Year: 2014
Type: article
Abstract: Increasing evidence indicates that Parkinson's disease (PD) and type 2 diabetes (T2DM) share dysregulated molecular networks. We identified 84 genes shared between PD and T2DM from curated disease-gene databases. Nitric oxide biosynthesis, lipid and carbohydrate metabolism, insulin secretion and inflammation were identified as common dysregulated pathways. A network prioritization approach was implemented to rank genes according to their distance to seed genes and their involvement in common biological pathways. Quantitative polymerase chain reaction assays revealed that a highly ranked gene, superoxide dismutase 2 (SOD2), is upregulated in PD patients compared to healthy controls in 192 whole blood samples from two independent clinical trials, the Harvard Biomarker Study (HBS) and the Diagnostic and Prognostic Biomarkers in Parkinson's disease (PROBE). The results from this study reinforce the idea that shared molecular networks between PD and T2DM provides an additional source of biologically meaningful biomarkers. Evaluation of this biomarker in de novo PD patients and in a larger prospective longitudinal study is warranted.
Source: PLoS ONE
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,382
Funders: Michael J. Fox Foundation for Parkinson's Research, Harvard NeuroDiscovery Center, Pfizer, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke, National Center for Complementary and Integrative Health, Medical Research and Materiel Command
Awards: Risk Marker for Parkinson's Disease: Enabling Novel Therapies, G1778344677, G2429896787, G276522564, G2886007300, A Next Generation of Biomarkers for Incipient Huntington Disease, Biomarkers for early intervention in Parkinson disease, G5132385799, G5850682332, Biomarkers for Huntington's Disease: Accelerating the Development of Therapies, Creatine Safety, Tolerability, and Efficacy in Huntington's Disease: CREST-E, Genome-wide analysis of tau neurotoxicity, Massachusetts Alzheimer's Disease Research Center, G7778722858, G8243195724, G8646438553, G9000085832, G9000208643
OpenAlex ID: W2132693527
