Central markers of neuroinflammation in alcohol use disorder: A meta‐analysis of neuroimaging, cerebral spinal fluid, and postmortem studies

Author:

Adams Claire12,Perry Nina1,Conigrave James12ORCID,Hurzeler Tristan12,Stevens Julia3,Yacou Dunbar Kristiane P.1,Sweeney Alicia3,Lee Kylie12,Sutherland Greg3,Haber Paul12,Morley Kirsten C.12ORCID

Affiliation:

1. Central Clinical School, Faculty of Medicine and Health The University of Sydney Sydney New South Wales Australia

2. Edith Collins Centre (Translational Research in Alcohol Drugs and Toxicology), Drug Health Services Sydney Local Health District Sydney New South Wales Australia

3. NSW Brain Tissue Resource Centre and School of Medical Sciences, Faculty of Medicine and Health The University of Sydney Sydney New South Wales Australia

Abstract

AbstractIntroduction and aimsThere is emerging evidence that heavy long‐term alcohol consumption may alter the neuroimmune profile. We conducted a meta‐analysis of the association between alcohol use disorder (AUD) and the extent of neuroinflammation using cerebrospinal (CSF), PET (Positron Emission Tomography), and postmortem studies.Design and methodsA comprehensive search of electronic databases was conducted using the Preferred Reporting Items for Systematic Review and Meta‐Analysis Protocols (PRISMA‐P) for AUD‐related terms in combination with neuroinflammatory markers and cytokine‐ and chemokine‐related terms for CSF, PET, and postmortem studies. Participants had to meet established criteria for AUD and/or heavy alcohol consumption with dependence features and be compared with healthy controls. Papers retrieved were assessed for inclusion criteria and a critical appraisal was completed using the Newcastle‐Ottawa Scale. A meta‐analysis was conducted on postmortem and PET studies.ResultsEleven papers met the inclusion criteria with CSF, PET, and postmortem studies included in the final analysis. Postmortem studies demonstrate significant heterogeneity (𝑄 (14) = 62.02, 𝑝 < 0.001), with the alcohol group showing higher levels of neuroimmune markers than controls (𝑑 = 1.50 [95% CI 0.56, 2.45]). PET studies demonstrated a lower [11C] PBR28 total volume of distribution (V T) for translocator protein in the hippocampus (g = −1.95 [95% CI −2.72, −1.18], p < 0.001) of the alcohol group compared to controls.ConclusionThere is emerging evidence across multiple diagnostic modalities that alcohol impacts neuroimmune signaling in the human brain.

Publisher

Wiley

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