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Observational analysis links fish oil supplements to genetic variants affecting fatty acid traits in UK Biobank

Observational analysis links fish oil supplements to genetic variants affecting fatty acid traits in…
Photo by Nathan Rimoux / Unsplash
Key Takeaway
Note that this observational analysis identifies associations between fish oil supplements and genetic variants affecting fatty acid traits.

This publication is an observational analysis utilizing a subset of the UK Biobank comprising 200,478 participants. The study investigated the relationship between fish oil supplements (FOS) and genetic variants (vQTLs) regarding 14 plasma polyunsaturated fatty acid (PUFA) and monounsaturated fatty acid (MUFA) phenotypes. No specific follow-up duration or setting details were reported in the source material.

The primary findings highlighted the identification of 172 vQTL-trait pairs across all 14 traits at genome-wide significance, defined as p < 5.0 x 10-8. These results involved 46 non-overlapping loci with an average of 12 vQTLs per trait. Additionally, six significant interaction signals were observed in DHA, DHA%, Omega-3, Omega-3%, LA, and the Omega-6/Omega-3 ratio around the FADS1/2, ZPR1, and SUGP1/TM6SF2 genes.

The authors explicitly note that this is an observational study, meaning associations do not imply causation. No adverse events, tolerability data, or discontinuations were reported. Consequently, the practice relevance remains uncertain, and clinicians should interpret these genetic and supplement associations with caution rather than as evidence for therapeutic efficacy.

Study Details

Sample sizen = 24
EvidenceLevel 5
PublishedApr 2026
View Original Abstract ↓
Gene-environment interactions (GEI) contribute to circulating polyunsaturated fatty acid (PUFA) and monounsaturated fatty acid (MUFA) profiles. GEI may partly explain differences in trait variance across genotype groups. To identify GEI for circulating unsaturated fatty acids, we adopted a two-stage strategy. First, we detected quantitative trait loci associated with trait variance (vQTLs). Second, we tested these vQTLs for interaction with fish oil supplements (FOS). We performed genome-wide vQTL screens for 14 plasma PUFA and MUFA phenotypes in a UK Biobank subset of 200,478 participants. At the genome-wide significance threshold (p < 5.0 x 10-8), we identified 172 vQTL-trait pairs across all 14 traits, and 16 of these vQTLs had no marginal genetic effect on the corresponding trait. We found 46 non-overlapping loci across all phenotypes, with an average of 12 vQTLs per trait. Omega-6% and PUFA% had the most independent vQTLs (N = 24) while DHA% and Omega-3% had the least (N = 1 and 2, respectively). For each of the 172 vQTL-trait pairs, we tested the interaction effect of the vQTL with FOS on the corresponding trait. We found six significant interaction signals in DHA, DHA%, Omega-3, Omega-3%, LA, and Omega-6/Omega-3 ratio around the FADS1/2, ZPR1, and SUGP1/TM6SF2 genes. Our results provide a comprehensive resource of vQTLs and gene-FOS interactions shaping the circulating levels of unsaturated fatty acids.
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