Lipid Accumulation Product Is Associated with Insulin Resistance, Lipid Peroxidation, and Systemic Inflammation in Type 2 Diabetic Patients.
10.3803/EnM.2014.29.4.443
- Author:
Parvin MIRMIRAN
1
;
Zahra BAHADORAN
;
Fereidoun AZIZI
Author Information
1. Nutrition and Endocrine Research Center, and Obesity Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
- Publication Type:Original Article
- Keywords:
Diabetes mellitus, type 2;
Lipid accumulation product;
Subclinical inflammation;
Oxidative stress
- MeSH:
Body Mass Index;
C-Reactive Protein;
Cardiovascular Diseases;
Cholesterol;
Cholesterol, HDL;
Diabetes Mellitus, Type 2;
Fasting;
Female;
Glucose;
Homeostasis;
Humans;
Inflammation*;
Insulin;
Insulin Resistance*;
Lipid Accumulation Product*;
Lipid Peroxidation*;
Lipoproteins;
Male;
Malondialdehyde;
Oxidative Stress;
Triglycerides
- From:Endocrinology and Metabolism
2014;29(4):443-449
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Lipid accumulation product (LAP) is a novel biomarker of central lipid accumulation related to risk of diabetes and cardiovascular disease. In this study, we assessed the association of LAP with glucose homeostasis, lipid and lipid peroxidation, and subclinical systemic inflammation in diabetic patients. METHODS: Thirty-nine male and 47 female type 2 diabetic patients were assessed for anthropometrics and biochemical measurements. LAP was calculated as [waist circumference (cm)-65]x[triglycerides (mmol/L)] in men, and [waist circumference (cm)-58]x[triglycerides (mmol/L)] in women. Associations of LAP with fasting glucose, insulin, insulin resistance index, lipid and lipoprotein levels, malondialdehyde, and high-sensitive C-reactive protein (hs-CRP) were assessed. RESULTS: Mean age and LAP index were 53.6+/-9.6 and 51.9+/-31.2 years, respectively. After adjustments for age, sex and body mass index status, a significant positive correlation was observed between LAP index and fasting glucose (r=0.39, P<0.001), and homeostasis model assessment of insulin resistance (r=0.31, P<0.05). After additional adjustment for fasting glucose levels, antidiabetic and antilipidemic drugs, the LAP index was also correlated to total cholesterol (r=0.45, P<0.001), high density lipoprotein cholesterol (HDL-C) levels (r=-0.29, P<0.05), triglycerides to HDL-C ratio (r=0.89, P<0.001), malondialdehyde (r=0.65, P<0.001), and hs-CRP levels (r=0.27, P<0.05). CONCLUSION: Higher central lipid accumulation in diabetic patients was related to higher insulin resistance, oxidative stress and systemic inflammation.