Imperial College London

Dr David R Owen MD PhD

Faculty of MedicineDepartment of Brain Sciences

Reader in Molecular Pharmacology and Experimental Medicine
 
 
 
//

Contact

 

+44 (0)20 3313 6195d.owen Website

 
 
//

Location

 

G20AICTEM buildingHammersmith Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Kalk:2017:10.1038/tp.2016.264,
author = {Kalk, NJ and Guo, Q and Owen, D and Cherian, R and Erritzoe, D and Gilmour, A and Ribeiro, AS and McGonigle, J and Waldman, A and Matthews, P and Cavanagh, J and McInnes, I and Dar, K and Gunn, R and Rabiner, EA and Lingford-Hughes, AR},
doi = {10.1038/tp.2016.264},
journal = {Translational Psychiatry},
title = {Decreased hippocampal translocator protein (18 kDa) expression in alcohol dependence: a [(11)C]PBR28 PET study},
url = {http://dx.doi.org/10.1038/tp.2016.264},
volume = {7},
year = {2017}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Repeated withdrawal from alcohol is clinically associated with progressive cognitive impairment. Microglial activation occurring during pre-clinical models of alcohol withdrawal is associated with learning deficits. We investigated whether there was microglial activation in recently detoxified alcohol-dependent patients (ADP), using [(11)C]PBR28 positron emission tomography (PET), selective for the 18kDa translocator protein (TSPO) highly expressed in activated microglia and astrocytes. We investigated the relationship between microglial activation and cognitive performance. Twenty healthy control (HC) subjects (45±13; M:F 14:6) and nine ADP (45±6, M:F 9:0) were evaluated. Dynamic PET data were acquired for 90 min following an injection of 331±15 MBq [(11)C]PBR28. Regional volumes of distribution (VT) for regions of interest (ROIs) identified a priori were estimated using a two-tissue compartmental model with metabolite-corrected arterial plasma input function. ADP had an ~20% lower [(11)C]PBR28 VT, in the hippocampus (F(1,24) 5.694; P=0.025), but no difference in VT in other ROIs. Hippocampal [(11)C]PBR28 VT was positively correlated with verbal memory performance in a combined group of HC and ADP (r=0.720, P<0.001), an effect seen in HC alone (r=0.738; P=0.001) but not in ADP. We did not find evidence for increased microglial activation in ADP, as seen pre-clinically. Instead, our findings suggest lower glial density or an altered activation state with lower TSPO expression. The correlation between verbal memory and [(11)C]PBR28 VT, raises the possibility that abnormalities of glial function may contribute to cognitive impairment in ADP.
AU - Kalk,NJ
AU - Guo,Q
AU - Owen,D
AU - Cherian,R
AU - Erritzoe,D
AU - Gilmour,A
AU - Ribeiro,AS
AU - McGonigle,J
AU - Waldman,A
AU - Matthews,P
AU - Cavanagh,J
AU - McInnes,I
AU - Dar,K
AU - Gunn,R
AU - Rabiner,EA
AU - Lingford-Hughes,AR
DO - 10.1038/tp.2016.264
PY - 2017///
SN - 2158-3188
TI - Decreased hippocampal translocator protein (18 kDa) expression in alcohol dependence: a [(11)C]PBR28 PET study
T2 - Translational Psychiatry
UR - http://dx.doi.org/10.1038/tp.2016.264
UR - http://www.ncbi.nlm.nih.gov/pubmed/28072413
UR - http://hdl.handle.net/10044/1/44858
VL - 7
ER -