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Serum Fatty Acids and Inflammatory Patterns in Severe Obesity: A Preliminary Investigation in Women.

Authors :
Lima, Gislene B.
Figueiredo, Nayra
Kattah, Fabiana M.
Oliveira, Emilly S.
Horst, Maria A.
Dâmaso, Ana R.
Oyama, Lila M.
Whitton, Renata G. M.
de Souza, Gabriel I. M. H.
Lima, Glaucia C.
Mota, João F.
Campos, Raquel M. S.
Corgosinho, Flávia C.
Source :
Biomedicines; Oct2024, Vol. 12 Issue 10, p2248, 9p
Publication Year :
2024

Abstract

Background: Inflammation plays a central role in many chronic diseases that characterize modern society. Leptin/adiponectin and adiponectin/leptin ratios have been recognized as notable markers of dysfunctional adipose tissue and, consequently, an inflammatory state. Methods: Blood samples were collected from 41 adult volunteers (40.2 ± 8.3 years) diagnosed with severe obesity (BMI 46.99; 42.98–51.91 kg/m<superscript>2</superscript>). The adipokines were quantified using an enzyme-linked immunosorbent assay, while the serum fatty acid analysis was conducted using chromatography. Results: The results unveiled a positive correlation between the leptin/adiponectin ratio and the 20:3n6 fatty acid (r = 0.52, p = 0.001), as well as a similar positive correlation between the adiponectin/leptin ratio and the 22:6n3 fatty acid (r = 0.74, p = 0.001). In the regression analysis, the 22:6n3 fatty acid predicted the adiponectin/leptin ratio (β = 0.76, p < 0.001), whereas C20:3 n-6 was a predictor for inflammatory markers (β = 4.84, p < 0.001). Conclusions: In conclusion, the 22:6n3 fatty acid was demonstrated to be a predictive factor for the adiponectin/leptin ratio and C20:3 n-6 was a predictor for inflammatory markers. This discovery, novel within this population, can help develop new intervention strategies aimed at controlling the inflammatory status in individuals classified as having severe obesity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
12
Issue :
10
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
180525630
Full Text :
https://doi.org/10.3390/biomedicines12102248