Imperial College London

Professor Paul M. Matthews

Faculty of MedicineDepartment of Brain Sciences

Edmond and Lily Safra Chair, Head of Department
 
 
 
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Contact

 

+44 (0)20 7594 2855p.matthews

 
 
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Assistant

 

Ms Siobhan Dillon +44 (0)20 7594 2855

 
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Location

 

E502Burlington DanesHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Datta:2016:10.1177/1352458516681504,
author = {Datta, G and Violante, IR and Scott, G and Zimmerman, K and Santos-Ribeiro, A and Rabiner, EA and Gunn, RN and Malik, O and Ciccarelli, O and Nicholas, R and Matthews, PM},
doi = {10.1177/1352458516681504},
journal = {Multiple Sclerosis},
pages = {1469--1478},
title = {Translocator positron-emission tomography and magnetic resonance spectroscopic imaging of brain glial cell activation in multiple sclerosis.},
url = {http://dx.doi.org/10.1177/1352458516681504},
volume = {23},
year = {2016}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - BACKGROUND: Multiple sclerosis (MS) is characterised by a diffuse inflammatory response mediated by microglia and astrocytes. Brain translocator protein (TSPO) positron-emission tomography (PET) and [myo-inositol] magnetic resonance spectroscopy (MRS) were used together to assess this. OBJECTIVE: To explore the in vivo relationships between MRS and PET [(11)C]PBR28 in MS over a range of brain inflammatory burden. METHODS: A total of 23 patients were studied. TSPO PET imaging with [(11)C]PBR28, single voxel MRS and conventional magnetic resonance imaging (MRI) sequences were undertaken. Disability was assessed by Expanded Disability Status Scale (EDSS) and Multiple Sclerosis Functional Composite (MSFC). RESULTS: [(11)C]PBR28 uptake and [ myo-inositol] were not associated. When the whole cohort was stratified by higher [(11)C]PBR28 inflammatory burden, [ myo-inositol] was positively correlated to [(11)C]PBR28 uptake (Spearman's ρ = 0.685, p = 0.014). Moderate correlations were found between [(11)C]PBR28 uptake and both MRS creatine normalised N-acetyl aspartate (NAA) concentration and grey matter volume. MSFC was correlated with grey matter volume (ρ = 0.535, p = 0.009). There were no associations between other imaging or clinical measures. CONCLUSION: MRS [ myo-inositol] and PET [(11)C]PBR28 measure independent inflammatory processes which may be more commonly found together with more severe inflammatory disease. Microglial activation measured by [(11)C]PBR28 uptake was associated with loss of neuronal integrity and grey matter atrophy.
AU - Datta,G
AU - Violante,IR
AU - Scott,G
AU - Zimmerman,K
AU - Santos-Ribeiro,A
AU - Rabiner,EA
AU - Gunn,RN
AU - Malik,O
AU - Ciccarelli,O
AU - Nicholas,R
AU - Matthews,PM
DO - 10.1177/1352458516681504
EP - 1478
PY - 2016///
SN - 1352-4585
SP - 1469
TI - Translocator positron-emission tomography and magnetic resonance spectroscopic imaging of brain glial cell activation in multiple sclerosis.
T2 - Multiple Sclerosis
UR - http://dx.doi.org/10.1177/1352458516681504
UR - http://hdl.handle.net/10044/1/51598
VL - 23
ER -