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        <identifier>oai:figshare.com:article/34041811</identifier>
        <datestamp>2026-10-01T09:40:03Z</datestamp>
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          <dc:title>Identification of clinical phenotypes and development of a predictive model for rapid lung function decline in COPD patients</dc:title>
          <dc:creator>Zehua Yang (1621204)</dc:creator>
          <dc:creator>Wei Li (7081)</dc:creator>
          <dc:creator>Yanan Cui (3643606)</dc:creator>
          <dc:creator>Tingting Huang (496866)</dc:creator>
          <dc:creator>Xingyao Tang (10009711)</dc:creator>
          <dc:creator>Yaodie Peng (16910712)</dc:creator>
          <dc:creator>Rui Su (822125)</dc:creator>
          <dc:creator>Xu Chu (2818645)</dc:creator>
          <dc:creator>Yong Li (15029)</dc:creator>
          <dc:creator>Chunyu Zhang (118320)</dc:creator>
          <dc:creator>Cunbo Jia (25155646)</dc:creator>
          <dc:creator>Ke Huang (110341)</dc:creator>
          <dc:creator>Ting Yang (189879)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Information Systems not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>Chronic obstructive pulmonary disease</dc:subject>
          <dc:subject>clinical phenotypes</dc:subject>
          <dc:subject>lung function decline</dc:subject>
          <dc:subject>predictive models</dc:subject>
          <dc:subject>machine learning</dc:subject>
          <dc:description>&lt;p&gt;Chronic obstructive pulmonary disease (COPD) exhibits significant clinical heterogeneity. This study integrates phenotype identification with longitudinal lung function analysis to develop a prediction tool for rapid decline in a large Chinese cohort.&lt;/p&gt; &lt;p&gt;This study included 38,863 COPD patients from a national multicenter screening program. Latent class analysis identified clinical phenotypes. Among 1,215 patients with baseline and 24-month follow-up spirometry, rapid decline was defined as annual FEV&lt;sub&gt;1&lt;/sub&gt; decline ≥40 mL or FEV&lt;sub&gt;1&lt;/sub&gt;% predicted decline &gt;1.5%. LASSO regression and the Boruta algorithm selected predictive variables. Six machine learning models were constructed and evaluated for discrimination, calibration, and utility. SHAP analysis was employed for interpretation.&lt;/p&gt; &lt;p&gt;Three distinct phenotypes were identified: Phenotype 1 (GOLD Stage 2, non-smoking females, 25.8%), Phenotype 2 (GOLD Stage 1, smoking males, 44.8%), and Phenotype 3 (GOLD Stage 3, severe smokers, 29.4%). Phenotype 2 exhibited the highest rapid decline rate (55.8%). The CatBoost model achieved optimal performance (AUC 0.712) using six variables: region, fuel type, income level, wheezing, hip circumference, and baseline FEV&lt;sub&gt;1&lt;/sub&gt;. SHAP identified baseline FEV&lt;sub&gt;1&lt;/sub&gt; as the top predictor. At a threshold of 0.365, the model attained 95.5% sensitivity and 86.4% negative predictive value, with significant net benefit.&lt;/p&gt; &lt;p&gt;Three clinical phenotypes were identified among COPD patients. Phenotype 2 exhibits the highest risk of rapid progression, representing a key target group for intervention. The predictive model, based on six simple indicators, serves as a valuable tool for screening high-risk rapid decliners.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T09:40:03Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.34041811.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Identification_of_clinical_phenotypes_and_development_of_a_predictive_model_for_rapid_lung_function_decline_in_COPD_patients/34041811</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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