4.6 Article

Peripheral inflammation levels associated with degree of advanced brain aging in schizophrenia

期刊

FRONTIERS IN PSYCHIATRY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2022.966439

关键词

inflammation; brain; schizophrenia; aging; MRI; TNF alpha; negative symptoms; cognition

资金

  1. Swiss National Science Foundation (SNSF)
  2. Novartis Foundation for Medical-Biological Research Fellowship [P2ZHP3_181506]
  3. NIMH
  4. Sam and Rose Stein Institute for Research on Aging [2 R01 MH094151-08]
  5. Desert-Pacific Mental Illness Research, Education, and Clinical Center Pala Pilot grant
  6. Swiss National Science Foundation (SNF) [P2ZHP3_181506] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

This study investigated the relationship between brain aging, peripheral inflammation, and symptoms of schizophrenia. The results showed that patients with schizophrenia had a higher degree of brain aging compared to healthy controls, and advanced brain age was associated with higher levels of peripheral TNF alpha. However, there was no strong evidence for a relationship between brain aging and cognitive or negative symptoms.
Brain structural abnormalities have been demonstrated in schizophrenia (SZ); these resemble those seen in typical aging, but are seen at younger ages. Furthermore, SZ is associated with accelerated global brain aging, as measured by brain structure-based brain predicted age difference (Brain-PAD). High heterogeneity exists in the degree of brain abnormalities in SZ, and individual differences may be related to levels of peripheral inflammation and may relate to cognitive deficits and negative symptoms. The goal of our study was to investigate the relationship between brain aging, peripheral inflammation, and symptoms of SZ. We hypothesized older brain-PAD in SZ vs. healthy comparison (HC) participants, as well as positive relationships of brain-PAD with peripheral inflammation markers and symptoms in SZ. We analyzed data from two cross-sectional studies in SZ (n = 26; M/F: 21/5) and HC (n = 28; 20/8) (22-64 years). Brain-PAD was calculated using a previously validated Gaussian process regression model applied to raw T1-weighted MRI data. Plasma levels of inflammatory biomarkers (CRP, Eotaxin, Fractalkine, IP10, IL6, IL10, ICAM1, IFN gamma, MCP1, MIP1 beta, SAA, TNF alpha, VEGF, VCAM1) and cognitive and negative symptoms were assessed. We observed a higher brain-PAD in SZ vs. HC, and advanced brain age relative to chronological age was related to higher peripheral levels of TNF alpha in the overall group and in the SZ group; other inflammatory markers were not related to brain-PAD. Within the SZ group, we observed no association between cognitive or negative symptoms and brain-PAD. These results support our hypothesis of advanced brain aging in SZ. Furthermore, our findings on the relationship of the pro-inflammatory cytokine TNF alpha with higher brain-PAD of SZ are relevant to explain heterogeneity of brain ages in SZ, but we did not find strong evidence for cognitive or negative symptom relationships with brain-PAD.

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