Obesity-Related Changes in Human Plasma Lipidome Determined by the Lipidyzer Platform.
Peter PikoLászló PálSándor SzűcsZsigmond KósaJános SándorRoza AdanyPublished in: Biomolecules (2021)
Obesity is an increasing public health concern both in the developed and developing countries. Previous studies have demonstrated that considerable alterations in lipid metabolism and consequently marked changes in lipid profile are associated with the onset and progression of obesity-related complications. To characterize the full spectrum of obesity-induced changes in lipid metabolism, direct infusion tandem mass spectrometry analysis is the most promising approach. To better understand which of the many lipid species are the most strongly associated with obesity, the aim of our work was to measure and profile plasma lipids in normal (n = 57), overweight (n = 31), and obese (n = 48) individuals randomly selected from samples of Hungarian general and Roma populations by using the targeted quantitative lipidomics platform, the Lipidyzer. Principal component and stepwise regression analyses were used to identify the most significant clusters and species of lipids by increasing body mass index (BMI). From the 18 clusters identified four key lipid species (PE P-16:0/20:3, TG 20:4_33:1, TG 22:6_36:4, TG 18:3_33:0) showed a strong significant positive and three others (Hex-Cer 18:1;O2/22:0, LPC 18:2, PC 18:1_18:1) significant negative association with BMI. Compared to individual lipid species alone, the lipid species ratio (LSR) we introduced showed an extremely strong, at least 9 orders of magnitude stronger, association with BMI. The LSR can be used as a sensitive and predictive indicator to monitor obesity-related alterations in human plasma and control the effectiveness of treatment of obesity associated non-communicable diseases.
Keyphrases
- weight gain
- weight loss
- metabolic syndrome
- insulin resistance
- body mass index
- type diabetes
- high fat diet induced
- public health
- fatty acid
- systematic review
- adipose tissue
- randomized controlled trial
- high resolution
- low dose
- skeletal muscle
- high throughput
- drug induced
- simultaneous determination
- gas chromatography
- replacement therapy
- global health
- obese patients