Murphy D G, Mentis M J, Pietrini P, Grady C, Daly E, Haxby J V, De La Granja M, Allen G, Largay K, White B J, Powell C M, Horwitz B, Rapoport S I, Schapiro M B
Department of Psychological Medicine, Institute of Psychiatry, London, U.K.
Biol Psychiatry. 1997 Feb 1;41(3):285-98. doi: 10.1016/s0006-3223(95)00660-5.
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and behavioral abnormalities because they lack one/part of one X chromosome, and endogenous estrogen. We studied 13 healthy controls (mean age +/- SD, 28 +/- 6 years) and 16 TS subjects (mean age +/- SD, 26 +/- 6 years). We measured cognitive abilities using neuropsychological tests, and cerebral metabolic rates for glucose with positron emission tomography. Compared to controls, TS subjects had significant absolute hypermetabolism in most brain areas; however, normalized metabolism was significantly lower in TS subjects than controls in the insula and association neocortices bilaterally, and there were significant differences in functional metabolic associations of brain region pairs originating in occipital cortex bilaterally, and within the right hemisphere. There were significant correlations between right-left cognitive and metabolic asymmetries in the TS group. Also, within TS a preliminary analysis demonstrated "X chromosome dosage" effects in language ability and left temporal metabolism, asymmetry of right-left test scores, and parietal metabolism. We hypothesize that within TS: i) generalized brain hypermetabolism reflects global abnormalities in neuron packing; ii) neuronal abnormalities occur in association neocortex that differ in nature or extent from whole brain and are associated with significant differences in normalized metabolism; iii) cognitive deficits are related to brain metabolic abnormalities; and iv) social-behavioral problems may be related to abnormalities of brain metabolism. Moreover, in human brain the X chromosome involved in development of the association neocortices.
患有特纳综合征(TS)的女性使我们能够研究认知和行为异常的神经生物学关联,因为她们缺少一条X染色体或其一部分,且缺乏内源性雌激素。我们研究了13名健康对照者(平均年龄±标准差,28±6岁)和16名TS患者(平均年龄±标准差,26±6岁)。我们使用神经心理学测试测量认知能力,并通过正电子发射断层扫描测量大脑葡萄糖代谢率。与对照组相比,TS患者在大多数脑区存在明显的绝对代谢亢进;然而,TS患者双侧脑岛和联合新皮质的标准化代谢显著低于对照组,并且双侧枕叶皮质及右侧半球内脑区对的功能代谢关联存在显著差异。TS组左右认知和代谢不对称之间存在显著相关性。此外,在TS患者中,初步分析显示了“X染色体剂量”对语言能力、左侧颞叶代谢、左右测试分数不对称以及顶叶代谢的影响。我们假设在TS患者中:i)广泛大脑代谢亢进反映了神经元堆积的整体异常;ii)联合新皮质中发生的神经元异常在性质或程度上与全脑不同,且与标准化代谢的显著差异相关;iii)认知缺陷与脑代谢异常有关;iv)社会行为问题可能与脑代谢异常有关。此外,在人类大脑中,X染色体参与联合新皮质的发育。