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Understanding sex/gender differences in intelligence profiles of children with Autism: A comprehensive WISC meta-analysis 了解自闭症儿童智力特征的性别差异:WISC 综合荟萃分析。
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-10-09 DOI: 10.1016/j.ridd.2024.104854
David Giofrè , Rachele Lievore , Katie Allen , Irene Tonizzi , Irene Cristina Mammarella , Enrico Toffalini

Background

Intelligence assessment in children with autism spectrum disorders (ASD) often sparks debates about sex/gender differences. Specifically, the question arises whether girls exhibit lower performance on intelligence scales compared to boys. This meta-analysis examines nine studies (N=1105; 809 boys and 296 girls) to quantify sex/gender differences on the Wechsler Intelligence Scale for Children (WISC) in children with ASD, comparing their results to typically developing children.

Method and procedures

Random-effects meta-analyses on WISC indices and subtests were conducted to address the heterogeneity across effect sizes. Results for children with ASD were compared to those of typically developing children.

Outcomes and results

Findings revealed no significant differences in general intellectual functioning (full-scale IQ), verbal comprehension, working memory, or processing speed between boys and girls in children with ASD. Boys showed an advantage only in the perceptual reasoning index. At the subtest level, boys outperformed on certain tasks, while girls excelled in others.

Conclusions and implications

The observed pattern of differences in the ASD population aligns quantitatively with those in typically developing populations. Differences, if present, are specific to certain indices rather than general intelligence. These insights contribute to a nuanced understanding of gender-related cognitive variations in the context of ASD.
背景:自闭症谱系障碍(ASD)儿童的智力评估经常引发有关性/性别差异的争论。具体来说,问题在于女孩在智力量表上的表现是否低于男孩。本荟萃分析考察了九项研究(N=1105;809名男孩和296名女孩),以量化自闭症儿童在韦氏儿童智力量表(WISC)上的性别差异,并将其结果与发育正常的儿童进行比较:对WISC指数和分测验进行随机效应荟萃分析,以解决效应大小的异质性问题。将患有自闭症的儿童的结果与发育正常儿童的结果进行比较:研究结果表明,患有 ASD 的男孩和女孩在一般智力功能(全面智商)、言语理解能力、工作记忆或处理速度方面没有明显差异。男孩仅在感知推理指数方面表现出优势。在子测试层面,男孩在某些任务中表现优异,而女孩则在其他任务中表现突出:在 ASD 群体中观察到的差异模式在数量上与典型发育人群中的差异模式一致。即使存在差异,也是特定指标的差异,而不是一般智力的差异。这些见解有助于深入理解在 ASD 背景下与性别相关的认知差异。
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引用次数: 0
Vulnerability to depression and resolution in mothers of children with cerebral palsy 脑瘫儿童母亲的抑郁易感性和解决方法。
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-10-08 DOI: 10.1016/j.ridd.2024.104852
Tatjana Krstić , Sanja Batić Očovaj , Nina Brkić Jovanović , Ljiljana Mihić

Background

This study investigated associations between Self-Criticism and Dependency as factors of vulnerability to depression and maternal resolution. Resolution entails parental cognitive and emotional acceptance of the child's developmental disability.

Methods

Our sample included 100 mothers whose children had a diagnosis of cerebral palsy. The Reaction to Diagnosis Interview, the Depressive Experiences Questionnaire and the Depression Scale were administered.

Results

The results showed that unresolved mothers scored higher on the dimensions of Self-Criticism and Dependency compared to their resolved counterparts. The hierarchical cluster analysis yielded three maternal profiles based on the scores obtained on the dimensions of vulnerability to depression, regardless of maternal resolution status. The first profile was labeled Low Vulnerability and was characterized by low scores on Self-Criticism and Dependency. The second profile was labeled Dependent and it included mothers with higher scores on Dependency and lower scores on Self-Criticism. The third profile comprised mothers with higher scores on both Self-Criticism and Dependency. The smallest proportion of unresolved mothers belonged to the third, most vulnerable profile labeled Double Vulnerability.

