Early childhood socioeconomic status is associated with circulating interleukin-6 among mid-life adults.

TitleEarly childhood socioeconomic status is associated with circulating interleukin-6 among mid-life adults.
Publication TypeJournal Article
Year of Publication2011
AuthorsCarroll JE, Cohen S, Marsland AL
JournalBrain Behav Immun
Volume25
Issue7
Pagination1468-74
Date Published2011 Oct
ISSN1090-2139
KeywordsAdolescent, Adult, Child, Child, Preschool, Disease Susceptibility, Educational Status, Female, Humans, Infant, Inflammation, Interleukin-6, Male, Middle Aged, Poverty, Residence Characteristics, Social Class, Social Environment, Socioeconomic Factors
Abstract

It is proposed that socioeconomic conditions in early childhood effect immune programming, with poorer conditions resulting in adult phenotypes that are prone to inflammation. Recent evidence supports this possibility, showing an inverse association of childhood SES with adult markers of systemic inflammation. In this study, we further investigate this association, extending prior studies to include an examination of multiple indices of SES across distinct periods of childhood. Subjects were 112 men and women, 40-60 years of age (88.6% Caucasian). Childhood SES was indexed by a composite of three indicators of parental wealth (parental home and vehicle ownership, and number of bedrooms per child in the family home) averaged across 2 year periods of childhood between 1 and 18 years old. Higher adult serum concentrations of interleukin (IL)-6 were associated with lower SES in early childhood (years 1-2) (β=-.05, p<.05), associations that were independent of adult age, personal income, educational attainment, gender, race, body mass index, and physical activity. These associations support recent suggestions that the early environment may program immune phenotypes that contribute to disease risk.

DOI10.1016/j.bbi.2011.05.016
Alternate JournalBrain Behav. Immun.
PubMed ID21672624
PubMed Central IDPMC3175292
Grant ListNR008237 / NR / NINR NIH HHS / United States
R01 NR008237 / NR / NINR NIH HHS / United States
R01 NR008237-05 / NR / NINR NIH HHS / United States
T32 MH019925 / MH / NIMH NIH HHS / United States
T32 MH019925-12 / MH / NIMH NIH HHS / United States
T32-MH19925 / MH / NIMH NIH HHS / United States