Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease : a nationwide registry study. / Vilstrup, Frida; Heerfordt, Christian Kjer; Kamstrup, Peter; Hedsund, Caroline; Biering-Sørensen, Tor; Sørensen, Rikke; Kolekar, Shailesh; Hilberg, Ole; Pedersen, Lars; Lund, Thomas Kromann; Klausen, Tobias Wirenfeldt; Skaarup, Kristoffer Grundtvig; Eklöf, Josefin; Sivapalan, Pradeesh; Jensen, Jens Ulrik Stæhr.

In: BMJ Open Respiratory Research, Vol. 10, No. 1, e001428, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Vilstrup, F, Heerfordt, CK, Kamstrup, P, Hedsund, C, Biering-Sørensen, T, Sørensen, R, Kolekar, S, Hilberg, O, Pedersen, L, Lund, TK, Klausen, TW, Skaarup, KG, Eklöf, J, Sivapalan, P & Jensen, JUS 2023, 'Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study', BMJ Open Respiratory Research, vol. 10, no. 1, e001428. https://doi.org/10.1136/bmjresp-2022-001428

APA

Vilstrup, F., Heerfordt, C. K., Kamstrup, P., Hedsund, C., Biering-Sørensen, T., Sørensen, R., Kolekar, S., Hilberg, O., Pedersen, L., Lund, T. K., Klausen, T. W., Skaarup, K. G., Eklöf, J., Sivapalan, P., & Jensen, J. U. S. (2023). Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study. BMJ Open Respiratory Research, 10(1), [e001428]. https://doi.org/10.1136/bmjresp-2022-001428

Vancouver

Vilstrup F, Heerfordt CK, Kamstrup P, Hedsund C, Biering-Sørensen T, Sørensen R et al. Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study. BMJ Open Respiratory Research. 2023;10(1). e001428. https://doi.org/10.1136/bmjresp-2022-001428

Author

Vilstrup, Frida ; Heerfordt, Christian Kjer ; Kamstrup, Peter ; Hedsund, Caroline ; Biering-Sørensen, Tor ; Sørensen, Rikke ; Kolekar, Shailesh ; Hilberg, Ole ; Pedersen, Lars ; Lund, Thomas Kromann ; Klausen, Tobias Wirenfeldt ; Skaarup, Kristoffer Grundtvig ; Eklöf, Josefin ; Sivapalan, Pradeesh ; Jensen, Jens Ulrik Stæhr. / Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease : a nationwide registry study. In: BMJ Open Respiratory Research. 2023 ; Vol. 10, No. 1.

Bibtex

@article{10b68a103dd44bdfac998b5c4b1eb941,
title = "Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study",
abstract = "Objective The renin-angiotensin system (RAS) has been shown to play a role in the pathogenesis of chronic obstructive pulmonary disease (COPD) because of the inflammatory properties of the system. Many patients with COPD use RAS-inhibiting (RASi) treatment. The aim was to determine the association between treatment with RASi and the risk of acute exacerbations and mortality in patients with severe COPD. Methods Active comparator analysis by propensity-score matching. Data were collected in Danish national registries, containing complete information on health data, prescriptions, hospital admissions and outpatient clinic visits. Patients with COPD (n=38 862) were matched by propensity score on known predictors of the outcome. One group was exposed to RASi treatment (cases) and the other was exposed to bendroflumethiazide as an active comparator in the primary analysis. Results The use of RASi was associated with a reduced risk of exacerbations or death in the active comparator analysis at 12 months follow-up (HR 0.86, 95% CI 0.78 to 0.95). Similar results were evident in a sensitivity analysis of the propensity-score-matched population (HR 0.89, 95% CI 0.83 to 0.94) and in an adjusted Cox proportional hazards model (HR 0.93, 95% CI 0.89 to 0.98). Conclusion In the current study, we found that the use of RASi treatment was associated with a consistently lower risk of acute exacerbations and death in patients with COPD. Explanations to these findings include real effect, uncontrolled biases, and - less likely - chance findings. ",
keywords = "COPD epidemiology, COPD Exacerbations, COPD Pathology, COPD Pharmacology",
author = "Frida Vilstrup and Heerfordt, {Christian Kjer} and Peter Kamstrup and Caroline Hedsund and Tor Biering-S{\o}rensen and Rikke S{\o}rensen and Shailesh Kolekar and Ole Hilberg and Lars Pedersen and Lund, {Thomas Kromann} and Klausen, {Tobias Wirenfeldt} and Skaarup, {Kristoffer Grundtvig} and Josefin Ekl{\"o}f and Pradeesh Sivapalan and Jensen, {Jens Ulrik St{\ae}hr}",
note = "Publisher Copyright: {\textcopyright} 2023 Author(s). Published by BMJ.",
year = "2023",
doi = "10.1136/bmjresp-2022-001428",
language = "English",
volume = "10",
journal = "B M J Open Respiratory Research",
issn = "2052-4439",
publisher = "B M J Group",
number = "1",

