Causality of Genetically Determined Monounsaturated Fatty Acids on Risk of Cardiovascular Disease: A Mendelian Randomization Study
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Background/Aim
The possible association between serum monounsaturated fatty acids (MUFAs) and the risk of cardiovascular diseases (CVDs) has been examined in observational studies, which indicate controversial findings. In the current study, we used the Mendelian randomization (MR) analysis to determine the causal relationship of genetically determined serum MUFAs with the risk of various CVD outcomes, including angina, atherosclerotic, ischemic heart disease (IHD), myocardial infarction (MI), and high blood pressure (BP).
Method
The summary statistics dataset on the genetic variants related to serum MUFAs was used from the published GWAS of European descent in UK Biobank participants (N=114,999). Genetic variants underlying angina, atherosclerotic, IHD, MI, and BP events were ascertained using a GWAS dataset of 461,880 (case= 14,828, control= 447,052), 463,010 (case= 12,171, control= 450,839), 361,194 (case= 20,857, control= 340,337), 462,933 (case= 10,616, control= 452,317), and 461,880 (case= 124,227, control= 337,653) European descent participants from the UK Biobank, respectively.
Results
Our results showed that MUFAs were associated with angina [OR IVW = 1.005, 95% CI: 1.003– 1.007, p = <0.001; Cochran’s Q=23.89, p=0.717, I 2 =0.0%; Egger intercept= -0.0003, p=0.289], atherosclerotic [OR IVW = 1.005, 95% CI: 1.003–1.007, p = <0.001; Cochran’s Q=42.71, p=0.078, I 2 =27.4%; Egger intercept= -0.0004, p=0.146], IHD [OR IVW = 1.004, 95% CI: 1.001–1.007, p = 0.005; Cochran’s Q=42.75, p=0.172, I 2 =18.1%; Egger intercept= -0.0001, p=0.827], MI [OR IVW = 1.001, 95% CI: 0.999– 1.003, p = 0.199; Cochran’s Q= 23.03, p=0.631, I 2 =0.0%; Egger intercept= -0.0003, p=0.196], and BP [OR WM = 1.008, 95% CI: 1.001–1.015, p = 0.022; Cochran’s Q= 52.87, p=0.015, I 2 = 37.6%; Egger intercept= 0.0002, p=0.779]. These results remained consistent using different Mendelian randomization methods and sensitivity analyses.
Conclusion
In the present MR analysis, serum MUFA levels were associated with the risk of angina, atherosclerotic, IHD, MI, and BP. These findings prompt significant questions about the function of MUFAs in the progression of CVD events. Further research is required to elucidate the connections between MUFAs and CVD to contribute to health policy decisions in reducing CVD risk.
