Elevated inflammation levels in depressed adults with a history of childhood maltreatment

被引:478
作者
Danese, Andrea [1 ]
Moffitt, Terrie E. [1 ,3 ,4 ,5 ,6 ]
Pariante, Carmine M. [2 ]
Ambler, Antony [1 ]
Poulton, Richie [7 ]
Caspi, Avshalom [1 ,3 ,4 ,5 ,6 ]
机构
[1] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London SE5 8AF, England
[2] Kings Coll London, Inst Psychiat, Dept Med Psychol, London SE5 8AF, England
[3] Duke Univ, Dept Psychol, Durham, NC USA
[4] Duke Univ, Dept Neurosci, Durham, NC USA
[5] Duke Univ, Dept Psychiat & Behav Sci, Durham, NC USA
[6] Duke Univ, Inst Genome Sci & Policy, Durham, NC USA
[7] Univ Otago, Dunedin Sch Med, Dunedin, New Zealand
基金
英国医学研究理事会;
关键词
D O I
10.1001/archpsyc.65.4.409
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: The association between depression and inflammation is inconsistent across research samples. Objective: To test whether a history of childhood maltreatment could identify a subgroup of depressed individuals with elevated inflammation levels, thus helping to explain previous inconsistencies. Design: Prospective longitudinal cohort study. Setting: New Zealand. Participants: A representative birth cohort of 1000 individuals was followed up to age 32 years as part of the Dunedin Multidisciplinary Health and Development Study. Study members were assessed for history of childhood maltreatment and current depression. Main Outcome Measures: Inflammation was assessed using a clinically relevant categorical measure of high-sensitivity C-reactive protein (>3 mg/L) and a dimensional inflammation factor indexing the shared variance of continuous measures of high-sensitivity C-reactive protein, fibrinogen, and white blood cells. Results: Although depression was associated with high levels of high-sensitivity C-reactive protein (relative risk, 1.45; 95% confidence interval, 1.06-1.99), this association was significantly attenuated and no longer significant when the effect of childhood maltreatment was taken into account. Individuals with current depression and a history of childhood maltreatment were more likely to have high levels of high-sensitivity C-reactive protein compared with control subjects (n = 27; relative risk, 2.07; 95% confidence interval, 1.23-3.47). In contrast, individuals with current depression only had a nonsignificant elevation in risk (n = 109; relative risk, 1.40; 95% confidence interval, 0.97-2.01). Results were generalizable to the inflammation factor. The elevated inflammation levels in individuals who were both depressed and maltreated were not explained by correlated risk factors such as depression recurrence, low socioeconomic status in childhood or adulthood, poor health, or smoking. Conclusions: A history of childhood maltreatment contributes to the co-occurrence of depression and inflammation. Information about experiences of childhood maltreatment may help to identify depressed individuals with elevated inflammation levels and, thus, at greater risk of cardiovascular disease.
引用
收藏
页码:409 / 416
页数:8
相关论文
共 40 条
  • [1] American Psychiatric Association, 2013, Diagnostic and statistical manual of mental disorders: DSM-5, DOI [10.1176/appi.books.9780890425596, 10.1176/appi.books.9780890425596.x00diagnosticclassification]
  • [2] American Psychiatric Association, 2013, Diagnostic and statistical manual of mental disorders: DSM-5, V5th ed.
  • [3] Adverse childhood experiences and smoking during adolescence and adulthood
    Anda, RF
    Croft, JB
    Felitti, VJ
    Nordenberg, D
    Giles, WH
    Williamson, DF
    Giovino, GA
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (17): : 1652 - 1658
  • [4] Berkman LF, 2003, JAMA-J AM MED ASSOC, V289, P3106
  • [5] Role of genotype in the cycle of violence in maltreated children
    Caspi, A
    McClay, J
    Moffitt, TE
    Mill, J
    Martin, J
    Craig, IW
    Taylor, A
    Poulton, R
    [J]. SCIENCE, 2002, 297 (5582) : 851 - 854
  • [6] COSTELLO E, 1982, NATL I MENTAL HLTH D
  • [7] Childhood maltreatment predicts adult inflammation in a life-course study
    Danese, Andrea
    Pariante, Carmine M.
    Caspi, Avshalom
    Taylor, Alan
    Poulton, Richie
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (04) : 1319 - 1324
  • [8] Association of fibrinogen, C-reactive protein, albumin, or leukocyte count with coronary heart disease - Meta-analyses of prospective studies
    Danesh, J
    Collins, R
    Appleby, P
    Peto, R
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (18): : 1477 - 1482
  • [9] DAVIS P, 2003, NZ SOCIOECONOMICS IN
  • [10] Insights into causal pathways for ischemic heart disease - Adverse childhood experiences study
    Dong, MX
    Giles, WH
    Felitti, VJ
    Dube, SR
    Williams, JE
    Chapman, DP
    Anda, RF
    [J]. CIRCULATION, 2004, 110 (13) : 1761 - 1766