Department of Molecular Biology and Genetics, School of Biomedicine, MNUMS, Ulaanbaatar, Mongolia.
Department of Biochemistry, School of Medicine, International University of Health and Welfare, Narita, Japan.
Int J Chron Obstruct Pulmon Dis. 2021 Oct 18;16:2857-2868. doi: 10.2147/COPD.S320841. eCollection 2021.
Chronic obstructive pulmonary disease (COPD) is a multifactorial disorder which is affected by external and internal risk factors. People with no external risk factors may be significantly affected and develop pulmonary disease. The study aimed to define gene-gene and gene-environmental effects on COPD.
A case control study involved 181 COPD patients and 292 healthy individuals, with peripheral blood sampling and adequate questionnaires. Genotyping was done with various types of PCR design for (null del), (null del), (rs2234922 and rs1051740), (rs1695 and rs1138272), (rs1051730 and rs12914385), (rs16969968 and rs17486278), and (rs1799895 and rs699473) gene polymorphisms. Gene-gene and gene-environmental interactions were investigated using multidimensional regression analysis.
Frequency of risk alleles of rs1051730 (p = 0.001), rs16969968 (p <0.001), and rs1799895 (p <0.001) polymorphisms were significant in univariate analysis. For gene-gene interaction, null, rs1051730, rs16969968, and rs1799895 polymorphisms independently contributed to risk of COPD and any combinations of the risk genotypes have a higher risk of disease. A cumulative effect of the four risk polymorphisms increased the risk of COPD for the smoking index (cOR = 13.6, p <0.001), cigarettes per day (cOR = 32.08, p <0.01), nicotine dependence (cOR = 12.0, p <0.01), and smoking status (cOR = 17.02, p <0.01) for gene-environmental interaction.
Several pivotal genes showed distinct effects for COPD, and some synergistic effects affected the disease progression. The development of COPD was synergistically increased with gene-gene and gene-environmental risk factors.
慢性阻塞性肺疾病(COPD)是一种受多种内外因素影响的多因素疾病。没有外在风险因素的人可能会受到显著影响并患上肺部疾病。本研究旨在确定 COPD 的基因-基因和基因-环境效应。
一项病例对照研究纳入了 181 名 COPD 患者和 292 名健康对照者,进行外周血采样和充分的问卷调查。采用各种类型的 PCR 设计对 (null del)、(null del)、(rs2234922 和 rs1051740)、(rs1695 和 rs1138272)、(rs1051730 和 rs12914385)、(rs16969968 和 rs17486278) 和 (rs1799895 和 rs699473) 基因多态性进行基因分型。采用多维回归分析研究基因-基因和基因-环境相互作用。
rs1051730(p=0.001)、rs16969968(p<0.001)和 rs1799895(p<0.001)多态性的风险等位基因频率在单因素分析中均有显著差异。对于基因-基因相互作用,null、rs1051730、rs16969968 和 rs1799895 多态性独立导致 COPD 发病风险增加,任何风险基因型的组合均具有更高的疾病风险。四种风险多态性的累积效应增加了吸烟指数(cOR=13.6,p<0.001)、每天吸烟量(cOR=32.08,p<0.01)、尼古丁依赖(cOR=12.0,p<0.01)和吸烟状况(cOR=17.02,p<0.01)的 COPD 发病风险。
几个关键基因对 COPD 有明显影响,一些协同作用影响疾病进展。COPD 的发展是基因-基因和基因-环境危险因素协同增加的结果。