Yalçın Çapan Özlem
Department of Medical Biology, Faculty of Medicine, Tekirdağ Namık Kemal University, Tekirdağ, Türkiye.
J Mol Neurosci. 2025 Feb 13;75(1):19. doi: 10.1007/s12031-024-02299-z.
Mutations in the CDKL5 gene are associated with developmental and epileptic encephalopathy (DEE), a severe disorder characterized by developmental delay and epileptic activity. In genetic analyses of DEEs, variants classified as pathogenic confirm the diagnosis of the disease while Variants of Uncertain Significance (VUS) remain in a gray area due to insufficient evidence. This study aimed to optimize the interpretation of VUS in the CDKL5 gene by evaluating the performance of 22 in silico prediction tools using 186 known pathogenic or benign missense variants from the ClinVar database. The best-performing tools were then applied to analyze CDKL5 VUS variants, complemented by the evaluation of evolutionary conservation, structural analyses, and molecular dynamics simulations to assess their impact on protein structure and function. The results identified SNPred as the most reliable tool, achieving 100% accuracy, sensitivity, and specificity. Other high-performing tools, including ESM-1v, AlphaMissense, EVE, and ClinPred, demonstrated over 98% accuracy. Among 44 CDKL5 VUS variants evaluated, 20 were initially classified as pathogenic by these tools. However, further evaluation using stringent criteria-incorporating conservation scores, structural disruptions identified by Missense3D and PyMol, and molecular dynamics simulation results-led to the reclassification of 8 VUS variants as "potentially pathogenic" and the remaining 12 as "variants with conflicting data". This comprehensive approach provides a robust framework for the classification of VUS in the CDKL5 gene, offering critical insights for accurate diagnosis and treatment strategies in DEE. These findings will serve as a valuable resource for clinicians and geneticists in resolving the diagnostic ambiguity associated with VUS.
CDKL5基因的突变与发育性和癫痫性脑病(DEE)相关,这是一种以发育迟缓与癫痫活动为特征的严重疾病。在DEE的基因分析中,被归类为致病性的变异可确诊疾病,而意义未明的变异(VUS)由于证据不足仍处于灰色地带。本研究旨在通过使用来自ClinVar数据库的186个已知致病性或良性错义变异评估22种计算机预测工具的性能,来优化对CDKL5基因中VUS的解读。然后应用性能最佳的工具来分析CDKL5 VUS变异,并辅以进化保守性评估、结构分析和分子动力学模拟,以评估它们对蛋白质结构和功能的影响。结果确定SNPred为最可靠的工具,准确率、灵敏度和特异性均达到100%。其他高性能工具,包括ESM-1v、AlphaMissense、EVE和ClinPred,准确率超过98%。在评估的44个CDKL5 VUS变异中,有20个最初被这些工具归类为致病性。然而,使用严格标准进行进一步评估——纳入保守性评分、由Missense3D和PyMol确定的结构破坏以及分子动力学模拟结果——导致8个VUS变异被重新归类为“潜在致病性”,其余12个被归类为“数据冲突的变异”。这种综合方法为CDKL5基因中VUS的分类提供了一个强大的框架,为DEE的准确诊断和治疗策略提供了关键见解。这些发现将为临床医生和遗传学家解决与VUS相关的诊断模糊性提供宝贵资源。