Discussion

We discussed the implications of the obtained results in light of a need for psychotherapeutic interventions that would focus on individual differences when providing support to parental resolution.
研究背景本研究调查了作为抑郁症易感因素的自我批评和依赖性与母亲解决之间的关联。解决意味着父母在认知和情感上接受孩子的发育障碍:我们的样本包括 100 名子女被诊断为脑瘫的母亲。方法:我们的样本包括 100 名其子女被诊断为脑瘫的母亲,对她们进行了诊断反应访谈、抑郁经历问卷和抑郁量表:结果表明,在自我批评和依赖性方面,未解决问题的母亲得分高于解决问题的母亲。分层聚类分析根据母亲在抑郁易感性维度上的得分得出了三种母亲特征,与母亲的解压状态无关。第一种情况被称为 "低脆弱性",其特点是自我批评和依赖性得分较低。第二种情况被称为依赖型,包括依赖性得分较高而自我批评得分较低的母亲。第三种情况是自我批评和依赖性得分都较高的母亲。第三种情况是最脆弱的,被称为 "双重脆弱":我们讨论了所得结果的影响,认为在为父母解决问题提供支持时,有必要采取注重个体差异的心理治疗干预措施。
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引用次数: 0
Obstacle negotiation while dual-tasking in children with Developmental Coordination Disorder (DCD): An augmented-reality approach 发育协调障碍(DCD)儿童在执行双重任务时的障碍协商:增强现实方法
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-10-04 DOI: 10.1016/j.ridd.2024.104853
Emily Subara-Zukic , Thomas B. McGuckian , Michael H. Cole , Peter Wilson

Background

Children with Developmental Coordination Disorder (DCD) exhibit deficits in predictive motor control, balance, and aspects of cognitive control, which are important for safely negotiating obstacles while walking. As concurrent performance of cognitive and motor tasks (dual-tasking) may exacerbate these deficits, we examined motor and cognitive dual-tasking differences between children with DCD and their typically developing (TD) peers during obstacle negotiation.

Methods

34 children aged 6–12 years (16 TD, 18 DCD) walked along a 12 m path, stepping over an obstacle (30 % or 50 % of leg length) at its mid-point. On dual-task trials, participants completed a simple or complex (cognitive) visual discrimination task presented via an augmented reality headset. Proportional dual-task costs (pDTCs) were measured on cognitive and gait outcomes over three phases: pre-obstacle, obstacle step-over, and post-obstacle.

Results

During the obstacle step-over phase, both groups increased their leading leg clearance when dual-tasking, while the DCD group had larger pDTC than TD for the high obstacle under simple stimulus conditions (viz simple-high combination). The complex cognitive task produced larger pDTCs than the simple one on leading leg clearance and post-obstacle gait variability.

