» Articles » PMID: 39133724

Relationship Between Types and Levels of Free Fatty Acids, Peripheral Insulin Resistance, and Oxidative Stress in T2DM: A Case-control Study

Overview
Journal PLoS One
Date 2024 Aug 12
PMID 39133724
Authors
Affiliations
Soon will be listed here.
Abstract

Free Fatty Acids (FFAs) are vital for energy homeostasis and the pathogenesis of a variety of diseases, including diabetes. For the first time, we presumed and investigated the types and levels of FFAs and their links to Insulin Resistance (IR) and Oxidative Stress (OS) in T2DM. A case-control study was conducted on 60 individuals with diabetes, 60 prediabetics with IFG, and 60 control groups. A Gas Chromatography Flame Ionization Detector (GC-FID) was used to estimate FFAs, which were then classified based on length and saturation. Indeed, antioxidant parameters such as TAC, MDA levels, PON-1, SOD-3, and CAT activity were assessed. Higher levels of LCFFA, SFFA, USFFA, and total FFA were found in people with diabetes and prediabetes. These levels were also linked to higher levels of HOMA-IR, BMI, FBS, HbA1C, and MDA, but lower levels of antioxidants. Furthermore, adjusting the above FFAs with age, sex, and antihypertensive medication increased T2DM development. SCFFA and ω3/6 fatty acids had a negative relationship with HOMA-IR, FBS, and insulin and a positive relationship with TAC. Adjusted SCFFA reduces T2DM risk. According to our models, total FFA is utilized to diagnose diabetes (AUC = 83.98, cut-off > 919 μM) and SCFFA for prediabetes (AUC = 82.32, cut-off < 39.56 μM). Total FFA (≥ 776 μM), LCFFA (≥ 613 μM), SFFA (≥ 471 μM), and USFFA (≥ 398 μM) all increase the risk of T2DM by increasing OS, BMI, and HOMA-IR. On the other hand, SCFFAs (≥ 38.7 μM) reduce the risk of T2DM by reducing BMI, HOMA-IR, and OS. SCFFAs and total FFAs can be used for the diagnosis of prediabetes and diabetes, respectively.

Citing Articles

Effect of plasma free fatty acids on lung function in male COPD patients.

Yazdani R, Fallah H, Yazdani S, Shahouzehi B, Danesh B Sci Rep. 2025; 15(1):3377.

PMID: 39870734 PMC: 11772598. DOI: 10.1038/s41598-025-86628-1.


Research progress on the relationship between free fatty acid profile and type 2 diabetes complicated by coronary heart disease.

Liu X, Gong M, Wu N Front Endocrinol (Lausanne). 2024; 15:1503704.

PMID: 39713052 PMC: 11658973. DOI: 10.3389/fendo.2024.1503704.


Microbial and proteomic signatures of type 2 diabetes in an Arab population.

Murugesan S, Yousif G, Djekidel M, Gentilcore G, Grivel J, Al Khodor S J Transl Med. 2024; 22(1):1132.

PMID: 39707404 PMC: 11662572. DOI: 10.1186/s12967-024-05928-8.


Gastrodin attenuates diabetic cardiomyopathy characterized by myocardial fibrosis by inhibiting the KLK8-PAR1 signaling axis.

Zhang M, Zhang Y, He J, Wang X, Wang Y, Li L Chin Med. 2024; 19(1):164.

PMID: 39578836 PMC: 11583739. DOI: 10.1186/s13020-024-01035-4.

References
1.
Petersen M, Shulman G . Mechanisms of Insulin Action and Insulin Resistance. Physiol Rev. 2018; 98(4):2133-2223. PMC: 6170977. DOI: 10.1152/physrev.00063.2017. View

2.
Zhu L, Sha L, Li K, Wang Z, Wang T, Li Y . Dietary flaxseed oil rich in omega-3 suppresses severity of type 2 diabetes mellitus via anti-inflammation and modulating gut microbiota in rats. Lipids Health Dis. 2020; 19(1):20. PMC: 7006389. DOI: 10.1186/s12944-019-1167-4. View

3.
Gehrmann W, Wurdemann W, Plotz T, Jorns A, Lenzen S, Elsner M . Antagonism Between Saturated and Unsaturated Fatty Acids in ROS Mediated Lipotoxicity in Rat Insulin-Producing Cells. Cell Physiol Biochem. 2015; 36(3):852-65. DOI: 10.1159/000430261. View

4.
Alhazmi A, Stojanovski E, Garg M, McEvoy M . Fasting whole blood fatty acid profile and risk of type 2 diabetes in adults: a nested case control study. PLoS One. 2014; 9(5):e97001. PMC: 4016225. DOI: 10.1371/journal.pone.0097001. View

5.
Guasch-Ferre M, Hruby A, Toledo E, Clish C, Martinez-Gonzalez M, Salas-Salvado J . Metabolomics in Prediabetes and Diabetes: A Systematic Review and Meta-analysis. Diabetes Care. 2016; 39(5):833-46. PMC: 4839172. DOI: 10.2337/dc15-2251. View