Elevated Angiotensin 1-7/Angiotensin II Ratio Predicts Favorable Outcomes in Patients With Heart Failure.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 26 6 2020
medline: 21 11 2020
entrez: 26 6 2020
Statut: ppublish

Résumé

ACE2 (angiotensin-converting enzyme 2) and Ang 1-7 (angiotensin 1-7) are endogenous negative regulators of the renin-angiotensin system exerting cardioprotective effects in models of heart failure. Recombinant human ACE2 markedly increased plasma Ang 1-7 and lowered Ang II levels in phase II clinical trials. We hypothesize that the dynamic state of this renin-angiotensin system protective arm could influence long-term outcomes in patients with heart failure. One hundred ten patients with heart failure were prospectively enrolled from our outpatient clinic and the emergency department. Comprehensive circulating and equilibrium levels of plasma angiotensin peptide profiles were assessed using novel liquid chromatography-mass spectrometry/mass spectroscopy techniques. Plasma aldosterone, B-type natriuretic peptide, active renin concentration, and clinical profiles were captured at baseline. During a median follow-up of 5.1 years (interquartile range, 4.7-5.7 years), composite clinical outcomes were assessed using all-cause in-patient hospitalizations and mortality. Circulating and equilibrium angiotensin peptide levels strongly correlated in our patient cohort. Adjusting for covariates, elevated equilibrium (hazard ratio, 0.38 [95% CI, 0.18-0.81] We extensively profiled plasma angiotensin peptides in patients with heart failure and identified elevated Ang 1-7/Ang II ratio, as an independent and incremental predictor of beneficial outcomes, higher survival rate, and decreased hospitalization duration. These findings provide important clinical evidence supporting strategies aiming to promote the beneficial Ang 1-7/Mas axis concurrent with renin-angiotensin system blockade therapies inhibiting the detrimental Ang II/AT

Sections du résumé

BACKGROUND
ACE2 (angiotensin-converting enzyme 2) and Ang 1-7 (angiotensin 1-7) are endogenous negative regulators of the renin-angiotensin system exerting cardioprotective effects in models of heart failure. Recombinant human ACE2 markedly increased plasma Ang 1-7 and lowered Ang II levels in phase II clinical trials. We hypothesize that the dynamic state of this renin-angiotensin system protective arm could influence long-term outcomes in patients with heart failure.
METHODS
One hundred ten patients with heart failure were prospectively enrolled from our outpatient clinic and the emergency department. Comprehensive circulating and equilibrium levels of plasma angiotensin peptide profiles were assessed using novel liquid chromatography-mass spectrometry/mass spectroscopy techniques. Plasma aldosterone, B-type natriuretic peptide, active renin concentration, and clinical profiles were captured at baseline. During a median follow-up of 5.1 years (interquartile range, 4.7-5.7 years), composite clinical outcomes were assessed using all-cause in-patient hospitalizations and mortality.
RESULTS
Circulating and equilibrium angiotensin peptide levels strongly correlated in our patient cohort. Adjusting for covariates, elevated equilibrium (hazard ratio, 0.38 [95% CI, 0.18-0.81]
CONCLUSIONS
We extensively profiled plasma angiotensin peptides in patients with heart failure and identified elevated Ang 1-7/Ang II ratio, as an independent and incremental predictor of beneficial outcomes, higher survival rate, and decreased hospitalization duration. These findings provide important clinical evidence supporting strategies aiming to promote the beneficial Ang 1-7/Mas axis concurrent with renin-angiotensin system blockade therapies inhibiting the detrimental Ang II/AT

Identifiants

pubmed: 32580658
doi: 10.1161/CIRCHEARTFAILURE.120.006939
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0
Biomarkers 0
Peptide Fragments 0
Angiotensin II 11128-99-7
Angiotensin I 9041-90-1
angiotensin I (1-7) IJ3FUK8MOF

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e006939

Subventions

Organisme : CIHR
Pays : Canada

Auteurs

Kaiming Wang (K)

Division of Cardiology, Department of Medicine (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.
Mazankowski Alberta Heart Institute (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.

Ratnadeep Basu (R)

Division of Cardiology, Department of Medicine (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.
Mazankowski Alberta Heart Institute (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.

Marko Poglitsch (M)

Attoquant Diagnostics, Vienna, Austria (M.P.).

Jeffrey A Bakal (JA)

Alberta Strategy for Patient Oriented Research (SPOR) Unit (J.A.B.), University of Alberta, Edmonton, Canada.

Gavin Y Oudit (GY)

Division of Cardiology, Department of Medicine (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.
Mazankowski Alberta Heart Institute (K.W., R.B., G.Y.O.), University of Alberta, Edmonton, Canada.

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Classifications MeSH