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Influence of X chromosome and hormones on human brain development: A magnetic resonance imaging and proton magnetic resonance spectroscopy study of Turner syndrome
被引:81
作者:
Cutter, WJ
Daly, EM
Robertson, DMW
Chitnis, XA
van Amelsvoort, TAMJ
Simmons, A
Ng, VWK
Williams, BS
Shaw, P
Conway, GS
Skuse, DH
Collier, DA
Craig, M
Murphy, DGM
机构:
[1] Inst Psychiat, Sect Brain Maturat, London SE5 8AF, England
[2] Inst Psychiat, Sect Cognit Neuropsychiat, Dept Psychol Med, London, England
[3] Inst Psychiat, Neuroimaging Res Grp, London, England
[4] Inst Psychiat, Dept Neurol & Social, Genet & Dev Psychiat Res Ctr, London, England
[5] Middlesex Hosp, Dept Endocrinol, London, England
[6] Inst Child Hlth, Behav Sci Unit, London, England
[7] Univ Amsterdam, Acad Med Ctr, Dept Psychiat, Amsterdam, Netherlands
关键词:
Turner syndrome;
brain;
magnetic resonance imaging;
magnetic resonance spectroscopy;
X chromosome;
D O I:
10.1016/j.biopsych.2005.06.026
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Background: Women with Turner syndrome (TS; 45,X) lack a normal second X chromosome, and many are prescibed exogenous sex and growth hormones (GH). Hence, the allow its an opportunity to investigate genetic and endocrine influences on brain development. Methods: We examined brain anatomy and metabolism in 27 adult monosomic TS women and 21 control subjects with volumetric magnetic resonance imaging and magnetic resonance spectroscopy. Results: In TS women, regional gray matter volume was significantly smaller in parieto-occipital cortex and caudate nucleus and larger in cerebellar hemispheres. White matter was reduced in the cerebellar hemispheres, parieto-occipital regions, and splenium of the corpus callosum but was increased in the temporal and orbitofrontal lobes and genui of corpus callosum. Women with TS bad a significantly lower parietal lobe concentration of N-acetyl aspartate, and higher hippocampal choline. Also, among women with TS, there were significant differences in regional gray matter volumes and/or neuronal integrity, depending upon. parental origin of X chromosome and oxandrolone and GH use. Conclusions. X chromosome monosomy, imprinting and neuroendocrine milieu modulate human brain development-perhaps in a regionally specific manner.
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页码:273 / 283
页数:11
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