Abstract
Introduction: Although several mechanisms confirm the cardioprotective role of omega-3 fatty acids (n-3 PUFA), there is still controversy regarding its impact on cardiovascular outcomes. We hypothesized that the n-3 PUFA in erythrocytes membranes reflect better intake and metabolization of these fatty acids, allowing identify their cardiovascular benefits. Objective: To evaluate the association of the n-3 PUFA with cardiometabolic biomarkers and absolute cardiovascular risk. Methods: A crossectional study based on the baseline time of CARDIONUTRI clinical trial (n = 356) with individuals of both sexes (30-74 years) who showed at least one of the following risk factors: smoking, hypertension, dyslipidemias, diabetes mellitus or obesity, but without previous cardiovascular events, monitored by clinical evaluation and ECG. By direct interviews, information about demographic data, medication, blood pressure, diet, and physical activity were investigated by physician and dietician. After 12h of fasting, the lipid profile, lipoprotein sub fractions, LDL(-), glucose, HbA1c, insulin, HOMA-IR and inflammation biomarkers were analyzed by standard and validated methods. After lipid extraction from erythrocytes, fatty acids were analyzed by gas chromatography using internal (C17) and external (FAME 37) standard. The 10-years projection of absolute cardiovascular risk was estimated by the Framingham (FRS), Reynolds (RRS) and ACC/AHA 2013 risk scores. Association between fatty acids, biomarkers and cardiovascular risk scores were performed by linear and logistic regression models and factorial analysis (SPSS v.20.0 and Stata v.14.0). Results: Individuals with n-3 PUFA > 6.24% and n-6/n-3 ≤ 1.27 had less plasma non-HDL cholesterol, Apo B, TG, LDL(-) and highest LDL size. Regarding FRS, the total n-3 PUFA had association with lower cardiovascular risk (OR=0.811; IC95%=0.675- 0.976) and the membrane 1 model rich in n-6 was and poor in n-3 PUFA was associated with higher risk (OR=1.469; IC95%=1.056-2.043). Regarding RRS, the same membrane model was associated with higher risk (OR: 1.276; IC95%=1.010-1.612) while the opposite pattern was observed for membrane 2 model (rich in n-3 and poor in n-6 PUFA), had association with lower risk (OR=0,747; IC95%=0,589-0,948). Conclusion: High content of n-3 in erythrocyte membranes containing was associated with a lipid profile characterized by less plasma atherogenic lipoproteins, reduced TG and modified LDL. This profile was associated with reduced chance to be classified as moderate or higher cardiovascular risk by the Reynolds and Framingham Risk Scores.
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