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首页> 外文期刊>Scientific reports. >Computational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy
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Computational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy

机译:DP140诱导Duchenne肌营养不良工作记忆变化的计算认知建模与验证

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Duchenne Muscular Dystrophy has emerged as a model to assess cognitive domains. The DMD gene variant location and its association with variable degrees of cognitive impairment necessitate identification of a common denominator. Computer architectures provide a framework to delineate the mechanisms involved in the cognitive functioning of the human brain. Copy number variations in the 79 exons of DMD gene were screened in 84 DMD subjects by Multiplex Ligation-dependent Probe Amplification (MLPA). DMD subjects were categorized based on the presence or absence of DP140 isoform. The cognitive and neuropsychological assessments were carried out as per inclusion criteria using standard scales. Instance-based learning theory (IBLT) based on the partial matching process was developed to mimic Stroop Color and Word Task (SCWT) performance on Adaptive Control of Thought-Rational (ACT-R) cognitive architecture based on IBLT. Genotype–phenotype correlation was conducted based on the mutation location in DMD gene. Assessment of specific cognitive domains in DP140???ve group corresponded to the involvement of multiple brain lobes including temporal (verbal and visual learning and memory), parietal (visuo-conceptual and visuo-constructive abilities) and frontal (sustained and focused attention, verbal fluency, cognitive control). Working memory axis was found to be the central domain through tasks including RAVLT trial 1, recency effect, digit span backward, working memory index, arithmetic subtests in the Dp140???ve group. IBLT validated the non-reliance of DMD subjects on recency indicating affected working memory domain. Modeling strategy revealed altered working memory processes in DMD cases with affected Dp140 isoform. DMD brain was observed to rely on primacy than the recency suggesting alterations in working memory capacity. Modeling revealed lowered activation of DMD brain with Dp140???ve in order to retrieve the instances.
机译:Duchenne肌肉营养不良症已成为评估认知域的模型。 DMD基因变体位置及其与可变认知损伤的可变程度的关联需要识别共同的母细胞。计算机架构提供了一个框架,用于描绘人类脑的认知功能所涉及的机制。通过多重连接依赖性探针扩增(MLPA)在84dMD受试者中筛选DMD基因79个外显子的拷贝数变异。根据DP140同种型的存在或不存在,对DMD受试者进行分类。根据使用标准尺度的含有标准进行认知和神经心理学评估。基于部分匹配进程的基于实例的学习理论(IBLT)是为基于IBLT的思想 - 理性(ACT-R)认知体系结构的自适应控制而模拟了用于模拟的争吵颜色和单词任务(SCWT)性能。基于DMD基因的突变位置进行基因型 - 表型相关性。 DP140的特异性认知结构域的评估对应于多个脑裂片的参与,包括时间(口头和视觉学习和记忆),前(Visuo-概念和潜视 - 建设能力)和额度(持续和重点关注,口头流畅,认知控制)。找到工作存储轴是中央域通过包括RACLT试用版1,后续效果,数字跨度向后,工作内存索引,DP140中的算术子测试的任务。 IBLT验证了DMD对象对指示受影响的工作存储器域的非依赖性。建模策略显示DMD案例中的改变工作记忆过程,具有受影响的DP140同种型。观察到DMD大脑依赖于PRIMACY而不是新近度建议改变工作记忆力。模型显示DP140的DMD大脑的激活降低了,以便检索该实例。

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