Back to Search Start Over

Volume, metabolites and neuroinflammation of the hippocampus in bipolar disorder - A combined magnetic resonance imaging and positron emission tomography study

Authors :
Bartholomeus C M Haarman
Jan-Bernard C Marsman
Remco J. Renken
Rixt F. Riemersma-van der Lek
Janine Doorduin
Jan Cees de Groot
Erik F. J. de Vries
Anita Sibeijn-Kuiper
Hemmo A. Drexhage
Willem A. Nolen
Richard Mendes
Huibert Burger
Immunology
Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE)
Life Course Epidemiology (LCE)
Perceptual and Cognitive Neuroscience (PCN)
Molecular Neuroscience and Ageing Research (MOLAR)
Guided Treatment in Optimal Selected Cancer Patients (GUTS)
​Basic and Translational Research and Imaging Methodology Development in Groningen (BRIDGE)
Clinical Cognitive Neuropsychiatry Research Program (CCNP)
Source :
Brain Behavior & Immunity, 56, 21-33. Academic Press, Brain behavior and immunity, 56, 21-33. ACADEMIC PRESS INC ELSEVIER SCIENCE
Publication Year :
2016

Abstract

Background: The hippocampus is one of the brain regions that is involved in several pathophysiological theories about bipolar disorder (BD), such as the neuroinflammation theory and the corticolimbic metabolic dysregulation theory. We compared hippocampal volume and hippocampal metabolites in bipolar I disorder (BD-I) patients versus healthy controls (HCs) with magnetic resonance imaging (MRI) and spectroscopy (MRS). We post hoc investigated whether hippocampal volume and hippocampal metabolites were associated with microglial activation and explored if potential illness modifying factors affected these hippocampal measurements and whether these were associated with experienced mood and functioning.Materials and methods: Twenty-two BD-I patients and twenty-four HCs were included in the analyses. All subjects underwent psychiatric interviews as well as an MRI scan, including a T1 scan and PRESS magnetic resonance spectroscopy (MRS). Volumetric analysis was performed with Freesurfer. MRS quantification was performed with LC Model. A subgroup of 14 patients and 11 HCs also underwent a successful [C-11]-(R)PK11195 neuroinflammation positron emission tomography scan.Results: In contrast to our hypothesis, hippocampal volumes were not decreased in patients compared to HC after correcting for individual whole-brain volume variations. We demonstrated decreased N-acetylaspartate (NAA) + N-acetyl-aspartyl-glutamate (NAAG) and creatine (Cr) + phosphocreatine (PCr) concentrations in the left hippocampus. In the explorative analyses in the left hippocampus we identified positive associations between microglial activation and the NAA + NAAG concentration, between alcohol use and NM + NAAG concentration, between microglial activation and the depression score and a negative relation between Cr + PCr concentration and experienced occupational disability. Duration of illness associated positively with volume bilaterally.Conclusion: Compared to HCs, the decreased NAA + NAAG concentration in the left hippocampus of BD-I patients suggests a decreased neuronal integrity in this region. In addition we found a positive relation between microglial activation and neuronal integrity in vivo, corresponding to a differentiated microglial function where some microglia induce apoptosis while others stimulate neurogenesis. (C) 2015 Elsevier Inc. All rights reserved.

Details

ISSN :
08891591
Database :
OpenAIRE
Journal :
Brain Behavior & Immunity, 56, 21-33. Academic Press, Brain behavior and immunity, 56, 21-33. ACADEMIC PRESS INC ELSEVIER SCIENCE
Accession number :
edsair.doi.dedup.....5d9fb74957b3b3314b9ee8416903476a