c-reactive protein, endothelial function and genetic influence: association with obesity

Clicks: 294
ID: 258732
2013
Article Quality & Performance Metrics
Overall Quality Improving Quality
0.0 /100
Combines engagement data with AI-assessed academic quality
AI Quality Assessment
Not analyzed
Abstract
Obesity is a multifactor chronic disease and its incidence has been increasing over the years and is being considered a public health problem. It is characterized by a chronic state of low grade inflammation, in which the C-reactive protein levels are usually increased. This inflammatory process can change the endothelial function in these individuals, since elevated levels of C-reactive protein are related to a low production of nitric oxide, which is responsible for the endothelium vasodilation. Several studies have demonstrated the influence of polymorphisms in the genes of C-reactive protein and of the endothelial nitric oxide synthesis enzyme in obese and healthy individuals. Thus this literature review aims at discussing the relationship between obesity and C-reactive protein levels and endothelial function, as well as to elucidate the association of genetic factors. Scientific articles from the databases PubMed, Science Direct and Scielo were consulted, using the following keywords and combinations of them: C-reactive protein, function/endothelial dysfunction, polymorphism and obesity. Thus, we concluded that obese individuals have elevated levels of C-reactive protein as a result of excess of body fat and this implies a reduction in nitric oxide synthesis. All these factors can be influenced by polymorphisms in regulatory genes of the production of these proteins.
Reference Key
abreu2013revistac-reactive Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Fabiana Guichard de Abreu;Leandro Silva de Lemos;Alana Schraiber Colato;Niara da Silva Medeiros;Marilu Fiegenbaum;Caroline Dani;Alessandra Peres;Jerri Luiz Ribeiro
Journal Inorganic chemistry
Year 2013
DOI
10.25061/2527-2675/ReBraM/2013.v16i1.44
URL
Keywords

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.