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Associations between indicators of socioeconomic position and DNA methylation: a scoping review

期刊

CLINICAL EPIGENETICS
卷 13, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13148-021-01189-0

关键词

Socioeconomic factors; DNA methylation; Epigenetics; Systematic review

资金

  1. Russell Sage Foundation [96-17-05]
  2. Ford Foundation
  3. [R01MH113930]

向作者/读者索取更多资源

The evidence suggests that socioeconomic position influences DNA methylation, with variations in patterns depending on the timing, duration, and type of socioeconomic indicator. However, longitudinal studies examining repeated socioeconomic position and DNA methylation measures are generally lacking. Conceptual and methodological diversity in prior studies limits the interpretability of findings related to these three features of socioeconomic position.
Background Socioeconomic position (SEP) is a major determinant of health across the life course. Yet, little is known about the biological mechanisms explaining this relationship. One possibility widely pursued in the scientific literature is that SEP becomes biologically embedded through epigenetic processes such as DNA methylation (DNAm), wherein the socioeconomic environment causes no alteration in the DNA sequence but modifies gene activity in ways that shape health. Methods To understand the evidence supporting a potential SEP-DNAm link, we performed a scoping review of published empirical findings on the association between SEP assessed from prenatal development to adulthood and DNAm measured across the life course, with an emphasis on exploring how the developmental timing, duration, and type of SEP exposure influenced DNAm. Results Across the 37 identified studies, we found that: (1) SEP-related DNAm signatures varied across the timing, duration, and type of SEP indicator; (2) however, longitudinal studies examining repeated SEP and DNAm measures are generally lacking; and (3) prior studies are conceptually and methodologically diverse, limiting the interpretability of findings across studies with respect to these three SEP features. Conclusions Given the complex relationship between SEP and DNAm across the lifespan, these findings underscore the importance of analyzing SEP features, including timing, duration, and type. To guide future research, we highlight additional research gaps and propose four recommendations to further unravel the relationship between SEP and DNAm.

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