Mid-regional pro-atrial natriuretic peptide and copeptin as indicators of disease severity and therapy response in CTEPH.
Journal
ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
05
06
2020
accepted:
18
08
2020
entrez:
2
12
2020
pubmed:
3
12
2020
medline:
3
12
2020
Statut:
epublish
Résumé
Chronic thromboembolic pulmonary hypertension (CTEPH) leads to right heart failure. Pulmonary endarterectomy (PEA) or balloon pulmonary angioplasty (BPA) restore pulmonary haemodynamics and allow cardiac recovery. This study examined the relationship of copeptin and mid-regional pro-atrial natriuretic peptide (MR-proANP) levels to disease severity and therapy response. This observational cohort study included 125 patients (55 PEA/70 BPA) who underwent treatment and completed a 6-/12-month follow-up. Biomarkers, measured at baseline, prior to every BPA and at follow-up, were compared to 1) severe disease at baseline (right atrial pressure (RAP) ≥8 mmHg and cardiac index ≤2.4 L·min Severely diseased patients had higher levels of MR-proANP (320 (246-527) pmol·L MR-proANP and copeptin levels are affected in CTEPH and decrease after therapy. MR-proANP identifies a severe disease status and optimal therapy response.
Sections du résumé
BACKGROUND
BACKGROUND
Chronic thromboembolic pulmonary hypertension (CTEPH) leads to right heart failure. Pulmonary endarterectomy (PEA) or balloon pulmonary angioplasty (BPA) restore pulmonary haemodynamics and allow cardiac recovery. This study examined the relationship of copeptin and mid-regional pro-atrial natriuretic peptide (MR-proANP) levels to disease severity and therapy response.
METHODS
METHODS
This observational cohort study included 125 patients (55 PEA/70 BPA) who underwent treatment and completed a 6-/12-month follow-up. Biomarkers, measured at baseline, prior to every BPA and at follow-up, were compared to 1) severe disease at baseline (right atrial pressure (RAP) ≥8 mmHg and cardiac index ≤2.4 L·min
RESULTS
RESULTS
Severely diseased patients had higher levels of MR-proANP (320 (246-527) pmol·L
CONCLUSION
CONCLUSIONS
MR-proANP and copeptin levels are affected in CTEPH and decrease after therapy. MR-proANP identifies a severe disease status and optimal therapy response.
Identifiants
pubmed: 33263045
doi: 10.1183/23120541.00356-2020
pii: 00356-2020
pmc: PMC7682678
pii:
doi:
Types de publication
Journal Article
Langues
eng
Informations de copyright
Copyright ©ERS 2020.
Déclaration de conflit d'intérêts
Conflict of interest: S.D. Kriechbaum has nothing to disclose. Conflict of interest: L. Scherwitz has nothing to disclose. Conflict of interest: C.B. Wiedenroth reports personal fees from Actelion, Bayer, MSD, Pfizer and BTG outside the submitted work. Conflict of interest: F. Rudolph has nothing to disclose. Conflict of interest: S. Wolter has nothing to disclose. Conflict of interest: M. Haas reports personal fees from Daiichi-Sankyo and Pfizer outside the submitted work. Conflict of interest: U. Fischer-Rasokat has nothing to disclose. Conflict of interest: A. Rolf reports personal fees from Astra Zeneca, Boehringer Ingelheim and Pfizer-Bristol-Myers Squibb outside the submitted work;. Conflict of interest: C.W. Hamm reports personal fees from BRAHMS/Thermo Fisher outside the submitted work. Conflict of interest: E. Mayer reports grants from Deutsche Forschungsgesellschaft during the conduct of the study; and personal fees from Actelion, Bayer, MSD and Pfizer outside the submitted work. Conflict of interest: S. Guth reports personal fees from Actelion, Bayer, GSK, MSD and Pfizer outside the submitted work. Conflict of interest: T. Keller reports personal fees from Abbott and Brahms outside the submitted work. Conflict of interest: S.V. Konstantinides reports grants from German Federal Ministry of Education and Research (BMBF 01EO1503) during the conduct of the study; and grants and personal fees from Bayer, personal fees from Pfizer Bristol Myers Suqibb, grants and personal fees from Boehringer Ingelheim, personal fees from Daiichi Sankyo and MSD, and grants from Actelion, outside the submitted work;. Conflict of interest: M. Lankeit reports grants from German Federal Ministry of Education and Research (BMBF 01EO1503) during the conduct of the study; and grants and personal fees from Bayer, personal fees from Pfizer Bristol Myers Squibb, personal fees from Daiichi Sankyo and MSD, grants and personal fees from Thermo Fisher Scientific, and personal fees from Actelion, outside the submitted work. Conflict of interest: C. Liebetrau reports personal fees from Bayer, Pfizer-Bristol-Myers Squibb, GSK, Abott, AstraZeneca, Berlin Chemie, Daiichi-Sankyo and Boehringer Ingelheim outside the submitted work.
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