Law Nicole, Greenberg Mark, Bouffet Eric, Laughlin Suzanne, Taylor Michael D, Malkin David, Liu Fang, Moxon-Emre Iska, Scantlebury Nadia, Skocic Jovanka, Mabbott Donald
Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Psychology, Collaborative Program in Neuroscience, University of Toronto, Toronto, Ontario, Canada.
Hum Brain Mapp. 2015 Jul;36(7):2615-28. doi: 10.1002/hbm.22795. Epub 2015 Apr 14.
Detailed information regarding the neuroanatomy of reciprocal cerebrocerebellar pathways is based on well-documented animal models. This knowledge has not yet been fully translated to humans, in that the structure of reciprocal cerebrocerebellar pathways connecting the cerebellum with frontal lobe has not been shown in its entirety. We investigated the impact of injury and age on cerebrocerebellar pathway microstructure using diffusion tensor imaging (DTI) and probabilistic tractography. We used medulloblastoma (MB) as an injury model due to the known impact of tumor/treatment on the cerebellum, one of the main nodes of cerebrocerebellar pathways. We delineated and segmented reciprocal cerebrocerebellar pathways connecting the cerebellum with frontal lobe in 38 healthy children (HC) and 34 children treated for MB, and compared pathway segment DTI measures between HC and MB and across three age cohorts: childhood, early adolescence, and late adolescence. Pathway compromise was evident for the MB group compared to HC, particularly within posterior segments (Ps<0.01). Though we found no age effect, group differences in microstructure were driven by pathway segment (posterior) and age cohort (adolescence), which may reflect the extent of injury to the posterior fossa following treatment for MB and age cohort differences in radiation treatment protocol in our sample. We have examined the microstructure of reciprocal cerebrocerebellar connections in the pediatric brain and have found that these pathways are injured in MB, a clinical population treated with surgery, radiation, and chemotherapy. Our findings support the late effects literature describing white matter injury emergence in the years following treatment for MB.
关于相互连接的大脑小脑通路神经解剖学的详细信息基于充分记录的动物模型。这一知识尚未完全转化到人类身上,因为连接小脑与额叶的相互大脑小脑通路的结构尚未完全展现。我们使用扩散张量成像(DTI)和概率性纤维束成像研究了损伤和年龄对大脑小脑通路微观结构的影响。由于肿瘤/治疗对小脑(大脑小脑通路的主要节点之一)的已知影响,我们将髓母细胞瘤(MB)用作损伤模型。我们在38名健康儿童(HC)和34名接受MB治疗的儿童中描绘并分割了连接小脑与额叶的相互大脑小脑通路,并比较了HC和MB之间以及三个年龄组(儿童期、青春期早期和青春期晚期)之间通路节段的DTI测量值。与HC相比,MB组的通路受损明显,尤其是在后段(P<0.01)。虽然我们没有发现年龄效应,但微观结构的组间差异由通路节段(后段)和年龄组(青春期)驱动,这可能反映了MB治疗后后颅窝的损伤程度以及我们样本中放射治疗方案的年龄组差异。我们研究了小儿大脑中相互连接的大脑小脑连接的微观结构,发现这些通路在接受手术、放疗和化疗治疗的临床人群MB中受到损伤。我们的研究结果支持了关于MB治疗后数年出现白质损伤的晚期效应文献。