Mariana Rabelo de Brito, Thiago Junqueira R Rezende, Stephany da Silva Passos, Cristina Iwabe, Alberto R M Martinez, Anamarli Nucci, Marcondes Cavalcante França
{"title":"DMD致病变异女性携带者的认知改变和脑结构异常。","authors":"Mariana Rabelo de Brito, Thiago Junqueira R Rezende, Stephany da Silva Passos, Cristina Iwabe, Alberto R M Martinez, Anamarli Nucci, Marcondes Cavalcante França","doi":"10.1007/s00415-025-12896-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Skeletal and cardiac muscle damage have been increasingly recognized in female carriers of DMD pathogenic variants (DMDc). Little is known about cognitive impairment in these women or whether they have structural brain damage.</p><p><strong>Objective: </strong>To characterize the cognitive profile in a Brazilian cohort of DMDc and determine whether they have structural brain abnormalities using multimodal MRI.</p><p><strong>Methods: </strong>Thirty-three DMDc and 33 age-matched healthy women were recruited. The Addenbrooke cognitive examination revised (ACE-R) and the Beck depression inventory (BDI) were used to assess cognition and depressive symptoms. 3T Brain MRI was acquired for both groups. Using volumetric T1 sequence, we computed cerebral cortical thickness (FreeSurfer), basal ganglia (T1 Multi-atlas) and cerebellar (Cerebnet) volumetry. Diffusion tensor imaging (DTI) assessed white-matter integrity (DTI Multi-atlas). Groups were compared using a generalized linear model with Bonferroni-corrected p values < 0.05.</p><p><strong>Results: </strong>Mean age of DMDc was 38.2 ± 8.2 years, 48.5% of them had abnormal cognition, but only 15% showed meaningful depressive symptoms. Multiple cognitive domains were affected: Attention in 51.5%, Verbal Fluency in 36.4%, Visuospatial Ability in 36.4%, Language in 27.3%, and Memory in 21.2%. Multimodal MRI revealed bilateral, symmetric atrophy in parieto-occipital cortices in DMDc relative to controls, but no basal ganglia, white matter, or cerebellar changes. Parietal cortex thinning correlated with attention, memory, and verbal fluency scores.</p><p><strong>Interpretation: </strong>DMDc should no longer be seen as 'asymptomatic'. They have cognitive abnormalities and cerebral structural changes compared to healthy women. These manifestations should be actively identified and managed in clinical practice.</p>","PeriodicalId":16558,"journal":{"name":"Journal of Neurology","volume":"272 2","pages":"152"},"PeriodicalIF":4.8000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cognitive changes and brain structural abnormalities in female carriers of DMD pathogenic variants.\",\"authors\":\"Mariana Rabelo de Brito, Thiago Junqueira R Rezende, Stephany da Silva Passos, Cristina Iwabe, Alberto R M Martinez, Anamarli Nucci, Marcondes Cavalcante França\",\"doi\":\"10.1007/s00415-025-12896-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Skeletal and cardiac muscle damage have been increasingly recognized in female carriers of DMD pathogenic variants (DMDc). Little is known about cognitive impairment in these women or whether they have structural brain damage.</p><p><strong>Objective: </strong>To characterize the cognitive profile in a Brazilian cohort of DMDc and determine whether they have structural brain abnormalities using multimodal MRI.</p><p><strong>Methods: </strong>Thirty-three DMDc and 33 age-matched healthy women were recruited. The Addenbrooke cognitive examination revised (ACE-R) and the Beck depression inventory (BDI) were used to assess cognition and depressive symptoms. 3T Brain MRI was acquired for both groups. Using volumetric T1 sequence, we computed cerebral cortical thickness (FreeSurfer), basal ganglia (T1 Multi-atlas) and cerebellar (Cerebnet) volumetry. Diffusion tensor imaging (DTI) assessed white-matter integrity (DTI Multi-atlas). Groups were compared using a generalized linear model with Bonferroni-corrected p values < 0.05.</p><p><strong>Results: </strong>Mean age of DMDc was 38.2 ± 8.2 years, 48.5% of them had abnormal cognition, but only 15% showed meaningful depressive symptoms. Multiple cognitive domains were affected: Attention in 51.5%, Verbal Fluency in 36.4%, Visuospatial Ability in 36.4%, Language in 27.3%, and Memory in 21.2%. Multimodal MRI revealed bilateral, symmetric atrophy in parieto-occipital cortices in DMDc relative to controls, but no basal ganglia, white matter, or cerebellar changes. Parietal cortex thinning correlated with attention, memory, and verbal fluency scores.</p><p><strong>Interpretation: </strong>DMDc should no longer be seen as 'asymptomatic'. They have cognitive abnormalities and cerebral structural changes compared to healthy women. These manifestations should be actively identified and managed in clinical practice.</p>\",\"PeriodicalId\":16558,\"journal\":{\"name\":\"Journal of Neurology\",\"volume\":\"272 2\",\"pages\":\"152\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00415-025-12896-6\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00415-025-12896-6","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Cognitive changes and brain structural abnormalities in female carriers of DMD pathogenic variants.
Background: Skeletal and cardiac muscle damage have been increasingly recognized in female carriers of DMD pathogenic variants (DMDc). Little is known about cognitive impairment in these women or whether they have structural brain damage.
Objective: To characterize the cognitive profile in a Brazilian cohort of DMDc and determine whether they have structural brain abnormalities using multimodal MRI.
Methods: Thirty-three DMDc and 33 age-matched healthy women were recruited. The Addenbrooke cognitive examination revised (ACE-R) and the Beck depression inventory (BDI) were used to assess cognition and depressive symptoms. 3T Brain MRI was acquired for both groups. Using volumetric T1 sequence, we computed cerebral cortical thickness (FreeSurfer), basal ganglia (T1 Multi-atlas) and cerebellar (Cerebnet) volumetry. Diffusion tensor imaging (DTI) assessed white-matter integrity (DTI Multi-atlas). Groups were compared using a generalized linear model with Bonferroni-corrected p values < 0.05.
Results: Mean age of DMDc was 38.2 ± 8.2 years, 48.5% of them had abnormal cognition, but only 15% showed meaningful depressive symptoms. Multiple cognitive domains were affected: Attention in 51.5%, Verbal Fluency in 36.4%, Visuospatial Ability in 36.4%, Language in 27.3%, and Memory in 21.2%. Multimodal MRI revealed bilateral, symmetric atrophy in parieto-occipital cortices in DMDc relative to controls, but no basal ganglia, white matter, or cerebellar changes. Parietal cortex thinning correlated with attention, memory, and verbal fluency scores.
Interpretation: DMDc should no longer be seen as 'asymptomatic'. They have cognitive abnormalities and cerebral structural changes compared to healthy women. These manifestations should be actively identified and managed in clinical practice.
期刊介绍:
The Journal of Neurology is an international peer-reviewed journal which provides a source for publishing original communications and reviews on clinical neurology covering the whole field.
In addition, Letters to the Editors serve as a forum for clinical cases and the exchange of ideas which highlight important new findings. A section on Neurological progress serves to summarise the major findings in certain fields of neurology. Commentaries on new developments in clinical neuroscience, which may be commissioned or submitted, are published as editorials.
Every neurologist interested in the current diagnosis and treatment of neurological disorders needs access to the information contained in this valuable journal.