Evidence map›Paper›PMID 25585248›Full record

ArticleBone2015

Prevention of glucocorticoid induced bone changes with beta-ecdysone.

Weiwei Dai, Li Jiang, Yu-An Evan Lay, Haiyan Chen, Guoqin Jin, Hongliang Zhang, Alexander Kot, Robert O Ritchie, Nancy E Lane, Wei Yao

Abstract read
In one paragraph

Article in Bone, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  13. Sclerostin-antibody treatment of glucocorticoid-induced osteoporosis maintained bone mass and strength.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    Article
  14. β-Ecdysone Augments Peak Bone Mass in Mice of Both Sexes.Clinical orthopaedics and related research · 2015
    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

10 authors at 3 institutions in 2 countries.

Weiwei DaiCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA; Department of Science and Technology, Longhua Hospital Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China.
Li JiangCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Yu-An Evan LayCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Haiyan ChenCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Guoqin JinDepartment of Science and Technology, Longhua Hospital Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China.
Hongliang ZhangCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Alexander KotCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Robert O RitchieDepartment of Materials Science and Engineering, University of California at Berkeley, Berkeley, CA 94720, USA.
Nancy E LaneCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA.
Wei YaoCenter for Musculoskeletal Health, Internal Medicine, University of California at Davis Medical Center, Sacramento, CA 95817, USA. Electronic address: wei.yao@ucdmc.ucdavis.edu.
University of California Davis Medical Center · USShanghai University of Traditional Chinese Medicine · CNUniversity of California, Berkeley · US

Funding

Sex Differences in response to an exercise for hyperkyphosisP50AR063043 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GOLD, ELLEN B. · 2012 to 2017
$5.7M
3D IN VIVO MORPHOMETRY OF TRABECULAR MICROSTRUCTURER01AR043052 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI LANE, NANCY E · 1995 to 2014
$5.0M
Midcareer Investigator Award Patient-Oriented ResearchK24AR048841 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI LANE, NANCY E · 2002 to 2013
$1.4M
Directing mesenchymal stem cells to bone to augment bone formationR01AR061366 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI YAO, WEI · 2012 to 2015
$1.1M
NIAMS NIH HHS 1P50AR063043NIAMS NIH HHS K24 AR048841NIAMS NIH HHS P50 AR063043NIAMS NIH HHS R01 AR043052NIAMS NIH HHS R01 AR061366NIAMS NIH HHS R01-AR43052
6 · The paper itself

Abstract

Beta-ecdysone (βEcd) is a phytoecdysteroid found in the dry roots and seeds of the asteraceae and achyranthes plants, and is reported to increase osteogenesis in vitro. Since glucocorticoid (GC) excess is associated with a decrease in bone formation, the purpose of this study was to determine if treatment with βEcd could prevent GC-induced osteoporosis. Two-month-old male Swiss-Webster mice (n=8-10/group) were randomized to either placebo or slow release prednisolone pellets (3.3mg/kg/day) and treated with vehicle control or βEcd (0.5mg/kg/day) for 21days. GC treatment inhibited age-dependent trabecular gain and cortical bone expansion and this was accompanied by a 30-50% lower bone formation rate (BFR) at both the endosteal and periosteal surfaces. Mice treated with only βEcd significantly increased bone formation on the endosteal and periosteal bone surfaces, and increased cortical bone mass were their controls to compare to GC alone. Concurrent treatment of βEcd and GC completely prevented the GC-induced reduction in BFR, trabecular bone volume and partially prevented cortical bone loss. In vitro studies determined that βEcd prevented the GC increase in autophagy of the bone marrow stromal cells as well as in whole bone. In summary, βEcd prevented GC induced changes in bone formation, bone cell viability and bone mass. Additional studies are warranted of βEcd for the treatment of GC induced bone loss.

Indexed as

AnimalsAutophagyBiomechanical PhenomenaBody WeightBone and BonesBone RemodelingCell DifferentiationEcdysteroneGlucocorticoidsHormonesMaleMesenchymal Stem CellsMiceOrgan SizeOsteoblastsOsteogenesisEcdysteroneGlucocorticoidsHormonesAutophagyBeta-ecdysone (βEcd)Bone formationGlucocorticoid

Identifiers

PMID25585248
PMCPMC4355031
OpenAlexW2125913965

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.