Holzapfel Marie, Barnea-Goraly Naama, Eckert Mark A, Kesler Shelli R, Reiss Allan L
Center for Interdisciplinary Brain Sciences Research, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California 94305-5719, USA.
J Neurosci. 2006 Jun 28;26(26):7007-13. doi: 10.1523/JNEUROSCI.1764-06.2006.
Turner syndrome (TS) is a neurogenetic disorder characterized by impaired spatial, numerical, and motor functioning but relatively spared verbal ability. Results from previous neuroimaging studies suggest that gray matter alterations in parietal and frontal regions may contribute to atypical visuospatial and executive functioning in TS. Recent findings in TS also indicate variations in the shape of parietal gyri and white matter microstructural anomalies of the temporal lobe. Diffusion tensor imaging and structural imaging methods were used to determine whether 10 females with TS and 10 age- and gender-matched control subjects exhibited differences in fractional anisotropy, white matter density, and local brain shape. Relative to controls, females with TS had lower fractional anisotropy (FA) values in the deep white matter of the left parietal-occipital region extending anteriorly along the superior longitudinal fasciculus into the deep white matter of the frontal lobe. In addition, decreased FA values were located bilaterally in the internal capsule extending into the globus pallidus and in the right prefrontal region. Voxel-based morphometry (VBM) analysis showed corresponding white matter density differences in the internal capsules and left centrum semiovale. Tensor-based morphometry analysis indicated that the FA and VBM results were not attributable to differences in the local shape of brain structures. Compared with controls, females with TS had increases in FA values and white matter density in language-related areas of the inferior parietal and temporal lobes. These complementary analyses provide evidence for alterations in white matter pathways that subserve affected and preserved cognitive functions in TS.
特纳综合征(TS)是一种神经遗传性疾病,其特征为空间、数字和运动功能受损,但语言能力相对保留。以往神经影像学研究结果表明,顶叶和额叶区域的灰质改变可能导致特纳综合征患者出现非典型的视觉空间和执行功能。特纳综合征的最新研究结果还表明,顶叶脑回形状存在差异,颞叶白质微结构异常。采用扩散张量成像和结构成像方法,以确定10名特纳综合征女性患者以及10名年龄和性别匹配的对照受试者在分数各向异性、白质密度和局部脑形状方面是否存在差异。与对照组相比,特纳综合征女性患者沿上纵束向前延伸至额叶深部白质的左侧顶枕叶深部白质中的分数各向异性(FA)值较低。此外,双侧内囊延伸至苍白球以及右侧前额叶区域的FA值降低。基于体素的形态学测量(VBM)分析显示,内囊和左侧半卵圆中心存在相应的白质密度差异。基于张量的形态学测量分析表明,FA和VBM结果并非归因于脑结构局部形状的差异。与对照组相比,特纳综合征女性患者顶叶下部和颞叶与语言相关区域的FA值和白质密度增加。这些互补性分析为特纳综合征中服务于受影响和保留的认知功能的白质通路改变提供了证据。