Rationale and design of a longitudinal study of cerebral small vessel diseases, clinical and imaging outcomes in patients presenting with mild ischaemic stroke: Mild Stroke Study 3

Author:

Clancy Una1ORCID,Garcia Daniela Jaime1,Stringer Michael S1,Thrippleton Michael J1,Valdés-Hernández Maria C1,Wiseman Stewart1,Hamilton Olivia KL1ORCID,Chappell Francesca M1,Brown Rosalind1,Blair Gordon W1,Hewins Will1,Sleight Emilie1,Ballerini Lucia1ORCID,Bastin Mark E1,Maniega Susana Munoz1,MacGillivray Tom1,Hetherington Kirstie1,Hamid Charlene1,Arteaga Carmen1,Morgan Alasdair G1,Manning Cameron1,Backhouse Ellen1,Hamilton Iona1,Job Dominic1,Marshall Ian1,Doubal Fergus N1,Wardlaw Joanna M1ORCID

Affiliation:

1. Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK

Abstract

Background Cerebral small vessel disease is a major cause of dementia and stroke, visible on brain magnetic resonance imaging. Recent data suggest that small vessel disease lesions may be dynamic, damage extends into normal-appearing brain and microvascular dysfunctions include abnormal blood–brain barrier leakage, vasoreactivity and pulsatility, but much remains unknown regarding underlying pathophysiology, symptoms, clinical features and risk factors of small vessel disease. Patients and Methods: The Mild Stroke Study 3 is a prospective observational cohort study to identify risk factors for and clinical implications of small vessel disease progression and regression among up to 300 adults with non-disabling stroke. We perform detailed serial clinical, cognitive, lifestyle, physiological, retinal and brain magnetic resonance imaging assessments over one year; we assess cerebrovascular reactivity, blood flow, pulsatility and blood–brain barrier leakage on magnetic resonance imaging at baseline; we follow up to four years by post and phone. The study is registered ISRCTN 12113543. Summary Factors which influence direction and rate of change of small vessel disease lesions are poorly understood. We investigate the role of small vessel dysfunction using advanced serial neuroimaging in a deeply phenotyped cohort to increase understanding of the natural history of small vessel disease, identify those at highest risk of early disease progression or regression and uncover novel targets for small vessel disease prevention and therapy.

Funder

Dunhill Medical Trust

the UK Dementia Research Institute which receives its funding from DRI Ltd, funded by the UK MRC, Alzheimer’s Society and Alzheimer’s Research UK

Muir Maxwell Research Fund

Edinburgh and Lothians Health Foundation

NHS Lothian Research and Development Office

British Heart Foundation

Horizon 2020 Framework Programme

Medical Research Scotland

Chief Scientist Office

Scottish Funding Council through the Scottish Imaging Network, A Platform for Scientific Excellence (SINAPSE) Collaboration

Medical Research Council

Wellcome Trust

University Of Edinburgh

NHS Research Scotland

Mrs Gladys Row Fogo Charitable Trust

The Stroke Association

Fondation Leducq

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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