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The impact of comorbidities on selexipag treatment effect in patients with pulmonary arterial hypertension: insights from the GRIPHON study

dc.contributor.authorRosenkranz, Stephan
dc.contributor.authorChannick, Richard
dc.contributor.authorChin, Kelly M.
dc.contributor.authorJenner, Bartosz
dc.contributor.authorGaine, Sean
dc.contributor.authorGaliè, Nazzareno
dc.contributor.authorGhofrani, Hossein-Ardeschir
dc.contributor.authorHoeper, Marius M.
dc.contributor.authorMcLaughlin, Vallerie V.
dc.contributor.authorDu Roure, Camille
dc.contributor.authorRubin, Lewis J.
dc.contributor.authorSitbon, Olivier
dc.contributor.authorTapson, Victor
dc.contributor.authorLang, Irene M.
dc.date.accessioned2022-02-07T20:24:08Z
dc.date.available2023-02-07 15:24:07en
dc.date.available2022-02-07T20:24:08Z
dc.date.issued2022-01
dc.identifier.citationRosenkranz, Stephan; Channick, Richard; Chin, Kelly M.; Jenner, Bartosz; Gaine, Sean; Galiè, Nazzareno ; Ghofrani, Hossein-Ardeschir ; Hoeper, Marius M.; McLaughlin, Vallerie V.; Du Roure, Camille; Rubin, Lewis J.; Sitbon, Olivier; Tapson, Victor; Lang, Irene M. (2022). "The impact of comorbidities on selexipag treatment effect in patients with pulmonary arterial hypertension: insights from the GRIPHON study." European Journal of Heart Failure 24(1): 205-214.
dc.identifier.issn1388-9842
dc.identifier.issn1879-0844
dc.identifier.urihttps://hdl.handle.net/2027.42/171572
dc.description.abstractAimsThe number of pulmonary arterial hypertension (PAH) patients with comorbidities is increasing and there are limited data on response to PAH- targeted therapies in this population. These post hoc analyses explored the effect of selexipag in PAH patients with cardiovascular comorbidities in the GRIPHON study.Methods and resultsRandomized patients (n = 1156) were classified using three methods: (i) by subgroups defined according to previously published comorbidity count and restrictive haemodynamic criteria: Subgroup A (<3 comorbidities and haemodynamic criteria met; n = 962) and Subgroup B (- ¥3 comorbidities and/or haemodynamic criteria not met; n = 144); comorbidities included body mass index - ¥30- kg/m2, essential hypertension, diabetes, history of coronary artery disease; (ii) by number of comorbidities, with addition of atrial fibrillation (0, 1, 2, 3, 4, or 5); (iii) by presence of individual comorbidities. Selexipag to placebo hazard ratios (HR) and 95% confidence intervals (CI) for morbidity/mortality (primary composite endpoint) were estimated using Cox regression adjusting selexipag effect for baseline covariates. Approximately half of the patients in GRIPHON (n = 584; 50.5%) had comorbidities. Selexipag reduced the risk of a morbidity/mortality event compared with placebo in both Subgroup A (HR 0.66, 95% CI 0.53, 0.82) and Subgroup B (HR 0.50, 95% CI 0.26, 0.96), with no evidence of an inconsistent treatment effect between subgroups (interaction p = 0.432). Consistent results were observed in analyses by number and by specific type of comorbidity.ConclusionSelexipag reduces the risk of a morbidity/mortality event vs. placebo irrespective of patient comorbidity status, suggesting that comorbidity status does not influence the treatment effect of selexipag.Selexipag reduced the risk of morbidity/mortality events in patients with pulmonary arterial hypertension (PAH) independently of the patients’ comorbidity status. CI, confidence interval; LVEDP, left ventricular end- diastolic pressure; PAWP, pulmonary arterial wedge pressure; RCT, randomized controlled trial.
dc.publisherJohn Wiley & Sons, Ltd.
dc.subject.otherSelexipag
dc.subject.otherComorbidities
dc.subject.otherPulmonary arterial hypertension
dc.subject.otherPost hoc analysis
dc.subject.otherRandomized controlled trial
dc.titleThe impact of comorbidities on selexipag treatment effect in patients with pulmonary arterial hypertension: insights from the GRIPHON study
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelCardiovascular Medicine
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/171572/1/ejhf2369.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/171572/2/ejhf2369_am.pdf
dc.identifier.doi10.1002/ejhf.2369
dc.identifier.sourceEuropean Journal of Heart Failure
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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