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哥本哈根男性研究中慢性支气管炎和呼气峰值流速的遗传标记

Genetic markers for chronic bronchitis and peak expiratory flow in the Copenhagen Male Study.

作者信息

Vestbo J, Hein H O, Suadicani P, Sørensen H, Gyntelberg F

机构信息

Department of Occupational Medicine, Rigshospitalet, Copenhagen.

出版信息

Dan Med Bull. 1993 Jun;40(3):378-80.

PMID:8339607
Abstract

The associations between four major blood groups, ABH secretor status, and complement C3, and chronic bronchitis and peak expiratory flow were examined in 3387 men, aged 55-74 years. Presence of chronic bronchitis was assessed using the British Medical Research Council (BMRC) questionnaire. Men with NS- in the MNS system had significantly less chronic bronchitis than others, i.e. 11.4% versus 16.0% (p < 0.0005). In heavy smokers, both men with NS- and NS+ had significantly less chronic bronchitis than others. Also, Rhesus positive men had less chronic bronchitis than Rhesus negative men, 28.0% versus 38.3% (p < 0.05). Absence of the complement C3 allele C3F was associated with a higher prevalence of chronic bronchitis. No association with chronic bronchitis was found for the AB0 system or the ABH secretor system. No convincing associations were found between genetic markers and mean peak flow. In conclusion, this study has suggested new genetic markers for respiratory disease indicating a partly genetic aetiology of chronic respiratory disease. The MNS, and to some extent the Rhesus blood groups, were associated with chronic bronchitis in middle-aged men. However, this study demonstrates once again that no single blood type can act as a risk indicator of chronic respiratory disease.

摘要

在3387名年龄在55至74岁之间的男性中,研究了四种主要血型、ABH分泌状态、补体C3与慢性支气管炎及呼气峰值流量之间的关联。使用英国医学研究委员会(BMRC)问卷评估慢性支气管炎的存在情况。MNS系统中为NS-的男性患慢性支气管炎的比例显著低于其他男性,即分别为11.4%和16.0%(p<0.0005)。在重度吸烟者中,MNS系统中为NS-和NS+的男性患慢性支气管炎的比例均显著低于其他男性。此外,Rh阳性男性患慢性支气管炎的比例低于Rh阴性男性,分别为28.0%和38.3%(p<0.05)。补体C3等位基因C3F的缺失与慢性支气管炎的较高患病率相关。未发现AB0系统或ABH分泌系统与慢性支气管炎有关联。未发现遗传标记与平均峰值流量之间有令人信服的关联。总之,本研究提出了呼吸系统疾病的新遗传标记,表明慢性呼吸系统疾病有部分遗传病因。MNS血型以及在一定程度上Rh血型与中年男性的慢性支气管炎有关。然而,本研究再次表明,没有单一血型可作为慢性呼吸系统疾病的风险指标。

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