Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2022 Mar 16;23(1):59.
doi: 10.1186/s12931-022-01981-3.

Comorbidities in unclassifiable interstitial lung disease

Affiliations
Multicenter Study

Comorbidities in unclassifiable interstitial lung disease

Thomas Skovhus Prior et al. Respir Res. .

Abstract

Background: Comorbidities are common in interstitial lung diseases (ILD) and have an important association with survival, but the frequency and prognostic impact of comorbidities in unclassifiable interstitial lung disease (uILD) remains elusive. We aimed to describe the prevalence of comorbidities and assess the impact on survival in patients with uILD. Furthermore, we aimed to identify and characterize potential phenotypes based on clusters of comorbidities and examine their association with disease progression and survival.

Methods: Incident patients diagnosed with uILD were identified at two ILD referral centers in Denmark and Germany from 2003 to 2018. The diagnosis uILD was based on multidisciplinary team meetings. Clinical characteristics and comorbidities were extracted from ILD registries and patient case files. Survival analyses were performed using Cox regression analyses, disease progression was analyzed by linear mixed effects models, and clusters of comorbidities were analyzed using self-organizing maps.

Results: A total of 249 patients with uILD were identified. The cohort was dominated by males (60%), former (49%) or current (15%) smokers, median age was 70 years, mean FVC was 75.9% predicted, and mean DLCO was 49.9% predicted. One-year survival was 89% and three-year survival was 73%. Eighty-five percent of the patients had ≥ 1 comorbidities, 33% had ≥ 3 comorbidities and 9% had ≥ 5 comorbidities. The only comorbidity associated with excess mortality was dyslipidemia. No association between survival and number of comorbidities or the Charlson comorbidity index was observed. Three clusters with different comorbidities profiles and clinical characteristics were identified. A significant annual decline in FVC and DLCO % predicted was observed in cluster 1 and 2, but not in cluster 3. No difference in mortality was observed between the clusters.

Conclusions: The comorbidity burden in uILD is lower than reported in other types of ILD and the impact of comorbidities on mortality needs further clarification. Three clusters with distinct comorbidity profiles were identified and could represent specific phenotypes. No difference in mortality was observed between clusters, but slower disease progression was observed in cluster 3. Better understanding of disease behavior and mortality will require further studies of subgroups of uILD with longer observation time.

Keywords: Cluster analyses; Comorbidities; Disease course; Mortality; Unclassifiable interstitial lung disease.

PubMed Disclaimer

Conflict of interest statement

TSP reports personal fees from Galapagos, and grants and personal fees from Boehringer Ingelheim outside the submitted work; SKW reports grants from Roche during the conduct of the study, and personal fees from Roche and Bohringer Ingelheim outside the submitted work; EB reports grants from Roche during the conduct of the study, and grants and personal fees from Boehringer Ingelheim, grants and personal fees from Roche, and personal fees from Galapagos outside the submitted work; MK reports grants from Roche during the conduct of the study, and personal fees from Roche and Boehringer Ingelheim outside the submitted work; CH, SET and CG has nothing to disclose.

Figures

Fig. 1
Fig. 1
Total and specific comorbidities in the cohort. Data are presented as a percentage of all patients. A Total number of comorbidities per patient. B Spectrum of comorbidities in the uILD cohort. Multiple comorbidities could be reported
Fig. 2
Fig. 2
Comorbidity clusters and heat maps of each comorbidity. Cluster borders are indicated by the black lines. Each patient is placed in the same area on all maps. Red colors indicate a high frequency of the specific comorbidity, while blue colors indicate absence of the comorbidity. C1: Cluster 1; C2: Cluster 2; C3: Cluster 3; GERD: Gastro-esophageal reflux disease; CAD: Coronary artery disease; VTE: Venous thromboembolism
Fig. 3
Fig. 3
Survival in the three clusters

References

    1. Hyldgaard C, Hilberg O, Bendstrup E. How does comorbidity influence survival in idiopathic pulmonary fibrosis? Respir Med. 2014;108:647–653. doi: 10.1016/j.rmed.2014.01.008. - DOI - PubMed
    1. Kreuter M, Ehlers-Tenenbaum S, Palmowski K, Bruhwyler J, Oltmanns U, Muley T, et al. Impact of comorbidities on mortality in patients with idiopathic pulmonary fibrosis. PLoS ONE. 2016;11:e0151425. doi: 10.1371/journal.pone.0151425. - DOI - PMC - PubMed
    1. Wälscher J, Gross B, Morisset J, Johannson KA, Vasakova M, Bruhwyler J, et al. Comorbidities and survival in patients with chronic hypersensitivity pneumonitis. Respir Res. 2020;21:12. doi: 10.1186/s12931-020-1283-8. - DOI - PMC - PubMed
    1. Prior TS, Hoyer N, Hilberg O, Shaker SB, Davidsen JR, Rasmussen F, et al. Clusters of comorbidities in idiopathic pulmonary fibrosis. Respir Med. 2021;185:106490. doi: 10.1016/j.rmed.2021.106490. - DOI - PubMed
    1. Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, et al. An Official American Thoracic Society/European Respiratory Society Statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013;188:733–748. doi: 10.1164/rccm.201308-1483ST. - DOI - PMC - PubMed

Publication types