Evidence map›Paper›PMID 34930956›Full record

ArticleScientific reports2021

Evidence of feedback regulation of C-type natriuretic peptide during Vosoritide therapy in Achondroplasia.

Timothy C R Prickett, Eric A Espiner, Melita Irving, Carlos Bacino, John A Phillips, Ravi Savarirayan, Jonathan R S Day, Elena Fisheleva, Kevin Larimore, Ming Liang Chan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. C-type natriuretic peptide and collagen X marker are aberrant in skeletal dysplasias.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    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

11 authors at 6 institutions in 4 countries.

Timothy C R PrickettDepartment of Medicine, University of Otago, Christchurch, PO Box 4345, Christchurch, 8140, New Zealand. tim.prickett@otago.ac.nz.
Eric A EspinerDepartment of Medicine, University of Otago, Christchurch, PO Box 4345, Christchurch, 8140, New Zealand.
Melita IrvingGuy's and St. Thomas' NHS Foundation Trust, Evelina Children's Hospital, London, UK.
Carlos BacinoBaylor College of Medicine, Houston, TX, USA.
John A PhillipsVanderbilt University Medical Center, Nashville, TN, USA.
Ravi SavarirayanMurdoch Children's Research Institute, Royal Children's Hospital Victoria, University of Melbourne, Parkville, VIC, Australia.
Jonathan R S DayBioMarin Pharmaceutical, Novato, CA, USA.
Elena FishelevaBioMarin Pharmaceutical, Novato, CA, USA.
Kevin LarimoreBioMarin Pharmaceutical, Novato, CA, USA.
Ming Liang ChanBioMarin Pharmaceutical, Novato, CA, USA.
George S JehaBioMarin Pharmaceutical, Novato, CA, USA.
BioMarin (United States) · USUniversity of Otago · NZBaylor College of Medicine · USGuy's and St Thomas' NHS Foundation Trust · GBUniversity of Melbourne · AUVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence from genetic disorders of CNP signalling suggests that plasma concentrations of CNP are subject to feedback regulation. In subjects with Achondroplasia (Ach), CNP intracellular activity is suppressed and plasma concentrations are raised but the therapeutic impact of exogenous CNP agonists on endogenous CNP is unknown. In this exploratory dose finding and extension study of 28 Ach children receiving Vosoritide over a 5 year period of treatment, endogenous CNP production was assessed using measurements of plasma aminoterminal proCNP (NTproCNP) adjusted for age and sex and normalised as standard deviation score (SDS), and then related to skeletal growth. Before treatment NTproCNP SDS was raised. Within the first 3 months of accelerating growth, levels were significantly reduced. Across the 5 years of sustained growth, levels varied widely and were markedly increased in some subjects during adolescence. Plasma NTproCNP was suppressed at 4 h post-injection in proportion to the prevailing level of hormone resistance as reflected by SDS before injection. We conclude CNP remains subject to regulation during growth promoting doses of Vosoritide. Fall in CNP during accelerating growth is consistent with an indirect feedback whereas the fall at 4 h is likely to be a direct effect from removal of intra cellular CNP resistance.

Indexed as

AchondroplasiaAdolescentBone and BonesBone DevelopmentChildChild, PreschoolFeedbackFemaleGrowth DisordersHumansMaleNatriuretic Peptide, C-TypeTime FactorsTreatment OutcomeNatriuretic Peptide, C-Typevosoritide

Identifiers

PMID34930956
PMCPMC8688426
OpenAlexW4200421343

What Socratic 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 Socratic graph.