Longitudinal association between inflammatory markers and specific symptoms of depression in a prospective birth cohort
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
MR/L010305/1
Medical Research Council - United Kingdom
201486/Z/16/Z
Wellcome Trust - United Kingdom
G9815508
Medical Research Council - United Kingdom
088869/Z/09/Z
Wellcome Trust - United Kingdom
095844/Z/11/Z
Wellcome Trust - United Kingdom
PubMed
30414442
PubMed Central
PMC6363967
DOI
10.1016/j.bbi.2018.11.007
PII: S0889-1591(18)30789-X
Knihovny.cz E-zdroje
- Klíčová slova
- ALSPAC, C-reactive protein, Cohort study, Depression, Immunopsychiatry, Inflammation, Interleukin 6, Neurovegetative Symptoms, Psychological Symptoms, Somatic symptoms,
- MeSH
- antiflogistika MeSH
- biologické markery krev MeSH
- C-reaktivní protein analýza metabolismus MeSH
- deprese krev imunologie metabolismus MeSH
- depresivní poruchy imunologie metabolismus MeSH
- dítě MeSH
- interleukin-6 analýza krev MeSH
- kohortové studie MeSH
- lidé MeSH
- longitudinální studie MeSH
- mladiství MeSH
- prospektivní studie MeSH
- únava MeSH
- zánět imunologie metabolismus MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Anglie MeSH
- Názvy látek
- antiflogistika MeSH
- biologické markery MeSH
- C-reaktivní protein MeSH
- interleukin-6 MeSH
BACKGROUND: Low-grade inflammation is associated with depression, but studies of specific symptoms are relatively scarce. Association between inflammatory markers and specific symptoms may provide insights into potential mechanism of inflammation-related depression. Using longitudinal data, we have tested whether childhood serum interleukin 6 (IL-6) and C-reactive protein (CRP) levels are associated with specific depressive symptoms in early adulthood. METHODS: In the ALSPAC birth cohort, serum IL-6 and CRP levels were assessed at age 9 years and 19 depressive symptoms were assessed at age 18 years. We used modified Poisson generalised linear regression with robust error variance to estimate the risk ratio (RR) and 95% confidence interval (95% CI) for each depressive symptom. In addition, we used confirmatory factor analysis to create two continuous latent variables representing somatic/neurovegetative and psychological dimension scores. Structural equation modelling was used to test the associations between IL-6 and these dimension scores. RESULTS: Based on data from 2731 participants, IL-6 was associated with diurnal mood variation, concentration difficulties, fatigue and sleep disturbances. The adjusted RRs for these symptoms at age 18 years for participants in top, compared with bottom, third of IL-6 at age 9 years were 1.75 (95% CI, 1.13-2.69) for diurnal mood variation, 1.50 (95% CI, 1.11-2.02) for concentration difficulties, 1.31 (95% CI, 1.12-1.54) for fatigue, and 1.24 (95% CI, 1.01-1.52) for sleep disturbances. At dimension level, IL-6 was associated with both somatic/neurovegetative (β = 0.059, SE = 0.024, P = 0.013) and psychological (β = 0.056, SE = 0.023, P = 0.016) scores. CONCLUSIONS: Inflammation is associated with specific symptoms of depression. Associations with so-called somatic/neurovegetative symptoms of depression such as fatigue, sleep disturbances and diurnal mood variation indicate that these symptoms could be useful treatment targets and markers of treatment response in clinical trials of anti-inflammatory treatment for depression.
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