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Integrative Personal Omics Profiles during Periods of Weight Gain and Loss.

Citation
Piening, B. D., et al. “Integrative Personal Omics Profiles During Periods Of Weight Gain And Loss.”. Cell Systems, pp. 157-170.e8.
Center Stanford University
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Author Brian D Piening, Wenyu Zhou, Kévin Contrepois, Hannes Röst, Gucci Jijuan Gu Urban, Tejaswini Mishra, Blake M Hanson, Eddy J Bautista, Shana Leopold, Christine Y Yeh, Daniel Spakowicz, Imon Banerjee, Cynthia Chen, Kimberly Kukurba, Dalia Perelman, Colleen Craig, Elizabeth Colbert, Denis Salins, Shannon Rego, Sunjae Lee, Cheng Zhang, Jessica Wheeler, Reza Sailani, Liang Liang, Charles Abbott, Mark Gerstein, Adil Mardinoglu, Ulf Smith, Daniel L Rubin, Sharon Pitteri, Erica Sodergren, Tracey L McLaughlin, George M Weinstock, Michael P Snyder
Keywords genomics, metabolomics, microbiome, obesity, proteomics, systems biology, type 2 diabetes
Abstract

Advances in omics technologies now allow an unprecedented level of phenotyping for human diseases, including obesity, in which individual responses to excess weight are heterogeneous and unpredictable. To aid the development of better understanding of these phenotypes, we performed a controlled longitudinal weight perturbation study combining multiple omics strategies (genomics, transcriptomics, multiple proteomics assays, metabolomics, and microbiomics) during periods of weight gain and loss in humans. Results demonstrated that: (1) weight gain is associated with the activation of strong inflammatory and hypertrophic cardiomyopathy signatures in blood; (2) although weight loss reverses some changes, a number of signatures persist, indicative of long-term physiologic changes; (3) we observed omics signatures associated with insulin resistance that may serve as novel diagnostics; (4) specific biomolecules were highly individualized and stable in response to perturbations, potentially representing stable personalized markers. Most data are available open access and serve as a valuable resource for the community.

Year of Publication
2018
Journal
Cell systems
Volume
6
Issue
2
Number of Pages
157-170.e8
Date Published
02/2018
ISSN Number
2405-4712
DOI
10.1016/j.cels.2017.12.013
Alternate Journal
Cell Syst
PMID
29361466
PMCID
PMC6021558
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