Framework for Clinical Trials in Cerebral Small Vessel Disease (FINESSE): A Review.
Journal
JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536
Informations de publication
Date de publication:
01 11 2022
01 11 2022
Historique:
pubmed:
16
8
2022
medline:
18
11
2022
entrez:
15
8
2022
Statut:
ppublish
Résumé
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. 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. 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.
Identifiants
pubmed: 35969390
pii: 2795400
doi: 10.1001/jamaneurol.2022.2262
doi:
Substances chimiques
finesse
76363-65-0
Types de publication
Review
Journal Article
Research Support, N.I.H., Intramural
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1187-1198Subventions
Organisme : Department of Health
ID : BRC-1215-20014
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/16/38/32080
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206589/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : G1000372
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/J006971/1
Pays : United Kingdom