Causal Relationships Between High-Altitude Adaptation, Metabolic Traits, and Tumors: Insights from Mendelian Randomization

孟德尔随机化 生物 遗传学 孟德尔遗传 计算生物学 疾病 遗传变异 生物信息学 梅德林 进化生物学 医学 上位性 全基因组关联研究 因果关系(物理学) 遗传变异 遗传遗传 遗传数据 遗传倾向 基因 多效性
作者
Xingkai Zhang,Liang He,Kai Li,Wen Li,Li Wang,Ling Chen,Qing Shi
出处
期刊:High Altitude Medicine & Biology [Mary Ann Liebert, Inc.]
卷期号:27 (1): 23-32
标识
DOI:10.1177/15578682251382795
摘要

Zhang, Xingkai, Liang He, Kai Li, Wen Li, Li Wang, Ling Chen, and Qinghai Shi. Causal relationships between high-altitude adaptation, metabolic traits, and tumors: insights from Mendelian randomization. High Alt Med Biol. 27:23–32, 2026. Background and Objectives: Previous studies suggest that high-altitude adaptation (HAA) and metabolic traits in high-altitude populations correlate with tumor risk, but causal mechanisms remain unclear. This Mendelian randomization (MR) study investigated genetic links between HAA, metabolic traits, and tumor susceptibility while exploring potential mediation effects. Methods: Genome-wide association studies data for HAA, metabolic traits, and tumors were sourced from public databases. Inverse variance weighting served as the primary analytical method, supplemented by weighted mode, MR-Egger, and weighted median. Sensitivity analyses and two-step MR (TSMR) assessed robustness and mediation pathways. Results: We identified a potential association between HAA and a decreased risk of pancreatic cancer (odds ratio [OR] = 8.94e-8, p = 0.011) and cervical cancer (OR = 8.04e-6, p = 0.005). In contrast, HAA showed a potential link to an increased risk of esophageal cancer (OR = 3230.25, p = 0.03) and hepatocellular carcinoma (OR = 2080.07, p = 0.015). Several metabolic traits, particularly platelet-related indices, were identified as potentially associated with tumorigenesis. However, although possible mediating pathways were suggested, no metabolic trait demonstrated a statistically significant mediating effect. Conclusion: These findings highlight HAA’s complex role in tumor susceptibility and provide a genetic framework for understanding tumor disparities in high-altitude regions.
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