Why the study?
Does life-course socioeconomic position predict inflammatory biomarkers (CRP and IL-6) in older age?
Does life-course socioeconomic position predict inflammatory biomarkers (CRP and IL-6) in older age?
Consistently high socioeconomic position throughout life is associated with significantly lower levels of inflammatory biomarkers (CRP and IL-6) in older age compared to persistently low socioeconomic position.
Answers are grounded in this paper and cite their sources.
Suggests lifelong socioeconomic advantage is linked to lower systemic inflammation in older adults; leaves open whether targeted.
BACKGROUND: Evidence of an association between low socioeconomic position (SEP) and inflammatory markers is scant. This study aimed to examine how life-course SEP predicted C-reactive protein (CRP) and interleukin (IL-6) in older age from a national cohort. METHODS: We collected data from 1036 participants in the Social Environment and Biomarkers of Aging Study in Taiwan. Four SEP time points, childhood, young adulthood, active professional life, and older age were measured retrospectively. A group-based trajectory analysis method was used to identify the distinct trajectories of life-course SEP, and trajectory group membership was used as the predictor of CRP and IL-6 levels in older age. RESULTS: Three trajectories of life-course SEP were identified within the total sample: Low-Low (36.5%), Low-High (26.8%), and High-High (36.7%). Participants in the High-High group had the lowest levels of CRP and IL-6. Compared with those in the Low-Low group, the participants in the Low-High group had a similar adjusted CRP [-0.032 ln mg/L; 95% confidence interval (CI) - 0.193, 0.128] and IL-6 (0.017 ln pg/mL; 95% CI -0.093, 0.128); the participants in the High-High group had a significantly lower level of adjusted CRP concentration (-0.279 ln mg/L; 95% CI: -0.434, -0.125) and similarly lower IL-6 concentration (-0.129 ln pg/mL; 95% CI -0.236, -0.023) . CONCLUSIONS: Life-course SEP is related to the level of CRP and IL-6 in older age. Our data support the notion that life-course SEP predicts inflammatory markers in older age. Low SEP in childhood is related to elevated inflammatory markers in older age. Even after the transition from low SEP in childhood to high SEP in older age, the risk remains. Further study on SEP and inflammation-related disease is warranted.
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Lin et al. (2017) studied this question.
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