Lu Jun, Li Li-ming, Zhan Si-yan, Yang Hui-ying, Li Xiao-hui, Cao Wei-hua, Hu Yong-hua
Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100083, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2003 Jun;24(6):498-502.
To investigate the associations between angiotensin converting enzyme inhibitors (ACEIs) related cough and ACE I/D and bradykinin beta(2) receptor (BDKRB2) C/T polymorphism.
A case-control study, nested in a 3-year community-based postmarketing surveillance of benazepril in 1 831 Chinese hypertensives was carried out. Three hundred and fifty-one cases having suffered benazepril related cough were identified and genotyped. Genotyped controls were selected through a stratified sampling design by age, sex and kidney function status.
The allele frequencies in cases were I 65.4%, D 34.6% and T 53.0%, C 47.0% and the genotype frequencies were II 42.2%, ID 46.4%, DD 11.4% (ACE) and CC 21.6%, CT 50.9%, TT 27.6% (BDKRB2), respectively. Genotype frequencies were both in Hardy-Weinberg equilibrium. According to stratified analyses by sex, kidney function status and age, no association was found between BDKRB2 C/T polymorphism and cough. For ACE I/D polymorphism, in men with decompensated kidney function, patients with ID or DD genotype having 4.805 times the risk of those with II genotype in developing cough. In women aged 35 to 49 years with normal or compensated kidney function, the OR of DD genotype was 5.128. No associations were detected in other subgroups.
It was suggested that kidney function status and some specific characteristics surrogated by age and sex had modified the effect of ACE I/D variant on cough.
探讨血管紧张素转换酶抑制剂(ACEIs)相关性咳嗽与ACE基因I/D多态性及缓激肽β2受体(BDKRB2)基因C/T多态性之间的关联。
开展一项病例对照研究,该研究嵌套于一项针对1831例中国高血压患者进行的为期3年的苯那普利上市后社区监测。确定351例发生苯那普利相关性咳嗽的患者并进行基因分型。通过按年龄、性别和肾功能状态进行分层抽样设计来选择基因分型对照。
病例组的等位基因频率分别为I 65.4%、D 34.6%以及T 53.0%、C 47.0%,基因型频率分别为II 42.2%、ID 46.4%、DD 11.4%(ACE基因)以及CC 21.6%、CT 50.9%、TT 27.6%(BDKRB2基因)。基因型频率均处于Hardy-Weinberg平衡。根据性别、肾功能状态和年龄进行分层分析,未发现BDKRB2基因C/T多态性与咳嗽之间存在关联。对于ACE基因I/D多态性,在肾功能失代偿的男性中,ID或DD基因型患者发生咳嗽的风险是II基因型患者的4.805倍。在肾功能正常或代偿的35至49岁女性中,DD基因型的比值比为5.128。在其他亚组中未检测到关联。
提示肾功能状态以及由年龄和性别所代表的一些特定特征改变了ACE基因I/D变异对咳嗽的影响。