Analysis of tissue lipidomics and computed tomography pulmonary fat attenuation volume (CTPFAV) in idiopathic pulmonary fibrosis

Author:

O'Callaghan Marissa12ORCID,Duignan John3,Tarling Elizabeth J.4,Waters Darragh K.3,McStay Megan3,O'Carroll Orla1,Bridges James P.5,Redente Elizabeth F.6,Franciosi Alessandro N.12ORCID,McGrath Emmet E.12,Butler Marcus W.12,Dodd Jonathan D.23,Fabre Aurelie27ORCID,Murphy David J.23,Keane Michael P.12ORCID,McCarthy Cormac12ORCID

Affiliation:

1. Department of Respiratory Medicine St. Vincent's University Hospital Dublin Ireland

2. School of Medicine University College Dublin Dublin Ireland

3. Department of Radiology St. Vincent's University Hospital Dublin Ireland

4. Division of Cardiology University of California Los Angeles California USA

5. Department of Medicine National Jewish Health Denver Colorado USA

6. Department of Pediatrics National Jewish Health Denver Colorado USA

7. Department of Histopathology St. Vincent's University Hospital Dublin Ireland

Abstract

AbstractBackground and ObjectiveThere is increasing interest in the role of lipids in processes that modulate lung fibrosis with evidence of lipid deposition in idiopathic pulmonary fibrosis (IPF) histological specimens. The aim of this study was to identify measurable markers of pulmonary lipid that may have utility as IPF biomarkers.Study Design and MethodsIPF and control lung biopsy specimens were analysed using a unbiased lipidomic approach. Pulmonary fat attenuation volume (PFAV) was assessed on chest CT images (CTPFAV) with 3D semi‐automated lung density software. Aerated lung was semi‐automatically segmented and CTPFAV calculated using a Hounsfield‐unit (−40 to −200HU) threshold range expressed as a percentage of total lung volume. CTPFAV was compared to pulmonary function, serum lipids and qualitative CT fibrosis scores.ResultsThere was a significant increase in total lipid content on histological analysis of IPF lung tissue (23.16 nmol/mg) compared to controls (18.66 mol/mg, p = 0.0317). The median CTPFAV in IPF was higher than controls (1.34% vs. 0.72%, p < 0.001) and CTPFAV correlated significantly with DLCO% predicted (R2 = 0.356, p < 0.0001) and FVC% predicted (R2 = 0.407, p < 0.0001) in patients with IPF. CTPFAV correlated with CT features of fibrosis; higher CTPFAV was associated with >10% reticulation (1.6% vs. 0.94%, p = 0.0017) and >10% honeycombing (1.87% vs. 1.12%, p = 0.0003). CTPFAV showed no correlation with serum lipids.ConclusionCTPFAV is an easily quantifiable non‐invasive measure of pulmonary lipids. In this pilot study, CTPFAV correlates with pulmonary function and radiological features of IPF and could function as a potential biomarker for IPF disease severity assessment.

Funder

Health Research Board

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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