Monocyte transcriptomic profile following EPA and DHA supplementation in men and women with low-grade chronic inflammation

• Published in: Atherosclerosis Vol. 388; p. 117407
• Main Authors: So, Jisun, Wu, Dayong, Tai, Albert K., Lichtenstein, Alice H., Matthan, Nirupa R., Lamon-Fava, Stefania
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.01.2024
• Subjects: Dietary Supplements; Docosahexaenoic Acids; Double-Blind Method; Eicosapentaenoic Acid - therapeutic use; Fatty Acids, Omega-3; Female; Gene Expression Profiling; Humans; Inflammation; Macrophages; Male; Monocytes; Omega-3 fatty acids; Specialized pro-resolving lipid mediators; Transcriptome; Transcriptomics; Monocytes; Macrophages; Transcriptomics; Specialized pro-resolving lipid mediators; Omega-3 fatty acids
• ISSN: 0021-9150; 1879-1484; 1879-1484
• DOI: 10.1016/j.atherosclerosis.2023.117407

Recent data indicate considerable variability in response to very long chain omega-3 fatty acid supplementation on cardiovascular disease risk. This inconsistency may be due to differential effects of EPA vs DHA and/or sex-specific responses. Sixteen subjects (eight men and eight women) 50–75 y and with low-grade chronic inflammation participated in a randomized controlled crossover trial comparing 3 g/d EPA, 3 g/d DHA, and placebo (3 g/d high oleic acid sunflower oil). Blood monocytes were isolated at the end of each phase for RNA-sequencing. Sex dimorphism in monocyte gene expression was observed, therefore, data for men and women were analyzed separately. 1088 genes were differentially expressed in men and 997 in women (p < 0.05). In both men and women, EPA and DHA repressed genes involved in protein turnover and mitochondrial energy metabolism, relative to placebo. In men only, EPA and DHA upregulated genes related to wound healing and PPARα activation. In women only, EPA and DHA activated genes related to ER stress response. Relative to DHA, EPA resulted in lower expression of genes involved in inflammatory processes in men, and lower expression of genes involved in ER stress response in women. EPA and DHA supplementation elicited both similar and differential effects on monocyte transcriptome, some of which were sex specific. The observed variability in response to EPA and DHA in men and women could in part explain the conflicting results from previous cardiovascular clinical trials using omega-3 fatty acids. [Display omitted] •EPA and DHA have shared and differential effects on monocyte gene expression.•The changes in monocyte gene expression caused by EPA and DHA are sex-specific.•EPA, vs DHA, lowers inflammatory pathways in men and ER stress pathways in women.