Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairment

被引:17
|
作者
Battini, R. [1 ,2 ]
Lenzi, S. [1 ]
Lucibello, S. [3 ,4 ]
Chieffo, D. [3 ,4 ]
Moriconi, F. [3 ,4 ]
Cristofani, P. [1 ]
Bulgheroni, S. [5 ]
Cumbo, F. [6 ]
Pane, M. [3 ,4 ]
Baranello, G. [5 ]
Alfieri, P. [6 ]
Astrea, G. [1 ]
Cioni, G. [1 ,2 ]
Vicari, S. [6 ,7 ]
Mercuri, E. [3 ,4 ]
机构
[1] IRCCS Fdn Stella Maris, Dept Dev Neurosci, Viale Tirreno 341-ABC, I-56128 Pisa, Italy
[2] Univ Pisa, Dept Clin & Expt Med, Via Savi10, I-56126 Pisa, Italy
[3] Catholic Univ, Pediat Neurol Unit, Largo Agostino Gemelli 8, Rome, Italy
[4] Policlin Univ Gemelli, Nemo Ctr, Largo Agostino Gemelli 8, Rome, Italy
[5] Fdn IRCCS Ist Neurol Carlo Besta, Dev Neurol Div, Via Celoria 11, Milan, Italy
[6] IRCCS Bambino Gesu Childrens Hosp, Dept Neurol & Psychiat Sci, Child & Adolescent Neuropsychiat Unit, Piazza St Onofrio 4, I-00165 Rome, Italy
[7] Catholic Univ, Dept Life Sci & Publ Hlth, Largo Agostino Gemelli 8, Rome, Italy
关键词
Duchenne muscular dystrophy (DMD); Neuropsychological profile; Executive functions; Working memory; Cerebellum; VERBAL WORKING-MEMORY; EXECUTIVE FUNCTION; CHILDREN; LOCALIZATION; INHIBITION;
D O I
10.1016/j.nmd.2021.01.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of the study was to re-assess neuropsychological profile in a group of boys with Duchenne muscular dystrophy without intellectual disability and neuropsychiatric disorder three years apart from a previous evaluation, to establish possible changes over time. We were also interested in defining more in detail correlation between genotype and neuropsychological phenotype. Thirty-three of the previous 40 subjects (mean age at follow up: 10 years and 7 months) agreed to participate in the follow up study and to perform the new assessment. The results confirm a typical neuropsychological profile, with difficulty in the manipulation of stored information, poor abstract reasoning and planning capacity and impulsiveness, supporting the involvement of a cerebellar striatal cortical network for these children. The more detailed description of subgroups of subjects, according to the real expression of Dp140, let to reveal possible genotype-neuropsychological phenotype correlations, and a more general neuropsychological impairment emerged in boys without Dp140 expression. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:319 / 327
页数:9
相关论文
共 50 条
  • [31] Evolution of neuropsychological and behavioral profile in a cohort of pediatric patients with Becker muscular dystrophy in a longitudinal study
    Cumbo, Francesca
    Tosi, Michele
    Catteruccia, Michela
    Diodato, Daria
    Nicita, Francesco
    Mizzoni, Irene
    De Luca, Giacomo
    Carlesi, Adelina
    Alfieri, Paolo
    Vicari, Stefano
    Bertini, Enrico Silvio
    D'Amico, Adele
    NEUROMUSCULAR DISORDERS, 2024, 36 : 33 - 37
  • [32] Pulmonary function characteristics of boys with Duchenne muscular dystrophy: Data from the CINRG longitudinal study project
    Abresch, R. T.
    McDonald, C. M.
    Henricson, E. K.
    Gustavo, N.
    Hu, F.
    Duong, T.
    Joyce, N.
    Mah, J.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 802 - 802
  • [33] A longitudinal study of body composition in glucocorticoid treated boys with Duchenne muscular dystrophy
    Turnbull, A.
    Denker, M.
    Joseph, S.
    Di Marco, M.
    Dunne, J.
    Gerasimidis, K.
    Horrocks, I.
    Mochrie, R.
    Ahmed, S. F.
    Wong, S. C.
    SCOTTISH MEDICAL JOURNAL, 2020, 65 (03) : NP8 - NP8
  • [34] Deflazacort benefits boys with Duchenne muscular dystrophy
    Biggar, WD
    Harris, V
    Alman, B
    Vasjar, J
    NEUROMUSCULAR DISORDERS, 2002, 12 (7-8) : 738 - 738
  • [35] Sleep disorders in boys with Duchenne muscular dystrophy
    Bloetzer, Clemens
    Jeannet, Pierre-Yves
    Lynch, Bryan
    Newman, Christopher J.
    ACTA PAEDIATRICA, 2012, 101 (12) : 1265 - 1269
  • [36] Electrocardiographic Trends in Boys with Duchenne Muscular Dystrophy
    Gambetta, K.
    Wittlieb-Weber, C. W.
    Villa, C. R.
    Conway, J.
    Johnson, J. N.
    Bock, M. J.
    Lal, A. K.
    Schumacher, K. R.
    Law, S. P.
    Deshpande, S.
    West, S. C.
    Friedland-Little, J. M.
    Friedland-Little, J. M.
    Lytrivi, I. D.
    Butts, R. J.
    Knecht, K. J.
    Michael, M. A.
    JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2019, 38 (04): : S465 - S465
  • [37] Pulmonary function in boys with Duchenne Muscular Dystrophy
    Wasilewska, E.
    Niedoszytko, M.
    Meyer-Szary, J.
    Sledzinska, K.
    Jassem, E.
    Wierzba, J.
    ALLERGY, 2018, 73 : 418 - 418
  • [38] Vertebral fractures in boys with Duchenne muscular dystrophy
    Bothwell, JE
    Gordon, KE
    Dooley, JM
    MacSween, J
    Cummings, EA
    Salisbury, S
    CLINICAL PEDIATRICS, 2003, 42 (04) : 353 - 356
  • [39] Impact of Genotype on Boys with Duchenne Muscular Dystrophy
    Gambetta, K.
    Wittlieb-Weber, C.
    Bock, M.
    Villa, C.
    Johnson, J.
    Lal, A.
    Schumacher, K.
    Law, S.
    Deshpande, S.
    West, S.
    Friedland-Little, J.
    Lytrivi, I.
    Butts, R.
    Cunningham, C.
    Knecht, K. R.
    McCullough, M.
    JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2018, 37 (04): : S122 - S122
  • [40] Supported Standing in Boys With Duchenne Muscular Dystrophy
    Townsend, Elise L.
    Bibeau, Christine
    Holmes, Tara M.
    PEDIATRIC PHYSICAL THERAPY, 2016, 28 (03) : 320 - 329