Evidence map›Paper›PMID 23559676›Full record

Trial reportClinical journal of the American Society of Nephrology : CJASN2013

The skeletal consequences of growth hormone therapy in dialyzed children: a randomized trial.

Justine Bacchetta, Katherine Wesseling-Perry, Beatriz Kuizon, Renata C Pereira, Barbara Gales, He-jing Wang, Robert Elashoff, Isidro B Salusky

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical journal of the American Society of Nephrology : CJASN, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the 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
2.8field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Treatment of hyperphosphatemia: the dangers of high PTH levels.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  9. Article
  10. Clinical practice recommendations for treatment with active vitamin D analogues in children with chronic kidney disease Stages 2-5 and on dialysis.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    Article
  11. Review
  12. Article
  13. Combining exercise and growth hormone therapy: how can we translate from animal models to chronic kidney disease children?Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2016
    Article
  14. Micro-CT in the Assessment of Pediatric Renal Osteodystrophy by Bone Histomorphometry.Clinical journal of the American Society of Nephrology : CJASN · 2016
    Article
  15. Management dilemmas in pediatric nephrology: Cystinosis.Pediatric nephrology (Berlin, Germany) · 2015
    Article
  16. Defective skeletal mineralization in pediatric CKD.Current osteoporosis reports · 2015
    Review
  17. Article
  18. The consequences of chronic kidney disease on bone metabolism and growth in children.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2012
    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

8 authors at 2 institutions in 1 country.

Justine BacchettaDepartment of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, California 90095, USA.
Katherine Wesseling-Perry
Beatriz Kuizon
Renata C Pereira
Barbara Gales
He-jing Wang
Robert Elashoff
Isidro B Salusky
University of California, Los Angeles · USKaiser Permanente · US

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
UCLA CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR033176 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2011 to 2011
$15.5M
Pathophysiology of PTH-related Protein (1-36) in HumansR01DK051081 · NIDDK · YALE UNIVERSITY · PI STEWART, ANDREW F. · 1996 to 2012
$5.0M
Regulation of Bone Mineralization in Renal OsteodystrophyR01DK035423 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SALUSKY, ISIDRO B. · 1986 to 2012
$4.9M
ROLE OF PTH IN RENAL OSTEODYSTROPHYR01DK067563 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SALUSKY, ISIDRO B. · 2005 to 2009
$1.9M
MODELING BONE FORMATION AND 125 VITAMIN D IN HUMORAL HYPERCALCEMIA OF MALIGNANCYR01DK073039 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEWART, ANDREW F. · 2006 to 2009
$1.2M
NCATS NIH HHS UL1 TR000124NCATS NIH HHS UL1TR000124NCRR NIH HHS UL1 RR-033176NCRR NIH HHS UL1 RR033176NIDDK NIH HHS DK-073039NIDDK NIH HHS DK-35423NIDDK NIH HHS DK-51081NIDDK NIH HHS DK-67563NIDDK NIH HHS R01 DK035423NIDDK NIH HHS R01 DK051081NIDDK NIH HHS R01 DK067563NIDDK NIH HHS R01 DK073039
6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe effects of recombinant human growth hormone on renal osteodystrophy are unknown; thus, the effects of growth hormone (GH) on bone histomorphometry were assessed in pediatric patients with ESRD. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Thirty-three patients who underwent bone biopsy between July 1994 and May 1999 were randomly assigned to therapy with or without GH. Patients were stratified by bone formation rate; all patients with high bone turnover received intraperitoneal calcitriol. Serum biochemical values were obtained monthly, and bone biopsy was repeated after 8 months.

resultsMedian patient age was 11.7 years (interquartile range [IQR], 7.6, 14.1 years); 45% of patients were male, and 52% were prepubertal. Median dialysis duration was 0.4 (IQR, 0.3, 0.8) year. Bone formation rate per bone surface increased from 15.0 (9.6, 21.8) to 154.6 (23.7, 174.3) μm(2)/μm(3) per year (P=0.05) in patients with low bone turnover treated with GH, decreased from 103.3 (57.0, 173.4) to 60.3 (20.3, 13.7) μm(2)/μm(3) per year in patients with high bone turnover receiving standard therapy (P=0.03), and was unchanged in the other two groups. Bone formation rates were higher with GH, irrespective of underlying bone histologic features (P=0.05). Parathyroid hormone did not differ between groups. GH therapy resulted in greater increases in height SD scores (estimated mean difference in change ± SD, 0.324±0.076; P<0.001), irrespective of underlying bone histologic features.

conclusionsGH therapy improves height in pediatric dialysis patients, irrespective of underlying bone histologic features. Bone formation rates are higher in GH recipients, and GH therapy alters the relationship between circulating parathyroid hormone values and bone turnover.

Indexed as

Peritoneal DialysisAdolescentAnalysis of VarianceBiomarkersBiopsyBody HeightBone and BonesChildChild, PreschoolChronic Kidney Disease-Mineral and Bone DisorderFemaleHuman Growth HormoneHumansKidney Failure, ChronicLos AngelesMaleBiomarkersHuman Growth HormoneParathyroid HormonePTH protein, humanRecombinant Proteins

Identifiers

PMID23559676
PMCPMC3641609
OpenAlexW2100018439

What OpenQuestion holds

Textmetadata
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.