. The Special Turku Coronary Risk Factor Intervention Project has been supported by the Academy of Finland (206374, 294834, 251360, 275595); Juho Vainio Foundation; Finnish Cultural Foundation; Finnish Foundation for Cardiovascular Research; Sigrid Jusélius Foundation; Yrjö Jahnsson Foundation; Finnish Diabetes Research Foundation; Novo Nordisk Foundation; Finnish Ministry of Education and Culture; Special Governmental Grants for Health Sciences Research, Turku University Hospital; and University of Turku Foundation. Project HeartBeat! has been supported by research awards from NIH and the Centers for Disease Control and Prevention (UO1 HL41166, 1 RO3 HL57101, and 1 RO3 HL59223 [cardiac development]) and Centers for Disease Control and Prevention contract PO# 0009966385, Intergovernmental Personnel Agreement 00IPA24501, and Cooperative Agreement U48/CCU609653. Additional support from the Compaq Computer Corporation and the University of Texas Health Science Center at Houston, School of Public Health, is also gratefully acknowledged.
Funding Information:
KP is funded by an Academy of Finland research fellowship (Number 322112).
Funding Information:
This work was supported by an American Heart Association Strategically Funded Prevention Research Network Center Grant to Northwestern (AHA Award #14SFRN20780002).
Publisher Copyright:
© 2021 American Journal of Preventive Medicine
PY - 2021/10
Y1 - 2021/10
N2 - Introduction: Childhood declines in cardiovascular health have been linked to the development of subclinical atherosclerosis; however, less is known about the timing and sequence of the decline of the specific cardiovascular health components. The study objective is to identify the patterns of decline and associations with adulthood subclinical atherosclerosis. Methods: Data were pooled from 5 cardiovascular cohorts. Clinical components of cardiovascular health (BMI, blood pressure, cholesterol, and blood glucose) were categorized as ideal or nonideal using American Heart Association definitions. Multitrajectory models simultaneously fitted the probability ideal for each factor. Adjusted associations between trajectory groups and carotid intima-media thickness were modeled. Data were pooled from December 1, 2015 to June 1, 2019; statistical analysis occurred between June 1, 2019 and June 1, 2020. Results: This study included 9,388 individuals (55% female, 66% White). A total of 5 distinct trajectory groups were created: 1 maintained the ideal levels of all the 4 health factors, 2 had risk onset of a single factor in childhood, 1 had risk onset of multiple factors in childhood, and 1 had risk onset in adulthood. Those with childhood multiple risk onset had 8.1% higher carotid intima-media thickness (95% CI=0.067, 0.095) than those in the ideal group, childhood cholesterol risk onset had 5.9% higher carotid intima-media thickness (95% CI=0.045, 0.072), childhood BMI risk onset had 5.5% higher carotid intima-media thickness (95% CI=0.041, 0.069), and early adulthood multiple risk onset had 2.7% higher carotid intima-media thickness (95% CI=0.013, 0.041). Conclusions: Those who lost the ideal status of cardiovascular health in childhood and early adulthood had more subclinical atherosclerosis than those who retained the ideal cardiovascular health across the life course, underscoring the importance of preserving the ideal cardiovascular health beginning in childhood and continued into adulthood.
AB - Introduction: Childhood declines in cardiovascular health have been linked to the development of subclinical atherosclerosis; however, less is known about the timing and sequence of the decline of the specific cardiovascular health components. The study objective is to identify the patterns of decline and associations with adulthood subclinical atherosclerosis. Methods: Data were pooled from 5 cardiovascular cohorts. Clinical components of cardiovascular health (BMI, blood pressure, cholesterol, and blood glucose) were categorized as ideal or nonideal using American Heart Association definitions. Multitrajectory models simultaneously fitted the probability ideal for each factor. Adjusted associations between trajectory groups and carotid intima-media thickness were modeled. Data were pooled from December 1, 2015 to June 1, 2019; statistical analysis occurred between June 1, 2019 and June 1, 2020. Results: This study included 9,388 individuals (55% female, 66% White). A total of 5 distinct trajectory groups were created: 1 maintained the ideal levels of all the 4 health factors, 2 had risk onset of a single factor in childhood, 1 had risk onset of multiple factors in childhood, and 1 had risk onset in adulthood. Those with childhood multiple risk onset had 8.1% higher carotid intima-media thickness (95% CI=0.067, 0.095) than those in the ideal group, childhood cholesterol risk onset had 5.9% higher carotid intima-media thickness (95% CI=0.045, 0.072), childhood BMI risk onset had 5.5% higher carotid intima-media thickness (95% CI=0.041, 0.069), and early adulthood multiple risk onset had 2.7% higher carotid intima-media thickness (95% CI=0.013, 0.041). Conclusions: Those who lost the ideal status of cardiovascular health in childhood and early adulthood had more subclinical atherosclerosis than those who retained the ideal cardiovascular health across the life course, underscoring the importance of preserving the ideal cardiovascular health beginning in childhood and continued into adulthood.
UR - http://www.scopus.com/inward/record.url?scp=85114111468&partnerID=8YFLogxK
U2 - 10.1016/j.amepre.2021.04.010
DO - 10.1016/j.amepre.2021.04.010
M3 - Article
C2 - 34238623
AN - SCOPUS:85114111468
SN - 0749-3797
VL - 61
SP - 545
EP - 553
JO - American Journal of Preventive Medicine
JF - American Journal of Preventive Medicine
IS - 4
ER -