Kim Jung-Sun, Cho Jung Rae, Park Sungha, Shim Jaemin, Kim Jin-Bae, Cho Deok-Kyu, Shin Hyun-Joon, Park Chan Mi, Ko Young-Guk, Ha Jong-Won, Choi Donghoon, Rim Se-Joong, Jang Yangsoo, Chung Namsik
Division of Cardiology, Yonsei University College of Medicine, Seoul, Korea.
Cardiovascular Genome Center, Yonsei Cardiovascular Center, Yonsei University College of Medicine, Seoul, Korea.
Yonsei Med J. 2007 Jun 30;48(3):389-395. doi: 10.3349/ymj.2007.48.3.389.
Hypertensive response to exercise (HRE) is known to be an adverse prognostic factor for future cardiovascular events and may be associated to endothelial dysfunction. Previous studies regarding endothelial nitric oxide synthase (eNOS) Glu298Asp polymorphism focused upon its relation to hypertension. In this study, we hypothesize that the polymorphism may be associated with inherent difference in endothelial response to exercise.
Two hundred sixty nine patients who underwent treadmill test were enrolled in this study; 77 patients (mean age 55.8 +/- 9.4 years) had hypertensive response (peak systolic BP of > or = 210 mmHg in men and > or = 190 mmHg in women). Pulse wave velocity (PWV) was measured on 153 patients of them. The Glu298Asp exchange in exon 7 was determined by the methods of single base extension with amplifying primers and probes for TaqMan.
The percentages of the GG, GT and TT genotypes were 81.0, 18.6 and 0.4 %, respectively. The presence of GT or TT genotype was independently associated with prevention of HRE when controlled for age, sex, baseline systolic BP and homeostatic model assessment (HOMA) index (OR=0.35, p=0.016). Subgroup analysis showed that preventive effect for HRE of T allele was significant in females (p < 0.001) and patients without insulin resistance (p=0.009).
In our study, eNOS Glu298Asp polymorphism was significantly associated with HRE. This result suggests that the presence of T allele of the Glu298Asp polymorphism may be a favorable factor to in preventing HRE, especially in female and patients without insulin resistance.
运动性高血压反应(HRE)是未来心血管事件的不良预后因素,可能与内皮功能障碍有关。以往关于内皮型一氧化氮合酶(eNOS)Glu298Asp多态性的研究主要关注其与高血压的关系。在本研究中,我们假设该多态性可能与内皮对运动反应的内在差异有关。
本研究纳入了269例行平板运动试验的患者;77例患者(平均年龄55.8±9.4岁)出现运动性高血压反应(男性收缩压峰值≥210 mmHg,女性收缩压峰值≥190 mmHg)。其中153例患者测量了脉搏波速度(PWV)。采用TaqMan扩增引物和探针单碱基延伸法测定第7外显子的Glu298Asp交换。
GG、GT和TT基因型的比例分别为81.0%、18.6%和0.4%。在控制年龄、性别、基线收缩压和稳态模型评估(HOMA)指数后,GT或TT基因型的存在与预防HRE独立相关(OR = 0.35,p = 0.016)。亚组分析显示,T等位基因对女性(p < 0.001)和无胰岛素抵抗患者(p = 0.009)的HRE预防作用显著。
在我们的研究中,eNOS Glu298Asp多态性与HRE显著相关。这一结果表明,Glu298Asp多态性T等位基因的存在可能是预防HRE的有利因素,尤其是在女性和无胰岛素抵抗的患者中。