Conclusions

In general, both DCD and TD groups showed similar pDTCs under complex conditions, while the specific deficit in DCD under the simple-high combination suggests a (default) compensatory strategy during step-over when attention is diverted to a secondary task. Competing cognitive and motor demands during obstacle negotiation present a potential safety risk for children.
背景:患有发育协调障碍(DCD)的儿童在预测性运动控制、平衡和认知控制方面表现出缺陷,而这些方面对于在行走过程中安全地绕过障碍非常重要。由于同时执行认知和运动任务(双重任务)可能会加剧这些缺陷,因此我们研究了发育协调障碍儿童和发育正常(TD)儿童在障碍协商过程中的运动和认知双重任务差异。方法:34 名 6-12 岁的儿童(16 名 TD,18 名 DCD)沿着一条 12 米长的路径行走,在中点跨过障碍物(腿长的 30% 或 50%)。在双重任务试验中,参与者通过增强现实耳机完成简单或复杂(认知)的视觉辨别任务。在障碍前、障碍跨步和障碍后三个阶段,测量了认知和步态结果的双任务成本比例(pDTC):在障碍跨越阶段,两组人在执行双重任务时都增加了前腿间隙,而在简单刺激条件下(即简单-高组合),DCD 组在高障碍上的 pDTC 比 TD 组大。在前腿间隙和障碍后步态变异性方面,复杂认知任务比简单认知任务产生更大的pDTC:总的来说,在复杂条件下,DCD 组和 TD 组显示出相似的 pDTC,而 DCD 组在简单-高组合条件下的特定缺陷表明,在跨步时,当注意力转移到次要任务时,存在(默认)补偿策略。在障碍协商过程中,认知需求和运动需求相互竞争,给儿童带来了潜在的安全风险。
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引用次数: 0
DNA methylation signatures of prenatal socioeconomic position associated with 36-month language outcomes 产前社会经济地位的 DNA 甲基化特征与 36 个月的语言结果有关。
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-10-01 DOI: 10.1016/j.ridd.2024.104846
Meghna Rajaprakash , Meredith Palmore , Kelly M. Bakulski , Ellen Howerton , Kristen Lyall , Rebecca J. Schmidt , Craig Newschaffer , Lisa A. Croen , Irva Hertz-Picciotto , Heather Volk , Christine Ladd-Acosta , M. Daniele Fallin

Background

Socioeconomic position (SEP), which reflects one’s position in society and access to resources, is strongly tied to neurodevelopment and is associated with epigenetic changes. AIM: This study examined whether DNA methylation signatures of prenatal SEP, measured in birth samples, are associated with child neurodevelopmental outcomes at 36 months of age. METHODS: Prenatal SEP DNA methylation scores were derived using 97 placenta and 127 cord blood biospecimens in the Early Autism Risk Longitudinal Investigation cohort. Participants completed the Mullen Scales of Early Learning (MSEL) and Vineland Adaptive Behavior Scales (VABS) at 36 months of age. Generalized regression analyses, adjusting for maternal age and race, were performed to test the association between SEP methylation score, for each birth biospecimen type, and MSEL and VABS scores. RESULTS: Significant associations were observed between placenta SEP methylation score and MSEL Expressive Language outcomes (beta = −2.7, p = 0.046, 95 % CI [- 5.43, −0.05]) and Receptive Language outcomes (beta = −2.5, p = 0.037, 95 % CI [-4.82, −0.16]). In cord blood, methylation-SEP scores were significantly associated with Receptive Language outcomes (beta = −2.0, p = 0.037, 95 % CI [-3.85, −0.12]). No significant associations were observed with VABS scores. CONCLUSION: Our results confirm associations between prenatal SEP and early childhood language development using a novel empiric DNA methylation measure of exposure
背景:社会经济地位(SEP)反映了一个人在社会中的地位和获得资源的机会,它与神经发育密切相关,并与表观遗传变化有关。目的:本研究探讨了出生样本中测得的产前社会经济地位DNA甲基化特征是否与36个月大时儿童的神经发育结果有关:产前 SEP DNA 甲基化评分是通过早期自闭症风险纵向调查队列中的 97 份胎盘样本和 127 份脐带血生物样本得出的。参与者在 36 个月大时完成了 Mullen 早期学习量表 (MSEL) 和 Vineland 适应行为量表 (VABS)。在对母亲年龄和种族进行调整后,进行了广义回归分析,以检验每种出生生物样本类型的SEP甲基化得分与MSEL和VABS得分之间的关联:胎盘 SEP 甲基化得分与 MSEL 表达性语言结果(beta = -2.7,p = 0.046,95 % CI [- 5.43,-0.05])和接受性语言结果(beta = -2.5,p = 0.037,95 % CI [-4.82,-0.16])之间存在显著关联。在脐带血中,甲基化-SEP 评分与感知语言结果(β = -2.0,p = 0.037,95 % CI [-3.85,-0.12])显著相关。结论:我们的研究结果证实了产前 SEP 与儿童早期语言发展之间的联系,并使用了一种新的 DNA 甲基化暴露经验测量方法。
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引用次数: 0
How do fine and gross motor skills develop in preschool boys with Duchenne Muscular Dystrophy? 患有杜兴氏肌肉萎缩症的学龄前男孩的精细和粗大运动技能是如何发展的?
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-27 DOI: 10.1016/j.ridd.2024.104845
Jasmine Hoskens , Ines Vandekerckhove , Liesbeth De Waele , Hilde Feys , Nathalie Goemans , Katrijn Klingels

Background

Boys with Duchenne Muscular Dystrophy (DMD) experience both fine and gross motor problems. Nowadays, early intervention focuses almost exclusively on gross motor skills.

