Naumov Denis E, Kotova Olesya O, Gassan Dina A, Sugaylo Ivana Y, Afanas'eva Evgeniya Y, Sheludko Elizaveta G, Perelman Juliy M
Far Eastern Scientific Center of Physiology and Pathology of Respiration, Laboratory of Molecular and Translational Research, 675000 Blagoveshchensk, Russia.
Far Eastern Scientific Center of Physiology and Pathology of Respiration, Laboratory of Functional Research of the Respiratory System, 675000 Blagoveshchensk, Russia.
J Pers Med. 2021 Feb 8;11(2):108. doi: 10.3390/jpm11020108.
Certain transient receptor potential (TRP) channels including and are widely expressed in the respiratory tract and have been shown to be the receptors of cigarette smoke and particulate matter-the main causative factors of chronic obstructive pulmonary disease (COPD). The aim of the study was to investigate the effect of and polymorphisms on COPD predisposition and lung function in COPD patients. The study enrolled 143 COPD patients and 104 smokers with post-bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) > 70%. Lung function was measured by spirometry. and polymorphisms were genotyped by LATE-PCR. None of the polymorphisms significantly influenced COPD predisposition after correction for covariates and multiple testing. Among COPD patients, the TT genotype of rs7819749 was significantly associated with higher degree of bronchial obstruction. In addition, we established that carriers of the C allele of rs11562975 more commonly had post-bronchodilator FEV1 < 60% (OR 3.2, 95%CI (1.14-8.94), = 0.03) and revealed the effect of rs959976 and rs17865682 on bronchodilator response in COPD. Thus, the obtained results suggest possible involvement of and in COPD pathogenesis, indicating the necessity to further investigate their functional role in this pathology.
某些瞬时受体电位(TRP)通道,包括[具体通道名称未给出]和[具体通道名称未给出],在呼吸道中广泛表达,并且已被证明是香烟烟雾和颗粒物(慢性阻塞性肺疾病(COPD)的主要致病因素)的受体。本研究的目的是调查[具体通道名称未给出]和[具体通道名称未给出]基因多态性对COPD易感性以及COPD患者肺功能的影响。该研究纳入了143例COPD患者和104例支气管扩张剂后一秒用力呼气量(FEV1)/用力肺活量(FVC)>70%的吸烟者。通过肺量计测量肺功能。通过LATE-PCR对[具体通道名称未给出]和[具体通道名称未给出]基因多态性进行基因分型。在校正协变量和多重检验后,没有一种多态性对COPD易感性有显著影响。在COPD患者中,[具体通道名称未给出] rs7819749的TT基因型与更高程度的支气管阻塞显著相关。此外,我们发现[具体通道名称未给出] rs11562975的C等位基因携带者更常见支气管扩张剂后FEV1<60%(比值比3.2,95%置信区间(1.14 - 8.94),P = 0.03),并揭示了[具体通道名称未给出] rs959976和[具体通道名称未给出] rs17865682对COPD患者支气管扩张剂反应的影响。因此,所获得的结果表明[具体通道名称未给出]和[具体通道名称未给出]可能参与了COPD的发病机制,表明有必要进一步研究它们在这种病理状况中的功能作用。