Department of Genetics, Franklin College of Arts and Sciences, University of Georgia, Athens, GA, United States.
Department of Epidemiology and Biostatistics, College of Public Health, University of Georgia, Athens, GA, United States.
Am J Clin Nutr. 2024 Sep;120(3):540-549. doi: 10.1016/j.ajcnut.2024.07.009. Epub 2024 Jul 15.
Dyslipidemia is a well-known risk factor for cardiovascular disease, the leading cause of mortality worldwide. Although habitual intake of fish oil is associated with cardioprotective effects through triglyceride reduction, the interactions of fish oil with the genetic predisposition to dysregulated lipids remain elusive.
We examined whether fish oil supplementation modifies the association between genetically predicted and observed concentrations of total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides.
A total of 441,985 participants with complete genetic and phenotypic data from the UK Biobank were included. Polygenic scores (PGS) of the 4 lipids were calculated in participants of diverse ancestries. For each lipid, multivariable linear regression models were used to assess if fish oil supplementation modified the association between PGS and the observed circulating concentration, with adjustment for relevant covariates.
Fish oil supplementation attenuates the associations between genetically predicted and observed circulating concentrations of total cholesterol, LDL cholesterol, and triglycerides while accentuating the corresponding association for HDL cholesterol among 424,090 participants of European ancestry. Consistent significant findings were obtained using PGS calculated based on multiple genome-wide association studies or alternative PGS methods. For triglycerides, each standard deviation (SD) increment in PGS is associated with 0.254 [95% confidence interval (CI): 0.248, 0.259] SD increase in the observed concentration among European-ancestry participants who reported fish oil usage. In contrast, a stronger association was observed in nonusers (0.267; 95% CI: 0.263, 0.270). Consistently, we showed that fish oil significantly attenuates the association between genetically predicted and observed concentrations of triglycerides in African-ancestry participants.
Fish oil supplementation attenuates the association between genetically predicted and observed circulating concentrations of total cholesterol, LDL cholesterol, and triglycerides while accentuating the corresponding association for HDL cholesterol in individuals of European ancestry. Further research is needed to understand the clinical implications of these findings.
血脂异常是心血管疾病的一个众所周知的危险因素,也是全球范围内导致死亡的主要原因。尽管习惯性摄入鱼油可通过降低甘油三酯来起到心脏保护作用,但鱼油与血脂失调的遗传易感性之间的相互作用仍不清楚。
我们研究了鱼油补充是否会改变遗传预测和观察到的总胆固醇、低密度脂蛋白(LDL)胆固醇、高密度脂蛋白(HDL)胆固醇和甘油三酯浓度之间的关联。
共纳入来自英国生物库的 441985 名具有完整遗传和表型数据的参与者。在不同血统的参与者中计算了 4 种脂质的多基因评分(PGS)。对于每种脂质,采用多变量线性回归模型来评估鱼油补充是否改变了 PGS 与观察到的循环浓度之间的关联,同时调整了相关协变量。
在 424090 名欧洲血统的参与者中,鱼油补充减弱了遗传预测和观察到的循环总胆固醇、LDL 胆固醇和甘油三酯浓度之间的关联,同时增强了相应的 HDL 胆固醇关联。使用基于多个全基因组关联研究或替代 PGS 方法计算的 PGS 得到了一致的显著发现。对于甘油三酯,在报告使用鱼油的欧洲血统参与者中,PGS 的每一个标准差(SD)增加与观察到的浓度增加 0.254[95%置信区间(CI):0.248,0.259]SD。相比之下,在未使用者中观察到更强的关联(0.267;95%CI:0.263,0.270)。一致地,我们表明鱼油显著减弱了非洲血统参与者中遗传预测和观察到的甘油三酯浓度之间的关联。
在欧洲血统的个体中,鱼油补充减弱了遗传预测和观察到的循环总胆固醇、LDL 胆固醇和甘油三酯浓度之间的关联,同时增强了 HDL 胆固醇的相应关联。需要进一步的研究来了解这些发现的临床意义。