Framework for Clinical Trials in Cerebral Small Vessel Disease (FINESSE)

Author:

Markus Hugh S.1,van Der Flier Wiesje M.1,Smith Eric E.2,Bath Philip3,Biessels Geert Jan4,Briceno Emily5,Brodtman Amy678,Chabriat Hugues9,Chen Christopher10,de Leeuw Frank-Erik11,Egle Marco12,Ganesh Aravind2,Georgakis Marios K.131415,Gottesman Rebecca F.1617,Kwon Sun18,Launer Lenore19,Mok Vincent20,O’Brien John21,Ottenhoff Lois22,Pendlebury Sarah23,Richard Edo11,Sachdev Perminder24,Schmidt Reinhold25,Springer Melanie26,Tiedt Stefan1315,Wardlaw Joanna M.27,Verdelho Ana28,Webb Alastair29,Werring David30,Duering Marco131531,Levine Deborah32,Dichgans Martin1315

Affiliation:

1. Alzheimer Center Amsterdam, Department of Neurology, Epidemiology and Data Science, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands

2. Department of Clinical Neurosciences and Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada

3. Stroke Trials Unit, Mental Health & Clinical Neuroscience, University of Nottingham, Nottingham, United Kingdom

4. Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands

5. Department of Physical Medicine & Rehabilitation, University of Michigan Medical School, Ann Arbor

6. Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia

7. University of Melbourne, Melbourne, Victoria, Australia

8. Monash University, Melbourne, Victoria, Australia

9. Department of Neurology, FHU NeuroVasc, APHP, University of Paris, Paris, France

10. Memory Aging and Cognition Centre, Departments of Pharmacology and Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore

11. Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijimegen, the Netherlands

12. Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom

13. Institute for Stroke and Dementia Research (ISD), LMU University Hospital, Munich, Germany

14. Center for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, Boston

15. Munich Cluster for Systems Neurology (SyNergy), Munich, Germany

16. Now with National Institute of Neurological Disorders and Stroke Intramural Research Program, Bethesda, Maryland

17. Johns Hopkins University School of Medicine, Baltimore, Maryland

18. University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea

19. Intramural Research Program, National Institute on Aging, Baltimore, Maryland

20. Gerald Choa Neuroscience Centre, Lui Che Woo Institute of Innovative Medicine, Margaret K.L. Cheung Research Centre for Management of Parkinsonism, Division of Neurology, Department of Medicine and Therapeutics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China

21. Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom

22. Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam and the Netherlands and Brain Research Center Amsterdam, the Netherlands

23. Wolfson Centre for Prevention of Stroke and Dementia, Nuffield Department of Clinical Neurosciences, University of Oxford, NIHR Oxford Biomedical Research Centre, Departments of General (internal) Medicine and Geratology, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom

24. Centre for Healthy Brain Ageing (CHeBA), University of New South Wales, Sydney, New South Wales, Australia

25. Department of Neurology, Clinical Division of Neurogeriatrics, Medical University Graz, Graz, Austria

26. Department of Neurology, University of Michigan, Ann Arbor

27. Centre for Clinical Brain Sciences, UK Dementia Research Institute Centre at the University of Edinburgh, Edinburgh, United Kingdom

28. Faculdade de Medicina, Department of Neurosciences and Mental Health, CHULN-Hospital de Santa Maria Instituto de Medicina Molecular (IMM) e Instituto de Saúde Ambiental (ISAMB), University of Lisbon, Lisbon, Portugal

29. Wolfson Centre for Prevention of Stroke and Dementia, Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom

30. Stroke Research Centre, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology and the National Hospital for Neurology and Neurosurgery, London, United Kingdom

31. Medical Image Analysis Center (MIAC AG) and Quantitative Biomedical Imaging Group, Department of Biomedical Engineering, University of Basel, Basel, Switzerland

32. Departments of Internal Medicine and Neurology, University of Michigan, Ann Arbor

Abstract

ImportanceCerebral small vessel disease (SVD) causes a quarter of strokes and is the most common pathology underlying vascular cognitive impairment and dementia. An important step to developing new treatments is better trial methodology. Disease mechanisms in SVD differ from other stroke etiologies; therefore, treatments need to be evaluated in cohorts in which SVD has been well characterized. Furthermore, SVD itself can be caused by a number of different pathologies, the most common of which are arteriosclerosis and cerebral amyloid angiopathy. To date, there have been few sufficiently powered high-quality randomized clinical trials in SVD, and inconsistent trial methodology has made interpretation of some findings difficult.ObservationsTo address these issues and develop guidelines for optimizing design of clinical trials in SVD, the Framework for Clinical Trials in Cerebral Small Vessel Disease (FINESSE) was created under the auspices of the International Society of Vascular Behavioral and Cognitive Disorders. Experts in relevant aspects of SVD trial methodology were convened, and a structured Delphi consensus process was used to develop recommendations. Areas in which recommendations were developed included optimal choice of study populations, choice of clinical end points, use of brain imaging as a surrogate outcome measure, use of circulating biomarkers for participant selection and as surrogate markers, novel trial designs, and prioritization of therapeutic agents using genetic data via Mendelian randomization.Conclusions and RelevanceThe FINESSE provides recommendations for trial design in SVD for which there are currently few effective treatments. However, new insights into understanding disease pathogenesis, particularly from recent genetic studies, provide novel pathways that could be therapeutically targeted. In addition, whether other currently available cardiovascular interventions are specifically effective in SVD, as opposed to other subtypes of stroke, remains uncertain. FINESSE provides a framework for design of trials examining such therapeutic approaches.

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

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