Naik Ashwin Ashok, Narayanan Aswath, Khanchandani Prakash, Sridharan Divya, Sukumar Piruthivi, Srimadh Bhagavatam Sai Krishna, Seshagiri Polani B, Sivaramakrishnan Venketesh
Disease Biology Lab, Department of Biosciences, Sri Sathya Sai Institute of Higher Learning, Prasanthinilayam, Andhra Pradesh, 515 134, India.
Department of Orthopedics, Sri Sathya Sai Institute of Higher Medical Sciences, Prasanthigram, Andhra Pradesh, 515 134, India.
Sci Rep. 2020 Oct 22;10(1):18099. doi: 10.1038/s41598-020-75197-0.
Avascular necrosis of femoral head (AVNFH) is a debilitating disease, which affects the middle aged population. Though the disease is managed using bisphosphonate, it eventually leads to total hip replacement due to collapse of femoral head. Studies regarding the association of single nucleotide polymorphisms with AVNFH, transcriptomics, proteomics, metabolomics, biophysical, ultrastructural and histopathology have been carried out. Functional validation of SNPs was carried out using literature. An integrated systems analysis using the available datasets might help to gain further insights into the disease process. We have carried out an analysis of transcriptomic data from GEO-database, SNPs associated with AVNFH, proteomic and metabolomic data collected from literature. Based on deficiency of vitamins in AVNFH, an enzyme-cofactor network was generated. The datasets are analyzed using ClueGO and the genes are binned into pathways. Metabolomic datasets are analyzed using MetaboAnalyst. Centrality analysis using CytoNCA on the data sets showed cystathionine beta synthase and methylmalonyl-CoA-mutase to be common to 3 out of 4 datasets. Further, the genes common to at least two data sets were analyzed using DisGeNET, which showed their involvement with various diseases, most of which were risk factors associated with AVNFH. Our analysis shows elevated homocysteine, hypoxia, coagulation, Osteoclast differentiation and endochondral ossification as the major pathways associated with disease which correlated with histopathology, IHC, MRI, Micro-Raman spectroscopy etc. The analysis shows AVNFH to be a multi-systemic disease and provides molecular signatures that are characteristic to the disease process.
股骨头缺血性坏死(AVNFH)是一种使人衰弱的疾病,影响中年人群。尽管该疾病使用双膦酸盐进行治疗,但由于股骨头塌陷,最终仍会导致全髋关节置换。已经开展了关于单核苷酸多态性与AVNFH的关联、转录组学、蛋白质组学、代谢组学、生物物理学、超微结构和组织病理学的研究。利用文献对单核苷酸多态性进行了功能验证。使用现有数据集进行综合系统分析可能有助于进一步深入了解疾病过程。我们对来自基因表达综合数据库(GEO)的转录组数据、与AVNFH相关的单核苷酸多态性、从文献中收集的蛋白质组学和代谢组学数据进行了分析。基于AVNFH中维生素的缺乏,生成了一个酶-辅因子网络。使用ClueGO对数据集进行分析,并将基因分类到不同途径中。使用MetaboAnalyst对代谢组学数据集进行分析。使用CytoNCA对数据集进行中心性分析,结果显示胱硫醚β合酶和甲基丙二酰辅酶A变位酶在4个数据集中的3个中是共同的。此外,使用DisGeNET对至少两个数据集共有的基因进行了分析,结果显示它们与各种疾病有关,其中大多数是与AVNFH相关的危险因素。我们的分析表明,高同型半胱氨酸血症、缺氧、凝血、破骨细胞分化和软骨内成骨是与该疾病相关的主要途径,这与组织病理学、免疫组化、磁共振成像、显微拉曼光谱等相关。分析表明AVNFH是一种多系统疾病,并提供了该疾病过程特有的分子特征。