Evidence map›Paper›PMID 23567489›Full record

Trial reportThe pharmacogenomics journal2014

Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndrome.

A Stevens, P Clayton, L Tatò, H W Yoo, M D Rodriguez-Arnao, J Skorodok, G R Ambler, M Zignani, J Zieschang, G Della Corte and 4 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IV
In one paragraph

Trial report in The pharmacogenomics journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00256126 (A Phase IV Open-label Study of Predictive Markers in Growth Hormone Deficient and Turner Syndrome Pre-pubertal Children Treated With SAIZEN®), which is not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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.

NCT00256126 phase4completednot on this map

A Phase IV Open-label Study of Predictive Markers in Growth Hormone Deficient and Turner Syndrome Pre-pubertal Children Treated With SAIZEN®

TypeinterventionalSponsorMerck KGaA, Darmstadt, GermanyRan2005 to 2007Enrolled318ConditionsGrowth Hormone Deficiency, Turner SyndromeArmsSaizen
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. [Turner syndrome and genetic polymorphism: a systematic review].Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. First Clinical Study on Long-Acting Growth Hormone Therapy in Children with Turner Sydrome.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2022
    Article
  8. Review
  9. A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness.The Journal of clinical endocrinology and metabolism · 2020
    Observational
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Sex, Sport, IGF-1 and the Community Effect in Height Hypothesis.International journal of environmental research and public health · 2015
    Article
  16. Article
  17. Article
  18. 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

14 authors at 8 institutions in 9 countries.

A StevensManchester Academic Health Sciences Centre, Royal Manchester Children's Hospital, Manchester, UK.
P ClaytonManchester Academic Health Sciences Centre, Royal Manchester Children's Hospital, Manchester, UK.
L TatòClinica Pediatrica, Università degli Studi di Verona, Verona, Italy.
H W YooDepartment of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
M D Rodriguez-ArnaoPaediatric Endocrine Unit, Hospital General Universitario Gregorio Marañón and Universidad Complutense, Madrid, Spain.
J SkorodokSt Petersburg State Pediatric Medical Academy, Department of Endocrinology, St Petersburg, Russia.
G R AmblerInstitute of Endocrinology and Diabetes, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.
M ZignaniMerck Serono S.A.-Geneva, Geneva, Switzerland.
J ZieschangMerck KGaA, Darmstadt, Germany.
G Della CorteMerck Serono S.A.-Geneva, Geneva, Switzerland.
B DestenavesMerck Serono S.A.-Geneva, Geneva, Switzerland.
A ChampigneulleMerck Serono S.A.-Geneva, Geneva, Switzerland.
J RaelsonGenizon Biosciences, St Laurent, Quebec, Canada.
P ChatelainDepartment Pediatrie, Service d'Endocrinologie & Diabétologie Pédiatriques, Hôpital Mère-Enfant-Université Claude Bernard, Lyon, France.
Merck Serono (Switzerland) · CHChildren's Hospital at Westmead · AUMerck (Germany) · DERoyal Manchester Children's Hospital · GBUlsan College · KRUniversité Claude Bernard Lyon 1 · FRHospital General Universitario Gregorio Marañón · ESUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individual responses to growth hormone (GH) treatment are variable. Short-term generation of insulin-like growth factor-I (IGF-I) is recognized as a potential marker of sensitivity to GH treatment. This prospective, phase IV study used an integrated genomic analysis to identify markers associated with 1-month change in IGF-I (ΔIGF-I) following initiation of recombinant human (r-h)GH therapy in treatment-naïve children with GH deficiency (GHD) (n=166) or Turner syndrome (TS) (n=147). In both GHD and TS, polymorphisms in the cell-cycle regulator CDK4 were associated with 1-month ΔIGF-I (P<0.05). Baseline gene expression was also correlated with 1-month ΔIGF-I in both GHD and TS (r=0.3; P<0.01). In patients with low IGF-I responses, carriage of specific CDK4 alleles was associated with MAPK and glucocorticoid receptor signaling in GHD, and with p53 and Wnt signaling pathways in TS. Understanding the relationship between genomic markers and early changes in IGF-I may allow development of strategies to rapidly individualize r-hGH dose.

Indexed as

Polymorphism, Single NucleotideAdolescentChildChild, PreschoolCyclin-Dependent Kinase 4FemaleGene Expression ProfilingGrowth DisordersHormone Replacement TherapyHuman Growth HormoneHumansInfantInsulin-Like Growth Factor IMaleProspective StudiesRecombinant ProteinsCDK4 protein, humanCyclin-Dependent Kinase 4Human Growth HormoneInsulin-Like Growth Factor IRecombinant Proteins

Identifiers

PMID23567489
PMCPMC3959225
OpenAlexW2063010074

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.