Neighborhood structural disadvantage and biological aging in a sample of Black middle age and young adults

2021 ◽  
pp. 114654
Author(s):  
Man-Kit Lei ◽  
Mark T. Berg ◽  
Ronald L. Simons ◽  
Steven R.H. Beach
Circulation ◽  
2019 ◽  
Vol 139 (Suppl_1) ◽  
Author(s):  
John N Booth ◽  
Joseph Schwartz ◽  
Norrina Allen ◽  
Bryron Jaeger ◽  
Cora Lewis ◽  
...  

Diabetes Care ◽  
2018 ◽  
Vol 41 (12) ◽  
pp. 2579-2585 ◽  
Author(s):  
Michael P. Bancks ◽  
Mercedes R. Carnethon ◽  
David R. Jacobs ◽  
Lenore J. Launer ◽  
Jared P. Reis ◽  
...  

2019 ◽  
Author(s):  
William C. Cockerham ◽  
Joseph D. Wolfe ◽  
Shawn Bauldry

A growing body of work identifies distinct health lifestyles among children, adolescents, and young adults and documents important social correlates. This study contributes to that line of research by identifying the health lifestyles of U.S. adults entering late-middle age, assessing structural predictors of membership in different health lifestyles in this understudied age group, and examining net associations between health lifestyles, chronic conditions, and physical health. The data come from the National Longitudinal Survey of Youth 1979 (NLSY-79) 50+ Health Module. The analysis is based on respondents who answered the 50+ Health Module in 2008, 2010, 2012, or 2014 (N = 7,234). The results confirm similar relationships between health lifestyles and structural factors like class, gender, and race that prior studies observe and also reveal a unique pattern of associations between health lifestyle and health status because of diagnosed conditions that impact health behaviors in adulthood.


2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Drew R. Nannini ◽  
Brian T. Joyce ◽  
Yinan Zheng ◽  
Tao Gao ◽  
Lei Liu ◽  
...  

Abstract Background The metabolic syndrome (MetS) is a collection of metabolic disturbances that can lead to various cardiovascular diseases. Previous studies have shown a more adverse metabolic risk profile is associated with more advanced biological aging. The associations between epigenetic biomarkers of age with MetS, however, are not well understood. We therefore investigated the associations between epigenetic age acceleration and MetS severity score and incident MetS. Results A subset of study participants with available whole blood at examination years 15 and 20 from the Coronary Artery Risk Development in Young Adults Study underwent epigenomic profiling using the Illumina MethylationEPIC Beadchip (~ 850,000 sites). Intrinsic and extrinsic epigenetic age acceleration (IEAA and EEAA) were calculated from DNA methylation levels. The MetS severity score was positively associated with IEAA at years 15 (P = 0.016) and 20 (P = 0.016) and EEAA at year 20 (P = 0.040) in cross-sectional analysis. IEAA at year 20 was significantly associated with incident MetS at year 30 (OR = 1.05 [95% CI 1.01, 1.10], P = 0.028). Conclusions To our knowledge, this is the first report of the longitudinal association between epigenetic age acceleration and MetS. These findings suggest that a higher MetS severity score is associated with accelerated epigenetic aging and such aging may play a role in the development of metabolic disorders, potentially serving as a useful biomarker of and early detection tool for future MetS.


Circulation ◽  
2017 ◽  
Vol 135 (suppl_1) ◽  
Author(s):  
Donald M Lloyd-Jones ◽  
Laura Colangelo ◽  
Beth Lewis ◽  
Pamela Schreiner ◽  
Stephen Sidney ◽  
...  

Background: Data are sparse regarding associations of risk factors (RF) across young adulthood with development of adverse left ventricular (LV) structure and function by middle age, and it is unclear whether baseline, cumulative, or longitudinal RF exposure patterns best represent that risk. Methods: We included up to 2335 CARDIA participants (ppts) who had echocardiographic data from exam year (Y)5, Y25, and Y30, and RF data from at least 3 exams including Y0 and Y25. Echo outcomes included Y30 indexed LV end-systolic (ESD/ht) and -diastolic (EDD/ht) dimensions, and LV mass (M/ht 2.7 ), septal and posterior wall thickness, ejection fraction (EF), and incident adverse geometry (defined as LV concentric remodeling [CR], concentric hypertrophy [cLVH], or eccentric hypertrophy [eLVH]). We used multivariable linear, logistic or polytomous regression (as appropriate to endpoint) to examine associations of RF exposures measured as: 1) baseline (Y0); 2) change from Y0 to Y25; 3) cumulative exposure from Y0 to Y25 (e.g., pack-yrs, mmHg-yrs); or 4) latent class trajectories (using PROC TRAJ) from Y0 to Y25, with adjustment for demographics and relevant Y5 echo measures. Results: At Y30, ppts were 55±4 yrs, 56% women and 44% black; 12% smoked, mean BMI was 30.4±7, 37% had hypertension, and 17% diabetes; 20.5% had incident LVH; 4.5% EF<50%; and 37.2% adverse LV geometry. Models representing cumulative RF exposures tended to have the highest adjusted R 2 and lowest AIC for continuous and categorical Y30 LV outcomes. The table shows associations of cumulative RFs from Y0 to Y25 with incident LVH, EF<50%, and adverse LV geometry at Y30. Few RFs were consistently associated with Y25-Y30 change in echo measures, but they included education and SBP. Conclusions: Among initially healthy young adults, cumulative risk factor exposures (often within clinically normative ranges) over 25 years are significantly associated with continuous LV echo measures and adverse LV outcomes by middle age, suggesting the importance of primordial prevention.


