Metabolomic Modularity Analysis (MMA) to Quantify Human Liver Perfusion Dynamics

DSpace/Manakin Repository

Metabolomic Modularity Analysis (MMA) to Quantify Human Liver Perfusion Dynamics

Citable link to this page


Title: Metabolomic Modularity Analysis (MMA) to Quantify Human Liver Perfusion Dynamics
Author: Sridharan, Gautham Vivek; Bruinsma, Bote Gosse; Bale, Shyam Sundhar; Swaminathan, Anandh; Saeidi, Nima; Yarmush, Martin L.; Uygun, Korkut

Note: Order does not necessarily reflect citation order of authors.

Citation: Sridharan, Gautham Vivek, Bote Gosse Bruinsma, Shyam Sundhar Bale, Anandh Swaminathan, Nima Saeidi, Martin L. Yarmush, and Korkut Uygun. 2017. “Metabolomic Modularity Analysis (MMA) to Quantify Human Liver Perfusion Dynamics.” Metabolites 7 (4): 58. doi:10.3390/metabo7040058.
Full Text & Related Files:
Abstract: Large-scale -omics data are now ubiquitously utilized to capture and interpret global responses to perturbations in biological systems, such as the impact of disease states on cells, tissues, and whole organs. Metabolomics data, in particular, are difficult to interpret for providing physiological insight because predefined biochemical pathways used for analysis are inherently biased and fail to capture more complex network interactions that span multiple canonical pathways. In this study, we introduce a nov-el approach coined Metabolomic Modularity Analysis (MMA) as a graph-based algorithm to systematically identify metabolic modules of reactions enriched with metabolites flagged to be statistically significant. A defining feature of the algorithm is its ability to determine modularity that highlights interactions between reactions mediated by the production and consumption of cofactors and other hub metabolites. As a case study, we evaluated the metabolic dynamics of discarded human livers using time-course metabolomics data and MMA to identify modules that explain the observed physiological changes leading to liver recovery during subnormothermic machine perfusion (SNMP). MMA was performed on a large scale liver-specific human metabolic network that was weighted based on metabolomics data and identified cofactor-mediated modules that would not have been discovered by traditional metabolic pathway analyses.
Published Version: doi:10.3390/metabo7040058
Other Sources:
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at
Citable link to this page:
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search