Sex-specific aspects in an unclassified population of patients with interstitial lung disease (ILD) undergoing transbronchial cryobiopsy (TCB)

<bold>Introduction:</bold> Sex-specific aspects of idiopathic pulmonary fibrosis (IPF) are well-documented. However, these have not been investigated in the assessment of previously undiagnosed ILDs. <bold>Methods:</bold> Patients with ILD who underwent BAL, TCB and, if necessary, surgical lung biopsy (SLB) at the Thoraxklinik Heidelberg from 11/17-12/2021 were analysed. Along with clinical parameters CT biomarkers were analyzed. These included visual analysis and fully automated segmentation using the YACTA QCT software tool with emphysema index (El% -950 HU) and 80th and 40th percentile of lung density, representative of fibrosis and ground-glass opacity (GGO), respectively. Final diagnoses were made by multidisciplinary discussion (MDD). <bold>Results:</bold> The study analysed data from 402 patients, comprising 248 males and 154 females with an average age of 68±12 years. QCT imaging did not reveal sex differences. GGO were equally prevalent in both sexes.SLB was administered to 18 patients (4.5%) in addition to TCB. A final diagnosis was possible in over 90% of cases, if including unclassifiable ILD. There were sex differences in diagnoses: ILD with a known cause was diagnosed in 12% of men and 15% of women, IIP in 59% of men and 38% of women, granulomatous ILD in 25% of men and 37% of women, and other forms in 2% of men and 4% of women (p<0.001). In women, NSIP and unclassifiable ILD were the most commonly diagnosed IIP, each accounting for 32% of cases, whereas in men, IPF was the most commonly diagnosed IIP, accounting for 37% of cases (p=0.008). <bold>Conclusion:</bold> There were significant sex differences in diagnoses in this heterogeneous patient population.

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Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa2445
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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article
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article

Sex-specific aspects in an unclassified population of patients with interstitial lung disease (ILD) undergoing transbronchial cryobiopsy (TCB)

Markus Polke, Katharina Buschulte, Mark Oliver Wielpütz, Felix Herth et al.
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Sex-specific aspects in an unclassified population of patients with interstitial lung disease (ILD) undergoing transbronchial cryobiopsy (TCB)

Markus Polke, Katharina Buschulte, Mark Oliver Wielpütz, Felix Herth, Konstantina Kontogianni, Kathrin Kahnert, Claus Peter Heußel, Franziska Christina Trudzinski, Monika Eichinger, Janna Reinhard, J Michels-Zetsche, Michael Kreuter, Laura Valentina Klotz, Ralf Eberhardt, Maximilian Güttlein
article en

Abstract

<bold>Introduction:</bold> Sex-specific aspects of idiopathic pulmonary fibrosis (IPF) are well-documented. However, these have not been investigated in the assessment of previously undiagnosed ILDs. <bold>Methods:</bold> Patients with ILD who underwent BAL, TCB and, if necessary, surgical lung biopsy (SLB) at the Thoraxklinik Heidelberg from 11/17-12/2021 were analysed. Along with clinical parameters CT biomarkers were analyzed. These included visual analysis and fully automated segmentation using the YACTA QCT software tool with emphysema index (El% -950 HU) and 80th and 40th percentile of lung density, representative of fibrosis and ground-glass opacity (GGO), respectively. Final diagnoses were made by multidisciplinary discussion (MDD). <bold>Results:</bold> The study analysed data from 402 patients, comprising 248 males and 154 females with an average age of 68±12 years. QCT imaging did not reveal sex differences. GGO were equally prevalent in both sexes.SLB was administered to 18 patients (4.5%) in addition to TCB. A final diagnosis was possible in over 90% of cases, if including unclassifiable ILD. There were sex differences in diagnoses: ILD with a known cause was diagnosed in 12% of men and 15% of women, IIP in 59% of men and 38% of women, granulomatous ILD in 25% of men and 37% of women, and other forms in 2% of men and 4% of women (p<0.001). In women, NSIP and unclassifiable ILD were the most commonly diagnosed IIP, each accounting for 32% of cases, whereas in men, IPF was the most commonly diagnosed IIP, accounting for 37% of cases (p=0.008). <bold>Conclusion:</bold> There were significant sex differences in diagnoses in this heterogeneous patient population.

Johannes Gutenberg University Mainz (DE), Heidelberg University (DE), University Hospital Heidelberg (DE), University Medical Center of the Johannes Gutenberg University Mainz (DE), Frauenklinik Heidelberg (DE), German Center for Lung Research (DE), Asklepios Klinik Barmbek (DE)
Gender equality
Openalex Percentile: Top 63%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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