}

RIS

TY - JOUR

T1 - Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease

T2 - a nationwide registry study

AU - Vilstrup, Frida

AU - Heerfordt, Christian Kjer

AU - Kamstrup, Peter

AU - Hedsund, Caroline

AU - Biering-Sørensen, Tor

AU - Sørensen, Rikke

AU - Kolekar, Shailesh

AU - Hilberg, Ole

AU - Pedersen, Lars

AU - Lund, Thomas Kromann

AU - Klausen, Tobias Wirenfeldt

AU - Skaarup, Kristoffer Grundtvig

AU - Eklöf, Josefin

AU - Sivapalan, Pradeesh

AU - Jensen, Jens Ulrik Stæhr

N1 - Publisher Copyright: © 2023 Author(s). Published by BMJ.

PY - 2023

Y1 - 2023

N2 - Objective The renin-angiotensin system (RAS) has been shown to play a role in the pathogenesis of chronic obstructive pulmonary disease (COPD) because of the inflammatory properties of the system. Many patients with COPD use RAS-inhibiting (RASi) treatment. The aim was to determine the association between treatment with RASi and the risk of acute exacerbations and mortality in patients with severe COPD. Methods Active comparator analysis by propensity-score matching. Data were collected in Danish national registries, containing complete information on health data, prescriptions, hospital admissions and outpatient clinic visits. Patients with COPD (n=38 862) were matched by propensity score on known predictors of the outcome. One group was exposed to RASi treatment (cases) and the other was exposed to bendroflumethiazide as an active comparator in the primary analysis. Results The use of RASi was associated with a reduced risk of exacerbations or death in the active comparator analysis at 12 months follow-up (HR 0.86, 95% CI 0.78 to 0.95). Similar results were evident in a sensitivity analysis of the propensity-score-matched population (HR 0.89, 95% CI 0.83 to 0.94) and in an adjusted Cox proportional hazards model (HR 0.93, 95% CI 0.89 to 0.98). Conclusion In the current study, we found that the use of RASi treatment was associated with a consistently lower risk of acute exacerbations and death in patients with COPD. Explanations to these findings include real effect, uncontrolled biases, and - less likely - chance findings.

AB - Objective The renin-angiotensin system (RAS) has been shown to play a role in the pathogenesis of chronic obstructive pulmonary disease (COPD) because of the inflammatory properties of the system. Many patients with COPD use RAS-inhibiting (RASi) treatment. The aim was to determine the association between treatment with RASi and the risk of acute exacerbations and mortality in patients with severe COPD. Methods Active comparator analysis by propensity-score matching. Data were collected in Danish national registries, containing complete information on health data, prescriptions, hospital admissions and outpatient clinic visits. Patients with COPD (n=38 862) were matched by propensity score on known predictors of the outcome. One group was exposed to RASi treatment (cases) and the other was exposed to bendroflumethiazide as an active comparator in the primary analysis. Results The use of RASi was associated with a reduced risk of exacerbations or death in the active comparator analysis at 12 months follow-up (HR 0.86, 95% CI 0.78 to 0.95). Similar results were evident in a sensitivity analysis of the propensity-score-matched population (HR 0.89, 95% CI 0.83 to 0.94) and in an adjusted Cox proportional hazards model (HR 0.93, 95% CI 0.89 to 0.98). Conclusion In the current study, we found that the use of RASi treatment was associated with a consistently lower risk of acute exacerbations and death in patients with COPD. Explanations to these findings include real effect, uncontrolled biases, and - less likely - chance findings.

KW - COPD epidemiology

KW - COPD Exacerbations

KW - COPD Pathology

KW - COPD Pharmacology

UR - http://www.scopus.com/inward/record.url?scp=85149529096&partnerID=8YFLogxK

U2 - 10.1136/bmjresp-2022-001428

DO - 10.1136/bmjresp-2022-001428

M3 - Journal article

C2 - 36882221

AN - SCOPUS:85149529096

VL - 10

JO - B M J Open Respiratory Research

JF - B M J Open Respiratory Research

SN - 2052-4439

IS - 1

M1 - e001428

ER -

ID: 340409641