Exposure to adversity and inflammatory outcomes in mid and late childhood.
Brain Behav Immun Health
; 9: 100146, 2020 Dec.
Article
in En
| MEDLINE
| ID: mdl-34589892
ABSTRACT
BACKGROUND:
We aimed to estimate the association between exposure to adversity and inflammatory markers in mid (4 years) and late (11-12 years) childhood, and whether effects differ by type and timing of exposure.METHODS:
Data sources Barwon Infant Study (BIS; Nâ¯=â¯510 analyzed) and Longitudinal Study of Australian Children (LSAC; Nâ¯=â¯1156 analyzed). Exposures Adversity indicators assessed from 0 to 4 (BIS) and 0-11 years (LSAC) parent legal problems, mental illness and substance abuse, anger in parenting responses, separation/divorce, unsafe neighborhood, and family member death; a count of adversities; and, in LSAC only, early (0-3), middle (4-7), or later (10-11) initial exposure.Outcomes:
Inflammation quantified by high sensitivity C-reactive protein (hsCRP, Log (ug/ml)) and glycoprotein acetyls (GlycA, Log (umol/L)). Analyses Linear regression was used to estimate relative change in inflammatory markers, adjusted for sociodemographic characteristics, with exposure to adversity. Outcomes were log-transformed.RESULTS:
Evidence of an association between adversity and hsCRP was weak and inconsistent (e.g., 3+ versus no adversity BIS 12% higher, 95%CI -49.4, 147.8; LSAC 4.6% lower, 95%CI -36.6, 48.3). A small positive association between adversity and GlycA levels was observed at both 4 years (e.g., 3+ versus no adversity 3.3% higher, 95%CI -3.0, 9.9) and 11-12 years (3.2% higher, 95%CI 0.8, 5.8). In LSAC, we did not find evidence that inflammatory outcomes differed by initial timing of adversity exposure.CONCLUSIONS:
Small positive associations between adversity and inflammation were consistently observed for GlycA, across two cohorts with differing ages. Further work is needed to understand mechanisms, clinical relevance, and to identify opportunities for early intervention.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Brain Behav Immun Health
Year:
2020
Document type:
Article
Affiliation country:
Australia
Country of publication:
EEUU
/
ESTADOS UNIDOS
/
ESTADOS UNIDOS DA AMERICA
/
EUA
/
UNITED STATES
/
UNITED STATES OF AMERICA
/
US
/
USA