Hungarian Research Network University of Debrecen, Public Health Research Group, Department of Public Health and Epidemiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Department of Public Health and Epidemiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Int J Mol Sci. 2024 Aug 6;25(16):8587. doi: 10.3390/ijms25168587.
Polymorphisms in the cholesteryl ester transfer protein () gene are known to be strongly associated with increased cardiovascular risk, primarily through their effects on the lipid profile and consequently on atherosclerotic risk. The acute heart rate response (AHRR) to physical activity is closely related to individual cardiovascular health. This study aimed to investigate the effect of gene polymorphisms on AHRR. Our analysis examines the association of five single nucleotide polymorphisms (SNPs; rs1532624, rs5882, rs708272, rs7499892, and rs9989419) and their haplotypes (H) in the gene with AHRR in 607 people from the Hungarian population. Individual AHRR in the present study was assessed using the YMCA 3-min step test and was estimated as the difference between resting and post-exercise heart rate, i.e., delta heart rate (ΔHR). To exclude the direct confounding effect of the gene on the lipid profile, adjustments for TG and HDL-C levels, next to conventional risk factors, were applied in the statistical analyses. Among the examined five SNPs, two showed a significant association with lower ΔHR (rs1532624-C: B = -8.41, < 0.001; rs708272-G: B = -8.33, < 0.001) and reduced the risk of adverse AHRR (rs1532624-C: OR = 0.44, = 0.004; rs708272-G: OR = 0.43, = 0.003). Among the ten haplotypes, two showed significant association with lower ΔHR (H3-CAGCA: B = -6.81, = 0.003; H9-CGGCG: B = -14.64, = 0.015) and lower risk of adverse AHRR (H3-CAGCA: OR = 0.58, = 0.040; H9-CGGCG: OR = 0.05, = 0.009) compared to the reference haplotype (H1-AGACG). Our study is the first to report a significant association between gene polymorphisms and AHRR. It also confirms that the association of the gene with cardiovascular risk is mediated by changes in heart rate in response to physical activity, in addition to its effect on lipid profile.
载脂蛋白酯酶基因()中的多态性与心血管风险增加密切相关,主要通过对血脂谱的影响,进而影响动脉粥样硬化风险。对体力活动的急性心率反应(AHRR)与个体心血管健康密切相关。本研究旨在探讨基因多态性对 AHRR 的影响。我们的分析研究了匈牙利人群中 607 人基因中的五个单核苷酸多态性(SNPs;rs1532624、rs5882、rs708272、rs7499892 和 rs9989419)及其单倍型(H)与 AHRR 的关联。本研究中个体 AHRR 使用 YMCA 3 分钟台阶测试进行评估,估计为静息和运动后心率之间的差异,即差心率(ΔHR)。为了排除基因对血脂谱的直接混杂影响,除了常规危险因素外,还对 TG 和 HDL-C 水平进行了调整,以进行统计分析。在所检查的五个 SNP 中,有两个 SNP 与较低的ΔHR 显著相关(rs1532624-C:B = -8.41,<0.001;rs708272-G:B = -8.33,<0.001),并降低了不良 AHRR 的风险(rs1532624-C:OR = 0.44,= 0.004;rs708272-G:OR = 0.43,= 0.003)。在十个单倍型中,有两个与较低的ΔHR 显著相关(H3-CAGCA:B = -6.81,= 0.003;H9-CGGCG:B = -14.64,= 0.015)和较低的不良 AHRR 风险(H3-CAGCA:OR = 0.58,= 0.040;H9-CGGCG:OR = 0.05,= 0.009)与参考单倍型(H1-AGACG)相比。本研究首次报道了载脂蛋白酯酶基因多态性与 AHRR 之间的显著关联。它还证实了基因与心血管风险的关联是通过对体力活动的心率反应的变化介导的,除了对血脂谱的影响外。