4.7 Article

Inflammatory cytokines and callosal white matter microstructure in adolescents

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 100, Issue -, Pages 321-331

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2021.12.003

Keywords

Interleukin-6; Tumur necrosis factor-alpha; Corpus callosum; Adolescence; Depression; Cytokines; Diffusion tensor imaging; White matter microstructure; Uncinate fasciculus

Funding

  1. National Institute of Mental Health [K01MH117442, R37MH101495]
  2. Klingenstein Third Generation Foundation
  3. Stanford's Child and Maternal Health Institute
  4. Ray and Dagmar Dolby Family Fund
  5. Human Biology Research Exploration Program 2018
  6. National Science Foundation [DGE-1752134]

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This study is the first to explore the relationship between peripheral inflammation and white matter microstructure in fronto-cingulatelimbic tracts in depressed and nondepressed adolescents. The results show that depressed adolescents had higher levels of inflammation compared to controls, but there was no significant difference in white matter connectivity between the two groups. While there was an association between inflammation levels and white matter structure, the diagnostic group did not moderate this relationship.
Adolescent depression is characterized by heightened inflammation and altered connectivity of fronto-cingulatelimbic tracts, including the genu of the corpus callosum (CCG) and the uncinate fasciculus (UF). No studies, however, have yet examined the association between inflammation, measured by peripheral levels of cytokines, and white matter connectivity of fronto-cingulate-limbic tracts in adolescents. Here, 56 depressed adolescents (32 females, 3 non-binary; 16.23 +/- 1.28 years) and 19 controls (10 females; 15.72 +/- 1.17 years) completed a diffusion-weighted MRI scan at 3 Tesla. We conducted deterministic tractography to segment bilateral corpus callosum (genu and splenium) and UF and computed mean fractional anisotropy (FA) in each tract. A subset of participants (43 depressed and 17 healthy controls) also provided dried blood spot samples from which we assayed interleukin 6 (IL-6) and tumor necrosis factor alpha (TNF-alpha) using a Luminex multiplex array. Depressed participants did not differ from controls in FA of the corpus callosum or UF (all FDR-corrected ps > 0.056) but exhibited higher levels of inflammation than did controls (IL-6: 13 = 0.91, FDR-corrected p = 0.006; TNF-alpha: 13 = 0.76, FDR-corrected p = 0.006). Although diagnostic group did not moderate the associations between inflammatory cytokines and FA in the CCG and UF, across both groups, greater peripheral inflammation was associated with lower FA in the CCG (IL-6: 13 = -0.38; FDR-corrected p = 0.044; TNF-alpha: 13 = -0.41, FDR-corrected p = 0.044). This study is the first to examine associations between peripheral inflammation and white matter microstructure of fronto-cingulate-limbic tracts in depressed and nondepressed adolescents. Future mechanistic studies are needed to confirm our findings; nevertheless, our results suggest that heightened inflammation is an important component of neurophenotypes that are relevant to adolescent depression.

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