首页> 外文期刊>American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics >Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies
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Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies

机译:哥斯达黎加多动症同胞对的神经心理学和维度行为特征概况:遗传研究的潜在中间表型

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Attention deficit hyperactivity disorder (ADHD) is associated with substantial functional impairment in children and in adults. Many individuals with ADHD have clear neurocognitive deficits, including problems with visual attention, processing speed, and set shifting. ADHD is etiologically complex, and although genetic factors play a role in its development, much of the genetic contribution to ADHD remains unidentified. We conducted clinical and neuropsychological assessments of 294 individuals (269 with ADHD) from 163 families (48 multigenerational families created using genealogical reconstruction, 78 affected sib pair families, and 37 trios) from the Central Valley of Costa Rica (CVCR). We used principal components analysis (PCA) to group neurocognitive and behavioral variables using the subscales of the Child Behavior Checklist (CBCL) and 15 neuropsychological measures, and created quantitative traits for heritability analyses. We identified seven cognitive and two behavioral domains. Individuals with ADHD were significantly more impaired than their unaffected siblings on most behavioral and cognitive domains. The verbal IQ domain had the highest heritability (92%), followed by auditory attention (87%), visual processing speed and problem solving (85%), and externalizing symptoms (81%). The quantitative traits identified here have high heritabilities, similar to the reported heritability of ADHD (70-90%), and may represent appropriate alternative phenotypes for genetic studies. The use of multigenerational families from a genetically isolated population may facilitate the identification of ADHD risk genes in the face of phenotypic and genetic heterogeneity. (c) 2015 Wiley Periodicals, Inc.
机译:注意缺陷多动障碍(ADHD)与儿童和成人的严重功能障碍有关。许多患有多动症的人都有明显的神经认知缺陷,包括视觉注意力,处理速度和组移位等问题。多动症的病因复杂,尽管遗传因素在其发展中起作用,但对多动症的许多遗传贡献仍未确定。我们对哥斯达黎加中央山谷(CVCR)的163个家庭(使用族谱重建创建的48个多代家庭,78个受影响的同胞对家庭和37个三重奏)中的294个人(269例患有ADHD)进行了临床和神经心理学评估。我们使用儿童行为清单(CBCL)和15种神经心理学指标的分量表,使用主成分分析(PCA)对神经认知和行为变量进行分组,并为遗传力分析创建了定量特征。我们确定了七个认知领域和两个行为领域。在大多数行为和认知领域,患有多动症的人比未受影响的兄弟姐妹受到的伤害明显更大。言语智商域的遗传力最高(92%),其次是听觉注意力(87%),视觉处理速度和问题解决能力(85%)以及外在症状(81%)。此处确定的定量性状具有较高的遗传力,与报道的ADHD遗传力相似(70-90%),并且可能代表了遗传研究的适当替代表型。面对遗传上的表型和遗传异质性,使用来自遗传分离群体的多代家庭可能有助于识别ADHD风险基因。 (c)2015年威利期刊有限公司

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