Center for Biomedical Technology, Technical University of Madrid, Campus Montegancedo 28223, Pozuelo de Alarcón, Madrid, Spain.
Chaos. 2011 Sep;21(3):033103. doi: 10.1063/1.3608126.
Congenital obstructive nephropathy (ON) is one of the most frequent nephropathy observed among newborns and children, and the first cause of end-stage renal diseases treated by dialysis or transplantation. This pathology is characterized by the presence of an obstacle in the urinary tract, e.g., stenosis or abnormal implantation of the urethra in the kidney. In spite of important advances, pathological mechanisms are not yet fully understood. In this contribution, the topology of complex networks created upon vectors of features for control and ON subjects is related with the severity of the pathology. Nodes in these networks represent genetic and metabolic profiles, while connections between them indicate an abnormal relation between their expressions. Resulting topologies allow discriminating ON subjects and detecting which genetic or metabolic elements are responsible for the malfunction.
先天性梗阻性肾病(ON)是新生儿和儿童中最常见的肾病之一,也是透析或移植治疗的终末期肾病的首要原因。这种病理表现为尿路存在梗阻,例如尿道狭窄或异常植入肾脏。尽管取得了重要进展,但病理机制仍未完全阐明。在本研究中,我们将控制组和 ON 组特征向量所构建的复杂网络拓扑与病理严重程度相关联。这些网络中的节点代表基因和代谢谱,而它们之间的连接则表明其表达之间存在异常关系。由此产生的拓扑结构可以区分 ON 患者,并检测出哪些遗传或代谢因素导致了功能障碍。