Gender differences in idiopathic pulmonary fibrosis (IPF) from the British Thoracic Society (BTS) UK ILD registry.

  • Leng Cheng Sia
  • , Paul Minnis
  • , Graham Bloye
  • , Helen Morris
  • , Marium Naqvi
  • , Clare Hodkinson
  • , Sophie Fletcher
  • , Felix Chua
  • , Gavin Thomas
  • , Richard Hewitt
  • , Fasihul Khan
  • , Gina Amanda
  • , Karol Bączek
  • , Andrew Achaiah
  • , Lucile Sesé
  • , Nazia Chaudhuri

Research output: Contribution to journalConference articlepeer-review

Abstract

Background: IPF is a male predominance disease and male gender is associated with poorer prognosis.

Objectives: This study aimed to explore gender differences in clinical characteristic, management, and outcomes among IPF patients in the BTS UK ILD registry.

Methods: Participating centres entered data into a central electronic database between January 2013 and May 2024. Informed consent was obtained from all participants. A cox proportional hazard analysis was performed separately for males and females.

Result: Among 6,666 patients, 77.9% were males. Smoking history was more common in males than females (69.9% vs. 59.9%, P<0.001). Males had higher rates of diabetes (19.7% vs. 14.6%, P<0.001) and ischemic heart disease (IHD) (19.9% vs. 11.2%, P<0.001), while hiatus hernia was more prevalent in females (8.0% vs. 6.4%, P=0.027). Baseline predicted forced vital capacity (FVC) % was lower in males than females (78.8±17.2 vs. 84.1±19.3, P<0.001). No difference was found in diffusion capacity for carbon monoxide (DLCO) and age between males and females. Males were more likely to receive antifibrotic therapy (47.2% vs. 41.6%, P<0.001). Males had a mean survival of 3.22 years compared to females of 3.46 years (P=0.003).

In males, IHD (HR 1.27, P=0.001), hiatus hernia (HR 0.74, P=0.033), lower baseline predicted % in FVC (HR 1.01, P<0.001), and DLCO (HR 1.024, P<0.001) predicted mortality. In females, symptom duration >12 months (HR 1.59, P=0.002) and lower baseline % predicted in DLCO (HR 1.023, P<0.001) were significant prognostic factors.

Conclusion: Gender differences in IPF emphasise the need for gender-specific approaches in its management.
Original languageEnglish
Article numberPA5071
JournalEuropean Respiratory Journal
Volume66
Issue numberSuppl 69
DOIs
Publication statusPublished online - 18 Nov 2025

Bibliographical note

This article was presented at the 2025 ERS Congress, in session “Clinical aspects in interstitial lung disease”.

This is an ERS Congress abstract. No full-text version is available. Related materials (such as slides or recordings) will be accessible via the ERS Respiratory Channel at https://channel.ersnet.org/programme-live-418

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