通过心理语言学和口腔面部相关性探索阅读障碍风险:个性化医学方法的神经发育见解。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Ștefan Lucian Burlea, Laura Elisabeta Checheriţă, Ovidiu Stamatin, Marius Văcaru, Ana Elena Sîrghe, Ioana Rudnic, Diana Andreea Ilinca, Violina Budu, Maria Antonela Beldiman, Vasilica Toma, Liana Aminov, Anamaria Ciubară
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引用次数: 0

摘要

背景/目的:阅读障碍和书写障碍是常见的儿童神经发育障碍,其特征是持续的阅读和写作困难,尽管智力正常,接受过教育。虽然通常被描述为认知语言缺陷,但新兴研究表明,这可能与口面部功能障碍和情绪调节问题有关。本研究探讨了学龄前儿童口颌异常、情绪失调和阅读-书写障碍风险早期指标之间的关系,旨在加强早期筛查和干预策略。方法:对罗马尼亚11所幼儿园689名5-7岁儿童进行横断面病例对照研究。筛选包括使用ACTIV-BURLEA心理测量电池来评估语言、运动和认知能力。临床评估的目标是牙弓形状、咬合平衡、舌头和嘴唇功能。使用标准化儿童行为量表评估情绪调节能力。32名儿童被确定为有阅读困难-书写困难的风险,并进行纵向跟踪,然后与匹配的对照组进行比较。统计分析采用卡方检验、Pearson相关检验、t检验和逻辑回归。结果:随访时,74.19%的高危儿童得到确诊。舌功能障碍(TD) (OR = 4.81, p = 0.06)和情绪调节障碍(ED) (OR = 3.94, p = 0.09)成为主要危险指标,但差异无统计学意义。舌功能障碍(TD)与逃避学业相关(r = 0.76, p < 0.01),咬合异常(OAs)与情绪困扰相关(r = 0.64, p < 0.05)。结论:研究结果表明,早期阅读困难-书写困难的风险涉及口面部和情绪因素。舌功能障碍(TD)、咬合障碍(OA)和情绪失调(ED)可能是重要的临床标志。将牙科和情感评估整合到学前筛查中可以改善早期识别并实现个性化干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring Dyslexia Risk Through Psycholinguistic and Orofacial Correlates: Neurodevelopmental Insights Toward a Personalized Medicine Approach.

Exploring Dyslexia Risk Through Psycholinguistic and Orofacial Correlates: Neurodevelopmental Insights Toward a Personalized Medicine Approach.

Exploring Dyslexia Risk Through Psycholinguistic and Orofacial Correlates: Neurodevelopmental Insights Toward a Personalized Medicine Approach.

Exploring Dyslexia Risk Through Psycholinguistic and Orofacial Correlates: Neurodevelopmental Insights Toward a Personalized Medicine Approach.

Background/Objectives: Dyslexia and dysgraphia are common childhood neurodevelopmental disorders characterized by persistent reading and writing difficulties, despite normal intelligence and access to education. While typically described as cognitive-linguistic deficits, emerging research suggests potential links to orofacial dysfunction and emotional regulation issues. This study examines associations between stomatognathic anomalies, emotional dysregulation, and early indicators of dyslexia-dysgraphia risk in preschool children, aiming to strengthen early screening and intervention strategies. Methods: A cross-sectional case-control study included 689 Romanian children aged 5-7 from 11 kindergartens. Screening involved the ACTIV-BURLEA psychometric battery to evaluate language, motor, and cognitive abilities. Clinical assessments targeted dental arch form, occlusal balance, and tongue and lip function. Emotional regulation was evaluated using a standardized child behavior scale. Thirty-two children were identified as at risk for dyslexia-dysgraphia and followed longitudinally, and then compared to matched controls. Statistical analysis employed chi-square tests, Pearson correlations, t-tests, and logistic regression. Results: At follow-up, 74.19% of at-risk children received confirmed diagnoses. Tongue dysfunction (TD) (OR = 4.81, p = 0.06) and emotional dysregulation (ED) (OR = 3.94, p = 0.09) emerged as key risk indicators, though not statistically significant. Tongue dysfunction (TD) correlated with school avoidance (r = 0.76, p < 0.01), while occlusal anomalies (OAs) correlated with emotional distress (ED) (r = 0.64, p < 0.05). Conclusions: The findings suggest that early dyslexia-dysgraphia risk involves orofacial and emotional components. Tongue dysfunction (TD), occlusal disturbances (OA), and emotional dysregulation (ED) may offer important clinical markers. Integrating dental and emotional assessments into preschool screening may improve early identification and enable personalized intervention.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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