4.7 Article

Reconsidering the reasons for heightened inflammation in major depressive disorder

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 282, 期 -, 页码 434-441

出版社

ELSEVIER
DOI: 10.1016/j.jad.2020.12.109

关键词

Inflammation; Major depressive disorder; Body mass index; Polygenic risk scores

资金

  1. Rayne Foundation Ph.D. studentship [TRT M14717]
  2. Medical Research Council Skills Development Fellowship [MR/N014863/1]
  3. Biomedical Research Nucleus data management and informatics facility at South London and Maudsley NHS Foundation Trust - National Institute for Health Research (NIHR) Mental Health Biomedical Research Center at South London and Maudsley NHS Foundation Trus
  4. Guy's and St Thomas' Charity
  5. Maudsley Charity
  6. National Institute for Health Research (NIHR) Mental Health Biomedical Research Center, South London and Maudsley NHS Foundation Trust and King's College London
  7. MRC [MR/N014863/1] Funding Source: UKRI

向作者/读者索取更多资源

The study reveals that polygenic risk scores for MDD and BMI have different impacts on adulthood inflammation levels. While MDD PRS affects certain inflammatory markers, BMI has a significant positive effect on a greater number of inflammatory markers.
Background: Increased circulating pro-inflammatory markers have repeatedly been associated with major depressive disorder (MDD). However, it remains unclear whether inflammation represents a causal mechanism for MDD, or whether the association is influenced by confounding factors such as body mass index (BMI). Methods: To better understand this complex relationship, we generated polygenic risk scores (PRS) for MDD and BMI in a population cohort and attempted to isolate the impact these potential risk factors have on adulthood inflammation. Peripheral blood samples were collected as part of the South East London Community Health study, where we generated individualized PRS for MDD and BMI and quantified inflammatory markers using multiplex ELISA-based technology. We performed linear regressions to investigate the effects of PRS for MDD and BMI on inflammatory marker levels. Results: Out of 35 inflammatory markers, we found a nominal effect of PRS for MDD on interleukin-10. We also found a significant positive effect of BMI on nine inflammatory markers, of which the two most strongly affected markers, interleukin-6 (IL-6) and C-reactive protein (CRP), were also nominally predicted by BMI PRS. Limitations: The study utilized a cross-sectional design with a moderately sized sample. Conclusions: Our findings suggest there may not be a shared genetic mechanism contributing to MDD and higher inflammatory marker levels. However, there may be shared genetic etiology between BMI and adulthood levels of CRP and IL-6. Therefore, polygenic risk scores for BMI may represent a useful indicator for heightened levels of inflammation in adulthood.

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