Abnormal Functional Brain Connectivity and Personality Traits in Myotonic Dystrophy Type 1

被引:56
作者
Serra, Laura [1 ]
Silvestri, Gabriella [2 ]
Petrucci, Antonio [3 ]
Basile, Barbara [1 ]
Masciullo, Marcella [2 ,4 ]
Makovac, Elena [1 ]
Torso, Mario [1 ]
Spano, Barbara [1 ]
Mastropasqua, Chiara [1 ]
Harrison, Neil A. [5 ]
Bianchi, Maria L. E. [2 ,6 ]
Giacanelli, Manlio [3 ]
Caltagirone, Carlo [7 ,8 ]
Cercignani, Mara [5 ]
Bozzali, Marco [1 ]
机构
[1] Ist Ricovero & Cura Carattere Sci IRCCS Santa Luc, Neuroimaging Lab, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Inst Neurol, Dept Geriatr Orthoped & Neurosci, I-00168 Rome, Italy
[3] Azienda Osped San Camillo Forlanini, Unita Operat Complessa Neurol & Neurofisiopatol, Rome, Italy
[4] IRCCS San Raffaele Pisana, Dept Neurorehabil, Rome, Italy
[5] Univ Sussex, Brighton & Sussex Med Sch, Clin Imaging Sci Ctr, Brighton, E Sussex, England
[6] Fdn Don C Gnocchi Onlus, Milan, Italy
[7] IRCCS Santa Lucia Fdn, Dept Clin & Behav Neurol, I-00179 Rome, Italy
[8] Univ Roma Tor Vergata, Dept Neurosci, Rome, Italy
关键词
COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; DEFAULT NETWORK; HUMAN STRIATUM; RATING-SCALE; CTG REPEAT; RELEVANCE; EXPANSION; STATE; MRI;
D O I
10.1001/jamaneurol.2014.130
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE Myotonic dystrophy type 1 (DM1), the most common muscular dystrophy observed in adults, is a genetic multisystem disorder affecting several other organs besides skeletal muscle, including the brain. Cognitive and personality abnormalities have been reported; however, no studies have investigated brain functional networks and their relationship with personality traits/disorders in patients with DM1. OBJECTIVE To use resting-state functional magnetic resonance imaging to assess the potential relationship between personality traits/disorders and changes to functional connectivity within the default mode network (DMN) in patients with DM1. DESIGN, SETTING, AND PARTICIPANTS We enrolled 27 patients with genetically confirmed DM1 and 16 matched healthy control individuals. Patients underwent personality assessment using clinical interview and Minnesota Multiphasic Personality Inventory-2 administration; all participants underwent resting-state functional magnetic resonance imaging. Investigations were conducted at the Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia Foundation, Catholic University of Sacred Heart, and Azienda Ospedaliera San Camillo Forlanini. INTERVENTION Resting-state functional magnetic resonance imaging. MAIN OUTCOMES AND MEASURES Measures of personality traits in patients and changes in functional connectivity within the DMN in patients and controls. Changes in functional connectivity and atypical personality traits in patients were correlated. RESULTS We combined results obtained from the Minnesota Multiphasic Personality Inventory-2 and clinical interview to identify a continuum of atypical personality profiles ranging from schizotypal personality traits to paranoid personality disorder within our DM1 patients. We also demonstrated an increase in functional connectivity in the bilateral posterior cingulate and left parietal DMN nodes in DM1 patients compared with controls. Moreover, patients with DM1 showed strong associations between DMN functional connectivity and schizotypal-paranoid traits. CONCLUSIONS AND RELEVANCE Our findings provide novel biological evidence that DM1 is a clinical condition that also involves an alteration of functional connectivity of the brain. We speculate that these functional brain abnormalities, similarly to frank psychiatric disorders, may account for the atypical personality traits observed in patients with DM1.
引用
收藏
页码:603 / 611
页数:9
相关论文
共 50 条
  • [21] Muscular disability and organ impairments in myotonic dystrophy type 1
    Pruna, L.
