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

被引:57
作者
Markus, Hugh S. [1 ]
van der Flier, Wiesje M. [1 ]
Smith, Eric E. [2 ,3 ]
Bath, Philip [4 ]
Biessels, Geert Jan [5 ]
Briceno, Emily [6 ]
Brodtman, Amy [7 ,8 ,9 ]
Chabriat, Hugues [10 ]
Chen, Christopher [11 ,12 ]
De Leeuw, Frank-Erik [13 ]
Egle, Marco [14 ]
Ganesh, Aravind [2 ,3 ]
Georgakis, Marios K. [15 ,16 ,17 ]
Gottesman, Rebecca F. [18 ,19 ]
Kwon, Sun [20 ]
Launer, Lenore [21 ]
Mok, Vincent [22 ]
O'Brien, John [23 ]
Ottenhoff, Lois [24 ,25 ]
Pendlebury, Sarah [26 ,27 ]
Richard, Edo [13 ]
Sachdev, Perminder [28 ]
Schmidt, Reinhold [29 ]
Springer, Melanie [30 ]
Tiedt, Stefan [15 ,17 ]
Wardlaw, Joanna M. [31 ]
Verdelho, Ana [32 ,33 ]
Webb, Alastair [34 ]
Werring, David [35 ,36 ]
Duering, Marco [15 ,17 ,37 ,38 ]
Levine, Deborah [39 ]
Dichgans, Martin [15 ,17 ]
机构
[1] Vrije Univ Amsterdam, Alzheimer Ctr Amsterdam, Dept Neurol Epidemiol & Data Sci, Amsterdam UMC,Amsterdam Neurosci, Amsterdam, Netherlands
[2] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[3] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[4] Univ Nottingham, Stroke Trials Unit, Mental Hlth & Clin Neurosci, Nottingham, England
[5] Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Neurol, Utrecht, Netherlands
[6] Univ Michigan Med Sch, Dept Phys Med & Rehabil, Ann Arbor, MI USA
[7] Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[8] Univ Melbourne, Melbourne, Vic, Australia
[9] Monash Univ, Melbourne, Vic, Australia
[10] Univ Paris, AP HP, Dept Neurol, FHU NeuroVasc, Paris, France
[11] Natl Univ Singapore, Memory Aging & Cognit Ctr, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[12] Natl Univ Singapore, Memory Aging & Cognit Ctr, Yong Loo Lin Sch Med, Dept Psychol Med, Singapore, Singapore
[13] Radboud Univ Nijmegen Med Ctr, Donders Inst Brain Cognit & Behav, Dept Neurol, Nijimegen, Netherlands
[14] Univ Cambridge, Dept Clin Neurosci, Cambridge Biomed Campus, Cambridge CB2 0QQ, Cambs, England
[15] LMU Univ Hosp, Inst Stroke & Dementia Res ISD, Munich, Germany
[16] Harvard Med Sch, Ctr Genom Med, Massachusetts Gen Hosp, Boston, MA 02115 USA
[17] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[18] NINDS, Intramural Res Program, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[19] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[20] Univ Ulsan, Asan Med Ctr, Coll Med, Seoul, South Korea
[21] NIA, Intramural Res Program, Baltimore, MD 21224 USA
[22] Chinese Univ Hong Kong, Fac Med, Gerald Choa Neurosci Ctr,Div Neurol,Dept Med & Th, Lui Che Woo Inst Innovat Med,Margaret KL Cheung R, Hong Kong, Peoples R China
[23] Univ Cambridge, Dept Psychiat, Cambridge, England
[24] Vrije Univ Amsterdam, Alzheimer Ctr Amsterdam, Dept Neurol, Amsterdam Neurosci, Amsterdam, Netherlands
[25] Brain Res Ctr Amsterdam, Amsterdam, Netherlands
[26] Univ Oxford, Oxford Univ Hosp NHS Fdn Trust, Wolfson Ctr Prevent Stroke & Dementia,Dept Gen In, NIHR Oxford Biomed Res Ctr,Nuffield Dept Clin Neu, Oxford, England
[27] Univ Oxford, Oxford Univ Hosp NHS Fdn Trust, Wolfson Ctr Prevent Stroke & Dementia,Dept Gerato, NIHR Oxford Biomed Res Ctr,Nuffield Dept Clin Neu, Oxford, England
[28] Univ New South Wales, Ctr Hlth Brain Ageing CHeBA, Sydney, NSW, Australia
[29] Med Univ Graz, Dept Neurol, Clin Div Neurogeriatr, Graz, Austria
[30] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[31] Univ Edinburgh, Ctr Clin Brain Sci, UK Dementia Res Inst Ctr, Edinburgh, Midlothian, Scotland
[32] Univ Lisbon, CHULN Hosp Santa Maria, Fac Med, Dept Neurosci & Mental Hlth,Inst Med Mol IMM, Lisbon, Portugal
[33] Univ Lisbon, Inst Saude Ambiental ISAMB, Lisbon, Portugal
[34] Univ Oxford, Wolfson Ctr Prevent Stroke & Dementia, Dept Clin Neurosci, Oxford, England
[35] UCL Queen Sq Inst Neurol, Dept Brain Repair & Rehabil, Stroke Res Ctr, London, England
[36] Natl Hosp Neurol & Neurosurg, London, England
[37] Univ Basel, Med Image Anal Ctr MIAC AG, Basel, Switzerland
[38] Univ Basel, Quantitat Biomed Imaging Grp, Dept Biomed Engn, Basel, Switzerland
[39] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
VASCULAR COGNITIVE IMPAIRMENT; TRANSIENT ISCHEMIC ATTACK; TELEPHONE INTERVIEW; DIAGNOSTIC-CRITERIA; LACUNAR STROKE; DISORDERS; RISK; CLASSIFICATION; DEFINITIONS; PROGRESSION;
D O I
10.1001/jamaneurol.2022.2262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE Cerebral 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. OBSERVATIONS To 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 RELEVANCE The 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.
引用
收藏
页码:1187 / 1198
页数:12
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