Facial emotion recognition and cerebral white matter lesions in myotonic dystrophy type 1
- PMID: 20006353
- DOI: 10.1016/j.jns.2009.11.011
Facial emotion recognition and cerebral white matter lesions in myotonic dystrophy type 1
Abstract
In order to investigate the cognitive and neurological bases of social cognitive impairment in myotonic dystrophy type 1 (DM1), we examined the facial expression recognition abilities and the cerebral lesions in a group of DM 1 (5 men, 4 women). We measured sensitivity to facial emotions and compared the findings with magnetic resonance image (MRI) findings evaluated using a semi-quantitative method. The DM1 patients showed lower sensitivity to disgusted and angry faces as compared to the healthy controls. The assessment of brain lesions revealed that more severe lesions occurred in the frontal, temporal, and insular white matters. Sensitivity to the emotion of disgust was negatively correlated with temporal lesions, and sensitivity to anger negatively correlated with frontal, temporal, and insular lesions. The results of this study indicate an association between lesions in the frontal, temporal, and insular subcortices and decreased emotional sensitivity to disgust and anger in DM1 patients. These areas are thought to play an important role in emotional processing in the normal brain. Our results suggest that social cognitive impairment in DM1 patients is attributable to impaired emotional processing linked to white matter lesions.
Similar articles
-
Lowered sensitivity to facial emotions in myotonic dystrophy type 1.J Neurol Sci. 2009 May 15;280(1-2):35-9. doi: 10.1016/j.jns.2009.01.014. Epub 2009 Feb 15. J Neurol Sci. 2009. PMID: 19223261
-
Cranial magnetic resonance imaging in genetically proven myotonic dystrophy type 1 and 2.J Neurol. 2004 Jun;251(6):710-4. doi: 10.1007/s00415-004-0408-1. J Neurol. 2004. PMID: 15311347
-
[Social Cognitive Impairment in Myotonic Dystrophy Type 1].Brain Nerve. 2016 Feb;68(2):137-44. doi: 10.11477/mf.1416200363. Brain Nerve. 2016. PMID: 26873233 Review. Japanese.
-
Hemispheric dominance for emotions, empathy and social behaviour: evidence from right and left handers with frontotemporal dementia.Neurocase. 2001;7(2):145-60. doi: 10.1093/neucas/7.2.145. Neurocase. 2001. PMID: 11320162
-
[Neurological disease and facial recognition].Brain Nerve. 2012 Jul;64(7):799-813. Brain Nerve. 2012. PMID: 22764352 Review. Japanese.
Cited by
-
Myotonic dystrophy-1 complicated by factor-v (leiden) mutation.Case Rep Med. 2015;2015:271639. doi: 10.1155/2015/271639. Epub 2015 Mar 30. Case Rep Med. 2015. PMID: 25918532 Free PMC article.
-
Theory of Mind in Myotonic Dystrophy Type 1 Is Associated With Cortical Gyrification and White Matter Hyperintensities.Eur J Neurol. 2025 May;32(5):e70216. doi: 10.1111/ene.70216. Eur J Neurol. 2025. PMID: 40407282 Free PMC article.
-
A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1.J Neuromuscul Dis. 2018;5(3):279-294. doi: 10.3233/JND-180310. J Neuromuscul Dis. 2018. PMID: 30040740 Free PMC article. Review.
-
Brain Pathogenesis and Potential Therapeutic Strategies in Myotonic Dystrophy Type 1.Front Aging Neurosci. 2021 Nov 15;13:755392. doi: 10.3389/fnagi.2021.755392. eCollection 2021. Front Aging Neurosci. 2021. PMID: 34867280 Free PMC article. Review.
-
Myotonic Dystrophies: State of the Art of New Therapeutic Developments for the CNS.Front Cell Neurosci. 2017 Apr 20;11:101. doi: 10.3389/fncel.2017.00101. eCollection 2017. Front Cell Neurosci. 2017. PMID: 28473756 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources