Development and validation of a nomogram for predicting intellectual disability in children with cerebral palsy

被引:0
|
作者
Yuan, Junying [1 ,2 ,3 ,4 ,5 ]
Wang, Gailing [5 ]
Li, Mengyue [6 ]
Zhang, Lingling [1 ,2 ,3 ,4 ]
He, Longyuan [5 ]
Xu, Yiran [1 ,2 ,3 ,4 ]
Zhu, Dengna [1 ,2 ,3 ,4 ,5 ]
Yang, Zhen [5 ]
Xin, Wending [5 ]
Sun, Erliang [5 ]
Zhang, Wei [5 ]
Li, Li [5 ]
Zhang, Xiaoli [1 ,2 ,3 ,4 ]
Zhu, Changlian [1 ,2 ,3 ,4 ,7 ]
机构
[1] Zhengzhou Univ, Henan Pediat Clin Res Ctr, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Inst Neurosci, Henan Key Lab Child Brain Injury, Zhengzhou 450052, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 3, Zhengzhou 450052, Peoples R China
[4] Zhengzhou Univ, Zhengzhou 450052, Peoples R China
[5] Zhengzhou Univ, Cerebral Palsy Rehabil Ctr, Affiliated Hosp 3, Zhengzhou 450052, Peoples R China
[6] Zhengzhou Univ, Affiliated Hosp 3, Ctr Child Behav Dev, Zhengzhou 450052, Peoples R China
[7] Univ Gothenburg, Inst Neurosci & Physiol, Ctr Brain Repair & Rehabil, S-40530 Gothenburg, Sweden
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
Cerebral palsy; Intellectual disability; Prediction model; MRICS; GMFCS; Epilepsy; RISK-FACTORS; MOTOR FUNCTION; GROSS MOTOR; CLASSIFICATION; RELIABILITY; DIAGNOSIS; SYSTEM; IMPACT; AGE;
D O I
10.1016/j.ijchp.2024.100493
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Intellectual disability (ID) is a prevalent comorbidity in children with cerebral palsy (CP), presenting significant challenges to individuals, families and society. This study aims to develop a predictive model to assess the risk of ID in children with CP. Methods: We analyzed data from 885 children diagnosed with CP, among whom 377 had ID. Using least absolute shrinkage and selection operator regression, along with univariate and multivariate logistic regression, we identified key predictors for ID. Model performance was evaluated through receiver operating characteristic curves, calibration plots, and decision curve analysis (DCA). Bootstrapping validation was also employed. Results: The predictive nomogram included variables such as preterm birth, CP subtypes, Gross Motor Function Classification System level, MRI classification category, epilepsy status and hearing loss. The model demonstrated strong discrimination with an area under the receiver operating characteristic curve (AUC) of 0.781 (95% CI: 0.7504-0.8116) and a bootstrapped AUC of 0.7624 (95% CI: 0.7216-0.8032). Calibration plots and the Hosmer-Lemeshow test indicated a good fit (chi(2)= 2 = 7.9061, p = 0.4427). DCA confirmed the model's clinical utility. The cases were randomly divided into test group and validation group at a 7:3 ratio, demonstrating strong discrimination, good fit and clinical utility; similar results were found when stratified by sex. Conclusions: This predictive model effectively identifies children with CP at a high risk for ID, facilitating early intervention strategies. Stratified risk categories provide precise guidance for clinical management, aiming to optimize outcomes for children with CP by leveraging neuroplasticity during early childhood.
引用
收藏
页数:9
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