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Utility of peripheral protein biomarkers for the prediction of incident interstitial features: a multicentre retrospective cohort study.
Ash, Samuel; Doyle, Tracy J; Choi, Bina; San Jose Estepar, Ruben; Castro, Victor; Enzer, Nicholas; Kalhan, Ravi; Liu, Gabrielle; Bowler, Russell; Wilson, David O; San Jose Estepar, Raul; Rosas, Ivan O; Washko, George R.
Affiliation
  • Ash S; Department of Critical Care Medicine, South Shore Hospital, South Weymouth, Massachusetts, USA sash@southshorehealth.org.
  • Doyle TJ; Tufts University School of Medicine, Boston, Massachusetts, USA.
  • Choi B; Pulmonary and Critical Care Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • San Jose Estepar R; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Castro V; Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Enzer N; Boston University School of Medicine, Boston, Massachusetts, USA.
  • Kalhan R; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Liu G; Division of Pulmonary/Critical Care, Northwestern University, Chicago, Illinois, USA.
  • Bowler R; Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Wilson DO; Medicine, National Jewish Health, Denver, Colorado, USA.
  • San Jose Estepar R; Medicine, Pulmonary Division, University of Pittsburgh, pittsburgh, Pennsylvania, USA.
  • Rosas IO; Applied Chest Imaging Laboratory, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Washko GR; Department of Medicine: Pulmonary, Critical Care and Sleep Medicine, Baylor College of Medicine, Houston, Texas, USA.
BMJ Open Respir Res ; 11(1)2024 Mar 14.
Article in En | MEDLINE | ID: mdl-38485250
ABSTRACT
INTRODUCTION/RATIONALE Protein biomarkers may help enable the prediction of incident interstitial features on chest CT.

METHODS:

We identified which protein biomarkers in a cohort of smokers (COPDGene) differed between those with and without objectively measured interstitial features at baseline using a univariate screen (t-test false discovery rate, FDR p<0.001), and which of those were associated with interstitial features longitudinally (multivariable mixed effects model FDR p<0.05). To predict incident interstitial features, we trained four random forest classifiers in a two-thirds random subset of COPDGene (1) imaging and demographic information, (2) univariate screen biomarkers, (3) multivariable confirmation biomarkers and (4) multivariable confirmation biomarkers available in a separate testing cohort (Pittsburgh Lung Screening Study (PLuSS)). We evaluated classifier performance in the remaining one-third of COPDGene, and, for the final model, also in PLuSS.

RESULTS:

In COPDGene, 1305 biomarkers were available and 20 differed between those with and without interstitial features at baseline. Of these, 11 were associated with feature progression over a mean of 5.5 years of follow-up, and of these 4 were available in PLuSS, (angiopoietin-2, matrix metalloproteinase 7, macrophage inflammatory protein 1 alpha) over a mean of 8.8 years of follow-up. The area under the curve (AUC) of classifiers using demographics and imaging features in COPDGene and PLuSS were 0.69 and 0.59, respectively. In COPDGene, the AUC of the univariate screen classifier was 0.78 and of the multivariable confirmation classifier was 0.76. The AUC of the final classifier in COPDGene was 0.75 and in PLuSS was 0.76. The outcome for all of the models was the development of incident interstitial features.

CONCLUSIONS:

Multiple novel and previously identified proteomic biomarkers are associated with interstitial features on chest CT and may enable the prediction of incident interstitial diseases such as idiopathic pulmonary fibrosis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteomics / Idiopathic Pulmonary Fibrosis Limits: Humans Language: En Journal: BMJ Open Respir Res Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteomics / Idiopathic Pulmonary Fibrosis Limits: Humans Language: En Journal: BMJ Open Respir Res Year: 2024 Type: Article Affiliation country: United States