期刊
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 -, 期 -, 页码 -出版社
ENDOCRINE SOC
DOI: 10.1210/clinem/dgad487
关键词
executive function; brain; inhibition; Klinefelter syndrome; sex chromosome aneuploidy; fMRI
Executive dysfunction is a common cognitive phenotype in adolescents with Klinefelter syndrome (KS), and it is associated with testicular failure. This study found that boys with KS have lower executive function and reduced brain activation in regions related to executive function. The severity of pubertal developmental delay, indicated by lower testosterone and testes volume, was associated with the magnitude of activation differences in boys with KS.
Context Executive dysfunction is a well-recognized component of the cognitive phenotype of Klinefelter syndrome (KS), yet the neural basis of KS-associated cognitive weaknesses, and their association with testicular failure is unknown.Objective We investigated executive function, brain activation, and pubertal development in adolescents with and without KS.Methods Forty-three adolescents with KS (mean age 12.3 & PLUSMN; 2.3 years) and 41 typically developing boys (mean age 11.9 & PLUSMN; 1.8 years) underwent pubertal evaluation, behavioral assessment, and completed functional magnetic resonance imaging (fMRI) as they performed an executive function task, the go/no-go task. Group differences in activation were examined. Associations among activation, executive function, and pubertal development measures were tested in secondary analyses.Results Boys with KS exhibited reduced executive function, as well as lower activation in brain regions subserving executive function, including the inferior frontal gyrus, anterior insula, dorsal anterior cingulate cortex, and caudate nucleus. Secondary analyses indicated that the magnitude of activation differences in boys with KS was associated with severity of pubertal developmental delay, as indexed by lower testosterone (t(36) = 2.285; P = .028) and lower testes volume (t(36) = 2.238; P = .031). Greater parent-reported attention difficulties were additionally associated with lower testicular volume (t(36) = -2.028; P = .050).Conclusion These findings indicate a neural basis for executive dysfunction in KS and suggest alterations in pubertal development may contribute to increased severity of this cognitive weakness. Future studies that examine whether these patterns change with testosterone replacement therapy are warranted.
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