Evidence map›Paper›PMID 19468288›Full record

ReviewNature reviews. Rheumatology2009

Fat targets for skeletal health.

Masanobu Kawai, Maureen J Devlin, Clifford J Rosen

Abstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
9.0field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Effects of risedronate on bone marrow adipocytes in postmenopausal women.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2011
    Trial
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. The role of bone health in low-velocity fractures and the effects of obesity on the growing skeleton.Journal of the Pediatric Orthopaedic Society of North America · 2024
    Article
  12. The essential roles of mGenes & diseases · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Osteocalcin and Metabolic Syndrome.Clinical medicine insights. Endocrinology and diabetes · 2023
    Article
  17. Article
  18. The mActa pharmacologica Sinica · 2022
    Article
  19. Article
  20. Role of m6A in osteoporosis, arthritis and osteosarcoma (Review).Experimental and therapeutic medicine · 2021
    Review

12 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Masanobu KawaiMaine Medical Center Research Institute, Scarborough, ME 04074-7205, USA.
Maureen J Devlin
Clifford J Rosen
Beth Israel Deaconess Medical Center · USMaine Medical Center Research Institute · 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
NIAMS NIH HHS AR 45433NIAMS NIH HHS AR 54604NIAMS NIH HHS R01 AR045433NIAMS NIH HHS R01 AR054604
6 · The paper itself

Abstract

Emerging evidence points to a critical role for the skeleton in several homeostatic processes, including energy balance. The connection between fuel utilization and skeletal remodeling begins in the bone marrow with lineage allocation of mesenchymal stem cells to adipocytes or osteoblasts. Mature bone cells secrete factors that influence insulin sensitivity, and fat cells synthesize cytokines that regulate osteoblast differentiation; thus, these two pathways are closely linked. The emerging importance of the bone-fat interaction suggests that novel molecules could be used as targets to enhance bone formation and possibly prevent fractures. In this article, we discuss three pathways that could be pharmacologically targeted for the ultimate goal of enhancing bone mass and reducing osteoporotic fracture risk: the leptin, peroxisome proliferator-activated receptor gamma and osteocalcin pathways. Not surprisingly, because of the complex interactions across homeostatic networks, other pathways will probably be activated by this targeting, which could prove to be beneficial or detrimental for the organism. Hence, a more complete picture of energy utilization and skeletal remodeling will be required to bring any potential agents into the future clinical armamentarium.

Indexed as

Adipose TissueAnimalsBone and BonesBone DensityBone RemodelingDisease Models, AnimalEnergy MetabolismFemaleHomeostasisHumansLeptinMaleMiceMice, KnockoutOsteocalcinOsteoporosisLeptinOsteocalcinPPAR gamma

Identifiers

PMID19468288
PMCPMC3661210
OpenAlexW2043432266

What OpenQuestion holds

Textmetadata
LicenceTDM
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.