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Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain

BACKGROUND: The impact of comorbidity on multiple sclerosis (MS) is a new area of interest. Limited data on the risk factors of metabolic syndrome (MetS) is currently available. The aim of this study was to estimate the presence of comorbid conditions and MetS in a sample of adult patients with MS....

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Autores principales: Sicras-Mainar, Antoni, Ruíz-Beato, Elena, Navarro-Artieda, Ruth, Maurino, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512748/
https://www.ncbi.nlm.nih.gov/pubmed/28716070
http://dx.doi.org/10.1186/s12883-017-0914-2
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author Sicras-Mainar, Antoni
Ruíz-Beato, Elena
Navarro-Artieda, Ruth
Maurino, Jorge
author_facet Sicras-Mainar, Antoni
Ruíz-Beato, Elena
Navarro-Artieda, Ruth
Maurino, Jorge
author_sort Sicras-Mainar, Antoni
collection PubMed
description BACKGROUND: The impact of comorbidity on multiple sclerosis (MS) is a new area of interest. Limited data on the risk factors of metabolic syndrome (MetS) is currently available. The aim of this study was to estimate the presence of comorbid conditions and MetS in a sample of adult patients with MS. METHODS: A retrospective, cohort study was conducted using electronic medical records from 19 primary care centres in Catalonia and Asturias, Spain. The number of chronic diseases (diagnoses), the Charlson Comorbidity Index and the individual Case-mix Index were used to assess general comorbidity variables. MetS was defined using the National Cholesterol Education Program Adult Treatment Panel III. Patients were distributed into two groups according to the Expanded Disability Status Scale (EDSS) score: 0–3.5 and 4–10. RESULTS: A total of 222 patients were studied (mean age = 45.5 (SD 12.5) years, 64.4% were female and 62.2% presented a diagnosis of relapsing-remitting MS). Mean EDSS score was 3.2 (SD 2.0). Depression (32.4%), dyslipidaemia (31.1%), hypertension (23.0%) and obesity (22.5%) were the most common comorbidities. Overall MetS prevalence was 31.1% (95% CI: 25.0–37.2%). Patients with an EDSS ≥ 4.0 showed a significantly higher number of comorbidities (OR=2.2; 95% CI: 1.7–3.0; p<0.001). CONCLUSION: MS patients had a high prevalence of MetS. Screening for comorbidity should be part of standard MS care. Further studies are necessary to confirm this association and the underlying mechanisms of MS and its comorbidities.
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spelling pubmed-55127482017-07-19 Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain Sicras-Mainar, Antoni Ruíz-Beato, Elena Navarro-Artieda, Ruth Maurino, Jorge BMC Neurol Research Article BACKGROUND: The impact of comorbidity on multiple sclerosis (MS) is a new area of interest. Limited data on the risk factors of metabolic syndrome (MetS) is currently available. The aim of this study was to estimate the presence of comorbid conditions and MetS in a sample of adult patients with MS. METHODS: A retrospective, cohort study was conducted using electronic medical records from 19 primary care centres in Catalonia and Asturias, Spain. The number of chronic diseases (diagnoses), the Charlson Comorbidity Index and the individual Case-mix Index were used to assess general comorbidity variables. MetS was defined using the National Cholesterol Education Program Adult Treatment Panel III. Patients were distributed into two groups according to the Expanded Disability Status Scale (EDSS) score: 0–3.5 and 4–10. RESULTS: A total of 222 patients were studied (mean age = 45.5 (SD 12.5) years, 64.4% were female and 62.2% presented a diagnosis of relapsing-remitting MS). Mean EDSS score was 3.2 (SD 2.0). Depression (32.4%), dyslipidaemia (31.1%), hypertension (23.0%) and obesity (22.5%) were the most common comorbidities. Overall MetS prevalence was 31.1% (95% CI: 25.0–37.2%). Patients with an EDSS ≥ 4.0 showed a significantly higher number of comorbidities (OR=2.2; 95% CI: 1.7–3.0; p<0.001). CONCLUSION: MS patients had a high prevalence of MetS. Screening for comorbidity should be part of standard MS care. Further studies are necessary to confirm this association and the underlying mechanisms of MS and its comorbidities. BioMed Central 2017-07-17 /pmc/articles/PMC5512748/ /pubmed/28716070 http://dx.doi.org/10.1186/s12883-017-0914-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sicras-Mainar, Antoni
Ruíz-Beato, Elena
Navarro-Artieda, Ruth
Maurino, Jorge
Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title_full Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title_fullStr Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title_full_unstemmed Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title_short Comorbidity and metabolic syndrome in patients with multiple sclerosis from Asturias and Catalonia, Spain
title_sort comorbidity and metabolic syndrome in patients with multiple sclerosis from asturias and catalonia, spain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512748/
https://www.ncbi.nlm.nih.gov/pubmed/28716070
http://dx.doi.org/10.1186/s12883-017-0914-2
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