Publication
C-Reactive Protein Causes Adult-Onset Obesity Through Chronic Inflammatory Mechanism
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- Persistent URL
- Last modified
- 05/21/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2020-02-20
- Publisher
- Frontiers Media S.A.
- Publication Version
- Copyright Statement
- © 2020 Li, Wang, Xu, Ma, Wang, Eatman, You, Zou, Champion, Zhao, Cui, Li, Deng, Ma, Wu, Wang, Zhang, Wang, Bayorh and Song.
- License
- Final Published Version (URL)
- Title of Journal or Parent Work
- Volume
- 8
- Start Page
- 18
- End Page
- 18
- Grant/Funding Information
- This work was supported by National Institutes of Health (SC2HL095098, G12MD007602, U54MD007590). This study was supported by the Key Research and Development Project of Shaanxi Provincial Science and Technology Department (2017ZDXM-SF-068), Shaanxi Provincial Collaborative Technology Innovation Plan (2017XT-026, 2018XT-002), and Medical Research Project of Xi'an Social Development Guidance Plan (2017117SF/YX011-3).
- Supplemental Material (URL)
- Abstract
- Obesity is characterized by low-grade chronic inflammation. As an acute-phase reactant to inflammation and infection, C-reactive protein (CRP) has been found to be the strongest factor associated with obesity. Here we show that chronic elevation of human CRP at baseline level causes the obesity. The obesity phenotype is confirmed by whole-body magnetic resonance imaging (MRI), in which the total fat mass is 6- to 9- fold higher in the CRP rats than the control rats. Univariate linear regression analysis showed different growth rates between the CRP rats and the control rats, and that the difference appears around 11 weeks old, indicating that they developed adult-onset obesity. We also found that chronic elevation of CRP can prime molecular changes broadly in the innate immune system, energy expenditure systems, thyroid hormones, apolipoproteins, and gut flora. Our data established a causal role of CRP elevation in the development of adult-onset obesity.
- Author Notes
- Keywords
- Research Categories
- Health Sciences, Immunology
- Health Sciences, Nutrition
- Health Sciences, Human Development
- Biology, Cell
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