1. Is Lipid Accumulation Product Associated with an Atherogenic Lipoprotein Profile in Brazilian Subjects?
- Author
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Nágila Raquel Teixeira Damasceno, Caroline Pappiani, Flávia de Conti Cartolano, Maria Camila Prupper de Freitas, Antônio Augusto Ferreira Carioca, and Antônio Martins Figueiredo Neto
- Subjects
Fatores de Risco ,Blood Glucose ,Male ,Dislipidemias ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Apolipoprotein B ,Doenças Cardiovasculares ,medicine.medical_treatment ,Fibrate ,Fatty Acids, Nonesterified ,030204 cardiovascular system & hematology ,chemistry.chemical_compound ,0302 clinical medicine ,Reference Values ,Risk Factors ,Insulin ,Anthropometry ,biology ,Lipoproteínas LDL ,Middle Aged ,Lipoproteins, LDL ,Cardiovascular Diseases ,Female ,lipids (amino acids, peptides, and proteins) ,Cardiology and Cardiovascular Medicine ,Lipoproteins, HDL ,Brazil ,Adult ,medicine.medical_specialty ,medicine.drug_class ,Resistência à Insulina ,030209 endocrinology & metabolism ,Risk Assessment ,03 medical and health sciences ,Sex Factors ,NEFA ,Insulin resistance ,Internal medicine ,medicine ,Humans ,Adults ,Adultos ,Lipoproteínas HDL ,Aged ,Apolipoproteins B ,Dyslipidemias ,Apolipoprotein A-I ,Cholesterol ,business.industry ,Cholesterol, HDL ,Cholesterol, LDL ,Original Articles ,Atherosclerosis ,medicine.disease ,Endocrinology ,chemistry ,lcsh:RC666-701 ,biology.protein ,Insulin Resistance ,Epidemiologic Methods ,Lipid Accumulation Product ,business ,Biomarkers ,Lipoprotein - Abstract
Background: Lipid accumulation product (LAP), a simple and low-cost tool, is a novel biomarker of central lipid accumulation and represents a potential surrogate marker for atherogenic lipoprotein profile. However, its association with lipoprotein subfractions has not been described in the literature. Objective: To determine whether LAP index could be used as a marker of low- and high-density lipoprotein (LDL and HDL) size in Brazilian individuals. Methods: This cross-sectional study included patients (n = 351) of both sexes and age between 30-74 years. Clinical and sociodemographic data and family history of diseases were evaluated. Lipoprotein size, and levels of total cholesterol (TC), lipoproteins, apolipoprotein AI and B (APO AI/APO B), glucose, insulin, insulin resistance index (HOMA-IR) and non-esterified fatty acids (NEFA) were assessed in blood samples. LAP was calculated by the formulas [(waist circumference[cm]-58) × (triglycerides[mmol/L]) for women and (waist circumference [cm]-65) × (triglycerides [mmol/L]) for men]. The association between LAP and metabolic parameters were tested by linear trend (general linear model, GLM test) before and after multiple adjustments for potential confounders (sex, age, smoking, statin, fibrate, and hypoglycemic drugs) at significant level p < 0.05. Results: LAP was positively associated with TC, APO B, NEFA, glucose, insulin and HOMA-IR values, and negatively associated with HDL-C. Higher central lipid accumulation was corelated with higher percentage of intermediate HDL and of small LDL and HDL and less amount of large HDL. LDL size was also reduced in greater LAP index values. The negative impact of LAP was maintained after adjustment for multiple variables. Conclusion: LAP was robustly associated with atherogenic profile of lipoprotein subfractions, independently of multiple confounders.
- Published
- 2018