Evidence map›Paper›PMID 42113746›Full record

ArticleRespiration; international review of thoracic diseases2026

Sex-Dependent Integration of Symptoms and Functional Vulnerability in Interstitial Lung Disease: eurILDreg Study.

Silke Tello, Anita C Windhorst, Heva Mustafa, Poornima Mahavadi, Tobias Veit, Juergen Behr, Bruno Crestani, Carlo Vancheri, Maria Molina Molina, Andreas Guenther and 1 more

Abstract read
In one paragraph

Article in Respiration; international review of thoracic diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Silke TelloEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Anita C WindhorstInstitute of Medical Informatics, Justus-Liebig University of Giessen, Giessen, Germany.
Heva MustafaEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Poornima MahavadiEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Tobias VeitEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Juergen BehrEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Bruno CrestaniEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Carlo VancheriEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Maria Molina MolinaEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Andreas GuentherEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany.
Ekaterina KraussEuropean IPF/ILD Registry and Biobank (eurIPFreg/bank, eurILDreg/bank), Giessen, Germany, ekaterina.krauss@innere.med.uni-giessen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn interstitial lung diseases (ILDs), patient-centred disease burden is only partly explained by physiological impairment, with considerable variability in symptoms, psychological distress, and functional limitation among patients with similar lung function. We investigated whether sex modifies longitudinal patient-centred outcomes in ILD and whether differences emerge in outcome structure and cross-domain integration.

methodsIn a prospective multicentre eurILDreg cohort, repeated measures of lung function, patient-reported outcome measures (K-BILD, EQ-5D-5L, LCQ), and the Clinical Frailty Scale (CFS) were analysed. Longitudinal trajectories and time × sex interactions were assessed using linear mixed-effects models. Sex-stratified correlation analyses examined cross-domain outcome structure and symptom-physiology integration.

resultsBaseline global PROM scores and functional vulnerability were comparable between women and men, including EQ-5D-5L index (p = 0.337), K-BILD total (66.4 ± 19.9 vs. 68.2 ± 18.6; p = 0.271), LCQ total (7.2 ± 3.0 vs. 7.0 ± 3.0; p = 0.107), and CFS (mean 3.24 in both sexes). Despite similar global scores, EQ-5D-5L domain profiles differed: women reported greater limitations in usual activities (2.04 vs. 1.90) and higher pain/discomfort (2.27 vs. 2.07), while mobility and self-care were similar. Anxiety/depression (AD ≥2) was more frequent in women, reaching borderline significance (χ2 = 3.71, p = 0.054). Sex differences were most evident in cross-domain outcome structure. Coupling between global health perception and ILD-specific psychological domains was stronger in women (EQ-5D × K-BILD psychological: r = 0.452 vs. 0.380; EQ-5D anxiety/depression × K-BILD psychological: r = -0.555 vs. -0.486), whereas men showed stronger coupling between psychological and physical cough domains (LCQ psychological × LCQ physical: r = 0.635 vs. 0.560). Longitudinal trajectories were largely similar by sex: EQ-5D-5L (p = 0.330) and LCQ (p = 0.105) remained stable. A borderline sex interaction was observed for K-BILD (time × sex -0.243 points/month; p = 0.053). CFS increased modestly over time (+0.0172 points/month; p = 0.0084) without sex differences.

conclusionsSex differences in ILD are not primarily reflected in overall disease severity, functional vulnerability, or average PROM trajectories, but in how patient-centred outcomes are organised and interconnected. These findings suggest sex-specific patterns in the experience of ILD, with women showing stronger links between global health perception and psychological burden and men between psychological and physical symptom domains. Recognising sex as a modifier of patient-reported outcomes may help refine interpretation of PROMs and support more personalised, sex-informed ILD care.

Indexed as

European idiopathic pulmonary fibrosis registryEuropean ILD registryHealth-related quality of lifeIdiopathic pulmonary fibrosisInterstitial lung disease

Identifiers

PMID42113746
PMCPMC13225801

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.