Clinical study on cognitive impairment in Duchenne muscular dystrophy

被引:4
|
作者
Zhang, Xiao-Fang [1 ]
Luo, Yuan-Yuan [1 ]
Jiang, Li [1 ]
Hong, Si-Qi [1 ,2 ]
机构
[1] Chongqing Med Univ, Childrens Hosp, Natl Clin Res Ctr Child Hlth & Disorders,China Int, Dept Neurol,Minist Educ,Key Lab Child Dev & Disord, Chongqing, Peoples R China
[2] Chongqing Med Univ, Childrens Hosp, 2nd Zhongshan Rd, Chongqing, Peoples R China
关键词
Duchenne muscular dystrophy; Dystrophin; Cognitive impairment; Glucocorticoids; MEMORY; PERFORMANCE; TRANSCRIPT; CHILDREN; GENE; DP71;
D O I
10.1016/j.nmd.2023.06.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our study aimed to explore the intellectual function of patients with Duchenne muscular dystrophy (DMD) in China and examine the correlation of full-scale intelligence quotient (FSIQ) with age, mutation locations, mutation class, and dystrophin isoforms. We assessed 64 boys with DMD using The Wechsler Intelligence Scales for Children-Fourth Edition and compared intellectual function at enrollment and follow-up in the 15 patients who completed the follow-up. Our findings confirm that boys with DMD may exhibit cognitive impairment, with the Working Memory Index being the most impaired. There was no significant correlation between FSIQ and age; however, a positive correlation was noted between age and the Verbal Comprehension Index. FSIQ was not associated with mutation class, the number of affected mutated exons, or mutation locations. However, there was a significant difference in FSIQ between the groups with intact and deficient Dp140. Fifteen participants adhered to glucocorticoid therapy throughout the two-year follow-up period, and eleven of them showed an improvement in FSIQ compared to their initial scores, with improvement ranging from 2 to 20. In conclusion, patients with the cumulative loss of isoforms in the brain are at a higher risk of cognitive deficits and may require early cognitive interventions.& COPY; 2023 Elsevier B.V. All rights reserved.
引用
收藏
页码:596 / 604
页数:9
相关论文
共 50 条
  • [21] Pragmatic cognitive and psychosocial health monitoring in clinical practice in Duchenne muscular dystrophy
    Thangarajh, M.
    Kaat, A.
    Hardy, K.
    Wagner, K.
    NEUROMUSCULAR DISORDERS, 2019, 29 : S148 - S149
  • [22] Duchenne Muscular Dystrophy: are we able to correlate cognitive impairment to site of mutations in the dystrophin gene?
    Wong, J. T. Y.
    Taylor, P. J.
    Pedersen, R. L.
    Betts, G. A.
    Mowat, D. R.
    Buckley, M. F.
    Johnson, H. M.
    NEUROMUSCULAR DISORDERS, 2006, 16 : S141 - S141
  • [23] Histoenzymatic study in Duchenne muscular dystrophy
    Sideeq, D
    Nashaat, N
    Ahmad, S
    Abdulla, N
    NEUROMUSCULAR DISORDERS, 2002, 12 (7-8) : 756 - 756
  • [24] CORRELATION OF DUCHENNE MUSCULAR-DYSTROPHY X-CHROMOSOME DELETION SITE WITH COGNITIVE IMPAIRMENT
    SMITH, SA
    SHAPIRO, EG
    BEST, K
    DEMARTINVILLE, B
    ANNALS OF NEUROLOGY, 1991, 30 (03) : 449 - 450
  • [25] Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairment
    Battini, R.
    Lenzi, S.
    Lucibello, S.
    Chieffo, D.
    Moriconi, F.
    Cristofani, P.
    Bulgheroni, S.
    Cumbo, F.
    Pane, M.
    Baranello, G.
    Alfieri, P.
    Astrea, G.
    Cioni, G.
    Vicari, S.
    Mercuri, E.
    NEUROMUSCULAR DISORDERS, 2021, 31 (04) : 319 - 327
  • [26] Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy
    Banihani, Rudaina
    Smile, Sharon
    Yoon, Grace
    Dupuis, Annie
    Mosleh, Maureen
    Snider, Andrea
    McAdam, Laura
    JOURNAL OF CHILD NEUROLOGY, 2015, 30 (11) : 1472 - 1482
  • [27] Clinical and spirometric alterations in Duchenne muscular dystrophy
    Andrada, LE
    DeVito, EL
    MEDICINA-BUENOS AIRES, 1996, 56 (05) : 463 - 471
  • [28] The NIH Toolbox for Cognitive Surveillance in Duchenne Muscular Dystrophy
    Thangarajh, Mathula
    Kaat, Aaron
    Bibat, Genila
    Hardy, Kristina
    Wagner, Kathryn
    NEUROLOGY, 2020, 94 (15)
  • [29] Cognitive, behavioral and emotional functioning in Duchenne muscular dystrophy
    Taneja, C.
    Donders, J.
    CLINICAL NEUROPSYCHOLOGIST, 2007, 21 (03) : 420 - 421
  • [30] Cognitive dysfunction in boys with Duchenne Muscular Dystrophy.
    Palumbo, D
    Pandya, S
    Moxley, R
    Silverstein, S
    ARCHIVES OF CLINICAL NEUROPSYCHOLOGY, 1996, 11 (05) : 431 - 431