Subacute Subclinical Brain Infarctions after Transcatheter Aortic Valve Implantation Negatively Impact Cognitive Function in Long-Term Follow-Up

To date every post-procedural cerebrovascular embolic event (CVE) is dreaded for its potential to accelerate cognitive decline after transcatheter aortic valve implantation (TAVI). This study differentiates the impact of acute (procedural) and post-acute cerebrovascular embolic events (CVEs) on cogn...

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Veröffentlicht in:PloS one 2017-01, Vol.12 (1), p.e0168852-e0168852
Hauptverfasser: Ghanem, Alexander, Dörner, Jonas, Schulze-Hagen, Leonie, Müller, Andreas, Wilsing, Marius, Sinning, Jan-Malte, Lütkens, Julian, Frerker, Christian, Kuck, Karl-Heinz, Gräff, Ingo, Schild, Hans, Werner, Nikos, Grube, Eberhard, Nickenig, Georg
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container_issue 1
container_start_page e0168852
container_title PloS one
container_volume 12
creator Ghanem, Alexander
Dörner, Jonas
Schulze-Hagen, Leonie
Müller, Andreas
Wilsing, Marius
Sinning, Jan-Malte
Lütkens, Julian
Frerker, Christian
Kuck, Karl-Heinz
Gräff, Ingo
Schild, Hans
Werner, Nikos
Grube, Eberhard
Nickenig, Georg
description To date every post-procedural cerebrovascular embolic event (CVE) is dreaded for its potential to accelerate cognitive decline after transcatheter aortic valve implantation (TAVI). This study differentiates the impact of acute (procedural) and post-acute cerebrovascular embolic events (CVEs) on cognitive performance. Magnetic resonance imaging (MRI) before, early and late after TAVI was performed to quantify embolic burden. Quantification of diffusion- and T1-weighted lesions, as well as white-matter and total brain volumes, as well as cognitive function testing (MMSE) were assessed in 28 patients with a medium follow-up period of 34 months. Procedural diffusion-weighted lesions were observed in 17 patients (61%), but demonstrated locoregional remnants only in a minority of patients in long-term follow-up (6.5%). Acute CVEs did not impact the trajectory of late silent brain infarctions (SBI), white-matter hyperintensities, and cerebral atrophy. Functionally, early CVEs did not affect cognitive function. In contrast, patients with "new" SBIs after TAVI had a trend to cognitive deterioration in long-term follow-up ("new"SBI: MMSE -1.4 / no "new"SBI: MMSE +1.5, p = 0.067). Interestingly, only a fraction of these "new" SBIs evolved from procedural CVEs (22.2%). Aquired SBIs after TAVI, but not DW-CVE per se are associated with functional impairment long-term after TAVI. In the context of subacute thrombosis seen in TAVI prostheses, these findings set the stage for tailored stroke prevention and comprehensive surrogate endpoint definitions in neuroprotective trials.
