Department of Psychiatry, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Biol Psychiatry. 2011 Nov 1;70(9):852-8. doi: 10.1016/j.biopsych.2011.05.038. Epub 2011 Jul 29.
Fragile X syndrome (FXS) is the most common known heritable cause of intellectual disability. Prior studies in FXS have observed a plateau in cognitive and adaptive behavioral development in early adolescence, suggesting that brain development in FXS may diverge from typical development during this period.
In this study, we examined adolescent brain development using structural magnetic resonance imaging data acquired from 59 individuals with FXS and 83 typically developing control subjects aged 9 to 22, a subset of whom were followed up longitudinally (1-5 years; typically developing: 17, FXS: 19). Regional volumes were modeled to obtain estimates of age-related change.
We found that while structures such as the caudate showed consistent volume differences from control subjects across adolescence, prefrontal cortex (PFC) gyri showed significantly aberrant maturation. Furthermore, we found that PFC-related measures of cognitive functioning followed a similarly aberrant developmental trajectory in FXS.
Our findings suggest that aberrant maturation of the PFC during adolescence may contribute to persistent or increasing intellectual deficits in FXS.
脆性 X 综合征(FXS)是已知的最常见的遗传性智力障碍病因。此前 FXS 的研究观察到青少年早期认知和适应行为发展趋于平稳,这表明在此期间 FXS 大脑的发育可能与典型发育不同。
本研究使用从 59 名 FXS 患者和 83 名正常发育对照者(年龄 9 至 22 岁)的结构磁共振成像数据,对青少年大脑发育进行了研究,其中一些参与者进行了纵向随访(1-5 年;正常发育:17 名,FXS:19 名)。对区域体积进行建模以获得与年龄相关的变化估计。
我们发现,虽然尾状核等结构在整个青春期都与对照组存在明显的体积差异,但前额叶皮层(PFC)脑回表现出明显的异常成熟。此外,我们发现 FXS 中的认知功能的 PFC 相关指标也呈现出类似的异常发育轨迹。
我们的研究结果表明,青少年时期 PFC 的异常成熟可能导致 FXS 中持续或增加的智力缺陷。