Systemic Inflammation Contributes to the Association Between Childhood Socioeconomic Disadvantage and Midlife Cardiometabolic Risk

被引:4
|
作者
Natale, Brianna N. [1 ]
Manuck, Stephen B. [1 ]
Shaw, Daniel S. [1 ]
Matthews, Karen A. [2 ]
Muldoon, Matthew F. [3 ]
Wright, Aidan G. C. [1 ]
Marsland, Anna L. [1 ]
机构
[1] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Psychiat, Sch Med, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Heart & Vasc Inst, Dept Med, Sch Med, Pittsburgh, PA 15213 USA
关键词
Phildhood socioeconomic disadvantage; Inflammation; Cardiometabolic health; C-REACTIVE PROTEIN; EARLY-LIFE STRESS; ADULT BODY-MASS; METABOLIC SYNDROME; ADIPOSE-TISSUE; CARDIOVASCULAR-DISEASE; PSYCHOLOGICAL STRESS; BIOLOGICAL RESIDUE; INSULIN-RESISTANCE; SLEEP DURATION;
D O I
10.1093/abm/kaac004
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Background Childhood socioeconomic disadvantage is associated with increased risk for chronic inflammation and cardiometabolic disease at midlife. Purpose As it is presently unknown whether inflammation mediates the relationship between childhood socioeconomic status (SES) and adulthood cardiometabolic risk, we investigated associations between retrospectively reported childhood SES, circulating levels of inflammatory markers, and a latent construct of cardiometabolic risk in midlife adults. Methods Participants were 1,359 healthy adults aged 30-54 (Adult Health and Behavior I & II; 52% women, 17% Black) who retrospectively reported childhood SES (parental education, occupational grade). Measures included plasma interleukin (IL)-6, C-reactive protein (CRP), and cardiometabolic risk factors. Structural equation modeling was conducted, with cardiometabolic risk modeled as a second-order latent variable with adiposity, blood lipids, glucose control, and blood pressure as first-order components. Results Lower childhood SES was associated with greater risk for cardiometabolic disease at midlife (beta = -0.08, CI[-0.04, -0.01], p = .01) in models adjusted for demographics, but this association was attenuated in models that adjusted for adulthood SES and health behaviors. In fully-adjusted models, the relationship between lower childhood SES and adult cardiometabolic risk was partially explained by higher circulating levels of CRP (beta = -0.05, CI[-0.02, -0.01], p = .001), but not by IL-6. In an exploratory model, lower adulthood SES was also found to independently contribute to the association between childhood SES and adult cardiometabolic risk (beta = -0.02, CI[-0.01, -0.001], p = .02). Conclusions The current study provides initial evidence that systemic inflammation may contribute to childhood socioeconomic disparities in cardiometabolic risk in midlife. Future work would benefit from prospective investigation of these relationships.
引用
收藏
页码:26 / 37
页数:12
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