Aims

We aimed to explore early motor development in preschool boys with DMD and investigate the influence of cognition.

Methods and procedures

Seventeen boys with DMD (11 months- 6 years) were compared to typically developing (TD) peers and followed-up with the Bayley Scales of Infant and Toddler Development (Bayley-III); Peabody developmental motor scales (PDMS-II) and Motor Function Measure (MFM-20). The longitudinal evolution of fine and gross motor skills was investigated using linear mixed effect models (LMM). Cognition was added to the LMM as a covariate.

Outcomes and results

Preschool boys with DMD scored lower compared to TD peers on both fine and gross motor skills (p<0.001). The evolution of motor development was subscale-dependent. A significant influence of cognition was found on different subscales (p= 0.002–0.04).

Conclusions and implications

Preschool boys with DMD do not achieve the same functioning level as TD boys. Cognition plays a crucial role in the evolution of motor skills. Our results suggest a shift to a broader psychomotor approach including both fine and gross motor skills, also considering the impact of cognition.

What this paper adds?

Our study provides a detailed mapping of early fine and gross motor development in preschool boys with Duchenne Muscular Dystrophy (DMD) and describes the influence of cognition on both fine and gross motor skills. Preschool boys with DMD do not achieve the same functioning level compared to typically developing boys. They score significantly lower on both fine and gross motor skills. The evolution of fine and gross motor development was subscale-dependent e.g. a negative-positive evolution was seen for grasping skills, with a tipping point around the age of four; stationary scaled scores decreased followed by a stabilization around the age four to five and locomotion scaled scores remained stable over time. Finally, we also found that cognition plays a crucial role in the evolution of both fine and gross motor skills. These new insights in the evolution of early motor development could be of added value for future clinical trials in young boys with DMD. Subsequently, increased alertness to early symptoms, e.g. developmental delay, may advance the age of diagnosis, as well as associated early intervention.
背景患有杜兴氏肌肉萎缩症(DMD)的男孩会出现精细和粗大运动问题。方法和程序将 17 名患有 DMD 的男孩(11 个月至 6 岁)与发育正常的同龄人(TD)进行比较,并使用贝利婴幼儿发育量表(Bayley-III)、皮博迪发育运动量表(PDMS-II)和运动功能测量(MFM-20)进行随访。采用线性混合效应模型(LMM)对精细和粗大运动技能的纵向发展进行了研究。结果DMD学龄前男孩的精细和粗大运动技能得分均低于TD同龄人(p<0.001)。运动发展的演变与分量表有关。结论和启示患有 DMD 的学龄前男孩无法达到与 TD 男孩相同的功能水平。认知在运动技能的发展过程中起着至关重要的作用。我们的研究详细描绘了患有杜兴氏肌肉营养不良症(DMD)的学龄前男孩的早期精细和粗大运动发育情况,并描述了认知对精细和粗大运动技能的影响。与发育正常的男孩相比,患有 DMD 的学龄前男孩无法达到相同的功能水平。他们在精细和粗大运动技能方面的得分都明显较低。精细和粗大运动能力的发展与分量表有关,例如,抓握能力的发展由负转正,在四岁左右达到临界点;静止能力的分量表得分下降,在四至五岁左右趋于稳定,而运动能力的分量表得分则随着时间的推移保持稳定。最后,我们还发现认知在精细和粗大运动技能的进化过程中起着至关重要的作用。这些对早期运动发育演变的新认识可能对未来针对 DMD 男孩的临床试验具有重要价值。随后,提高对早期症状(如发育迟缓)的警觉性可能会提高诊断年龄,并促进相关的早期干预。
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引用次数: 0
Do maternal and paternal education protect against developmental delays? 母亲和父亲的教育能防止发育迟缓吗?
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-26 DOI: 10.1016/j.ridd.2024.104848
Diane L. Putnick , Neil J. Perkins , Edwina Yeung , Shyamal D. Peddada

