Is Lipid Accumulation Product Associated with an Atherogenic Lipoprotein Profile in Brazilian Subjects?

Autor: Nágila Raquel Teixeira Damasceno, Caroline Pappiani, Flávia de Conti Cartolano, Maria Camila Prupper de Freitas, Antônio Augusto Ferreira Carioca, Antônio Martins Figueiredo Neto
Jazyk: angličtina
Rok vydání: 2018
Předmět:
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
Zdroj: Arquivos Brasileiros de Cardiologia v.110 n.4 2018
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Arquivos Brasileiros de Cardiologia, Vol 110, Iss 4, Pp 339-347
Popis: 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.
Databáze: OpenAIRE