    Machado, F.
    Louis, L.
    Vasse, G.
    Kaminsky, P.
    REVUE NEUROLOGIQUE, 2011, 167 (01) : 23 - 28
  • [22] Endocrine function in 97 patients with myotonic dystrophy type 1
    Orngreen, M. C.
    Arlien-Soborg, P.
    Duno, M.
    Hertz, J. M.
    Vissing, J.
    JOURNAL OF NEUROLOGY, 2012, 259 (05) : 912 - 920
  • [23] Technical standards and guidelines for myotonic dystrophy type 1 testing
    Prior, Thomas W.
    GENETICS IN MEDICINE, 2009, 11 (07) : 552 - 555
  • [24] Peripheral neuropathy in myotonic dystrophy type 1
    Hermans, Mieke C. E.
    Faber, Catharina G.
    Vanhoutte, Els K.
    Bakkers, Mayienne
    De Baets, Marc H.
    de Die-Smulders, Christine E. M.
    Merkies, Ingemar S. J.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2011, 16 (01) : 24 - 29
  • [25] High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2
    Hilbert, James E.
    Barohn, Richard J.
    Clemens, Paula R.
    Luebbe, Elizabeth A.
    Martens, William B.
    McDermott, Michael P.
    Parkhill, Amy L.
    Tawil, Rabi
    Thornton, Charles A.
    Moxley, Richard T., III
    NEUROLOGY, 2017, 89 (13) : 1348 - 1354
  • [26] Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort
    Chawla, Tanushree
    Reddy, Nishanth
    Jankar, Rahul
    Vengalil, Seena
    Polavarapu, Kiran
    Arunachal, Gautham
    Preethish-Kumar, Veeramani
    Nashi, Saraswati
    Bardhan, Mainak
    Rajeshwaran, Jamuna
    Afsar, Mohammad
    Warrier, Manjusha
    Thomas, Priya T.
    Thennarasu, Kandavel
    Nalini, Atchayaram
    NEUROLOGY INDIA, 2024, 72 (01) : 83 - 89
  • [27] A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1)
    Angeard, Nathalie
    Jacquette, Aurelia
    Gargiulo, Marcela
    Radvanyi, Helene
    Moutier, Sylvain
    Eymard, Bruno
    Heron, Delphine
    NEUROMUSCULAR DISORDERS, 2011, 21 (07) : 468 - 476
  • [28] Peripheral nerve involvement in myotonic dystrophy type 2-similar or different than in myotonic dystrophy type 1?
    Nojszewska, Monika
    Lusakowska, Anna
    Szmidt-Salkowska, Elzbieta
    Gawel, Malgorzata
    Lipowska, Marta
    Sulek, Anna
    Krysa, Wioletta
    Rajkiewicz, Marta
    Seroka, Andrzej
    Kaczmarek, Katarzyna
    Kaminska, Anna M.
    NEUROLOGIA I NEUROCHIRURGIA POLSKA, 2015, 49 (03) : 164 - 170
  • [29] Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2
    Mijajlovic, Milija
    Bozovic, Ivo
    Pavlovic, Aleksandra
    Rakocevic-Stojanovic, Vidosava
    Gluscevic, Sanja
    Stojanovic, Amalija
    Basta, Ivana
    Meola, Giovanni
    Peric, Stojan
    HELIYON, 2024, 10 (05)
  • [30] Toward Understanding Cognitive Impairment in Patients with Myotonic Dystrophy Type 1
    Zalonis, Ioannis
    Bonakis, Anastasios
    Christidi, Fotini
    Vagiakis, Emmanouil
    Papageorgiou, Sokratis G.
    Kalfakis, Nikolaos
    Manta, Panagiota
    Vassilopoulos, Dimitrios
    ARCHIVES OF CLINICAL NEUROPSYCHOLOGY, 2010, 25 (04) : 303 - 313