Marine Omega‐3 Supplementation and Cardiovascular Disease: An Updated Meta‐Analysis of 13 Randomized Controlled Trials Involving 127 477 Participants DOI Creative Commons
Yang Hu, Frank B. Hu, JoAnn E. Manson

et al.

Journal of the American Heart Association, Journal Year: 2019, Volume and Issue: 8(19)

Published: Sept. 30, 2019

Background Whether marine omega‐3 supplementation is associated with reduction in risk of cardiovascular disease (CVD) remains controversial. Methods and Results This meta‐analysis included study‐level data from 13 trials. The outcomes interest myocardial infarction, coronary heart (CHD) death, total CHD, stroke, CVD CVD, major vascular events. unadjusted rate ratios were calculated using a fixed‐effect meta‐analysis. A meta‐regression was conducted to estimate the dose–response relationship between dosage each prespecified outcome. During mean treatment duration 5.0 years, 3838 infarctions, 3008 CHD deaths, 8435 events, 2683 strokes, 5017 15 759 16 478 events documented. In analysis excluding REDUCE‐IT (Reduction Cardiovascular Events Icosapent Ethyl‐Intervention Trial), significantly lower infarction (rate ratio [RR] [95% CI]: 0.92 [0.86, 0.99]; P =0.020), death (RR 0.98]; =0.014), 0.95 [0.91, =0.008), 0.93 [0.88, =0.013), 0.97 [0.94, =0.015). Inverse associations for all strengthened after including while introducing statistically significant heterogeneity. Statistically linear relationships found analyses without REDUCE‐IT. Conclusions Marine lowers even exclusion Risk reductions appeared be linearly related dose.

Language: Английский

Omega-3 fatty acids for the primary and secondary prevention of cardiovascular disease DOI
Asmaa Abdelhamid, Tracey Brown, Julii Brainard

et al.

Cochrane library, Journal Year: 2018, Volume and Issue: unknown

Published: Nov. 30, 2018

Language: Английский

Citations

371

Updated Cardiovascular Prevention Guideline of the Brazilian Society of Cardiology - 2019 DOI Creative Commons
Dalton Bertolim Précoma, Gláucia Maria Moraes de Oliveira,

Antônio Felipe Simão

et al.

Arquivos Brasileiros de Cardiologia, Journal Year: 2019, Volume and Issue: unknown

Published: Jan. 1, 2019

Introducao A doenca cardiovascular (DCV) e a principal causa de morte no Brasil mundo, determinando aumento da morbidade incapacidade ajustadas pelos anos vida. Embora as taxas mortalidade disability-adjusted life year (DALY) padronizadas por idade estejam diminuindo Brasil, possivelmente como resultado politicas saude bem-sucedidas, o numero total destas esta aumentando principalmente devido ao envelhecimento adoecimento populacao. presenca dos fatores risco classicos (hipertensao, dislipidemia, obesidade, sedentarismo, tabagismo, diabetes [...]

Citations

367

Arachidonic Acid Metabolites in Cardiovascular and Metabolic Diseases DOI Open Access
Thomas Sonnweber, Alex Pizzini, Manfred Nairz

et al.

International Journal of Molecular Sciences, Journal Year: 2018, Volume and Issue: 19(11), P. 3285 - 3285

Published: Oct. 23, 2018

Lipid and immune pathways are crucial in the pathophysiology of metabolic cardiovascular disease. Arachidonic acid (AA) its derivatives link nutrient metabolism to immunity inflammation, thus holding a key role emergence progression frequent diseases such as obesity, diabetes, non-alcoholic fatty liver disease, We herein present synopsis AA human health, tissue homeostasis, immunity, explore metabolome diverse pathophysiological conditions diseases.

Language: Английский

Citations

355

The role of lipid metabolism in aging, lifespan regulation, and age‐related disease DOI Creative Commons
Adiv A. Johnson, Alexandra Stolzing

Aging Cell, Journal Year: 2019, Volume and Issue: 18(6)

Published: Sept. 27, 2019

Abstract An emerging body of data suggests that lipid metabolism has an important role to play in the aging process. Indeed, a plethora dietary, pharmacological, genetic, and surgical lipid‐related interventions extend lifespan nematodes, fruit flies, mice, rats. For example, impairment genes involved ceramide sphingolipid synthesis extends both worms flies. The overexpression fatty acid amide hydrolase or lysosomal lipase prolongs life Caenorhabditis elegans , while diacylglycerol enhances longevity C. Drosophila melanogaster . removal adipose tissue rats, increased expression apolipoprotein D survival flies mice. Mouse can be additionally extended by genetic deletion acyltransferase 1, treatment with steroid 17‐α‐estradiol, ketogenic diet. Moreover, phospholipase A2 receptor improves various healthspan parameters progeria mouse model. Genome‐wide association studies have found several variants associated human aging. epsilon 2 4 alleles E are extreme late‐onset neurodegenerative disease, respectively. In humans, blood triglyceride levels tend increase, lysophosphatidylcholine decrease age. Specific phospholipid profiles also been shown change age exceptional longevity. These suggest may improve lipids likely represent rich source biomarkers.

Language: Английский

Citations

342

Marine Omega‐3 Supplementation and Cardiovascular Disease: An Updated Meta‐Analysis of 13 Randomized Controlled Trials Involving 127 477 Participants DOI Creative Commons
Yang Hu, Frank B. Hu, JoAnn E. Manson

et al.

Journal of the American Heart Association, Journal Year: 2019, Volume and Issue: 8(19)

Published: Sept. 30, 2019

Background Whether marine omega‐3 supplementation is associated with reduction in risk of cardiovascular disease (CVD) remains controversial. Methods and Results This meta‐analysis included study‐level data from 13 trials. The outcomes interest myocardial infarction, coronary heart (CHD) death, total CHD, stroke, CVD CVD, major vascular events. unadjusted rate ratios were calculated using a fixed‐effect meta‐analysis. A meta‐regression was conducted to estimate the dose–response relationship between dosage each prespecified outcome. During mean treatment duration 5.0 years, 3838 infarctions, 3008 CHD deaths, 8435 events, 2683 strokes, 5017 15 759 16 478 events documented. In analysis excluding REDUCE‐IT (Reduction Cardiovascular Events Icosapent Ethyl‐Intervention Trial), significantly lower infarction (rate ratio [RR] [95% CI]: 0.92 [0.86, 0.99]; P =0.020), death (RR 0.98]; =0.014), 0.95 [0.91, =0.008), 0.93 [0.88, =0.013), 0.97 [0.94, =0.015). Inverse associations for all strengthened after including while introducing statistically significant heterogeneity. Statistically linear relationships found analyses without REDUCE‐IT. Conclusions Marine lowers even exclusion Risk reductions appeared be linearly related dose.

Language: Английский

Citations

338