» Articles » PMID: 24719245

Plasma Lipids, Lipoprotein Metabolism and HDL Lipid Transfers Are Equally Altered in Metabolic Syndrome and in Type 2 Diabetes

Overview
Journal Lipids
Specialty Biochemistry
Date 2014 Apr 11
PMID 24719245
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Metabolic syndrome (MetS) refers to states of insulin resistance that predispose to development of cardiovascular disease and type 2 diabetes (T2DM). The aim was to investigate whether plasma lipids and lipid metabolism differ in MetS patients compared to those with T2DM with poor glycemic control (glycated hemoglobin > 7.0). Eighteen patients with T2DM, 18 with MetS and 14 controls, paired for age (40-70 years) and body mass index (BMI), were studied. Plasma lipids and the kinetics of a triacylglycerol-rich emulsion labeled with [(3)H]-triolein ([(3)H]-TAG) and [(14)C]-cholesteryl esters ([(14)C]-CE) injected intravenously followed by one-hour blood sampling were determined. Lipid transfers from an artificial nanoemulsion donor to high-density lipoprotien (HDL) were assayed in vitro. Low-density lipoprotein (LDL) and HDL cholesterol (mg/dl) were not different in T2DM (128 ± 7; 42 ± 7) and MetS (142 ± 6; 39 ± 3), but triacylglycerols were even higher in MetS (215 ± 13) than in T2DM (161 ±11, p < 0.05). Fractional clearance rate (FCR, in min(1)) of [(3)H]-TAG and [(14)C]-CE were equal in T2DM (0.008 ± 0.018; 0.005 ± 0.024) and MetS (0.010 ± 0.016; 0.006 ± 0.013), and both were reduced compared to controls. The transfer of non-esterified cholesterol, phospholipids and triacylglycerols to HDL was higher in MetS and T2DM than in controls (p < 0.01). Cholesteryl ester transfer and HDL size were equal in all groups. Results imply that MetS is equal to poorly controlled T2DM concerning the disturbances of plasma lipid metabolism examined here, and suggest that there are different thresholds for the insulin action on glucose and lipids. These findings highlight the magnitude of the lipid disturbances in MetS, and may have implications in the prevention of cardiovascular diseases.

Citing Articles

Developing a risk model for early diagnosis of metabolic syndrome in Chinese adults aged 40 years and above based on BMI/HDL-C: a cross-sectional study.

Liu Y, Wang X, Mu J, Gu Y, Zhou S, Ma X BMC Endocr Disord. 2024; 24(1):223.

PMID: 39448988 PMC: 11515612. DOI: 10.1186/s12902-024-01752-9.

References
1.
Cooper A . Hepatic uptake of chylomicron remnants. J Lipid Res. 1997; 38(11):2173-92. View

2.
Ford E . Risks for all-cause mortality, cardiovascular disease, and diabetes associated with the metabolic syndrome: a summary of the evidence. Diabetes Care. 2005; 28(7):1769-78. DOI: 10.2337/diacare.28.7.1769. View

3.
Maranhao R, Roland I, Hirata M . Effects of Triton WR 1339 and heparin on the transfer of surface lipids from triglyceride-rich emulsions to high density lipoproteins in rats. Lipids. 1990; 25(11):701-5. DOI: 10.1007/BF02544037. View

4.
Ginsberg H, Huang L . The insulin resistance syndrome: impact on lipoprotein metabolism and atherothrombosis. J Cardiovasc Risk. 2001; 7(5):325-31. DOI: 10.1177/204748730000700505. View

5.
Preiss D, Sattar N . Lipids, lipid modifying agents and cardiovascular risk: a review of the evidence. Clin Endocrinol (Oxf). 2008; 70(6):815-28. DOI: 10.1111/j.1365-2265.2008.03490.x. View