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An integrative systems biology approach for precision medicine in diabetic kidney disease.

Citation
Mulder, S., et al. “An Integrative Systems Biology Approach For Precision Medicine In Diabetic Kidney Disease.”. Diabetes, Obesity & Metabolism, pp. 6-13.
Center University of Michigan
Author Skander Mulder, Habib Hamidi, Matthias Kretzler, Wenjun Ju
Keywords biomarkers, Chronic kidney disease, systems biology, type 2 diabetes
Abstract

Current therapeutic approaches are ineffective in many patients with established diabetic kidney disease (DKD), an epidemic affecting one in three patients with diabetes. Early identification of patients at high risk for progression and individualizing therapies have the potential to mitigate kidney complications due to diabetes. To achieve this, a better understanding of the complex pathophysiology of DKD is needed. A system biology approach integrating large-scale omic data is well suited to unravel the molecular mechanisms driving DKD and may offer new perspectives how to personalize therapy. Recent studies indeed show that integrating genome scale data sets generated from prospectively designed clinical cohort studies with model systems using innovative bioinformatics analysis revealed critical molecular pathways in DKD and led to the development of candidate prognostic molecular biomarkers. This review seeks to provide an overview of the recent progress in the application of the integrative systems biology approaches specifically in the field of molecular biomarkers for DKD. We will mainly focus the discussion on how to use integrative system biology approach to first identify patients at high risk of progression, and second to identify patients who may or may not respond to treatment. Challenges and opportunities in applying precision medicine in DKD will also be discussed.

Year of Publication
2018
Journal
Diabetes, obesity & metabolism
Volume
20 Suppl 3
Number of Pages
6-13
Date Published
12/2018
ISSN Number
1463-1326
DOI
10.1111/dom.13416
Alternate Journal
Diabetes Obes Metab
PMID
30294956
PMCID
PMC6541014
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