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ABSTRACT: Aims
Recently, dipeptidyl peptidase 3 (DPP3) has been discovered as the peptidase responsible for cleavage of angiotensin (1-7) [Ang (1-7)]. Ang (1-7) is part of the angiotensin-converting enzyme-Ang (1-7)-Mas pathway which is considered to antagonize the renin-angiotensin-aldosterone system (RAAS). Since DPP3 inhibits the counteracting pathway of the RAAS, we hypothesize that DPP3 might be deleterious in the setting of heart failure. However, no data are available on DPP3 in chronic heart failure. We therefore investigated the clinical characteristics and outcome related to elevated DPP3 concentrations in patients with worsening heart failure.Methods and results
Dipeptidyl peptidase 3 was measured in 2156 serum samples of patients with worsening heart failure using luminom
SUBMITTER: Boorsma EM
PROVIDER: S-EPMC8359955 | biostudies-literature | 2021 Jun
REPOSITORIES: biostudies-literature