4.5 Article

Lung proteomic biomarkers associated with chronic obstructive pulmonary disease

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.00198.2021

Keywords

chronic obstructive pulmonary disease; machine learning; mass spectrometry; proteomics

Funding

  1. NIH [R01 HL133135, R01 HL147148, R01 HL137927, R01 HL124233, R01 GM087221, S10 RR027584, P01 HL114501]
  2. National Heart, Lung, and Blood Institute (NHLBI)

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The study identified 25 proteins significantly associated with COPD in lung tissue samples, including interleukin 33. Machine learning models showed reasonable accuracy and area under the curve for predicting COPD. Mass spectrometry-based proteomic analysis of lung tissue holds promise for identifying biomarkers for COPD.
Identifying protein biomarkers for chronic obstructive pulmonary disease (COPD) has been challenging. Most previous studies have used individual proteins or preselected protein panels measured in blood samples. Mass spectrometry proteomic studies of lung tissue have been based on small sample sizes. We used mass spectrometry proteomic approaches to discover protein biomarkers from 150 lung tissue samples representing COPD cases and controls. Top COPD-associated proteins were identified based on multiple linear regression analysis with false discovery rate (FDR) < 0.05. Correlations between pairs of COPD-associated proteins were examined. Machine learning models were also evaluated to identify potential combinations of protein biomarkers related to COPD. We identified 4,407 proteins passing quality controls. Twenty-five proteins were significantly associated with COPD at FDR < 0.05, including interleukin 33, ferritin (light chain and heavy chain), and two proteins related to caveolae (CAV1 and CAVIN1). Multiple previously reported plasma protein biomarkers for COPD were not significantly associated with proteomic analysis of COPD in lung tissue, although RAGE was borderline significant. Eleven pairs of top significant proteins were highly correlated (r > 0.8), including several strongly correlated with RAGE (EHD2 and CAVIN1). Machine learning models using Random Forests with the top 5% of protein biomarkers demonstrated reasonable accuracy (0.707) and area under the curve (0.714) for COPD prediction. Mass spectrometry-based proteomic analysis of lung tissue is a promising approach for the identification of biomarkers for COPD.

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