Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30138
Title: Use of a Genomic Classifier in Patients with Interstitial Lung Disease: A Systematic Review and Meta-Analysis.
Austin Authors: Kheir, Fayez;Uribe Becerra, Juan Pablo;Bissell, Brittany;Ghazipura, Marya;Herman, Derrick;Hon, Stephanie M;Hossain, Tanzib;Khor, Yet H ;Knight, Shandra L;Kreuter, Michael;Macrea, Madalina;Mammen, Manoj J;Martinez, Fernando J;Poletti, Venerino;Troy, Lauren;Raghu, Ganesh;Wilson, Kevin C
Affiliation: Respiratory and Sleep Medicine
Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts
Acute Care Pharmacy Services, University of Kentucky HealthCare, University of Kentucky, Lexington, Kentucky
Respiratory Research@Alfred, Central Clinical School, Monash University, Melbourne, Victoria, Australia
Division of Thoracic Surgery and Interventional Pulmonology, Beth Israel Deaconess Medical Center and Harvard Medical School, Harvard University, Boston, Massachusetts
Pharmacy Practice and Science Department, College of Pharmacy, University of Kentucky, Lexington, Kentucky
ZS Associates, Global Health Economics and Outcomes Research, New York, New York
Department of Medicine, The Ohio State University, Columbus, Ohio
Department of Medicine, School of Medicine, Tufts University, Boston, Massachusetts
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Grossman School of Medicine, New York University Langone Health, New York, New York
Library and Knowledge Services, National Jewish Health, Denver, Colorado
Center for Interstitial and Rare Lung Diseases, Department of Pneumology, University Hospital Heidelberg and German Center for Lung Research, Heidelberg, Germany
Department of Medicine, Veterans Affairs Medical Center, Salem, Virginia
Department of Medicine, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York
Joan and Sanford I. Weill Department of Medicine, New York-Presbyterian Hospital and Weill Cornell Medical Center, Weill Cornell Medical College, Cornell University, New York, New York
Department of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmark
Department of Medicine, School of Medicine, University of Washington, Seattle, Washington
Department of Medicine, School of Medicine, Boston University, Boston, Massachusetts
Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia
Department of Respiratory and Thorax Diseases, GB Morgagni Hospital, Forlì, Italy
Issue Date: May-2022
Publication information: Annals of the American Thoracic Society 2022; 19(5): 827-832
Abstract: Background: Usual interstitial pneumonia (UIP) is the histopathologic hallmark of idiopathic pulmonary fibrosis (IPF), the prototypical interstitial lung disease (ILD). Diagnosis of IPF requires that a typical UIP pattern be identified by using high-resolution chest computed tomography or lung sampling. A genomic classifier for UIP has been developed to predict histopathologic UIP by using lung samples obtained through bronchoscopy. Objective: To perform a systematic review to evaluate genomic classifier testing in the detection of histopathologic UIP to inform new American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana del Tórax guidelines. Data Sources: Medline, Embase, and the Cochrane Central Register of Controlled Trials were searched through June 2020. Data Extraction: Data were extracted from studies that enrolled patients with ILD and reported the use of genomic classifier testing. Synthesis: Data were aggregated across studies via meta-analysis. The quality of the evidence was appraised by using the Grading of Recommendations, Assessment, Development, and Evaluation approach. Results: Genomic classifier testing had a sensitivity of 68% (95% confidence interval [CI], 55-73%) and a specificity of 92% (95% CI, 81-95%) in predicting the UIP pattern in ILD. Confidence in an IPF diagnosis increased from 43% to 93% in one cohort and from 59% to 89% in another cohort. Agreement levels in categorical IPF and non-IPF diagnoses measured by using a concordance coefficient were 0.75 and 0.64 in the two cohorts. The quality of evidence was moderate for test characteristics and very low for both confidence and agreement. Conclusions: Genomic classifier testing predicts histopathologic UIP in patients with ILD with a specificity of 92% and improves diagnostic confidence; however, sensitivity is only 68%, and testing is not widely available.
URI: https://ahro.austin.org.au/austinjspui/handle/1/30138
DOI: 10.1513/AnnalsATS.202102-197OC
ORCID: 0000-0002-4192-5080
0000-0002-7345-9731
0000-0003-4328-6822
0000-0002-0390-8407
0000-0002-1995-7828
0000-0002-5434-9342
0000-0002-4404-3833
0000-0002-5352-9587
0000-0003-0343-3234
0000-0002-7426-336X
0000-0001-7506-6643
0000-0003-4429-2266
Journal: Annals of the American Thoracic Society
PubMed URL: 34077697
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/34077697/
Type: Journal Article
Subjects: genomic classifier
idiopathic pulmonary fibrosis
interstitial lung disease
usual interstitial pneumonia
Appears in Collections:Journal articles

Show full item record

Page view(s)

14
checked on Nov 21, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.