Psychological characteristics of patients with myotonic dystrophy type 1. (11th December 2014)
- Record Type:
- Journal Article
- Title:
- Psychological characteristics of patients with myotonic dystrophy type 1. (11th December 2014)
- Main Title:
- Psychological characteristics of patients with myotonic dystrophy type 1
- Authors:
- Bertrand, J. A.
Jean, S.
Laberge, L.
Gagnon, C.
Mathieu, J.
Gagnon, J. F.
Richer, L. - Abstract:
- <abstract abstract-type="main" id="ane12356-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ane12356-sec-0001" sec-type="section"> <title>Objectives</title> <p>Myotonic dystrophy type 1 (DM1) is the most common adult‐onset muscular dystrophy. It is associated with motor symptoms but patients also display non‐motor symptoms such as particular personality traits. Studies have reported mixed results about personality characteristics which may be attributable to small sample sizes, different disease severity of groups studied, and use of different questionnaires or method. This study aimed to describe the psychological characteristics of a large cohort of patients with DM1, to characterize those at risk of developing a psychiatric disorder, and to compare characteristics between two DM1 phenotypes, a mild and more severe adult‐onset phenotype.</p> </sec> <sec id="ane12356-sec-0002" sec-type="section"> <title>Methods</title> <p>Two hundred patients with DM1 (152 adult‐onset; 48 mild) were asked to complete questionnaires assessing personality traits, psychological symptoms, self‐esteem, and suicidal risk. Neurological and neuropsychological assessments were performed to compare personality characteristics to clinical and cognitive measures.</p> </sec> <sec id="ane12356-sec-0003" sec-type="section"> <title>Results</title> <p>Patients with DM1 globally showed personality traits and psychological symptoms in the average range compared to normative data,<abstract abstract-type="main" id="ane12356-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ane12356-sec-0001" sec-type="section"> <title>Objectives</title> <p>Myotonic dystrophy type 1 (DM1) is the most common adult‐onset muscular dystrophy. It is associated with motor symptoms but patients also display non‐motor symptoms such as particular personality traits. Studies have reported mixed results about personality characteristics which may be attributable to small sample sizes, different disease severity of groups studied, and use of different questionnaires or method. This study aimed to describe the psychological characteristics of a large cohort of patients with DM1, to characterize those at risk of developing a psychiatric disorder, and to compare characteristics between two DM1 phenotypes, a mild and more severe adult‐onset phenotype.</p> </sec> <sec id="ane12356-sec-0002" sec-type="section"> <title>Methods</title> <p>Two hundred patients with DM1 (152 adult‐onset; 48 mild) were asked to complete questionnaires assessing personality traits, psychological symptoms, self‐esteem, and suicidal risk. Neurological and neuropsychological assessments were performed to compare personality characteristics to clinical and cognitive measures.</p> </sec> <sec id="ane12356-sec-0003" sec-type="section"> <title>Results</title> <p>Patients with DM1 globally showed personality traits and psychological symptoms in the average range compared to normative data, with normal levels of self‐esteem and suicidal ideation. However, 27% of patients were found to be at high risk of developing a psychiatric disorder. Moreover, psychological traits differed across phenotypes, with the most severe phenotype tending to show more severe psychological symptoms. The presence of higher phobic anxiety and lower self‐esteem was associated with lower education, a higher number of CTG repeats, more severe muscular impairment, and lower cognitive functioning (<italic>P</italic> &lt; 0.001).</p> </sec> <sec id="ane12356-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Different phenotypes should thus be taken into account in clinical settings for individual management of patients and optimizing therapeutic success.</p> </sec> </abstract> … (more)
- Is Part Of:
- Acta neurologica Scandinavica. Volume 132:Number 1(2015:Jul.)
- Journal:
- Acta neurologica Scandinavica
- Issue:
- Volume 132:Number 1(2015:Jul.)
- Issue Display:
- Volume 132, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 132
- Issue:
- 1
- Issue Sort Value:
- 2015-0132-0001-0000
- Page Start:
- 49
- Page End:
- 58
- Publication Date:
- 2014-12-11
- Subjects:
- Neurology -- Periodicals
616.8 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1111/ane.12356 ↗
- Languages:
- English
- ISSNs:
- 0001-6314
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0639.910000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3049.xml