Working memory and arithmetic impairments in children with FMR1 premutation and gray zone alleles.

Q3 Medicine
Aline Aparecida Silva Martins, Giulia Moreira Paiva, Carolina Guimarães Ramos Matosinho, Elisângela Monteiro Coser, Pablo Augusto de Souza Fonseca, Vitor Geraldi Haase, Maria Raquel Santos Carvalho
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引用次数: 1

Abstract

Expansive mutations in familial mental retardation 1 (FMR1) gene have been associated with different phenotypes. Full mutations are associated with intellectual disability and autism spectrum disorder; premutations are associated with math learning difficulties and working memory impairments. In gray zone, neuropsychological development has not yet been described.

Objectives: This study aimed to describe the frequency of FMR1 premutation and gray zone alleles in a school population sample representing a broad spectrum of variation in math achievement and detail school achievement and cognitive performance in the children identified with FMR1 premutation or gray zone alleles.

Methods: We described a two-phase study. In the first phase, 2,195 school-age children were screened for math achievement. In the second phase, 378 children with normal intelligence were neuropsychologically assessed and genotyped for FMR1. Of these, 121 children (61 girls) performed below percentile 25 in mathematics (MD group) and 257 children (146 girls) performed above percentile 25 (control group).

Results: Four pupils presented expanded alleles, one premutation and three gray zone alleles. The girl with the premutation and one boy with a gray zone allele presented impairments in working memory and arithmetic performance below percentile 6, compatible with the diagnosis of developmental dyscalculia. These children's difficulties were not associated with inaccuracy of nonsymbolic number representations or literacy impairments. Dyscalculia in these children seems to be associated mainly with working memory impairments.

Conclusions: FMR1 expansions in the gray zone may contribute to dyscalculia in otherwise healthy and normally intelligent children.

Abstract Image

携带FMR1前突变和灰色地带等位基因的儿童的工作记忆和算术障碍。
家族性智力迟钝1 (FMR1)基因的扩张性突变与不同的表型相关。全突变与智力残疾和自闭症谱系障碍有关;基因突变与数学学习困难和工作记忆障碍有关。在灰色地带,神经心理学的发展还没有被描述。目的:本研究旨在描述学校人群样本中FMR1预突变和灰色区域等位基因的频率,代表了数学成绩的广泛变异,并详细描述了被鉴定为FMR1预突变或灰色区域等位基因的儿童的学习成绩和认知表现。方法:我们进行了一项两期研究。在第一阶段,2195名学龄儿童接受了数学成绩的筛选。在第二阶段,对378名智力正常的儿童进行了神经心理学评估和FMR1基因分型。其中,121名儿童(61名女孩)的数学成绩低于百分位数25 (MD组),257名儿童(146名女孩)的数学成绩高于百分位数25(对照组)。结果:4名小学生出现扩增等位基因,1例前突变,3例灰色区等位基因。携带该基因突变的女孩和一个携带灰色地带等位基因的男孩在工作记忆和算术表现方面的损害低于百分位数6,与发育性计算障碍的诊断相一致。这些儿童的困难与非符号数字表征的不准确性或读写障碍无关。这些儿童的计算障碍似乎主要与工作记忆障碍有关。结论:FMR1在灰色区域的扩张可能导致其他健康和正常智力儿童的计算障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dementia e Neuropsychologia
Dementia e Neuropsychologia Medicine-Geriatrics and Gerontology
CiteScore
2.20
自引率
0.00%
发文量
58
审稿时长
8 weeks
期刊介绍: Dementia top Neuropsychologia the official scientific journal of the Cognitive Neurology and Ageing Department of the Brazilian Academy of Neurology and of the Brazilian Association of Geriatric Neuropsychiatry, is published by the "Associação Neurologia Cognitiva e do Comportamento", a nonprofit Brazilian association. Regularly published on March, June, September, and December since 2007.
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