Back to Search Start Over

Neprilysin activity is increased in metabolic dysfunction-associated steatotic liver disease and normalizes after bariatric surgery or GLP-1 therapy

Authors :
Sasha A.S. Kjeldsen
Lise L. Gluud
Mikkel P. Werge
Julie S. Pedersen
Flemming Bendtsen
Kleopatra Alexiadou
Tricia Tan
Signe S. Torekov
Eva W. Iepsen
Nicole J. Jensen
Michael M. Richter
Jens P. Goetze
Jørgen Rungby
Bolette Hartmann
Jens J. Holst
Birgitte Holst
Joachim Holt
Finn Gustafsson
Sten Madsbad
Maria S. Svane
Kirstine N. Bojsen-Møller
Nicolai J. Wewer Albrechtsen
Source :
iScience, Vol 26, Iss 11, Pp 108190- (2023)
Publication Year :
2023
Publisher :
Elsevier, 2023.

Abstract

Summary: Inhibitors of neprilysin improve glycemia in patients with heart failure and type 2 diabetes (T2D). The effect of weight loss by diet, surgery, or pharmacotherapy on neprilysin activity (NEPa) is unknown. We investigated circulating NEPa and neprilysin protein concentrations in obesity, T2D, metabolic dysfunction-associated steatotic liver disease (MASLD), and following bariatric surgery, or GLP-1-receptor-agonist therapy. NEPa, but not neprilysin protein, was enhanced in obesity, T2D, and MASLD. Notably, MASLD associated with NEPa independently of BMI and HbA1c. NEPa decreased after bariatric surgery with a concurrent increase in OGTT-stimulated GLP-1. Diet-induced weight loss did not affect NEPa, but individuals randomized to 52-week weight maintenance with liraglutide (1.2 mg/day) decreased NEPa, consistent with another study following 6-week liraglutide (3 mg/day). A 90-min GLP-1 infusion did not alter NEPa. Thus, MASLD may drive exaggerated NEPa, and lowered NEPa following bariatric surgery or liraglutide therapy may contribute to the reported improved cardiometabolic effects.

Details

Language :
English
ISSN :
25890042
Volume :
26
Issue :
11
Database :
Directory of Open Access Journals
Journal :
iScience
Publication Type :
Academic Journal
Accession number :
edsdoj.541de04b6ddd4e19900f1ffa4e360c15
Document Type :
article
Full Text :
https://doi.org/10.1016/j.isci.2023.108190