首页> 外文期刊>American Journal of Epidemiology >Development of predictive models for airflow obstruction in alpha-1-antitrypsin deficiency.
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Development of predictive models for airflow obstruction in alpha-1-antitrypsin deficiency.

机译:在α-1-抗胰蛋白酶缺乏的气流阻塞预测模型的开发。

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摘要

Alpha-1-antitrypsin deficiency is a genetic condition associated with severe, early-onset chronic obstructive pulmonary disease (COPD). However, there is significant variability in lung function impairment among persons with the protease inhibitor ZZ genotype. Early identification of persons at highest risk of developing lung disease could be beneficial in guiding monitoring and treatment decisions. Using a multicenter, family-based study sample (2002-2005) of 372 persons with the protease inhibitor ZZ genotype, the authors developed prediction models for forced expiratory volume in 1 second (FEV(1)) and the presence of severe COPD using demographic, clinical, and genetic variables. Half of the data sample was used for model development, and the other half was used for model validation. In the training sample, variables found to be predictive of both FEV(1) and severe COPD were age, sex, pack-years of smoking, bronchodilator responsiveness, chronic bronchitis symptoms, and index case status. In the validation sample, the predictive model for FEV(1) explained 50% of the variance in FEV(1), and the model for severe COPD exhibited excellent discrimination (c statistic = 0.88).
机译:α-1-抗胰蛋白酶缺乏症是与严重,早发的慢性阻塞性肺疾病(COPD)相关的遗传疾病。但是,具有蛋白酶抑制剂ZZ基因型的人的肺功能损害存在显着差异。尽早发现罹患肺部疾病风险最高的人可能有助于指导监测和治疗决策。作者使用多中心的基于家庭的研究样本(2002-2005年),对372名具有蛋白酶抑制剂ZZ基因型的人进行了研究,他们开发了预测模型,用于预测1秒钟内的强制呼气量(FEV(1))以及使用人口统计学分析的严重COPD的存在,临床和遗传变量。数据样本的一半用于模型开发,另一半用于模型验证。在训练样本中,发现可预测FEV(1)和严重COPD的变量是年龄,性别,吸烟包年,支气管扩张药反应性,慢性支气管炎症状和指数病例状态。在验证样本中,FEV(1)的预测模型解释了FEV(1)中50%的方差,而严重COPD的模型则显示出出色的判别力(c统计量= 0.88)。

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