Background

Parental education is linked to child development and wellbeing, but unique and combined contributions of maternal and paternal education have rarely been studied.

Aims

This study assessed the individual and joint associations of maternal and paternal education on children’s odds of a probable developmental delay.

Methods and procedures

Mothers (N = 3566) from the Upstate KIDS cohort study reported on theirs and the father’s highest level of education and completed the Ages and Stages Questionnaires up to 7 times when the child was 4- to 36-months-old. A nonparametric constrained inference technique assessed the association between education and probable developmental delays.

Outcomes and results

Higher levels of maternal and paternal education were protective against child probable developmental delays in years 2 (18, 24 months; p-trends<.001) and 3 (30, 36 months; p-trends<.001), but not year 1 (4, 8, 12 months; p-trend=.486–.832). Trends held adjusting for parental age and race. When adjusting for the other parent’s education, only maternal education had unique associations with delays. Among parents with the same or similar education levels, when both parents had one level higher education it was also protective.

Conclusions and implications

Both maternal and paternal education may protect against children’s developmental delays in toddlerhood, but maternal education may be particularly important.
背景父母的教育与儿童的发展和幸福息息相关,但很少有人研究过母亲和父亲教育的独特和综合贡献。方法和程序来自Upstate KIDS队列研究的母亲(N = 3566)报告了自己和父亲的最高教育水平,并在孩子4-36个月大时完成了多达7次年龄和阶段问卷调查。结果和结果母亲和父亲的教育水平越高,对第 2 年(18、24 个月;p-趋势< .001)和第 3 年(30、36 个月;p-趋势< .001)儿童可能出现的发育迟缓越有保护作用,但对第 1 年(4、8、12 个月;p-趋势=.486-.832)则没有保护作用。调整父母年龄和种族后,趋势保持不变。当调整父母另一方的教育程度时,只有母亲的教育程度与延迟有独特的联系。在教育水平相同或相似的父母中,如果父母双方的教育水平都高一级,也会对儿童的发育迟缓起到保护作用。
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引用次数: 0
Effects of a combined neuropsychological and cognitive behavioral group therapy on young adults with Fragile X Syndrome: An explorative study 神经心理和认知行为联合小组疗法对脆性 X 综合征年轻成人的影响:探索性研究
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-26 DOI: 10.1016/j.ridd.2024.104839
Federica Alice Maria Montanaro , Paolo Alfieri , Cristina Caciolo , Giuseppina Spano , Andrea Bosco , Stefano Vicari

Background

Fragile X Syndrome (FXS) is an X-linked neurodevelopmental disorder that leads to intellectual disability (ID) along with cognitive-behavioral difficulties. Research on psychosocial treatments in individuals FXS and ID is still lacking. This study aimed to investigate the effectiveness of a combined neuropsychological and cognitive behavioral group therapy (nCBT) among young adults with FXS.

Method

Ten young adults diagnosed with FXS took part in the second stage intervention of "Corp-osa-Mente" (CoM II), a group nCBT program previously outlined by Montanaro and colleagues in an earlier study, with the participants being the same as in the previous research. This report details the outcomes of an additional twelve-month group sections aimed at enhancing the ability to manage emotions and the socio-communicative skills of these young adults. Caregivers completed measures of adaptive functioning, emotional and behavior problems, executive function, communication skills and family quality of life at pre-treatment (T0) and post-treatment (T1).

