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A predictive model for the development of chronic obstructive pulmonary disease

机译:慢性阻塞性肺疾病发展的预测模型

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摘要

The screening of a person at risk for chronic obstructive pulmonary disease (COPD) and timely treatment may provide opportunities to delay the progressive destruction of lung function. Therefore, a model to predict the disease is required. We hypothesized that demographic and clinical information in combination with genetic markers would aid in the prediction of COPD development, prior to its onset. The aim of the present study was to create a predictive model for COPD development. Demographic, clinical presentation and genetic polymorphisms were recorded in COPD patients and control subjects. Nighty-six single-nucleotide polymorphisms of 46 genes were selected for genotyping in the case-control study. A predictive model was produced using logistic regression with a stepwise model-building approach and was validated. A total of 331 patients and 351 control subjects were included. The logistic regression identified the following predictors: Gender, respiratory infection in early life, low birth weight, smoking history and genotype polymorphisms (rs2070600, rs10947233, rs1800629, rs2241712 and rs1205). The model was established using the following formula: COPD = 1/[1 + exp (−2.4933–1.2197 gender + 1.1842 respiratory infection in early life + 2.4350 low birth weight + 1.8524 smoking − 1.1978 rs2070600 + 2.0270 rs10947233 + 1.1913 rs10947233 + 0.6468 rs1800629 + 0.5272 rs2241712 + 0.4024 rs1205)] (when the value is >0.5). The Hosmer-Lemeshow test showed no significant deviations between the observed and predicted events. Validation of the model in 50 patients showed a modest sensitivity and specificity. Therefore, a predictive model based on demographic, clinical and genetic information may identify COPD prior to its onset.
机译:对处于慢性阻塞性肺疾病(COPD)风险中的人进行筛查并及时治疗可能会为延迟逐步破坏肺功能提供机会。因此,需要一种预测疾病的模型。我们假设人口统计学和临床​​信息与遗传标志物结合将有助于预测COPD发病之前的发展。本研究的目的是为COPD的发展创建一个预测模型。在COPD患者和对照组中记录了人口统计学,临床表现和遗传多态性。在病例对照研究中,选择了46个基因的Nighty-six单核苷酸多态性的46个基因进行基因分型。使用逻辑回归和逐步模型构建方法生成了预测模型,并进行了验证。总共包括331名患者和351名对照对象。 Logistic回归确定了以下预测因素:性别,早年呼吸道感染,低出生体重,吸烟史和基因型多态性(rs2070600,rs10947233,rs1800629,rs2241712和rs1205)。使用以下公式建立模型:COPD = 1 / [1 + exp(−2.4933–1.2197性别+ 1.1842早期呼吸道感染+ 2.4350低出生体重+ 1.8524吸烟-− 1.1978 rs2070600 + 2.0270 rs10947233 + 1.1913 rs10947233 + 0.6468 rs1800629 + 0.5272 rs2241712 + 0.4024 rs1205)](当值> 0.5时)。 Hosmer-Lemeshow测试表明,观察到的事件与预测的事件之间没有显着偏差。该模型在50例患者中的验证显示出适度的敏感性和特异性。因此,基于人口统计学,临床和遗传信息的预测模型可在COPD发作之前对其进行识别。

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