Kesler Shelli R, Blasey Christine M, Brown Wendy E, Yankowitz Jerome, Zeng She Min, Bender Bruce G, Reiss Allan L
Stanford Psychiatry Neuroimaging Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California 94305-5719, USA.
Biol Psychiatry. 2003 Sep 15;54(6):636-46. doi: 10.1016/s0006-3223(03)00289-0.
Turner syndrome (TS) results from complete or partial monosomy X. The cognitive phenotype of TS involves preservation of verbal skills with visuospatial functioning deficits. The superior temporal gyrus (STG), which is involved in language capacities, has not been investigated in TS.
The STG was measured in 30 female subjects (mean age = 14.73 +/- 6.41; range = 7.56-33.30) with TS and 30 age-matched control subjects (mean age = 14.63 +/- 5.90; range = 6.35-32.65) using volumetric magnetic resonance imaging analyses.
-Right STG, including both gray and white matter volumes, was significantly larger in TS compared with control subjects. Overall left STG volume was not significantly different between groups, although left white matter volume was increased in the TS subjects. The TS subgroup with a maternally derived X chromosome (Xm) demonstrated more aberrant STG volumes compared with subjects with a paternally (Xp) derived X and control subjects. The difference in STG volumes between Xm and control subjects involved both white and gray matter. The Xm subjects differed from Xp subjects only in terms of gray matter.
These findings suggest that X-monosomy and X-linked imprinting negatively affect STG development, possibly by disrupting neural pruning mechanisms.
特纳综合征(TS)由X染色体完全或部分单体性所致。TS的认知表型包括言语技能保留但存在视觉空间功能缺陷。参与语言能力的颞上回(STG)在TS中尚未得到研究。
使用容积磁共振成像分析对30名患有TS的女性受试者(平均年龄 = 14.73 +/- 6.41;范围 = 7.56 - 33.30)和30名年龄匹配的对照受试者(平均年龄 = 14.63 +/- 5.90;范围 = 6.35 - 32.65)的STG进行测量。
与对照受试者相比,TS患者右侧STG(包括灰质和白质体积)明显更大。尽管TS受试者左侧白质体积增加,但两组之间总体左侧STG体积无显著差异。与父源X染色体(Xp)的受试者和对照受试者相比,母源X染色体(Xm)的TS亚组表现出更异常的STG体积。Xm受试者与对照受试者之间STG体积的差异涉及白质和灰质。Xm受试者与Xp受试者仅在灰质方面存在差异。
这些发现表明,X单体性和X连锁印记可能通过破坏神经修剪机制对STG发育产生负面影响。