Results

CoM II showed a decrease in depressive and anxiety symptoms from T0 to T1, along with increased socio-pragmatic and communication skills from pre-test to post-test intervention. Additionally, our analysis revealed improvements in the adapative behavior of participants and in the family quality of life.

Conclusions

These preliminary findings suggest that young adults with FXS and ID experienced positive outcomes through participation in CoM II, a group nCBT. However, it is recommended to undertake additional methodologically rigorous studies, such as randomized controlled trials (RCTs), to substantiate these initially promising findings.
背景脆弱X综合征(FXS)是一种X连锁神经发育障碍,会导致智力残疾(ID)和认知行为障碍。目前还缺乏针对 FXS 和 ID 患者的社会心理治疗研究。本研究旨在调查神经心理学和认知行为联合小组疗法(nCBT)在 FXS 患者中的有效性。方法十名被诊断患有 FXS 的年轻人参加了 "Corp-osa-Mente"(CoM II)的第二阶段干预,CoM II 是 Montanaro 及其同事在早期研究中概述的一种 nCBT 小组项目,参与者与之前的研究相同。本报告详细介绍了为期 12 个月的额外小组项目的成果,该项目旨在提高这些年轻人的情绪管理能力和社会交际技能。照顾者在治疗前(T0)和治疗后(T1)完成了适应功能、情绪和行为问题、执行功能、沟通技巧和家庭生活质量的测量。结果CoM II显示,从T0到T1,抑郁症状和焦虑症状有所减轻,社会实用性和沟通技巧也从治疗前提高到治疗后。此外,我们的分析还显示,参与者的适应行为和家庭生活质量都有所改善。结论这些初步研究结果表明,患有 FXS 和 ID 的年轻人通过参加 CoM II(一种 nCBT 小组疗法)取得了积极的成果。然而,我们建议开展更多方法严谨的研究,如随机对照试验(RCTs),以证实这些初步研究结果。
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引用次数: 0
Negative emotions reduce sensorimotor cortex activity during proprioceptive modulation of rolandic ∼20HZ beta rhythm in typically developing children and those with neurodevelopmental conditions 消极情绪会降低发育正常儿童和神经发育不良儿童在本体感觉调节萝兰∼20HZβ节律过程中的感觉运动皮层活动
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-25 DOI: 10.1016/j.ridd.2024.104842
Álvaro Sabater-Gárriz , Francesc Mestre-Sansó , Vicent Canals , José Antonio Mingorance , Pedro Montoya , Inmaculada Riquelme

Background

The Rolandic ∼20-Hz beta rhythm of the sensorimotor cortex is associated with motor function and perception. However, the modulation of this rhythm by different emotional stimuli is an innovative area of research.

Aims

This study aims at investigating the impact of affective pictures (positive, negative, and neutral) on the proprioceptive modulation of the Rolandic ∼20 Hz beta rhythm in typically developing children and children with neurodevelopmental disorders (i.e. cerebral palsy and autism).

Methods and procedures

EEG was recorded while participants experienced passive wrist movements during the simultaneous viewing of affective pictures. Time-frequency analysis of the sensorimotor oscillatory activity was performed.

Outcomes and results

Our findings revealed that pictures with negative emotional valence notably diminish event-related synchronization (ERS) amplitude during the perception of hand movement in all groups of children.

Conclusions and implications

These findings suggest that emotional stimuli, particularly the negative ones, could significantly influence brain's processing of proprioception, adding knowledge to the interaction of common comorbidities, such as sensorimotor disorders and emotional dysregulation, in children with neurodevelopmental disabilities.
背景感觉运动皮层的罗兰蒂克∼20赫兹β节律与运动功能和知觉有关。本研究旨在调查情感图片(积极、消极和中性)对典型发育儿童和神经发育障碍儿童(即脑瘫和自闭症儿童)Rolandic ∼20 Hz β节律本体感觉调制的影响。结论和启示这些研究结果表明,情绪刺激,尤其是负面情绪刺激,会显著影响大脑对本体感觉的处理,从而为神经发育障碍儿童常见合并症(如感觉运动障碍和情绪失调)之间的相互作用增添了新的知识。
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引用次数: 0
Motor development trajectories of children with cerebral palsy in a community-based early intervention program in rural South India 印度南部农村地区基于社区的早期干预计划中脑瘫儿童的运动发展轨迹
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-24 DOI: 10.1016/j.ridd.2024.104829
Marie Brien , Dinesh Krishna , Ramasubramanian Ponnusamy , Cathy Cameron , Rahim Moineddin , Franzina Coutinho

