Targeted rejection predicts decreased anti-inflammatory gene expression and increased symptom severity in youth with asthma.

TitleTargeted rejection predicts decreased anti-inflammatory gene expression and increased symptom severity in youth with asthma.
Publication TypeJournal Article
Year of Publication2015
AuthorsMurphy MLM, Slavich GM, Chen E, Miller GE
JournalPsychol Sci
Volume26
Issue2
Pagination111-21
Date Published2015 Feb
ISSN1467-9280
Abstract

Although responses to different stressors are sometimes assumed to be similar, recent research has demonstrated that certain types of stress, such as targeted rejection, are particularly potent. To test such associations in a chronic-disease model, we examined how noninterpersonal, interpersonal, and targeted-rejection major life events predicted changes in gene expression and symptom severity in 121 youths with asthma who were assessed every 6 months for 2 years. Youths who had recently experienced targeted rejection had lower messenger RNA expression for signaling molecules that control airway inflammation and obstruction (specifically, the glucocorticoid receptor and β2-adrenergic receptor) than youths who had not experienced targeted rejection. These associations were specific to targeted rejection and stronger for youths higher in subjective social status. Higher-status youths exposed to targeted rejection (but not other types of stress) also reported more asthma symptoms. These data demonstrate stressor-specific associations with molecular-signaling pathways and the severity of asthma, and they suggest that threats to the social self may be particularly deleterious.

DOI10.1177/0956797614556320
Alternate JournalPsychol Sci
PubMed ID25564524
PubMed Central IDPMC4350370
Grant ListK08 MH103443 / MH / NIMH NIH HHS / United States
R01 HD058502 / HD / NICHD NIH HHS / United States
R01 HL073975 / HL / NHLBI NIH HHS / United States
R01 HL108723 / HL / NHLBI NIH HHS / United States
R01-HD058502 / HD / NICHD NIH HHS / United States
R01-HL073975 / HL / NHLBI NIH HHS / United States
R01-HL108723 / HL / NHLBI NIH HHS / United States