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. 2024 Oct 29;16(21):3674.
doi: 10.3390/nu16213674.

Using Genetics to Assess the Role of Acetate in Ischemic Heart Disease, Diabetes, and Sex-Hormone-Related Cancers: A Mendelian Randomization Study

Affiliations

Using Genetics to Assess the Role of Acetate in Ischemic Heart Disease, Diabetes, and Sex-Hormone-Related Cancers: A Mendelian Randomization Study

Jie V Zhao et al. Nutrients. .

Abstract

Background: Acetate, a short-chain fatty acid, has gained attention for its contrasting roles, with evidence suggesting it may offer cardiovascular protection but also promote cancer, particularly those involving sex hormones. However, these influences have been scarcely assessed in epidemiological research.

Objective: To investigate the relationship between acetate and ischemic heart disease (IHD), diabetes, and cancers related to sex hormones.

Methods: Mendelian randomization (MR) was used to assess potential causal effects, selecting genetic variants without linkage disequilibrium (r2 < 0.001) and with genome-wide significance for acetate (p < 5 × 10-8). These variants were applied to large genome-wide association studies (GWAS) for ischemic heart disease (IHD; up to 154,373 cases), diabetes (109,731 cases), and five sex-hormone-related cancers (breast, colorectal, prostate, ovarian, and endometrial cancers, ranging from 8679 to 122,977 cases). We employed various methods for analysis, including penalized inverse variance weighting (pIVW), inverse variance weighting, weighted mode, and weighted median.

Results: This study indicates that acetate may be associated with a lower risk of ischemic heart disease (IHD), with an odds ratio (OR) of 0.62 per standard deviation (SD) increase in acetate and a 95% confidence interval (CI) of 0.39 to 0.98. Additionally, acetate was linked to a higher breast cancer risk, with an OR of 1.26 and a 95% CI ranging from 1.08 to 1.46. This association remained robust across multiple sensitivity analyses.

Conclusions: Acetate, along with factors that influence its activity, may serve as possible targets for breast cancer treatment and possibly IHD, offering opportunities for new drug development.

Keywords: acetate; cancer; heart disease; short-chain fatty acid.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Associations of genetic instruments for acetate with ischemic heart disease and breast cancer.
Figure 2
Figure 2
The overall association of genetically predicted acetate with ischemic heart disease and diabetes using inverse variance weighting.
Figure 3
Figure 3
The sex-specific association of genetically predicted acetate with ischemic heart disease and diabetes.
Figure 4
Figure 4
The association of genetically predicted acetate with prostate cancer, breast cancer (including overall and ER+, ER- breast cancer), endometrial cancer, ovarian cancer, and colorectal cancer [30].
Figure 5
Figure 5
The overall association of genetically predicted acetate with lipids, glycemic traits, blood pressure, and body mass index.
Figure 6
Figure 6
The sex-specific association of genetically predicted acetate with lipids, glycemic traits, blood pressure, and body mass index.

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References

    1. Eckel R.H., Grundy S.M., Zimmet P.Z. The metabolic syndrome. Lancet. 2005;365:1415–1428. doi: 10.1016/S0140-6736(05)66378-7. - DOI - PubMed
    1. Buddeke J., Bots M.L., van Dis I., Visseren F.L., Hollander M., Schellevis F.G., Vaartjes I. Comorbidity in patients with cardiovascular disease in primary care: A cohort study with routine healthcare data. Br. J. Gen. Pract. 2019;69:e398–e406. doi: 10.3399/bjgp19X702725. - DOI - PMC - PubMed
    1. Moffett J.R., Puthillathu N., Vengilote R., Jaworski D.M., Namboodiri A.M. Acetate Revisited: A Key Biomolecule at the Nexus of Metabolism, Epigenetics, and Oncogenesis—Part 2: Acetate and ACSS2 in Health and Disease. Front. Physiol. 2020;11:580171. doi: 10.3389/fphys.2020.580171. - DOI - PMC - PubMed
    1. Dangana E.O., Omolekulo T.E., Areola E.D., Olaniyi K.S., Soladoye A.O., Olatunji L.A. Sodium acetate protects against nicotine-induced excess hepatic lipid in male rats by suppressing xanthine oxidase activity. Chem. Biol. Interact. 2020;316:108929. doi: 10.1016/j.cbi.2019.108929. - DOI - PubMed
    1. Bose S., Ramesh V., Locasale J.W. Acetate Metabolism in Physiology, Cancer, and Beyond. Trends Cell Biol. 2019;29:695–703. doi: 10.1016/j.tcb.2019.05.005. - DOI - PMC - PubMed

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