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Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study

BACKGROUND: Myotonic dystrophy type 1 (Steinert’s disease or DM1), the most common form of autosomal dominant muscular dystrophy in adults, is a multisystem disorder, affecting skeletal muscle as well as eyes, heart, gastrointestinal tract, endocrine system, and central nervous system, finally respo...

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Autores principales: Baldanzi, Sigrid, Bevilacqua, Francesca, Lorio, Rita, Volpi, Leda, Simoncini, Costanza, Petrucci, Antonio, Cosottini, Mirco, Massimetti, Gabriele, Tognoni, Gloria, Ricci, Giulia, Angelini, Corrado, Siciliano, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820880/
https://www.ncbi.nlm.nih.gov/pubmed/27044540
http://dx.doi.org/10.1186/s13023-016-0417-z
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author Baldanzi, Sigrid
Bevilacqua, Francesca
Lorio, Rita
Volpi, Leda
Simoncini, Costanza
Petrucci, Antonio
Cosottini, Mirco
Massimetti, Gabriele
Tognoni, Gloria
Ricci, Giulia
Angelini, Corrado
Siciliano, Gabriele
author_facet Baldanzi, Sigrid
Bevilacqua, Francesca
Lorio, Rita
Volpi, Leda
Simoncini, Costanza
Petrucci, Antonio
Cosottini, Mirco
Massimetti, Gabriele
Tognoni, Gloria
Ricci, Giulia
Angelini, Corrado
Siciliano, Gabriele
author_sort Baldanzi, Sigrid
collection PubMed
description BACKGROUND: Myotonic dystrophy type 1 (Steinert’s disease or DM1), the most common form of autosomal dominant muscular dystrophy in adults, is a multisystem disorder, affecting skeletal muscle as well as eyes, heart, gastrointestinal tract, endocrine system, and central nervous system, finally responsible of increasing disabilities and secondary social consequences. To date, DM1-related brain involvement represents a challenging field of research. It is well known that DM1 patients frequently present neuropsychological disturbances and psychiatric comorbidities among which reduced awareness of disease burden and its progression, also defined as anosognosia, is common in clinical practice, this leading to secondary misattribution of symptoms, delay in timely diagnostic procedures and low compliance to treatment. METHODS: Here we present an observational cross sectional study in which disease-related cognitive dysfunctions and quality of life were assessed by a protocol finally designed to estimate the prevalence of disease awareness in a sample of 65 adult-onset DM1 patients. RESULTS: Our analysis showed that in DM1 patients several cognitive functions, including executive and mnesic domains with visuo-spatial involvement, were affected. The assessment of anosognosia revealed that a high percentage (51.6 %) of DM1 subjects was disease unaware. The reduced illness awareness occurs across different physical and life domains, and it appears more prominent in Activities and Independence domains investigated by the Individualized Neuromuscular Quality Of Life (INQoL) questionnaire. Moreover, the unawareness resulted significantly related (at p <0.05 and p < 0.01) to the performance failure in cognitive tests, specifically in the domains of visuo-spatial memory, cognitive flexibility and conceptualization. CONCLUSIONS: The obtained data confirm, by a systematic analysis, what’s the common clinical perceiving of disease unawareness in Steinert’s disease, this related to the already known cognitive-behavioural impairment of frontal type in affected patients. We believe that a deep knowledge of this aspect will be useful for medical practice in the management of patients with DM1, also for guidance in occupational and social interventions, definition of outcome measures and in preparation of trial readiness.
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spelling pubmed-48208802016-04-06 Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study Baldanzi, Sigrid Bevilacqua, Francesca Lorio, Rita Volpi, Leda Simoncini, Costanza Petrucci, Antonio Cosottini, Mirco Massimetti, Gabriele Tognoni, Gloria Ricci, Giulia Angelini, Corrado Siciliano, Gabriele Orphanet J Rare Dis Research BACKGROUND: Myotonic dystrophy type 1 (Steinert’s disease or DM1), the most common form of autosomal dominant muscular dystrophy in adults, is a multisystem disorder, affecting skeletal muscle as well as eyes, heart, gastrointestinal tract, endocrine system, and central nervous system, finally responsible of increasing disabilities and secondary social consequences. To date, DM1-related brain involvement represents a challenging field of research. It is well known that DM1 patients frequently present neuropsychological disturbances and psychiatric comorbidities among which reduced awareness of disease burden and its progression, also defined as anosognosia, is common in clinical practice, this leading to secondary misattribution of symptoms, delay in timely diagnostic procedures and low compliance to treatment. METHODS: Here we present an observational cross sectional study in which disease-related cognitive dysfunctions and quality of life were assessed by a protocol finally designed to estimate the prevalence of disease awareness in a sample of 65 adult-onset DM1 patients. RESULTS: Our analysis showed that in DM1 patients several cognitive functions, including executive and mnesic domains with visuo-spatial involvement, were affected. The assessment of anosognosia revealed that a high percentage (51.6 %) of DM1 subjects was disease unaware. The reduced illness awareness occurs across different physical and life domains, and it appears more prominent in Activities and Independence domains investigated by the Individualized Neuromuscular Quality Of Life (INQoL) questionnaire. Moreover, the unawareness resulted significantly related (at p <0.05 and p < 0.01) to the performance failure in cognitive tests, specifically in the domains of visuo-spatial memory, cognitive flexibility and conceptualization. CONCLUSIONS: The obtained data confirm, by a systematic analysis, what’s the common clinical perceiving of disease unawareness in Steinert’s disease, this related to the already known cognitive-behavioural impairment of frontal type in affected patients. We believe that a deep knowledge of this aspect will be useful for medical practice in the management of patients with DM1, also for guidance in occupational and social interventions, definition of outcome measures and in preparation of trial readiness. BioMed Central 2016-04-04 /pmc/articles/PMC4820880/ /pubmed/27044540 http://dx.doi.org/10.1186/s13023-016-0417-z Text en © Baldanzi et al. 2016 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
Baldanzi, Sigrid
Bevilacqua, Francesca
Lorio, Rita
Volpi, Leda
Simoncini, Costanza
Petrucci, Antonio
Cosottini, Mirco
Massimetti, Gabriele
Tognoni, Gloria
Ricci, Giulia
Angelini, Corrado
Siciliano, Gabriele
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title_full Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title_fullStr Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title_full_unstemmed Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title_short Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
title_sort disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820880/
https://www.ncbi.nlm.nih.gov/pubmed/27044540
http://dx.doi.org/10.1186/s13023-016-0417-z
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