doi_str_mv 10.1371/journal.pone.0168852
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This study differentiates the impact of acute (procedural) and post-acute cerebrovascular embolic events (CVEs) on cognitive performance. Magnetic resonance imaging (MRI) before, early and late after TAVI was performed to quantify embolic burden. Quantification of diffusion- and T1-weighted lesions, as well as white-matter and total brain volumes, as well as cognitive function testing (MMSE) were assessed in 28 patients with a medium follow-up period of 34 months. Procedural diffusion-weighted lesions were observed in 17 patients (61%), but demonstrated locoregional remnants only in a minority of patients in long-term follow-up (6.5%). Acute CVEs did not impact the trajectory of late silent brain infarctions (SBI), white-matter hyperintensities, and cerebral atrophy. Functionally, early CVEs did not affect cognitive function. In contrast, patients with "new" SBIs after TAVI had a trend to cognitive deterioration in long-term follow-up ("new"SBI: MMSE -1.4 / no "new"SBI: MMSE +1.5, p = 0.067). Interestingly, only a fraction of these "new" SBIs evolved from procedural CVEs (22.2%). Aquired SBIs after TAVI, but not DW-CVE per se are associated with functional impairment long-term after TAVI. 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In contrast, patients with "new" SBIs after TAVI had a trend to cognitive deterioration in long-term follow-up ("new"SBI: MMSE -1.4 / no "new"SBI: MMSE +1.5, p = 0.067). Interestingly, only a fraction of these "new" SBIs evolved from procedural CVEs (22.2%). Aquired SBIs after TAVI, but not DW-CVE per se are associated with functional impairment long-term after TAVI. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghanem, Alexander</au><au>Dörner, Jonas</au><au>Schulze-Hagen, Leonie</au><au>Müller, Andreas</au><au>Wilsing, Marius</au><au>Sinning, Jan-Malte</au><au>Lütkens, Julian</au><au>Frerker, Christian</au><au>Kuck, Karl-Heinz</au><au>Gräff, Ingo</au><au>Schild, Hans</au><au>Werner, Nikos</au><au>Grube, Eberhard</au><au>Nickenig, Georg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subacute Subclinical Brain Infarctions after Transcatheter Aortic Valve Implantation Negatively Impact Cognitive Function in Long-Term Follow-Up</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-01-05</date><risdate>2017</risdate><volume>12</volume><issue>1</issue><spage>e0168852</spage><epage>e0168852</epage><pages>e0168852-e0168852</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>To date every post-procedural cerebrovascular embolic event (CVE) is dreaded for its potential to accelerate cognitive decline after transcatheter aortic valve implantation (TAVI). This study differentiates the impact of acute (procedural) and post-acute cerebrovascular embolic events (CVEs) on cognitive performance. Magnetic resonance imaging (MRI) before, early and late after TAVI was performed to quantify embolic burden. Quantification of diffusion- and T1-weighted lesions, as well as white-matter and total brain volumes, as well as cognitive function testing (MMSE) were assessed in 28 patients with a medium follow-up period of 34 months. Procedural diffusion-weighted lesions were observed in 17 patients (61%), but demonstrated locoregional remnants only in a minority of patients in long-term follow-up (6.5%). Acute CVEs did not impact the trajectory of late silent brain infarctions (SBI), white-matter hyperintensities, and cerebral atrophy. Functionally, early CVEs did not affect cognitive function. In contrast, patients with "new" SBIs after TAVI had a trend to cognitive deterioration in long-term follow-up ("new"SBI: MMSE -1.4 / no "new"SBI: MMSE +1.5, p = 0.067). Interestingly, only a fraction of these "new" SBIs evolved from procedural CVEs (22.2%). Aquired SBIs after TAVI, but not DW-CVE per se are associated with functional impairment long-term after TAVI. In the context of subacute thrombosis seen in TAVI prostheses, these findings set the stage for tailored stroke prevention and comprehensive surrogate endpoint definitions in neuroprotective trials.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28056466</pmid><doi>10.1371/journal.pone.0168852</doi><tpages>e0168852</tpages><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Aged
Aged, 80 and over
Aorta
Aortic valve
Atrophy
Biology and Life Sciences
Brain
Brain Infarction - physiopathology
Brain Infarction - surgery
Cardiac arrhythmia
Cardiology
Cerebrovascular disease
Cerebrovascular system
Clinical trials
Cognition - physiology
Cognitive ability
Councils
Dementia
Diffusion
Diffusion Magnetic Resonance Imaging
Female
Follow-Up Studies
Heart
Heart valve diseases
Heart Valve Prosthesis Implantation
Humans
Implantation
Lesions
Magnetic resonance
Magnetic resonance imaging
Male
Medicine and Health Sciences
Morphology
Mortality
Neuroimaging
Neuroprotection
NMR
Nuclear magnetic resonance
Older people
Patients
Prostheses
Prosthetics
Research and Analysis Methods
Social Sciences
Stroke
Studies
Substantia alba
Surgery
Systematic review
Thromboembolism
Thrombosis
Transcatheter Aortic Valve Replacement - adverse effects
title Subacute Subclinical Brain Infarctions after Transcatheter Aortic Valve Implantation Negatively Impact Cognitive Function in Long-Term Follow-Up
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