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PPARA和EPAS1基因单核苷酸多态性与中国青年男性高原食欲减退的关联

Association Between Single Nucleotide Polymorphisms in PPARA and EPAS1 Genes and High-Altitude Appetite Loss in Chinese Young Men.

作者信息

Pan Wenxu, Liu Chuan, Zhang Jihang, Gao Xubin, Yu Shiyong, Tan Hu, Yu Jie, Qian Dehui, Li Jiabei, Bian Shizhu, Yang Jie, Zhang Chen, Huang Lan, Jin Jun

机构信息

Department of Cardiology, Xinqiao Hospital, Army Medical University (The Third Military Medical University), Chongqing, China.

Institute of Cardiovascular Diseases, Xinqiao Hospital, Army Medical University (The Third Military Medical University), Chongqing, China.

出版信息

Front Physiol. 2019 Feb 4;10:59. doi: 10.3389/fphys.2019.00059. eCollection 2019.

Abstract

Appetite loss is a common symptom that occurs in high altitude (HA) for lowlanders. Previous studies indicated that hypoxia is the initiating vital factor of HA appetite loss. , and play important roles in hypoxic responses. We aimed to explore the association of these hypoxia-related gene polymorphisms with HA appetite loss. In this study, we enrolled 416 young men who rapidly ascended to Lhasa (3700 m) from Chengdu (<500m) by plane. , and were genotyped by MassARRAY. Appetite scores were measured to identify HA appetite loss. Logistic regression and multiple genetic models were tested to evaluate the association between the single nucleotide polymorphisms (SNPs) and risk of HA appetite loss in crude and adjusted (age and SaO) analysis. Subsequently, Haploview software was used to analyze the linkage disequilibrium (LD), haplotype construction and the association of diverse haplotypes with the risk of HA appetite loss. Our results revealed that allele "A" in rs4253747 was significantly associated with the increased risk of HA appetite loss. Codominant, dominant, recessive, and log-additive models of rs4253747 showed the increased risk of HA appetite loss in the crude and adjusted analysis. However, only dominant, overdominant, and log-additive models of rs6756667 showed decreased risk of HA appetite loss in the crude and adjusted analysis. Moreover, the results from haplotype-based test showed that the rs7292407-rs6520015 haplotype "AC" was associated with HA appetite loss in the crude analysis rather than the adjusted analysis. In this study, we first established the association of SNPs in (rs4253747) and (rs6756667) genes with susceptibility to HA appetite loss in Han Chinese young men. These findings provide novel insights into understanding the mechanisms involved in HA appetite loss.

摘要

食欲减退是低landers在高海拔地区(HA)常见的症状。以往研究表明,缺氧是HA食欲减退的起始关键因素。 , 和 在缺氧反应中起重要作用。我们旨在探讨这些缺氧相关基因多态性与HA食欲减退的关联。在本研究中,我们招募了416名从成都(<500米)乘飞机迅速升至拉萨(3700米)的年轻男性。 , 和 通过MassARRAY进行基因分型。测量食欲评分以确定HA食欲减退情况。在粗分析和校正分析(年龄和SaO)中,采用逻辑回归和多种遗传模型来评估单核苷酸多态性(SNP)与HA食欲减退风险之间的关联。随后,使用Haploview软件分析连锁不平衡(LD)、单倍型构建以及不同单倍型与HA食欲减退风险的关联。我们的结果显示,rs4253747中的等位基因“A”与HA食欲减退风险增加显著相关。rs4253747的共显性、显性、隐性和对数加性模型在粗分析和校正分析中均显示HA食欲减退风险增加。然而,只有rs6756667的显性、超显性和对数加性模型在粗分析和校正分析中显示HA食欲减退风险降低。此外,基于单倍型的测试结果表明,rs7292407 - rs6520015单倍型“AC”在粗分析而非校正分析中与HA食欲减退相关。在本研究中,我们首次在汉族年轻男性中建立了 (rs4253747)和 (rs6756667)基因中的SNP与HA食欲减退易感性的关联。这些发现为理解HA食欲减退所涉及的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/6369186/e28e4f6f61ed/fphys-10-00059-g001.jpg

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