Genetically determined circulating micronutrients and the risk of nonalcoholic fatty liver disease
- PMID: 38212362
- PMCID: PMC10784479
- DOI: 10.1038/s41598-024-51609-3
Genetically determined circulating micronutrients and the risk of nonalcoholic fatty liver disease
Abstract
Evidence from epidemiological literature on the association of circulating micronutrients with risk of nonalcoholic fatty liver disease (NAFLD) is inconsistent. We aimed to elucidate the causal relationships using Mendelian randomization (MR). Single-nucleotide polymorphisms associated with 14 circulating micronutrients (β-carotene, calcium, copper, folate, iron, magnesium, phosphorus, selenium, vitamin B6, B12, C, D, K1 and zinc) were employed as instrumental variables. Summary level data for NAFLD were obtained from a genome-wide association study (GWAS) meta-analysis of 8434 cases and 770,180 controls (discovery stage) and another two datasets including 1483 NAFLD cases and 17,781 controls (replication stage 1) and 2134 NAFLD cases and 33,433 controls (replication stage 2). Inverse variance-weighted method (IVW) was used as primary analysis, supplemented with a series of sensitivity analysis. Genetically predicted higher β‑carotene levels were suggestively associated with reduced NAFLD risk [odds ratio (OR) 0.81, 95% confidence interval (CI) 0.66-0.99; P = 0.047], whereas the association did not survive the false discovery rates (FDR) correction (PFDR = 0.164). Genetically predicted circulating iron (OR 1.16, 95% CI 1.05-1.29; P = 0.006, PFDR = 0.028), selenium (OR 1.11, 95% CI 1.03-1.20; P = 0.005, PFDR = 0.028) and vitamin B12 (OR 1.08, 95% CI 1.03-1.13; P = 0.002, PFDR = 0.028) were significantly associated with increased risk of NAFLD. Moreover, the findings were consistent in individual datasets (Pheterogeneity > 0.05) and confirmed in sensitivity analysis. Our study provided evidence that circulating iron, selenium and vitamin B12 might be causally linked to the risk of NAFLD, which deserves further exploration of the potential biological mechanism.
© 2024. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
Figures
![Figure 1](https://www.ncbi.nlm.nih.gov/pmc/articles/instance/10784479/bin/41598_2024_51609_Fig1_HTML.gif)
![Figure 2](https://www.ncbi.nlm.nih.gov/pmc/articles/instance/10784479/bin/41598_2024_51609_Fig2_HTML.gif)
Similar articles
-
Iron, Copper, and Selenium: Cancer's Thing for Redox Bling.Cold Spring Harb Perspect Med. 2024 Apr 1;14(4):a041545. doi: 10.1101/cshperspect.a041545. Cold Spring Harb Perspect Med. 2024. PMID: 37932129 Review.
-
Unraveling the link between dietary factors and cardiovascular metabolic diseases: Insights from a two-sample Mendelian Randomization investigation.Heart Lung. 2024 Jan-Feb;63:72-77. doi: 10.1016/j.hrtlng.2023.09.012. Epub 2023 Oct 10. Heart Lung. 2024. PMID: 37826923 Review.
-
Investigating Causal Associations of Circulating Micronutrients Concentrations with the Risk of Lung Cancer: A Mendelian Randomization Study.Nutrients. 2022 Oct 31;14(21):4569. doi: 10.3390/nu14214569. Nutrients. 2022. PMID: 36364831 Free PMC article.
-
Diet-derived antioxidants and nonalcoholic fatty liver disease: a Mendelian randomization study.Hepatol Int. 2023 Apr;17(2):326-338. doi: 10.1007/s12072-022-10443-3. Epub 2022 Nov 10. Hepatol Int. 2023. PMID: 36352064
-
Genetically predicted circulating concentrations of micronutrients and risk of breast cancer: A Mendelian randomization study.Int J Cancer. 2021 Feb 1;148(3):646-653. doi: 10.1002/ijc.33246. Epub 2020 Aug 25. Int J Cancer. 2021. PMID: 32761610 Free PMC article.
References
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical