Denckla M B, Hofman K, Mazzocco M M, Melhem E, Reiss A L, Bryan R N, Harris E L, Lee J, Cox C S, Schuerholz L J
Kennedy Krieger Institute, Baltimore, Maryland 21205, USA.
Am J Med Genet. 1996 Feb 16;67(1):98-102. doi: 10.1002/(SICI)1096-8628(19960216)67:1<98::AID-AJMG17>3.0.CO;2-K.
To address the controversy regarding the relationship between cognitive impairment (lowering of IQ) and magnetic resonance imaging (MRI) characteristics (T2-weighted hyperintensities or unidentified bright objects [UBOs]) in children with neurofibromatosis-1 (NF-1), we used a pairwise NF-1/ sibling design; we set out to predict the lowering of IQ in each child with NF-1 as a discrepancy from the IQ of an unaffected sibling (D-SIQ). Our multiple regression model included the age of the child with NF-1, familial or sporadic nature of the NF-1, number of locations in the child's brain occupied by T2-weighted hyperintensities (UBOs), and the volumetric percentage of brain tissue occupied by T2-weighted hyperintensities (UBOs). Only the number of locations occupied by UBOs accounted for IQ lowering (D-SIQ) in children with NF-1 (42% of the variance in D-SIQ). This is the first report to confirm that a continuum of lowered IQs in NF-1-affected children exists in relation to the distribution of UBOs (range 0-7), not just presence (vs. absence) of any UBOs.
为了解决关于1型神经纤维瘤病(NF-1)患儿认知障碍(智商降低)与磁共振成像(MRI)特征(T2加权高信号或不明亮物体[UBO])之间关系的争议,我们采用了NF-1患儿与其同胞配对的设计;我们着手将每个NF-1患儿智商的降低预测为与其未受影响同胞智商的差异(D-SIQ)。我们的多元回归模型包括NF-1患儿的年龄、NF-1的家族性或散发性、T2加权高信号(UBO)在患儿大脑中占据的位置数量,以及T2加权高信号(UBO)占据的脑组织体积百分比。在NF-1患儿中,只有UBO占据的位置数量可解释智商降低(D-SIQ)情况(占D-SIQ方差的42%)。这是第一份证实NF-1患儿智商降低与UBO分布(范围0至7)相关,而非仅与是否存在任何UBO相关的报告。