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Comorbidities in patients with Unverricht–Lundborg disease (EPM1)
BACKGROUND: Unverricht‐Lundborg disease (EPM1) typically leads to accumulating disability. Disability may also be caused by comorbidities but there are no data available on these. AIMS OF THE STUDY: To investigate the frequency of comorbidities in EPM1. METHODS: Comorbidity data of a previously desc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826374/ https://www.ncbi.nlm.nih.gov/pubmed/36097839 http://dx.doi.org/10.1111/ane.13706 |
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author | Sipilä, Jussi O. T. Kälviäinen, Reetta |
author_facet | Sipilä, Jussi O. T. Kälviäinen, Reetta |
author_sort | Sipilä, Jussi O. T. |
collection | PubMed |
description | BACKGROUND: Unverricht‐Lundborg disease (EPM1) typically leads to accumulating disability. Disability may also be caused by comorbidities but there are no data available on these. AIMS OF THE STUDY: To investigate the frequency of comorbidities in EPM1. METHODS: Comorbidity data of a previously described cohort of 135 Finnish patients with EPM1 were retrieved from neurological, surgical (including subspecialities), internal medicine (including subspecialities) and intensive care patient charts of the treating hospitals. RESULTS: Mean follow‐up time was 31.4 years (SD 12.4 years, range 6.8–57.8 years), during which at least one comorbidity was observed in 107 patients (79%) and three or more in 53 (39%). The most common diagnostic categories were external injuries, mental and behavioural disorders and endocrine, nutritional and metabolic diseases. The most common single comorbid diagnosis was a fracture of the ankle (in 19% of all patients). The second most common single comorbid diagnosis in the cohort was diabetes (in 13% of all patients), and the third was depression, recorded for 13% of the cohort. Malignancies and cardiovascular end‐organ damage were rare, whereas phimosis/paraphimosis appeared more common than in general population. CONCLUSIONS: Patients with EPM1 often have comorbidities. Trauma and mental health risks should be especially followed and acted upon. Further studies are needed to more accurately comorbidity risks, characteristics and patient needs. |
format | Online Article Text |
id | pubmed-9826374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98263742023-01-09 Comorbidities in patients with Unverricht–Lundborg disease (EPM1) Sipilä, Jussi O. T. Kälviäinen, Reetta Acta Neurol Scand Clinical Commentary BACKGROUND: Unverricht‐Lundborg disease (EPM1) typically leads to accumulating disability. Disability may also be caused by comorbidities but there are no data available on these. AIMS OF THE STUDY: To investigate the frequency of comorbidities in EPM1. METHODS: Comorbidity data of a previously described cohort of 135 Finnish patients with EPM1 were retrieved from neurological, surgical (including subspecialities), internal medicine (including subspecialities) and intensive care patient charts of the treating hospitals. RESULTS: Mean follow‐up time was 31.4 years (SD 12.4 years, range 6.8–57.8 years), during which at least one comorbidity was observed in 107 patients (79%) and three or more in 53 (39%). The most common diagnostic categories were external injuries, mental and behavioural disorders and endocrine, nutritional and metabolic diseases. The most common single comorbid diagnosis was a fracture of the ankle (in 19% of all patients). The second most common single comorbid diagnosis in the cohort was diabetes (in 13% of all patients), and the third was depression, recorded for 13% of the cohort. Malignancies and cardiovascular end‐organ damage were rare, whereas phimosis/paraphimosis appeared more common than in general population. CONCLUSIONS: Patients with EPM1 often have comorbidities. Trauma and mental health risks should be especially followed and acted upon. Further studies are needed to more accurately comorbidity risks, characteristics and patient needs. John Wiley and Sons Inc. 2022-09-13 2022-11 /pmc/articles/PMC9826374/ /pubmed/36097839 http://dx.doi.org/10.1111/ane.13706 Text en © 2022 The Authors. Acta Neurologica Scandinavica published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Clinical Commentary Sipilä, Jussi O. T. Kälviäinen, Reetta Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title | Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title_full | Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title_fullStr | Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title_full_unstemmed | Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title_short | Comorbidities in patients with Unverricht–Lundborg disease (EPM1) |
title_sort | comorbidities in patients with unverricht–lundborg disease (epm1) |
topic | Clinical Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826374/ https://www.ncbi.nlm.nih.gov/pubmed/36097839 http://dx.doi.org/10.1111/ane.13706 |
work_keys_str_mv | AT sipilajussiot comorbiditiesinpatientswithunverrichtlundborgdiseaseepm1 AT kalviainenreetta comorbiditiesinpatientswithunverrichtlundborgdiseaseepm1 |