Background

Developmental trajectories are crucial for evidence-based prognostication, planning interventions, and monitoring progress in children with cerebral palsy (CP).

Aims

To describe gross motor development patterns of children with CP in rural South India for the five Gross Motor Function Classification System (GMFCS) levels.

Methods

Longitudinal cohort study of 302 children (176 males, 126 females) with CP aged 0 to 10 years, followed by a community-based early intervention program. GMFCS levels were 5.4 % level 1, 16.5 % level II, 22.8 % level III, 26.8 % level IV, and 28.5 % level V. Assessments were undertaken using the Gross Motor Function Measure (GMFM-66) at 6-month intervals between April 2017 and August 2020. Longitudinal analyses were performed using mixed-effects linear regression models.

Outcomes and results

Five distinct motor development curves were created for ages 0 to 10 years by GMFCS levels as a function of age and GMFM-66 with a stable limit model, variation in estimated limits and rates of development.

Conclusions and Implications

Motor development trajectories for CP in an LMIC differ from those reported in HICs. Consideration of how social determinants of health, environmental and personal factors impact motor development in low-resource contexts is crucial. Further work is needed to describe developmental trajectories of children for CP in LMICs.
背景发育轨迹对于脑瘫(CP)儿童的循证预后、干预规划和进展监测至关重要。方法对 302 名 0 至 10 岁的 CP 儿童(176 名男性,126 名女性)进行纵向队列研究,并对他们进行社区早期干预项目。在2017年4月至2020年8月期间,每隔6个月使用粗大运动功能测量法(GMFM-66)进行一次评估。采用混合效应线性回归模型进行纵向分析。结果按 GMFCS 水平创建了 0 至 10 岁的五条不同的运动发展曲线,作为年龄和 GMFM-66 的函数,并采用稳定极限模型、估计极限变化和发展速度。考虑健康的社会决定因素、环境和个人因素如何影响低资源环境中的运动发育至关重要。需要进一步开展工作,描述低收入与中等收入国家儿童的 CP 发育轨迹。
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引用次数: 0
Proxy- and self-report evaluation of quality of life in cerebral palsy: Using Spanish version of CPQOL for Children and adolescents 对脑瘫患者生活质量的代理和自我报告评估:使用西班牙语版儿童和青少年 CPQOL
IF 2.9 2区 医学 Q1 EDUCATION, SPECIAL Pub Date : 2024-09-24 DOI: 10.1016/j.ridd.2024.104844
Alba Aza , Inmaculada Riquelme , María Gómez Vela , Marta Badia

Background

Promoting quality of life (QoL) is one of the main goals in interventions carried out with children and adolescents with cerebral palsy (CP).

Aims

The aim of this study was to analyze the determinants of QoL in children with CP, including evaluations by the children themselves and their parents, and to identify discrepancies between evaluators.

Methods and procedures

The adapted Spanish version of the Cerebral Palsy Quality of Life (CP-QOL) for children and adolescents (self-report and primary caregiver-reports versions) was applied to a sample of 74 children with CP and their respective parents (totaling 222 participants), as well as instruments to measure functioning (i.e., GMFCS, MACS, CFCS and EDACS). The average age of the children was 12.50 (SD=4.07), with a higher number of boys (55.7 %).

Outcomes and results

The lowest QoL levels were found in the Functional dimension in both assessments (Mchildren/adolescents=70.21, Mparents=58.14). For children, the highest rated dimension was Social Well-being (M=74.54), while for parents it was School (M=71.03). The degree of agreement between evaluators was low in almost all dimensions (ICC≤.40). More satisfactory predictive models were constructed from the evaluations carried out by parents, except in the case of the Access to Services dimension, with functioning measures being the main predictors of QoL levels.

