Effects of Cilostazol and Isosorbide Mononitrate on Cerebral Hemodynamics in the LACI-1 Randomized Controlled Trial.
Aged
Cerebral Small Vessel Diseases
/ diagnostic imaging
Cilostazol
/ pharmacology
Female
Hemodynamics
/ drug effects
Humans
Isosorbide Dinitrate
/ analogs & derivatives
Lipoproteins
/ pharmacology
Magnetic Resonance Imaging
/ methods
Male
Middle Aged
Treatment Outcome
Vasodilator Agents
/ pharmacology
cerebral small vessel diseases
cilostazol
cognitive dysfunction
ischemic stroke
magnetic resonance imaging
Journal
Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266
Informations de publication
Date de publication:
01 2022
01 2022
Historique:
pubmed:
2
12
2021
medline:
17
2
2022
entrez:
1
12
2021
Statut:
ppublish
Résumé
Cerebral small vessel disease-a major cause of stroke and dementia-is associated with cerebrovascular dysfunction. We investigated whether short-term isosorbide mononitrate (ISMN) and cilostazol, alone or in combination, improved magnetic resonance imaging-measured cerebrovascular function in patients with lacunar ischemic stroke. Participants were randomized to ISMN alone, cilostazol alone, both ISMN and cilostazol, or no medication. Participants underwent structural, cerebrovascular reactivity (to 6% carbon dioxide) and phase-contrast pulsatility magnetic resonance imaging at baseline and after 8 weeks of medication. Of 27 participants (mean age, 68±7.7; 44% female), 22 completed cerebrovascular reactivity and pulsatility imaging with complete datasets. White matter cerebrovascular reactivity increased in the ISMN (β=0.021%/mm Hg [95% CI, 0.003-0.040]) and cilostazol (β=0.035%/mm Hg [95% CI, 0.014-0.056]) monotherapy groups and in those taking any versus no medication (β=0.021%/mm Hg [95% CI, 0.005-0.037]). While limited by small sample size, we demonstrate that measuring cerebrovascular function with magnetic resonance imaging is feasible in clinical trials and that ISMN and cilostazol may improve cerebrovascular function. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02481323. URL: www.isrctn.com; Unique identifier: ISRCTN12580546. URL: www.clinicaltrialsregister.eu; Unique identifier: EudraCT 2015-001953-33.
Sections du résumé
BACKGROUND AND PURPOSE
Cerebral small vessel disease-a major cause of stroke and dementia-is associated with cerebrovascular dysfunction. We investigated whether short-term isosorbide mononitrate (ISMN) and cilostazol, alone or in combination, improved magnetic resonance imaging-measured cerebrovascular function in patients with lacunar ischemic stroke.
METHODS
Participants were randomized to ISMN alone, cilostazol alone, both ISMN and cilostazol, or no medication. Participants underwent structural, cerebrovascular reactivity (to 6% carbon dioxide) and phase-contrast pulsatility magnetic resonance imaging at baseline and after 8 weeks of medication.
RESULTS
Of 27 participants (mean age, 68±7.7; 44% female), 22 completed cerebrovascular reactivity and pulsatility imaging with complete datasets. White matter cerebrovascular reactivity increased in the ISMN (β=0.021%/mm Hg [95% CI, 0.003-0.040]) and cilostazol (β=0.035%/mm Hg [95% CI, 0.014-0.056]) monotherapy groups and in those taking any versus no medication (β=0.021%/mm Hg [95% CI, 0.005-0.037]).
CONCLUSIONS
While limited by small sample size, we demonstrate that measuring cerebrovascular function with magnetic resonance imaging is feasible in clinical trials and that ISMN and cilostazol may improve cerebrovascular function. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02481323. URL: www.isrctn.com; Unique identifier: ISRCTN12580546. URL: www.clinicaltrialsregister.eu; Unique identifier: EudraCT 2015-001953-33.
Identifiants
pubmed: 34847709
doi: 10.1161/STROKEAHA.121.034866
pmc: PMC8700302
mid: EMS138069
doi:
Substances chimiques
Lipoproteins
0
Vasodilator Agents
0
lipoprotein-associated coagulation inhibitor
0
Isosorbide Dinitrate
IA7306519N
isosorbide-5-mononitrate
LX1OH63030
Cilostazol
N7Z035406B
Banques de données
ClinicalTrials.gov
['NCT02481323']
ISRCTN
['ISRCTN12580546']
EudraCT
['2015-001953-33']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
29-33Subventions
Organisme : Alzheimer's Society
ID : 252
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CS/15/5/31475
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : ETM/326
Pays : United Kingdom
Organisme : Medical Research Council
Pays : United Kingdom
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