PMID- 33238466 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20221216 IS - 2077-0383 (Print) IS - 2077-0383 (Electronic) IS - 2077-0383 (Linking) VI - 9 IP - 11 DP - 2020 Nov 23 TI - Automated CT Analysis of Major Forms of Interstitial Lung Disease. LID - 10.3390/jcm9113776 [doi] LID - 3776 AB - This study aimed to determine diagnostic and prognostic differences in major forms of interstitial lung disease using quantitative CT imaging. A retrospective study of 225 subjects with a multidisciplinary diagnosis of idiopathic pulmonary fibrosis (IPF), interstitial pneumonia with autoimmune features (IPAF), connective tissue disease (CTD), or chronic hypersensitivity pneumonitis (cHP) was conducted. Non-contrast CT scans were analyzed using the Computer Aided Lung Informatics for Pathology Evaluation and Rating (CALIPER) program. Resulting data were analyzed statistically using ANOVA and Student's t-test. Univariate, multivariable, and receiver operating characteristic analyses were conducted on patient mortality data. CALIPER analysis of axial distribution on CT scans in those with IPF demonstrated greater peripheral volumes of reticulation than either CTD (p = 0.033) or cHP (p = 0.007). CTD showed lower peripheral ground-glass opacity than IPF (p = 0.005) and IPAF (p = 0.004). Statistical analysis of zonal distributions revealed reduced lower zone ground-glass opacity in cHP than IPF (p = 0.044) or IPAF (p = 0.018). Analysis of pulmonary vascular-related structure (VRS) volume by diagnosis indicated greater VRS volume in IPF compared to CTD (p = 0.003) and cHP (p = 0.003) as well as in IPAF compared to CTD (p = 0.007) and cHP (p = 0.007). Increased reticulation (p = 0.043) and ground glass opacity (p = 0.032) were predictive of mortality on univariate analysis. Increased pulmonary VRS volume was predictive of mortality (p < 0.001) even after multivariate analysis (p = 0.041). Quantitative CT imaging revealed significant differences between ILD diagnoses in specific CT findings in axial and, to a lesser degree, zonal distributions. Increased pulmonary VRS volume seems to be associated with both diagnosis and survival. FAU - Crews, Marlee S AU - Crews MS AUID- ORCID: 0000-0002-2240-0983 AD - Department of Radiology, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Bartholmai, Brian J AU - Bartholmai BJ AUID- ORCID: 0000-0001-7834-6579 AD - Department of Radiology, Mayo Clinic, Rochester, MN 55902, USA. FAU - Adegunsoye, Ayodeji AU - Adegunsoye A AD - Department of Medicine, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Oldham, Justin M AU - Oldham JM AD - Department of Medicine, The University of California Davis, Sacramento, CA 95616, USA. FAU - Montner, Steven M AU - Montner SM AD - Department of Radiology, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Karwoski, Ronald A AU - Karwoski RA AD - Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN 55902, USA. FAU - Husain, Aliya N AU - Husain AN AD - Department of Pathology, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Vij, Rekha AU - Vij R AD - Department of Medicine, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Noth, Imre AU - Noth I AD - Department of Medicine, University of Virginia, Charlottesville, VA 22903, USA. FAU - Strek, Mary E AU - Strek ME AD - Department of Medicine, The University of Chicago Medicine, Chicago, IL 60637, USA. FAU - Chung, Jonathan H AU - Chung JH AD - Department of Radiology, The University of Chicago Medicine, Chicago, IL 60637, USA. LA - eng GR - K23 HL138190/HL/NHLBI NIH HHS/United States GR - R01 HL130796/HL/NHLBI NIH HHS/United States PT - Journal Article DEP - 20201123 PL - Switzerland TA - J Clin Med JT - Journal of clinical medicine JID - 101606588 PMC - PMC7700631 OTO - NOTNLM OT - connective tissue disease OT - high-resolution computed tomography OT - hypersensitivity pneumonitis OT - idiopathic pulmonary fibrosis OT - interstitial pneumonia with autoimmune features COIS- The authors declare no conflict of interest. EDAT- 2020/11/27 06:00 MHDA- 2020/11/27 06:01 PMCR- 2020/11/23 CRDT- 2020/11/26 01:01 PHST- 2020/10/22 00:00 [received] PHST- 2020/11/13 00:00 [revised] PHST- 2020/11/19 00:00 [accepted] PHST- 2020/11/26 01:01 [entrez] PHST- 2020/11/27 06:00 [pubmed] PHST- 2020/11/27 06:01 [medline] PHST- 2020/11/23 00:00 [pmc-release] AID - jcm9113776 [pii] AID - jcm-09-03776 [pii] AID - 10.3390/jcm9113776 [doi] PST - epublish SO - J Clin Med. 2020 Nov 23;9(11):3776. doi: 10.3390/jcm9113776.