Evidence map›Paper›PMID 29931461›Full record

ArticleCalcified tissue international2018

Sclerostin Antibody Reverses the Severe Sublesional Bone Loss in Rats After Chronic Spinal Cord Injury.

Wei Zhao, Xiaodong Li, Yuanzhen Peng, Yiwen Qin, Jiangping Pan, Jiliang Li, Aihua Xu, Michael S Ominsky, Christopher Cardozo, Jian Q Feng and 3 more

Open access · greenAbstract read
In one paragraph

Article in Calcified tissue international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
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  7. Role of the Osteocyte in Musculoskeletal Disease.Current osteoporosis reports · 2023
    Review
  8. Article
  9. Article
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  12. Review
  13. Implications of enolase in the RANKL-mediated osteoclast activity following spinal cord injury.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2021
    Article
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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

13 authors at 7 institutions in 2 countries.

Wei ZhaoNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Xiaodong LiAmgen Inc., Thousand Oaks, CA, USA.
Yuanzhen PengNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Yiwen QinNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Jiangping PanNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Jiliang LiIndiana University Purdue University Indianapolis, Indianapolis, IN, USA.
Aihua XuIndiana University Purdue University Indianapolis, Indianapolis, IN, USA.
Michael S OminskyAmgen Inc., Thousand Oaks, CA, USA.
Christopher CardozoNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Jian Q FengBaylor College of Dentistry, TX A&M, Dallas, TX, USA.
Hua Zhu KeUCB Pharma, Slough, UK.
William A BaumanNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA.
Weiping QinNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY, 10468, USA. weiping.qin@mssm.edu.
James J. Peters VA Medical Center · USIcahn School of Medicine at Mount Sinai · USAmgen (United States) · USBaylor University · USIndiana University – Purdue University Indianapolis · USUCB Pharma (United Kingdom) · GBUniversity of Indianapolis · US

Funding

Novel Pharmacological and Non-pharmacological Interventions for Bone Loss in SCII01RX002089 · VA · JAMES J PETERS VA MEDICAL CENTER · PI QIN, WEIPING · 2017 to 2023
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RRD VA I01 RX000687RRD VA I01 RX001313RRD VA I01 RX002089
6 · The paper itself

Abstract

To date, no efficacious therapy exists that will prevent or treat the severe osteoporosis in individuals with neurologically motor-complete spinal cord injury (SCI). Recent preclinical studies have demonstrated that sclerostin antibody (Scl-Ab) can prevent sublesional bone loss after acute SCI in rats. However, it remains unknown whether sclerostin inhibition reverses substantial bone loss in the vast majority of the SCI population who have been injured for several years. This preclinical study tested the efficacy of Scl-Ab to reverse the bone loss that has occurred in a rodent model after chronic motor-complete SCI. Male Wistar rats underwent either complete spinal cord transection or only laminectomy. Twelve weeks after SCI, the rats were treated with Scl-Ab at 25 mg/kg/week or vehicle for 8 weeks. In the SCI group that did not receive Scl-Ab, 20 weeks of SCI resulted in a significant reduction of bone mineral density (BMD) and estimated bone strength, and deterioration of bone structure at the distal femoral metaphysis. Treatment with Scl-Ab largely restored BMD, bone structure, and bone mechanical strength. Histomorphometric analysis showed that Scl-Ab increased bone formation in animals with chronic SCI. In ex vivo cultures of bone marrow cells, Scl-Ab inhibited osteoclastogenesis, and promoted osteoblastogenesis accompanied by increased Tcf7, ENC1, and the OPG/RANKL ratio expression, and decreased SOST expression. Our findings demonstrate for the first time that Scl-Ab reverses the sublesional bone loss when therapy is begun after relatively prolonged spinal cord transection. The study suggests that, in addition to being a treatment option to prevent bone loss after acute SCI, sclerostin antagonism may be a valid clinical approach to reverse the severe bone loss that invariably occurs in patients with chronic SCI.

Indexed as

AnimalsAntibodiesBone DensityBone Morphogenetic ProteinsBone ResorptionChronic DiseaseGenetic MarkersMaleOsteogenesisRatsRats, WistarSpinal Cord InjuriesAntibodiesBone Morphogenetic ProteinsGenetic MarkersSost protein, ratBone formationBone mineral densitySclerostinSpinal cord injuryTrabecular bone volume

Identifiers

PMID29931461
PMCPMC7891854
OpenAlexW2808830456

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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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.