Meng Xin, Shen Kailin, Fan Jiachen, Zhang Jingrui, Ma Jun, Li Xinyu, Wang Yonggong
School of Stomatology, Henan University, Kaifeng, Henan, China.
Department of Maxillofacial Surgery, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Medicine (Baltimore). 2025 Jul 25;104(30):e43601. doi: 10.1097/MD.0000000000043601.
This study aimed to investigate the potential causal relationship between lipid metabolism biomarkers and the risk of tongue cancer, providing a theoretical basis for future prevention and treatment strategies. A two-sample Mendelian randomization (MR) analysis was performed using large-scale genome-wide association study datasets to examine the causal relationship between 233 circulating metabolic markers and tongue cancer. Multiple MR methods were employed, including inverse-variance weighted, MR-Egger, weighted median, and Bayesian weighted MR. Sensitivity analyses were conducted to assess horizontal pleiotropy and heterogeneity, ensuring the robustness of the results. Genetically predicted higher levels of saturated fatty acids relative to total fatty acids, the ratio of phospholipids to total lipids in small very-low-density lipoproteins, and various cholesterol components in medium high-density lipoproteins (free cholesterol-to-total lipids, total cholesterol, and cholesterol esters in mHDL) were significantly associated with an increased risk of tongue cancer. Sensitivity analyses confirmed the stability and reliability of these associations. This study is the first to reveal a potential causal relationship between specific lipid metabolism biomarkers and tongue cancer. Notably, genetically elevated saturated fatty acids relative to total fatty acids ratios, cholesterol components in HDL (free cholesterol-to-total lipids, total cholesterol, and cholesterol esters in mHDL), and phospholipids to total lipids in small very-low-density lipoproteins were significantly associated with increased tongue cancer risk. Future research should focus on validating these findings in diverse populations and elucidating the underlying biological mechanisms, with the aim of developing early warning tools and potential intervention targets.
本研究旨在探讨脂质代谢生物标志物与舌癌风险之间的潜在因果关系,为未来的预防和治疗策略提供理论依据。使用大规模全基因组关联研究数据集进行了两样本孟德尔随机化(MR)分析,以检验233种循环代谢标志物与舌癌之间的因果关系。采用了多种MR方法,包括逆方差加权法、MR-Egger法、加权中位数法和贝叶斯加权MR法。进行了敏感性分析以评估水平多效性和异质性,确保结果的稳健性。遗传预测的相对于总脂肪酸的饱和脂肪酸水平升高、小极低密度脂蛋白中磷脂与总脂质的比率以及中高密度脂蛋白中的各种胆固醇成分(游离胆固醇与总脂质、总胆固醇以及中高密度脂蛋白中的胆固醇酯)与舌癌风险增加显著相关。敏感性分析证实了这些关联的稳定性和可靠性。本研究首次揭示了特定脂质代谢生物标志物与舌癌之间的潜在因果关系。值得注意的是,遗传上相对于总脂肪酸比率升高的饱和脂肪酸、高密度脂蛋白中的胆固醇成分(游离胆固醇与总脂质、总胆固醇以及中高密度脂蛋白中的胆固醇酯)以及小极低密度脂蛋白中磷脂与总脂质的比率与舌癌风险增加显著相关。未来的研究应集中在不同人群中验证这些发现并阐明潜在的生物学机制,以期开发预警工具和潜在的干预靶点。