Evidence map›Paper›PMID 40037846›Full record

ArticleESC heart failure2025

Mono and combination therapies in pulmonary arterial hypertension patients with comorbidities: A COMPERA analysis.

Dirk Skowasch, Christine Pausch, Doerte Huscher, David Pittrow, Judith Wede, Fabian Kreimendahl, Stephan Rosenkranz, Stephan Beckmann, Matthias Held, Ekkehard Grünig and 11 more

Abstract readMulticenter Study
In one paragraph

Article in ESC heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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

21 authors.

Dirk SkowaschDepartment of Internal Medicine II, Bonn, Germany.
Christine PauschGWT-TUD GmbH, Innovation Center Real World Evidence, Dresden, Germany.
Doerte HuscherInstitute of Biometry and Clinical Epidemiology, Berlin Institute of Health, Charité-Universitätsmedizin, Berlin, Germany.
David PittrowGWT-TUD GmbH, Innovation Center Real World Evidence, Dresden, Germany.
Judith WedeJanssen-Cilag GmbH, Neuss, Germany.
Fabian KreimendahlJanssen-Cilag GmbH, Neuss, Germany.
Stephan RosenkranzClinic III for Internal Medicine (Cardiology) and Center for Molecular Medicine (CMMC), and the Cologne Cardiovascular Research Center (CCRC), University of Cologne, Cologne, Germany.
Stephan BeckmannSpecialist Clinic Löwenstein, Löwenstein, Germany.
Matthias HeldDepartment of Internal Medicine, Respiratory Medicine and Ventilatory Support, Medical Mission Hospital, Central Clinic, Würzburg, Germany.
Ekkehard GrünigTranslational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Center for Pulmonary Hypertension, Thoraxklinik at Heidelberg University Hospital, Heidelberg, Germany.
H Ardeschir GhofraniDepartment of Internal Medicine, Justus-Liebig-University Giessen, Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany.
Hans KloseDepartment of Respiratory Medicine, Eppendorf University Hospital, Hamburg, Germany.
Andris SkrideRiga Stradiņš University, Riga, Latvia; Rare Diseases Unit VSIA Pauls Stradins Clinical University Hospital, Riga, Latvia.
Michael HalankMedical Clinic and Polyclinic I, University Hospital Carl Gustav Carus of the Technical University of Dresden, Dresden, Germany.
Stefan StadlerDepartment of Internal Medicine II, University Medical Center Regensburg, Regensburg, Germany.
Marion DelcroixClinical Department of Respiratory Diseases, University Hospitals of Leuven and Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism (CHROMETA), KU Leuven - University of Leuven, Leuven, Belgium.
Anton Vonk-NoordegraafDepartment of Pulmonary Medicine, Amsterdam Cardiovascular Sciences, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Ralf EwertDepartment of Respiratory Medicine, Clinic of Internal Medicine, University Medical Center Greifswald, Greifswald, Germany.
Grzegorz KopecDepartment of Cardiac and Vascular Diseases, Jagiellonian University Medical College, John Paul II Hospital in Krakow, Krakow, Poland.
Marius M HoeperDepartment of Respiratory Medicine and Infectious Diseases and German Center of Lung Research (DZL), Hannover Medical School, Hannover, Germany.
Karen M OlssonDepartment of Respiratory Medicine and Infectious Diseases and German Center of Lung Research (DZL), Hannover Medical School, Hannover, Germany.

Funding

German Centre of Lung Research (DZL)
6 · The paper itself

Abstract

aimsPulmonary arterial hypertension (PAH) is often diagnosed in elderly patients with comorbidities. Although initial monotherapy is recommended for these patients, the value of combination therapy remains unclear. Here, we compare the efficacy of initial monotherapy and combination therapy in PAH patients with cardiovascular comorbidities. METHODS AND

resultsData from adult patients with incident pre-capillary PAH and cardiovascular comorbidities from the COMPERA database (European registry for PH) were analysed. A matched-pair analysis of patients treated with monotherapy versus combination therapy based on age, sex, WHO functional class (FC) and 4-strata risk at baseline was performed. The matching strategy identified 216 pairs of PAH patients with cardiovascular comorbidities, who differed considerably from the enrolled patient population (n = 1871), especially in terms of mean age (mono: matched pairs 62.9 ± 13.5 years vs. 70.6 ± 11.4 years, combination: matched pairs 62.0 ± 13.6 years vs. 60.5 ± 14.9 years). In the matched-pair analysis, the initial combination therapy group showed more pronounced improvements in WHO-FC, N-terminal pro-B-type natriuretic peptide (BNP/NT-proBNP) and risk status than patients treated with initial monotherapy, with no significant differences in 6-min walk distance (6MWD), PAH-related hospitalisations, survival and drug discontinuation.

conclusionsThis analysis suggests that PAH patients with comorbidities may benefit more pronounced from combination therapy regarding WHO-FC, BNP/NT-pro-BNP and risk status without a significant difference in survival. Good tolerability is indicated. However, given the relatively younger patient matched subgroup, these findings may not necessarily apply to older patients with a wider range of comorbidities.

Indexed as

Antihypertensive AgentsPulmonary Arterial HypertensionRegistriesAgedAged, 80 and overComorbidityDrug Therapy, CombinationEuropeFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntihypertensive AgentsCOMPERA databaseinitial monotherapy and combination therapymatched‐pair analysisPAH and comorbidities

Identifiers

PMID40037846
PMCPMC12287794

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Registered trials

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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.