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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.
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页码:596 / 604
页数:9
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