Evidence map›Paper›PMID 30644553›Full record

ArticleAnnals of the New York Academy of Sciences2019

Retention of osteocytic micromorphology by sclerostin antibody in a concurrent ovariectomy and functional disuse model.

Dongye Zhang, Mariana Miranda, Xiaofei Li, Jiangmeng Han, Yueli Sun, Nancy Rojas, Shan He, Minyi Hu, Liangjun Lin, Xiaodong Li and 2 more

Open access · greenAbstract read
In one paragraph

Article in Annals of the New York Academy of Sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. 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

12 authors at 2 institutions in 2 countries.

Dongye ZhangDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Mariana MirandaDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Xiaofei LiDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Jiangmeng HanDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Yueli SunDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Nancy RojasDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Shan HeDepartment of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York.
Minyi HuDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Liangjun LinDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Xiaodong LiDepartment of Metabolic Disorders, Amgen, Inc., Thousand Oaks, California.
Hua Zhu KeUCB Pharma, Slough, UK.
Yi-Xian QinDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York.
Stony Brook University · USUCB Pharma (United Kingdom) · GB

Funding

Functional Fluid Flow Regulated Bone RegenerationR01AR061821 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI QIN, YI-XIAN · 2012 to 2016
$1.7M
Role of Musculo-Dynamics in Bone Fluid Flow, Circulation and AdaptationR01AR052379 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI QIN, YI-XIAN · 2005 to 2009
$1.7M
Bone Fluid Flow and its Regulatory Role in AdaptationR01AR049286 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI QIN, YI-XIAN · 2003 to 2006
$1.1M
Amgen, IncNIAMS NIH HHS R01 AR049286NIAMS NIH HHS R01 AR052379NIAMS NIH HHS R01 AR061821US Army Medical Research and Materiel Command
6 · The paper itself

Abstract

Prolonged mechanical unloading in bedridden patients and concurrent hormonal dysregulation represents the cause of one of the severest forms of osteoporosis, a condition for which there are very few efficacious interventions available to date. Sclerostin, a Wnt antagonist, acts as a negative regulator of bone formation. Sclerostin antibody (Scl-Ab)-mediated blockade of sclerostin can dramatically enhance bone formation and reduce bone resorption. This study was designed to investigate the therapeutic effect of the Scl-Ab on severe bone loss induced by concurrent mechanical unloading and estrogen deficiency in a hindlimb-suspended and ovariectomized rat model, and to study the cellular mechanisms underlying severe osteoporosis and Scl-Ab action. Unloading and ovariectomy resulted in severe loss of trabecular and cortical bone mass and strength; Scl-Ab can significantly counteract the deterioration of bone in unloaded and/or ovariectomized rats, with noticeably increased cortical bone formation. Scanning electron microscopy analysis revealed that unloading and ovariectomy lead to multiple morphological and structural abnormalities of osteocytes in cortical bone and the abnormalities were abolished by Scl-Ab administration. This study extends our previous conclusion that Scl-Ab represents a promising therapeutic approach for severe bone loss that occurs after being exposed to estrogen deficiency and prolonged mechanical unloading.

Indexed as

OvariectomyAnimalsAntibodiesBone Morphogenetic ProteinsFemaleGenetic MarkersMiceOrgan SizeOsteocytesOsteoporosisRatsRats, Sprague-DawleyAntibodiesBone Morphogenetic ProteinsGenetic MarkersSost protein, ratestrogen deficiencymechanical unloadingosteocytescanning electron microscopysclerostin antibodysevere osteoporosis

Identifiers

PMID30644553
PMCPMC6465143
OpenAlexW2908939289

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.