Evidence map›Paper›PMID 9024217›Full record

ArticleThe Journal of clinical endocrinology and metabolism1997

Growth hormone (GH) retesting and auxological data in 131 GH-deficient patients after completion of treatment.

M Tauber, P Moulin, C Pienkowski, B Jouret, P Rochiccioli

Registry-linked trialOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01237041 (Free Fatty Acids, Body Weight, and Growth Hormone Secretion in Children), which is not on this map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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.

NCT01237041 phase1 / phase2terminatedstarted 2011, after this paper: background citation

Free Fatty Acids, Body Weight, and Growth Hormone Secretion in Children

Ran2011Enrolled37Registered outcomes4Posted comparisons4ConditionsGrowth Hormone Deficiency, Obesity, Short StatureArmsDose-Establishing Study 1 Niacin 250mg, Dose-Establishing Study 1 Niacin 500mg, Dose-Establishing Study 2 Niacin 500mg, Niacin First, Placebo First
PMID 16912138PMID 27654882PMID 18782877other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 205 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition.The Journal of clinical endocrinology and metabolism · 2022
    Article
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Article
  17. Relevance of Pituitary Gland Magnetic Resonance Imaging Results with Clinical and Laboratory Findings in Growth Hormone Deficiency.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  18. Article
  19. Article
  20. Update on GH therapy in adults.F1000Research · 2017
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

M TauberService de Pédiatrie Endocrinologie, Centre, Hospitalier Universitoine, Purpan, Toulouse, France.
P Moulin
C Pienkowski
B Jouret
P Rochiccioli
Centre Hospitalier Universitaire de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GH state and auxological data after completion of GH therapy are reported in 131 patients (79 males, 52 females). They were treated from 1980-1994 for partial (n = 98) or complete (n = 33) GH deficiency (GHD), either idiopathic (n = 121) or organic (n = 10). A single stimulation test (clonidine+betaxolol) was used, and only 50 patients (38%) maintained a blunted response (GH peak below 10 micrograms/L). Although 9 of the 10 patients with organic GHD had an abnormal low GH peak, 67% of patients with idiopathic GHD normalized their GH secretion. This was particularly true of partial GHD patients (71% vs. 36% of complete GH-deficient patients). Based on a retest GH peak below 5 micrograms/L, only 23% of the patients were considered to be GH deficient and therefore candidates for GH treatment during adulthood. We found no significant difference between hormonal state at completion of treatment and initial GH deficiency, pubertal state, or sex, although we did find a significantly lower GH peak value before and after treatment in patients with elevated body mass index. Of the 14 obese children who were treated, 50% had an abnormally low serum insulin-like growth factor-I level, arguing for true GHD, and only two children remained obese at cessation of treatment. Auxological data showed that with a mean duration of treatment of 3.6 +/- 2.0 yr, patients classified as having complete GHD before treatment had significantly greater catch-up growth as expressed in SDS for height than patients with partial GHD (0.6 +/- 1.1 vs. 1.1 +/- 0.7 SDS, P < 0.05), and that boys grew better than girls (1.4 +/- 0.8 vs. 1.6 +/- 0.6 SDS) for height, P < 0.01). That catch-up growth was not correlated with the result of GH peak after cessation of treatment.

Indexed as

Child DevelopmentAdolescentBody Mass IndexChildCohort StudiesFemaleHuman Growth HormoneHumansInsulin-Like Growth Factor IMaleMetabolism, Inborn ErrorsPubertyHuman Growth HormoneInsulin-Like Growth Factor I

Identifiers

PMID9024217
OpenAlexW1983635847

What OpenQuestion holds

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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.