Center of Neurodevelopmental Disorders (KIND), Division of Neuropsychiatry, Centre for Psychiatry Research, Department of Women's and Children's Health, Karolinska Institutet and Stockholm Health Care Services, Region Stockholm, Gävlegatan 22B, 113 30, Stockholm, Sweden.
Department of Nursing, Gustavus Adolphus College, 800 College Avenue West, St. Peter, MN, USA.
Sci Rep. 2020 Dec 29;10(1):22417. doi: 10.1038/s41598-020-79959-8.
While previous research has investigated neuroradiological findings in autism spectrum disorder (ASD) and attention-deficit hyperactivity disorder (ADHD), the entire range of neurodevelopmental disorders (NDDs) has not yet been well-studied using magnetic resonance imaging (MRI). Considering the overlap among NDDs and simultaneous development of the brain and face, guided by molecular signaling, we examined the relationship of actionable and incidental (non-actionable) MRI findings and NDD diagnoses together with facial morphological variants and genetic copy number variants (CNVs). A cross-sectional study was conducted with a twin cohort 8-36 years of age (57% monozygotic, 40% dizygotic), including 372 subjects (46% with NDDs; 47% female) imaged by MRI, 280 with data for facial morphological variants, and 183 for CNVs. Fifty-one percent of participants had MRI findings. Males had a statistically significantly higher percentage of MRI findings (57.7%) compared with females (43.8%, p = 0.03). Twin zygosity was not statistically significantly correlated with incidence or severity of specific MRI findings. No statistically significant association was found between MRI findings and any NDD diagnosis or facial morphological variants; however, MRI findings were statistically significantly associated with the number of CNVs (OR 1.20, 95% CI 1.00-1.44, p = 0.05, adjusted OR for sex 1.24, 95% CI 1.03-1.50, p = 0.02). When combining the presence of MRI findings, facial morphological variants, and CNVs, statistically significant relationships were found with ASD and ADHD diagnoses (p = 0.0006 and p = 0.002, respectively). The results of this study demonstrate that the ability to identify NDDs from combined radiology, morphology, and CNV assessments may be possible. Additionally, twins do not appear to be at increased risk for neuroradiological variants.
虽然先前的研究已经调查了自闭症谱系障碍(ASD)和注意缺陷多动障碍(ADHD)的神经影像学发现,但使用磁共振成像(MRI)对整个神经发育障碍(NDD)进行全面研究尚未得到很好的研究。考虑到 NDD 之间的重叠以及大脑和面部的同时发育,受分子信号指导,我们研究了可操作和偶发(不可操作)MRI 发现与 NDD 诊断以及面部形态变异和遗传拷贝数变异(CNV)之间的关系。对 8-36 岁的双胞胎队列进行了横断面研究(57%为同卵双胞胎,40%为异卵双胞胎),其中包括 372 名接受 MRI 成像的受试者(46%患有 NDD;47%为女性),280 名具有面部形态变异数据,183 名具有 CNV 数据。51%的参与者有 MRI 发现。与女性(43.8%)相比,男性的 MRI 发现比例具有统计学意义上的显著升高(57.7%,p=0.03)。双胞胎的同卵性与特定 MRI 发现的发生率或严重程度没有统计学上的显著相关性。MRI 发现与任何 NDD 诊断或面部形态变异之间没有发现统计学上的显著关联;然而,MRI 发现与 CNV 的数量存在统计学显著关联(OR 1.20,95%CI 1.00-1.44,p=0.05,调整性别后 OR 为 1.24,95%CI 1.03-1.50,p=0.02)。当将 MRI 发现、面部形态变异和 CNV 结合起来时,与 ASD 和 ADHD 诊断存在统计学显著的关系(p=0.0006 和 p=0.002)。这项研究的结果表明,从联合放射学、形态学和 CNV 评估中识别 NDD 的能力可能是可行的。此外,双胞胎似乎没有增加神经影像学变异的风险。