Evidence map›Paper›PMID 29500454›Full record

Trial reportScientific reports2018

The effects of angiotensin receptor neprilysin inhibition by sacubitril/valsartan on adipose tissue transcriptome and protein expression in obese hypertensive patients.

R Stinkens, B W van der Kolk, J Jordan, T Jax, S Engeli, T Heise, J W Jocken, M May, C Schindler, B Havekes and 8 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Angiotensin receptor-neprilysin inhibitors: Comprehensive review and implications in hypertension treatment.Hypertension research : official journal of the Japanese Society of Hypertension · 2021
    Review
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

18 authors at 6 institutions in 3 countries.

R StinkensDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.ORCID 0000-0001-9382-2457
B W van der KolkDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.
J JordanInstitute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany.
T JaxProfil GmbH, Neuss, Germany.
S EngeliInstitute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany.
T HeiseProfil GmbH, Neuss, Germany.
J W JockenDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.
M MayClinical Research Center Hannover, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-7513-4244
C SchindlerClinical Research Center Hannover, Hannover Medical School, Hannover, Germany.
B HavekesDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.
N SchaperDepartment of Internal Medicine, Division of Endocrinology, Maastricht University Medical Center+, Maastricht, The Netherlands.
D AlbrechtTranslational Medicine, Novartis Institutes for Biomedical Research, Basel, Switzerland.
S KaiserTranslational Medicine, Novartis Institutes for Biomedical Research, Basel, Switzerland.
N HartmannTranslational Medicine, Novartis Institutes for Biomedical Research, Basel, Switzerland.
M LetzkusTranslational Medicine, Novartis Institutes for Biomedical Research, Basel, Switzerland.
T H LangenickelTranslational Medicine, Novartis Institutes for Biomedical Research, Basel, Switzerland.
G H GoossensDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.
E E BlaakDepartment of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands. e.blaak@maastrichtuniversity.nl.
Maastricht University · NLNovartis (Switzerland) · CHMedizinische Hochschule Hannover · DEMaastricht University Medical Centre · NLProfil Institute for Metabolic Research · DEDeutsches Zentrum für Luft- und Raumfahrt e. V. (DLR) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased activation of the renin-angiotensin system is involved in the onset and progression of cardiometabolic diseases, while natriuretic peptides (NP) may exert protective effects. We have recently demonstrated that sacubitril/valsartan (LCZ696), a first-in-class angiotensin receptor neprilysin inhibitor, which blocks the angiotensin II type-1 receptor and augments natriuretic peptide levels, improved peripheral insulin sensitivity in obese hypertensive patients. Here, we investigated the effects of sacubitril/valsartan (400 mg QD) treatment for 8 weeks on the abdominal subcutaneous adipose tissue (AT) phenotype compared to the metabolically neutral comparator amlodipine (10 mg QD) in 70 obese hypertensive patients. Abdominal subcutaneous AT biopsies were collected before and after intervention to determine the AT transcriptome and expression of proteins involved in lipolysis, NP signaling and mitochondrial oxidative metabolism. Both sacubitril/valsartan and amlodipine treatment did not significantly induce AT transcriptional changes in pathways related to lipolysis, NP signaling and oxidative metabolism. Furthermore, protein expression of adipose triglyceride lipase (ATGL) (P

Indexed as

TranscriptomeAdipose TissueAdultAminobutyratesAmlodipineAngiotensin Receptor AntagonistsBiphenyl CompoundsDouble-Blind MethodDrug CombinationsFemaleHumansHypertensionMaleMiddle AgedNeprilysinObesityAminobutyratesAmlodipineAngiotensin Receptor AntagonistsBiphenyl CompoundsDrug CombinationsNeprilysinProteinssacubitril and valsartan sodium hydrate drug combinationTetrazolesValsartan

Identifiers

PMID29500454
PMCPMC5834447
OpenAlexW2806179649

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.