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Connectomic profile and clinical phenotype in newly diagnosed glioma patients

机译:初诊神经胶质瘤患者的结缔组织谱和临床表型

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Gliomas are primary brain tumors, originating from the glial cells in the brain. In contrast to the more traditional view of glioma as a localized disease, it is becoming clear that global brain functioning is impacted, even with respect to functional communication between brain regions remote from the tumor itself. However, a thorough investigation of glioma-related functional connectomic profiles is lacking. Therefore, we constructed functional brain networks using functional MR scans of 71 glioma patients and 19 matched healthy controls using the automated anatomical labelling (AAL) atlas and interregional Pearson correlation coefficients. The frequency distributions across connectivity values were calculated to depict overall connectomic profiles and quantitative features of these distributions (full-width half maximum (FWHM), peak position, peak height) were calculated. Next, we investigated the spatial distribution of the connectomic profile. We defined hub locations based on the literature and determined connectivity (1) between hubs, (2) between hubs and non-hubs, and (3) between non-hubs. Results show that patients had broader and flatter connectivity distributions compared to controls. Spatially, glioma patients particularly showed increased connectivity between non-hubs and hubs. Furthermore, connectivity distributions and hub-non-hub connectivity differed within the patient group according to tumor grade, while relating to Karnofsky performance status and progression-free survival. In conclusion, newly diagnosed glioma patients have globally altered functional connectomic profiles, which mainly affect hub connectivity and relate to clinical phenotypes. These findings underscore the promise of using connectomics as a future biomarker in this patient population. Highlights ? Glioma patients have altered connectomic profiles. ? Connectivity between hub and non-hub regions is increased in glioma patients. ? Connectivity between hub regions is decreased in glioma patients. ? Alterations in the connectomic profile relate to clinical phenotypes.
机译:神经胶质瘤是原发性脑部肿瘤,起源于大脑中的神经胶质细胞。与神经胶质瘤作为一种局部疾病的传统观点相反,越来越明显的是,甚至在远离肿瘤本身的大脑区域之间的功能交流方面,全球脑功能也会受到影响。但是,缺乏对神经胶质瘤相关功能性结缔组织谱的彻底研究。因此,我们使用自动解剖标记(AAL)地图集和区域间皮尔逊相关系数,对71位神经胶质瘤患者和19位匹配的健康对照进行功能MR扫描,构建功能性大脑网络。计算跨连接性值的频率分布,以描绘整个连接体轮廓,并计算这些分布的定量特征(半峰全宽(FWHM),峰位置,峰高)。接下来,我们研究了连接体轮廓的空间分布。我们根据文献定义了枢纽位置,并确定了枢纽之间的连通性(1),枢纽和非枢纽之间的连通性(2)和非枢纽之间的连通性(3)。结果表明,与对照组相比,患者的连接分布范围更广,更平坦。在空间上,神经胶质瘤患者尤其显示出非枢纽和枢纽之间的连通性增加。此外,在患者组中,根据肿瘤级别,连通性分布和集线器与非集线器的连通性也有所不同,但与卡诺夫斯基的机能状态和无进展生存期有关。总之,新诊断的神经胶质瘤患者的功能性连接体谱发生了整体变化,这主要影响枢纽连接性并与临床表型有关。这些发现凸显了将Connectomics用作该患者人群中未来生物标志物的希望。强调 ?胶质瘤患者的结缔组织谱改变。 ?胶质瘤患者中枢纽与非枢纽区域之间的连通性增加。 ?胶质瘤患者中枢区域之间的连通性降低。 ?结缔组织谱的改变与临床表型有关。

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