2021 ◽  
Vol 14 ◽  
Author(s):  
Shweta Shenoy ◽  
Prachi Khandekar ◽  
Abhinav Sathe

: Sustained attention (SA) is a construct of cognition that tends to decline with age. There is a lack of literature regarding the neural correlates of SA in middle age, a link between young and old age. This study evaluated the differences in SA ability and its neural correlates using functional near-infrared spectroscopy (fNIRS) between young and middle-aged adults. 38 young and 25 middle-aged adults were evaluated for the changes in neural correlates (oxy and deoxyhemoglobin concentration in the prefrontal cortex) during a SA task known as cognition. The results showed that young adults performed significantly better than middle-aged adults on the SA task with no gender difference in their performance. There was a significant difference in the prefrontal activation pattern between young and middle-aged adults. We found right prefrontal dominance in young adults and left the prefrontal authority in middle-aged adults. This study concludes that the ability to maintain SA diminishes with age, advancing from young to middle age. Hemodynamic findings confirmed significant differences in neural resources in the prefrontal cortical areas between young and middle age. Findings document the neurobiological basis of age-related decline in the middle-aged population to understand changes in the brain's functioning during SA-related cognitive tasks.


Circulation ◽  
2020 ◽  
Vol 141 (Suppl_1) ◽  
Author(s):  
Nagisa Morikawa ◽  
Michael P. Bancks ◽  
Yuichiro Yano ◽  
Masanori Kuwabara ◽  
Angelo L. Gaffo ◽  
...  

Introduction: Higher levels of serum urate (UA) obtained on a single occasion have been shown to be associated with a higher risk of cardiovascular disease (CVD) events among middle-aged or older adults. However, little is known regarding UA trajectory patterns during young adulthood and their associations with CVD outcomes by middle age. Hypothesis: We hypothesize that higher UA trajectory is associated with a higher risk for CVD events compared to lower UA trajectories. Methods: We included data from 4845 CARDIA Study participants (mean age at the Year 20 exam 44.8±3.7 (37-55) years; 50.8% African American; 55.6% female). Sex-specific UA trajectories were assessed using group-based trajectory modeling (PROC TRAJ in SAS version 9.4) based on UA levels obtained at baseline (Year 0) and 10, 15, 20 years later. Covariates included age, sex, race, and clinical characteristics at Year 20 (body mass index, diabetes and creatinine). We estimated hazard ratios (HR) for CVD events (coronary heart disease, heart failure, and stroke) from Year 20 (2005-06) through 2017. Results: We identified 3 UA trajectories in men and 3 similar but lower UA trajectories in women, characterized by low-increasing (men: 30%; n=652, mean UA 5.1; women 43%, n=1191, mean UA 3.9), moderate-increasing (men: 52%; n=1290, mean UA 6.4; women 45%, n=1284, mean UA 5.0), and high-increasing UA (men: 17%; n=377, mean UA 8.0; women 12%, n=305, mean UA 6.4) (Figure 1). Sex-specific trajectories were pooled. Over a median follow-up of 10.9 years, 203 incident CVD events occurred. The adjusted HRs for CVD events were 0.98 (95%CI, 0.66-1.45) for the pooled moderate-increasing group and 1.77 (95%CI, 1.10-2.84) for the pooled high-increasing group compared to the pooled low-increasing group. Conclusions: High-increasing UA trajectory during young adulthood was associated with an greater risk of CVD events by middle age. Modeling UA trajectories may help identify young adults at higher risk for CVD events.


2019 ◽  
Vol 105 (6) ◽  
pp. 2053-2059 ◽  
Author(s):  
Stephany H Donze ◽  
Veryan Codd ◽  
Layla Damen ◽  
Wesley J Goedegebuure ◽  
Matthew Denniff ◽  
...  

Abstract Objective Adults with Prader–Willi syndrome (PWS) are at increased risk of developing age-associated diseases early in life and, like in premature aging syndromes, aging might be accelerated. We investigated leukocyte telomere length (LTL), a marker of biological age, in young adults with PWS and compared LTL to healthy young adults of similar age. As all young adults with PWS were treated with growth hormone (GH), we also compared LTL in PWS subjects to GH-treated young adults born short for gestational age (SGA). Design Cross-sectional study in age-matched young adults; 47 with PWS, 135 healthy, and 75 born SGA. Measurements LTL measured by quantitative polymerase chain reaction, expressed as telomere/single copy gene ratio. Results Median (interquartile range) LTL was 2.6 (2.4–2.8) at a median (interquartile range) age of 19.2 (17.7–21.3) years in PWS, 3.1 (2.9–3.5) in healthy young adults and 3.1 (2.8–3.4) in the SGA group. Median LTL in PWS was significantly lower compared to both control groups (P &lt; .01). In PWS, a lower LTL tended to be associated with a lower total IQ (r = 0.35, P = .08). There was no association between LTL and duration of GH treatment, cumulative GH dose, or several risk factors for type 2 diabetes mellitus or cardiovascular disease. Conclusions Young adults with PWS have significantly shorter median LTL compared to age-matched healthy young adults and GH-treated young adults born SGA. The shorter telomeres might play a role in the premature aging in PWS, independent of GH. Longitudinal research is needed to determine the influence of LTL on aging in PWS.


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