Evidence map›Paper›PMID 18948404›Full record

ArticleEndocrinology2009

Strain-specific effects of rosiglitazone on bone mass, body composition, and serum insulin-like growth factor-I.

Cheryl L Ackert-Bicknell, Keith R Shockley, Lindsay G Horton, Beata Lecka-Czernik, Gary A Churchill, Clifford J Rosen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

60 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Bone marrow-derived IGF-1 orchestrates maintenance and regeneration of the adult skeleton.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. The benefits of adipocyte metabolism in bone health and regeneration.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Sclerostin-Neutralizing Antibody Treatment Rescues Negative Effects of Rosiglitazone on Mouse Bone Parameters.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. BMC biomedical engineering · 2019
    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

6 authors at 2 institutions in 1 country.

Cheryl L Ackert-BicknellThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Keith R Shockley
Lindsay G Horton
Beata Lecka-Czernik
Gary A Churchill
Clifford J Rosen
Jackson Laboratory · USUniversity of Toledo Medical Center · US

Funding

Genetics of IGF1 and Bone Density: The Role of NocturninR01AR045433 · NIAMS · MAINEHEALTH · PI ROSEN, CLIFFORD JAMES · 1998 to 2012
$6.8M
MOUSE MODELS TO DELINEATE A UNIQUE METABOLIC AND SKELETAL NETWORKR01AR054604 · NIAMS · MAINEHEALTH · PI ROSEN, CLIFFORD JAMES · 2007 to 2010
$2.3M
The effects of allelic variation in Pparg on skeletal metabolismF31AG030910 · NIA · JACKSON LABORATORY · PI ACKERT-BICKNELL, CHERYL LYNNE · 2007 to 2007
$17k
NIAMS NIH HHS AR05460NIAMS NIH HHS AR45433NIAMS NIH HHS R01 AR045433NIAMS NIH HHS R01 AR054604NIA NIH HHS F31 AG030910
6 · The paper itself

Abstract

Activation of peroxisome proliferator activated receptor-gamma (PPARG) is required for the differentiation of marrow mesenchymal stem cell into adipocytes and is associated with the development of age-related marrow adiposity in mice. Thiazolidinediones are agonists for PPARG and have a heterogeneous effect on bone mineral density (BMD). We postulated that genetic determinants influence the skeletal response to thiazolidinediones. We examined the effects of rosiglitazone (3 mg/kg . d for 8 wk) on BMD, body composition, and serum IGF-I in adult female mice from four inbred strains. C3H/HeJ mice showed the most significant response to treatment, exhibiting decreased femoral and vertebral BMD, reduced distal femoral bone volume fraction and a decrease in serum IGF-I. In DBA/2J, there were no changes in femoral BMD or bone volume fraction, but there was a decrease in vertebral BMD. C57BL/6J mice showed increases in marrow adiposity, without associated changes in trabecular bone volume; the skeletal effects from rosiglitazone in A/J mice were minimal. No association between trabecular bone volume and marrow adiposity was found. The effect of rosiglitazone on gene expression in the femur was then examined in the C3H/HeJ and C57BL/6J strains by microarray. Increased gene expression was observed in the PPARG signaling pathway and fatty acid metabolism in both C3H/HeJ and C57BL/6J, but a significant down-regulation of genes associated with cell cycle was noted only in the C3H/HeJ strain. The divergent skeletal responses to rosiglitazone in this study suggest the existence of a strong genetic background effect.

Indexed as

AdiposityAnimalsBody CompositionBone and BonesBone DensityFemaleFemurHypoglycemic AgentsInsulin-Like Growth Factor IMiceMice, Inbred C3HMice, Inbred C57BLMice, Inbred DBAMice, Inbred StrainsOrgan SizeRosiglitazoneHypoglycemic AgentsInsulin-Like Growth Factor IRosiglitazoneThiazolidinediones

Identifiers

PMID18948404
PMCPMC2654751
OpenAlexW2163861731

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.