Soluble Neprilysin in the General Population: Clinical Determinants and Its Relationship to Cardiovascular Disease.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
06 08 2019
Historique:
entrez: 27 7 2019
pubmed: 28 7 2019
medline: 5 1 2021
Statut: ppublish

Résumé

Background Neprilysin is a metalloprotease involved in proteolysis of numerous peptides, including natriuretic peptides, and is of prognostic and therapeutic importance in heart failure with reduced ejection fraction. No studies have investigated circulating neprilysin in the community, its clinical correlates, or its relationship to cardiovascular disease in the general population. Methods and Results Plasma neprilysin was measured in 1536 participants from Olmsted County, Minnesota, using a commercially available sandwich ELISA assay. Clinical and echocardiographic correlates and subsequent outcomes were determined. Soluble neprilysin is non-normally distributed in the community (median: 3.9 ng/mL; interquartile range: 1.0-43.0 ng/mL). There was no relationship between plasma neprilysin and age (Spearman correlation: -0.04, P=0.16); body mass index (Spearman correlation: -0.04, P=0.16); glomerular filtration rate (Spearman correlation: -0.007, P=0.8); or A-, B-, or C-type natriuretic peptides (Spearman correlation: 0.03, P=0.22; -0.001, P=0.96; 0.01, P=0.67, respectively). Among tertiles of neprilysin, the lowest tertile group had the highest prevalence of smokers (P<0.001), hypertension (P=0.04), dyslipidemia (P=0.03), and diastolic dysfunction (P=0.02). Soluble neprilysin was not prospectively associated with death or heart failure over a median of 10.7 years. Conclusions In a large community-based cohort, for the first time, we described the distribution of circulating neprilysin in the general community. We observed that neprilysin does not correlate with natriuretic peptide levels and is not independently associated with adverse outcomes. The novel associations observed between low soluble neprilysin levels and an adverse cardiometabolic and smoking profile requires further investigation.

Identifiants

pubmed: 31345101
doi: 10.1161/JAHA.119.012943
pmc: PMC6761669
doi:

Substances chimiques

Neprilysin EC 3.4.24.11

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e012943

Subventions

Organisme : NIA NIH HHS
ID : R01 AG034676
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG053512
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007111
Pays : United States

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Auteurs

Yogesh N V Reddy (YNV)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.

Seethalakshmi R Iyer (SR)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.

Christopher G Scott (CG)

Division of Biomedical Statistics and Informatics Mayo Clinic Rochester MN.

Richard J Rodeheffer (RJ)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.

Kent Bailey (K)

Division of Biomedical Statistics and Informatics Mayo Clinic Rochester MN.

Gregory Jenkins (G)

Division of Biomedical Statistics and Informatics Mayo Clinic Rochester MN.

Anthony Batzler (A)

Division of Biomedical Statistics and Informatics Mayo Clinic Rochester MN.

Margaret M Redfield (MM)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.

John C Burnett (JC)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.

Naveen L Pereira (NL)

The Department of Cardiovascular Medicine Mayo Clinic Rochester MN.
Department of Molecular Pharmacology and Experimental Therapeutics Mayo Clinic Rochester MN.

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Classifications MeSH