Using DTI to assess white matter microstructure in cerebral small vessel disease (SVD) in multicentre studies

Author:

Croall Iain D.1,Lohner Valerie1,Moynihan Barry2,Khan Usman3,Hassan Ahamad4,O’Brien John T.5,Morris Robin G.6,Tozer Daniel J.1,Cambridge Victoria C.1,Harkness Kirsty7,Werring David J.8,Blamire Andrew M.9,Ford Gary A.10,Barrick Thomas R.11,Markus Hugh S.1

Affiliation:

1. Department of Clinical Neuroscience, Stroke Research Group, University of Cambridge, Cambridge, U.K.

2. Neurosciences Research Centre, St. George's, University of London, London, U.K.

3. Stroke and Dementia Research Centre, St George’s, University of London, London, U.K.

4. Department of Neurology, Leeds General Infirmary, Leeds Teaching Hospitals NHS Trust, Leeds, U.K.

5. Department of Psychiatry, University of Cambridge, Cambridge, U.K.

6. Department of Psychology, Kings' College London, Institute of Psychiatry, Psychology and Neuroscience, London, U.K.

7. Department of Neurology, Royal Hallamshire Hospital, Sheffield, U.K.

8. Department of Brain Repair and Rehabilitation, Stroke Research Centre, UCL Institute of Neurology, London, U.K.

9. Magnetic Resonance Centre, Institute of Cellular Medicine, Newcastle University, Newcastle, U.K.

10. Medical Sciences Division, University of Oxford, Oxford, U.K., & Oxford University Hospitals NHS Foundation Trust

11. Molecular and Clinical Science Research Institute, St George’s, University of London, London, U.K.

Abstract

Diffusion tensor imaging (DTI) metrics such as fractional anisotropy (FA) and mean diffusivity (MD) have been proposed as clinical trial markers of cerebral small vessel disease (SVD) due to their associations with outcomes such as cognition. However, studies investigating this have been predominantly single-centre. As clinical trials are likely to be multisite, further studies are required to determine whether associations with cognition of similar strengths can be detected in a multicentre setting. One hundred and nine patients (mean age =68 years) with symptomatic lacunar infarction and confluent white matter hyperintensities (WMH) on MRI was recruited across six sites as part of the PRESERVE DTI substudy. After handling missing data, 3T-MRI scanning was available from five sites on five scanner models (Siemens and Philips), alongside neuropsychological and quality of life (QoL) assessments. FA median and MD peak height were extracted from DTI histogram analysis. Multiple linear regressions were performed, including normalized brain volume, WMH lesion load, and n° lacunes as covariates, to investigate the association of FA and MD with cognition and QoL. DTI metrics from all white matter were significantly associated with global cognition (standardized β =0.268), mental flexibility (β =0.306), verbal fluency (β =0.376), and Montreal Cognitive Assessment (MoCA) (β =0.273). The magnitudes of these associations were comparable with those previously reported from single-centre studies found in a systematic literature review. In this multicentre study, we confirmed associations between DTI parameters and cognition, which were similar in strength to those found in previous single-centre studies. The present study supports the use of DTI metrics as biomarkers of disease progression in multicentre studies.

Publisher

Portland Press Ltd.

Subject

General Medicine

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