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Functional brain activation during arithmetic processing in females with fragile X syndrome is related to FMR1 protein expression

机译:脆性X综合征女性在算术处理过程中的功能性大脑激活与FMR1蛋白表达有关

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摘要

Arithmetic processing deficits in persons with fragile X Syndrome (fraX), the most common heritable cause of mental retardation, are well known. In this study, we characterize the neural underpinnings of these performance deficits using functional MRI. Given that a single gene defect ( ) is known to be responsible for this disorder, we also assess whether brain activation in arithmetic processing areas is related to amount of protein expression (FMRP). Subjects included 16 females with fraX, and 16 female age‐matched controls. Subjects viewed arithmetic equations with two (1 + 3 = 4) or three (2 + 3 − 1 = 5) operands, and were asked to judge whether the results were correct or not. Subjects with fraX showed significant impairment in behavioral performance on the 3‐operand but not the 2‐operand arithmetic equations. Significant brain activation was observed bilaterally in the prefrontal and parietal cortices for unaffected subjects, and bilateral prefrontal and left angular gyrus for subjects with fraX, for both trial types. Subjects with fraX exhibited less overall activation than did unaffected subjects in both types of trials; and, unlike the unaffected group, did not show increased extent of activation in association with greater task difficulty. During the 3‐operand trials, activation in bilateral prefrontal and motor/premotor, and left supramarginal and angular gyri were positively correlated with FMRP, suggesting that decreased protein expression underlies deficits in math performance in persons with fraX. More broadly, this investigation demonstrates a unique bridging of cognitive and molecular neuroscience and represents a useful approach for the study of brain development and function. Hum. Brain Mapping 16:206–218, 2002. © 2002 Wiley‐Liss, Inc.
机译:脆性X综合征(fraX)是最常见的可遗传性智力低下的原因,人们的算术处理缺陷是众所周知的。在这项研究中,我们使用功能性MRI表征了这些表现缺陷的神经基础。鉴于已知单个基因缺陷()导致了这种疾病,我们还评估了算术处理区域的大脑激活是否与蛋白质表达量(FMRP)有关。受试者包括16名患有fraX的女性和16名年龄匹配的女性。受试者查看了具有两个(1 + 3 = 4)或三个(2 + 3-1 = 5)操作数的算术方程,并被要求判断结果是否正确。患有fraX的受试者在3操作数而非2操作数算术方程式上表现出明显的行为障碍。对于这两种试验类型,未受影响的受试者在前额皮层和顶叶皮层的两侧均观察到明显的大脑激活,而对于fraX受试者则在双侧前额叶和左角回中观察到。在这两种类型的试验中,患有fraX的受试者的总体活化程度均低于未受影响的受试者。而且,与未受影响的人群不同,他们没有表现出更大的活动难度以及更大的任务难度。在3操作数试验中,双侧前额叶和运动/前运动的激活以及左上argargy和角回回与FMRP正相关,这表明fraX蛋白表达下降是数学表现不足的基础。更广泛地说,这项研究证明了认知和分子神经科学的独特桥梁,是研究大脑发育和功能的一种有用方法。哼。 Brain Mapping 16:206–218,2002.©2002 Wiley-Liss,Inc.

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