Evidence map›Paper›PMID 38348796›Full record

ArticleJournal of the American Heart Association2024

Angiotensin Receptor-Neprilysin Inhibition (Sacubitril/Valsartan) Reduces Structural Arterial Stiffness in Middle-Aged Mice.

Isabel N Schellinger, Angelika Dannert, Annet Hoffmann, Giriprakash Chodisetti, Karin Mattern, Anne Petzold, Nora Klöting, Andreas Schuster, Markus U Wagenhäuser, Fabian Emrich and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Vascular (dys)function in the failing heart.Nature reviews. Cardiology · 2025
    Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Isabel N SchellingerDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.
Angelika DannertDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.ORCID 0000-0002-0902-3044
Annet HoffmannDepartment for Endocrinology, Nephrology and Rheumatology University Medical Center Leipzig, University of Leipzig Leipzig Germany.ORCID 0000-0002-8467-6758
Giriprakash ChodisettiDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.
Karin MatternDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.
Anne PetzoldDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.
Nora KlötingDepartment for Endocrinology, Nephrology and Rheumatology University Medical Center Leipzig, University of Leipzig Leipzig Germany.
Andreas SchusterDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.ORCID 0000-0003-1508-1125
Markus U WagenhäuserDepartment of Vascular and Endovascular Surgery University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf Germany.
Fabian EmrichDepartment of Cardiothoracic and Vascular Surgery Goethe University Hospital Frankfurt Frankfurt Germany.
Michael StumvollDepartment for Endocrinology, Nephrology and Rheumatology University Medical Center Leipzig, University of Leipzig Leipzig Germany.
Gerd HasenfußDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.
Uwe RaazDepartment of Cardiology and Pneumology Heart Center at the University Medical Center Göttingen Göttingen Germany.ORCID 0000-0003-2237-7653
Universitätsmedizin Göttingen · DEUniversity Hospital Leipzig · DEDüsseldorf University Hospital · DEGoethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing arterial stiffness is a prominent feature of the aging cardiovascular system. Arterial stiffening leads to fundamental alterations in central hemodynamics with widespread detrimental implications for organ function resulting in significant morbidity and death, and specific therapies to address the underlying age-related structural arterial remodeling remain elusive. The present study investigates the potential of the recently clinically available dual angiotensin receptor-neprilysin inhibitor (ARNI) sacubitril/valsartan (LCZ696) to counteract age-related arterial fibrotic remodeling and stiffening in 1-year-old mice. METHODS AND

resultsTreatment of in 1-year-old mice with ARNI (sacubitril/valsartan), in contrast to angiotensin receptor blocker monotherapy (valsartan) and vehicle treatment (controls), significantly decreases structural aortic stiffness (as measured by in vivo pulse-wave velocity and ex vivo aortic pressure myography). This phenomenon appears, at least partly, independent of (indirect) blood pressure effects and may be related to a direct antifibrotic interference with aortic smooth muscle cell collagen production. Furthermore, we find aortic remodeling and destiffening due to ARNI treatment to be associated with improved parameters of cardiac diastolic function in aged mice.

conclusionsThis study provides preclinical mechanistic evidence indicating that ARNI-based interventions may counteract age-related arterial stiffening and may therefore be further investigated as a promising strategy to improve cardiovascular outcomes in the elderly.

Indexed as

AminobutyratesHeart FailureVascular StiffnessAgedAngiotensin Receptor AntagonistsAngiotensinsAnimalsBiphenyl CompoundsDrug CombinationsHumansInfantMiceMiddle AgedNeprilysinReceptors, AngiotensinStroke VolumeAminobutyratesAngiotensin Receptor AntagonistsAngiotensinsBiphenyl CompoundsDrug CombinationsNeprilysinReceptors, Angiotensinsacubitrilsacubitril and valsartan sodium hydrate drug combinationTetrazolesValsartanagingangiotensin receptor antagonistsfibrosismiceneprilysinpulse wave analysisvascular stiffness

Identifiers

PMID38348796
PMCPMC11010079
OpenAlexW4391779997

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.