Beverage consumption and facial skin aging: Evidence from Mendelian randomization analysis

孟德尔随机化 全基因组关联研究 单核苷酸多态性 混淆 多效性 遗传关联 观察研究 医学 荟萃分析 多元分析 遗传学 生物 内科学 基因型 基因 遗传变异 表型
作者
Xuanchen Liu,Xin Li,Jiguang Ma
出处
期刊:Journal of Cosmetic Dermatology [Wiley]
卷期号:23 (5): 1800-1807 被引量:1
标识
DOI:10.1111/jocd.16153
摘要

Abstract Background Observational studies have linked coffee, alcohol, tea, and sugar‐sweetened beverage (SSB) consumption to facial skin aging. However, confounding factors may influence these studies. The present two‐sample Mendelian randomization (MR) investigated the potential causal association between beverage consumption and facial skin aging. Methods The single‐nucleotide polymorphisms (SNPs) associated with coffee, alcohol, and tea intake were derived from the IEU project. The SSB‐associated SNPs were selected from a genome‐wide association study (GWAS). Data on facial skin aging were derived from the largest GWAS involving 16 677 European individuals. The inverse variance‐weighted (IVW) was the main MR analysis method, supplemented by other methods (MR‐Egger, weighted median, simple mode, and weighted mode). The MR‐Egger intercept analysis was used for sensitivity analysis. Moreover, we conducted a replication analysis using data from another GWAS dataset on coffee consumption to validate our findings. Results Four instrumental variables (IVs) sets were used to examine the causal association between beverage consumption (coffee, alcohol, tea, SSB) and facial skin aging. Our results revealed that genetically predicted higher coffee consumption reduced the risk of facial skin aging (OR: 0.852; 95% CI: 0.753–0.964; p = 0.011, IVW method). The sensitivity analysis confirmed the robustness of the findings, with no evidence of pleiotropy or heterogeneity. The results of replicated MR analysis on coffee consumption were consistent with the initial analysis (OR = 0.997; 95% CI = 0.996–0.999; p = 0.003, IVW method). Conclusions This study manifests that higher coffee consumption is significantly associated with a reduced risk of facial skin aging. These findings can offer novel strategies for identifying the underlying etiology of facial skin aging.
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