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A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis

Background. Cardiovascular comorbidities have been associated with cognitive decline in the general population. Objectives. To evaluate the associations between cardiovascular risk and neuropsychological performances in MS. Methods. This is a retrospective study, including 69 MS patients. For all pa...

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Autores principales: Reia, Antonio, Petruzzo, Martina, Falco, Fabrizia, Costabile, Teresa, Conenna, Matteo, Carotenuto, Antonio, Petracca, Maria, Servillo, Giuseppe, Lanzillo, Roberta, Brescia Morra, Vincenzo, Moccia, Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071566/
https://www.ncbi.nlm.nih.gov/pubmed/33923390
http://dx.doi.org/10.3390/brainsci11040502
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author Reia, Antonio
Petruzzo, Martina
Falco, Fabrizia
Costabile, Teresa
Conenna, Matteo
Carotenuto, Antonio
Petracca, Maria
Servillo, Giuseppe
Lanzillo, Roberta
Brescia Morra, Vincenzo
Moccia, Marcello
author_facet Reia, Antonio
Petruzzo, Martina
Falco, Fabrizia
Costabile, Teresa
Conenna, Matteo
Carotenuto, Antonio
Petracca, Maria
Servillo, Giuseppe
Lanzillo, Roberta
Brescia Morra, Vincenzo
Moccia, Marcello
author_sort Reia, Antonio
collection PubMed
description Background. Cardiovascular comorbidities have been associated with cognitive decline in the general population. Objectives. To evaluate the associations between cardiovascular risk and neuropsychological performances in MS. Methods. This is a retrospective study, including 69 MS patients. For all patients, we calculated the Framingham risk score, which provides the 10-year probability of developing macrovascular disease, using age, sex, diabetes, smoking, systolic blood pressure, and cholesterol levels as input variables. Cognitive function was examined with the Brief International Cognitive Assessment for MS (BICAMS), including the Symbol Digit Modalities Test (SDMT), the California Verbal Learning Test-II (CVLT-II), and the Brief Visuospatial Memory Test-Revised (BVMT-R). Results. Each point increase of the Framingham risk score corresponded to 0.21 lower CVLT-II score. Looking at Framingham risk score components, male sex and higher total cholesterol levels corresponded to lower CVLT scores (Coeff = −8.54; 95%CI = −15.51, −1.57; and Coeff = −0.11; 95%CI = −0.20, −0.02, respectively). No associations were found between cardiovascular risk and SDMT or BVMT-R. Conclusions. In our exploratory analyses, cardiovascular risk was associated with verbal learning dysfunction in MS. Lifestyle and pharmacological interventions on cardiovascular risk factors should be considered carefully in the management of MS, given the possible effects on cognitive function.
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spelling pubmed-80715662021-04-26 A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis Reia, Antonio Petruzzo, Martina Falco, Fabrizia Costabile, Teresa Conenna, Matteo Carotenuto, Antonio Petracca, Maria Servillo, Giuseppe Lanzillo, Roberta Brescia Morra, Vincenzo Moccia, Marcello Brain Sci Article Background. Cardiovascular comorbidities have been associated with cognitive decline in the general population. Objectives. To evaluate the associations between cardiovascular risk and neuropsychological performances in MS. Methods. This is a retrospective study, including 69 MS patients. For all patients, we calculated the Framingham risk score, which provides the 10-year probability of developing macrovascular disease, using age, sex, diabetes, smoking, systolic blood pressure, and cholesterol levels as input variables. Cognitive function was examined with the Brief International Cognitive Assessment for MS (BICAMS), including the Symbol Digit Modalities Test (SDMT), the California Verbal Learning Test-II (CVLT-II), and the Brief Visuospatial Memory Test-Revised (BVMT-R). Results. Each point increase of the Framingham risk score corresponded to 0.21 lower CVLT-II score. Looking at Framingham risk score components, male sex and higher total cholesterol levels corresponded to lower CVLT scores (Coeff = −8.54; 95%CI = −15.51, −1.57; and Coeff = −0.11; 95%CI = −0.20, −0.02, respectively). No associations were found between cardiovascular risk and SDMT or BVMT-R. Conclusions. In our exploratory analyses, cardiovascular risk was associated with verbal learning dysfunction in MS. Lifestyle and pharmacological interventions on cardiovascular risk factors should be considered carefully in the management of MS, given the possible effects on cognitive function. MDPI 2021-04-16 /pmc/articles/PMC8071566/ /pubmed/33923390 http://dx.doi.org/10.3390/brainsci11040502 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reia, Antonio
Petruzzo, Martina
Falco, Fabrizia
Costabile, Teresa
Conenna, Matteo
Carotenuto, Antonio
Petracca, Maria
Servillo, Giuseppe
Lanzillo, Roberta
Brescia Morra, Vincenzo
Moccia, Marcello
A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title_full A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title_fullStr A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title_full_unstemmed A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title_short A Retrospective Exploratory Analysis on Cardiovascular Risk and Cognitive Dysfunction in Multiple Sclerosis
title_sort retrospective exploratory analysis on cardiovascular risk and cognitive dysfunction in multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071566/
https://www.ncbi.nlm.nih.gov/pubmed/33923390
http://dx.doi.org/10.3390/brainsci11040502
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