Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Relationships of Overt and Silent Brain Lesions With Cognitive Function in Patients With Atrial Fibrillation
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4523872
Author(s) Conen, David; Rodondi, Nicolas; Müller, Andreas; Beer, Juerg H.; Ammann, Peter; Moschovitis, Giorgio; Auricchio, Angelo; Hayoz, Daniel; Kobza, Richard; Shah, Dipen; Novak, Jan; Schläpfer, Jürg; Di Valentino, Marcello; Aeschbacher, Stefanie; Blum, Steffen; Meyre, Pascal; Sticherling, Christian; Bonati, Leo H.; Ehret, Georg; Moutzouri, Elisavet; Fischer, Urs; Monsch, Andreas U.; Stippich, Christoph; Wuerfel, Jens; Sinnecker, Tim; Coslovsky, Michael; Schwenkglenks, Matthias; Kühne, Michael; Osswald, Stefan; Swiss-AF Study Investigators,
Author(s) at UniBasel Schwenkglenks, Matthias
Aeschbacher, Stefanie
Blum, Steffen
Braun-Meyre, Pascal
Sticherling, Christian
Bonati, Leo
Osswald, Stefan
Kühne, Michael
Monsch, Andreas U.
Conen, David
Year 2019
Title Relationships of Overt and Silent Brain Lesions With Cognitive Function in Patients With Atrial Fibrillation
Journal Journal of the American College of Cardiology
Volume 73
Number 9
Pages / Article-Number 989-999
Keywords atrial fibrillation; cognitive dysfunction; microbleeds; silent cerebral infarcts; white matter lesions
Mesh terms Aged; Atrial Fibrillation, complications; Brain, pathology; Cerebral Infarction, diagnosis; Cognition, physiology; Cognitive Dysfunction, physiopathology; Female; Follow-Up Studies; Humans; Magnetic Resonance Imaging, methods; Male; Neuropsychological Tests; Prospective Studies; Risk Factors
Abstract Patients with atrial fibrillation (AF) have an increased risk of cognitive decline, potentially resulting from clinically unrecognized vascular brain lesions.; This study sought to assess the relationships between cognitive function and vascular brain lesions in patients with AF.; Patients with known AF were enrolled in a multicenter study in Switzerland. Brain magnetic resonance imaging (MRI) and cognitive testing using the Montreal Cognitive Assessment (MoCA) were performed in all participants. Large noncortical or cortical infarcts (LNCCIs), small noncortical infarcts (SNCIs), microbleeds, and white matter lesions were quantified by a central core laboratory. Clinically silent infarcts were defined as infarcts on brain MRI in patients without a clinical history of stroke or transient ischemic attack.; The study included 1,737 patients with a mean age of 73 ± 8 years (28% women, 90% taking oral anticoagulant agents). On MRI, LNCCIs were found in 387 patients (22%), SNCIs in 368 (21%), microbleeds in 372 (22%), and white matter lesions in 1715 (99%). Clinically silent infarcts among the 1,390 patients without a history of stroke or transient ischemic attack were found in 201 patients with LNCCIs (15%) and 245 patients with SNCIs (18%). The MoCA score was 24.7 ± 3.3 in patients with and 25.8 ± 2.9 in those without LNCCIs on brain MRI (p < 0.001). The difference in MoCA score remained similar when only clinically silent LNCCIs were considered (24.9 ± 3.1 vs. 25.8 ± 2.9; p < 0.001). In a multivariable regression model including all vascular brain lesion parameters, LNCCI volume was the strongest predictor of a reduced MoCA (β = -0.26; 95% confidence interval: -0.40 to -0.13; p < 0.001).; Patients with AF have a high burden of LNCCIs and other brain lesions on systematic brain MRI screening, and most of these lesions are clinically silent. LNCCIs were associated with worse cognitive function, even among patients with clinically silent infarcts. Our findings raise the question of MRI screening in patients with AF.
Publisher Elsevier
ISSN/ISBN 0735-1097
edoc-URL https://edoc.unibas.ch/74431/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.jacc.2018.12.039
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/30846109
Document type (ISI) Journal Article, Multicenter Study
 
   

MCSS v5.8 PRO. 0.457 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
11/05/2024