Conclusions and implications

The CP-QOL in its two available versions is a useful and specific instrument for assessing QoL in children with CP in both research and professional fields.
背景提高生活质量(QoL)是对脑瘫(CP)儿童和青少年进行干预的主要目标之一。目的本研究旨在分析脑瘫儿童生活质量的决定因素,包括儿童本人及其父母的评价,并找出评价者之间的差异。方法和程序对 74 名 CP 儿童及其父母(共 222 名参与者)以及功能测量工具(即:GMFCS、MACS、MACS)进行抽样调查,并采用改编的西班牙文版儿童和青少年脑瘫生活质量(CP-QOL)(自我报告版和主要照顾者报告版)、GMFCS、MACS、CFCS 和 EDACS)。儿童的平均年龄为 12.50 岁(SD=4.07),男孩的比例较高(55.7%)。结果在两次评估中,功能维度的 QoL 水平最低(儿童/青少年的 M=70.21,家长的 M=58.14)。对儿童而言,评分最高的维度是 "社会福祉"(M=74.54),而对家长而言,评分最高的维度是 "学校"(M=71.03)。在几乎所有维度上,评价者之间的一致程度都很低(ICC≤.40)。除了 "获得服务 "维度外,由家长进行的评价建立的预测模型更令人满意,功能测量是预测 QoL 水平的主要因素。
{"title":"Proxy- and self-report evaluation of quality of life in cerebral palsy: Using Spanish version of CPQOL for Children and adolescents","authors":"Alba Aza ,&nbsp;Inmaculada Riquelme ,&nbsp;María Gómez Vela ,&nbsp;Marta Badia","doi":"10.1016/j.ridd.2024.104844","DOIUrl":"10.1016/j.ridd.2024.104844","url":null,"abstract":"<div><h3>Background</h3><div>Promoting quality of life (QoL) is one of the main goals in interventions carried out with children and adolescents with cerebral palsy (CP).</div></div><div><h3>Aims</h3><div>The aim of this study was to analyze the determinants of QoL in children with CP, including evaluations by the children themselves and their parents, and to identify discrepancies between evaluators.</div></div><div><h3>Methods and procedures</h3><div>The adapted Spanish version of the Cerebral Palsy Quality of Life (CP-QOL) for children and adolescents (self-report and primary caregiver-reports versions) was applied to a sample of 74 children with CP and their respective parents (totaling 222 participants), as well as instruments to measure functioning (i.e., GMFCS, MACS, CFCS and EDACS). The average age of the children was 12.50 (<em>SD=</em>4.07), with a higher number of boys (55.7 %).</div></div><div><h3><em>Outcomes and results</em></h3><div>The lowest QoL levels were found in the Functional dimension in both assessments (<em>M</em><sub><em>children/adolescents</em></sub>=70.21, <em>M</em><sub><em>parents</em></sub>=58.14). For children, the highest rated dimension was Social Well-being (<em>M</em>=74.54), while for parents it was School (<em>M</em>=71.03). The degree of agreement between evaluators was low in almost all dimensions (ICC≤.40). More satisfactory predictive models were constructed from the evaluations carried out by parents, except in the case of the Access to Services dimension, with functioning measures being the main predictors of QoL levels.</div></div><div><h3>Conclusions and implications</h3><div>The CP-QOL in its two available versions is a useful and specific instrument for assessing QoL in children with CP in both research and professional fields.</div></div>","PeriodicalId":51351,"journal":{"name":"Research in Developmental Disabilities","volume":"154 ","pages":"Article 104844"},"PeriodicalIF":2.9,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0891422224001768/pdfft?md5=793c8eeeebb6ac460b7591d9768c38bd&pid=1-s2.0-S0891422224001768-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142315674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Research in Developmental Disabilities
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