Life-Course Glucose Trajectory and Cognitive Function in Middle Age—Evidence from the Bogalusa Heart Study

Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 1474-P
Author(s):  
PATRICK STUCHLIK ◽  
OWEN CARMICHAEL ◽  
EMILY HARVILLE ◽  
HUA HE ◽  
MARYELLEN ROMERO ◽  
...  
2018 ◽  
Vol 2 (suppl_1) ◽  
pp. 709-709
Author(s):  
P Stuchlik ◽  
E Harville ◽  
M Romero ◽  
H He ◽  
W Chen ◽  
...  

2020 ◽  
Vol 75 (11) ◽  
pp. 2074
Author(s):  
Alexander C. Razavi ◽  
Tanika N. Kelly ◽  
Jiang He ◽  
Camilo Fernandez – Alonso ◽  
Lydia Bazzano

2021 ◽  
Vol 17 (S10) ◽  
Author(s):  
Robert L Newton ◽  
Kathryn L Gwizdala ◽  
Lydia Bazzano ◽  
Owen T Carmichael

Circulation ◽  
2020 ◽  
Vol 141 (Suppl_1) ◽  
Author(s):  
Alexander C Razavi ◽  
Mengyao Shi ◽  
Lydia A Bazzano ◽  
Jiang He ◽  
Jovia L Nierenberg ◽  
...  

Introduction: Variability in lipid levels is decreased in childhood compared to adulthood. However, few studies have assessed whether genetic information may help to predict hyperlipidemia beyond measured lipid values at this critical developmental stage. Hypothesis: We hypothesized that a low-density lipoprotein cholesterol (LDL-C) genetic risk score (GRS) would predict hyperlipidemia and LDL-C over the life course, even after adjustment for childhood measures. Methods: The analysis included 651 Bogalusa Heart Study participants (63% women, 31% African American, baseline age=9.8 + 3.1 years, median follow-up=40 years) with genome-wide association study (GWAS) data and at least one childhood and one adulthood measure of LDL-C. A weighted LDL-C GRS was constructed using loci from previous GWAS meta-analyses. Hyperlipidemia was defined as an LDL-C > 130 mg/dL or statin use. Cox proportional hazards regression models examined the associations between GRS and hyperlipidemia. Linear and mixed linear regression models were employed to examine the associations of GRS with adulthood LDL-C and life-course LDL-C trajectory, respectively. All models adjusted for age, sex, and childhood LDL-C. Results: Among participants of European ancestry, increasing GRS tertile conferred strong, dose-response increases in the hazards of hyperlipidemia ( Figure ). Similarly, the highest GRS tertile was associated with a 20 mg/dl increased LDL-C level in middle-aged adults compared to the lowest tertile (P<0.0001). Each tertile increase in GRS was also associated with 5.5 mg/dL larger 10-year increase in LDL-C (interaction-P=0.04). No associations were observed among participants of African ancestry. Conclusions: A LDL-C GRS was associated with adulthood LDL-C phenotypes independently of childhood LDL-C values in participants of European but not African ancestry. These findings highlight a need for increased genomics research in diverse populations and suggest a predictive utility of genetic information in childhood.


2016 ◽  
Vol 11 (6) ◽  
pp. 535-542 ◽  
Author(s):  
L. A. Bazzano ◽  
T. Hu ◽  
S. M. Bertisch ◽  
L. Yao ◽  
E. W. Harville ◽  
...  

2021 ◽  
Vol 17 (S10) ◽  
Author(s):  
Lydia Bazzano ◽  
Kathryn L Gwizdala ◽  
Owen T Carmichael ◽  
Robert L Newton

2009 ◽  
Vol 5 (4S_Part_13) ◽  
pp. P387-P387
Author(s):  
Jeanette Gustat ◽  
Janet Rice ◽  
Benjamin Seltzer ◽  
Maryellen Romero ◽  
Jennifer J. Vasterling ◽  
...  

Circulation ◽  
2015 ◽  
Vol 132 (suppl_3) ◽  
Author(s):  
Patrick Stuchlik ◽  
Norrina Allen ◽  
Emily Harville ◽  
Wei Chen ◽  
Lydia Bazzano

Introduction: It is well known that depression and heart disease are closely linked. However, it remains unclear whether changes in cardiovascular (CV) risk factors over time may be related to depression. Few studies have examined the long term patterns of CV risk factors in relation to depression in middle age. Hypothesis: The trajectories of cardiovascular risk factors are associated with depression and depressive symptoms. Methods: We examined data from the Bogalusa Heart Study, a long-term community-based observational study of a biracial cohort, with first measurements in childhood in 1976. Men and women who completed the CES-D in 2010 with at least two childhood and two adult CV measurements (n=913) were included. Age, systolic blood pressure, antihypertensive treatment status, smoking status, total and HDL cholesterol, were used to calculate standardized 10-year Framingham CV risk scores at each follow-up. CES-D scores were categorized using established cut points (<8, 8-15, >15). Discrete mixture modeling was employed to identify trajectory groupings of CV risk. The association between CV risk score trajectory and CES-D were determined using multivariable logistic regression adjusted for smoking, education, physical activity, and BMI in 2010. Results: Mean (±SD) age was 43.06±4.48 years, 57.9% were female, and 31.7% were black race. 27.7% of participants were current smokers in 2010. Mean (±SD) BMI was 30.97±7.73. We identified three CV risk patterns: stable (63.8%), slightly elevated (28.8%), and increasingly elevated (7.5%). Relative to stable CV risk, the multivariable adjusted odds ratio of higher CES-D categorization, i.e. more depressed, for slightly elevated was 1.49 (95% CI, 1.08-2.06), and for increasingly elevated, 1.53 (95% CI, 0.90-2.59). Smokers had increased odds of higher CES-D categorization over nonsmokers (OR=2.16, 95% CI 1.58-2.95). One-unit increases of BMI were associated with 1.02 times greater odds of higher CES-D categorization (95% CI, 1.01-1.04). Conclusions: Trajectories of cardiovascular risk from childhood through adulthood are associated with depression in middle age. Individuals with elevated or increasing cardiovascular risk profiles may benefit from depression screening in early middle age.


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