Vanderbilt Brain Institute, 465 21(st) Avenue South, Nashville, TN 37212, USA.
Department of Electrical Engineering and Computer Science, Vanderbilt University, 2301Vanderbilt Place, Nashville, TN 37235, USA; Vanderbilt Kennedy Center, 110 Magnolia Circle, Nashville, TN 37203, USA.
Magn Reson Imaging. 2023 May;98:17-25. doi: 10.1016/j.mri.2022.12.022. Epub 2023 Jan 3.
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous syndrome that affects multiple organ systems resulting in widespread symptoms, including cognitive deficits. In addition to the criteria required for an NF1 diagnosis, approximately 70% of children with NF1 present with Unidentified Bright Objects (UBOs) or Focal Areas of Signal Intensity, which are hyperintense bright spots seen on T2-weighted magnetic resonance images and seen more prominently on FLAIR magnetic resonance images (Sabol et al., 2011). Current findings relating the presence/absence, quantities, sizes, and locations of these bright spots to cognitive abilities are mixed. To contribute to and hopefully disentangle some of these mixed findings, we explored potential relationships between metrics related to UBOs and cognitive abilities in a sample of 28 children and adolescents with NF1 (M=12.52 years; SD=3.18 years; 16 male). We used the Lesion Segmentation Tool (LST) to automatically detect and segment the UBOs. The LST was able to qualitatively and quantitatively reliably detect UBOs in images of children with NF1. Using these automatically detected and segmented lesions, we found that while controlling for age, biological sex, perceptual IQ, study, and scanner, "total UBO volume", defined as the sum of all the voxels representing all of the UBOs for each participant, helped explain differences in word reading, phonological awareness, and visuospatial skills. These findings contribute to the emerging NF1 literature and help parse the specific deficits that children with NF1 have, to then help improve the efficacy of reading interventions for children with NF1.
神经纤维瘤病 1 型(NF1)是一种常染色体显性神经皮肤综合征,影响多个器官系统,导致广泛的症状,包括认知缺陷。除了 NF1 诊断所需的标准外,大约 70%的 NF1 患儿存在未识别的明亮物体(UBO)或信号强度灶,这些是 T2 加权磁共振图像上看到的高亮亮点,在 FLAIR 磁共振图像上更为明显(Sabol 等人,2011 年)。目前的研究结果将这些亮点的存在/缺失、数量、大小和位置与认知能力联系起来,结果喜忧参半。为了进一步阐明这些混杂的发现,我们在 28 名 NF1 患儿和青少年(M=12.52 岁;SD=3.18 岁;16 名男性)样本中探索了与 UBO 相关的指标与认知能力之间的潜在关系。我们使用病变分割工具(LST)自动检测和分割 UBO。LST 能够可靠地定性和定量检测 NF1 儿童的 UBO。使用这些自动检测和分割的病变,我们发现,在控制年龄、生物性别、知觉智商、研究和扫描仪的情况下,“总 UBO 体积”(定义为每个参与者代表所有 UBO 的所有体素的总和)有助于解释阅读、语音意识和视觉空间技能的差异。这些发现为新兴的 NF1 文献做出了贡献,并有助于分析 NF1 患儿的具体缺陷,从而有助于提高 NF1 患儿阅读干预的效果。