Maternal warmth buffers the effects of low early-life socioeconomic status on pro-inflammatory signaling in adulthood

E. Chen*, G. E. Miller, M. S. Kobor, S. W. Cole

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

274 Scopus citations

Abstract

The notion that family support may buffer individuals under adversity from poor outcomes has been theorized to have important implications for mental and physical health, but little is known about the biological mechanisms that explain these links. We hypothesized that adults who grew up in low socioeconomic status (SES) households but who experienced high levels of maternal warmth would be protected from the pro-inflammatory states typically associated with low SES. A total of 53 healthy adults (aged 25-40 years) low in SES early in life were assessed on markers of immune activation and systemic inflammation. Genome-wide transcriptional profiling also was conducted. Low early-life SES individuals who had mothers, who expressed high warmth toward them, exhibited less Toll-like receptor-stimulated production of interleukin 6, and reduced bioinformatic indications of pro-inflammatory transcription factor activity (NF-κB) and immune activating transcription factor activity (AP-1) compared to those who were low in SES early in life but experienced low maternal warmth. To the extent that such effects are causal, they suggest the possibility that the detrimental immunologic effects of low early-life SES environments may be partly diminished through supportive family climates.

Original languageEnglish (US)
Pages (from-to)729-737
Number of pages9
JournalMolecular Psychiatry
Volume16
Issue number7
DOIs
StatePublished - Jul 2011

Funding

This work was supported by NIH Grants HD058502, CA116778, and AG107265; BC Ministry of Child and Family Development through the Human Early Learning Partnership; and the Allergy, Genes, & Environment Research Network.

Keywords

  • immune
  • maternal warmth
  • socioeconomic status

ASJC Scopus subject areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience
  • Psychiatry and Mental health

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