Evidence map›Paper›PMID 32736144›Full record

ArticleBone2020

Region-dependent bone loss in the lumbar spine following femoral fracture in mice.

Erica V Ely, Benjamin Osipov, Armaun J Emami, Blaine A Christiansen

Open access · greenAbstract read
In one paragraph

Article in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

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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

4 authors at 3 institutions in 1 country.

Erica V ElyDepartment of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, United States of America. Electronic address: evely@wustl.edu.
Benjamin OsipovDepartment of Orthopaedic Surgery, University of California Davis Health, Sacramento, CA, United States of America. Electronic address: bosipov@ucdavis.edu.
Armaun J EmamiDepartment of Orthopaedic Surgery, University of California Davis Health, Sacramento, CA, United States of America. Electronic address: ajemami@ucdavis.edu.
Blaine A ChristiansenDepartment of Orthopaedic Surgery, University of California Davis Health, Sacramento, CA, United States of America. Electronic address: bchristiansen@ucdavis.edu.
University of California System · USUniversity of California, Davis · USWashington University in St. Louis · US

Funding

Mechanisms of Systemic Bone Loss Following Femur Fracture in MiceR01AR071459 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHRISTIANSEN, BLAINE A. · 2017 to 2021
$1.8M
NIAMS NIH HHS R01 AR071459
6 · The paper itself

Abstract

We previously showed that after femur fracture, mice lose bone at distant skeletal sites, including the lumbar vertebrae. This bone loss may increase the risk of subsequent vertebral fractures, particularly if bone is lost from high-strain bone regions, which are most commonly found adjacent to the superior and inferior endplates of the vertebral body. To determine regional bone loss from the lumbar spine following femur fracture, we evaluated the cranial, center, and caudal portions of the L5 vertebral bodies of Young (3 month-old) and Middle-Aged (12 month-old) female C57BL/6 mice two weeks after a transverse femur fractures compared to Young and Middle-Aged uninjured control mice. We hypothesized that greater bone loss would be observed in the cranial and caudal regions than in the center region in both Young and Middle-Aged mice. Trabecular and cortical bone microstructure were evaluated using micro-computed tomography, and osteoclast number and eroded surface were evaluated histologically. In Young Mice, fracture led to decreased trabecular and cortical bone microstructure primarily in the cranial and caudal regions, but not the center region, while Middle-Aged mice demonstrated decreases in trabecular bone in all regions, but did not exhibit any changes in cortical bone microstructure after fracture. No significant differences in osteoclast number or eroded surface were observed at this time point. These data suggest that bone loss following fracture in Young Mice is concentrated in areas that contain a large amount of high-strain tissue, whereas bone loss in Middle-Aged mice is less region-dependent and is restricted to the trabecular bone compartment. These results illustrate how systemic bone loss after fracture could lead to decreases in vertebral strength, and how distinct regional patterns and age-dependent differences in bone loss may differentially affect vertebral fracture risk.

Indexed as

Bone Diseases, MetabolicFemoral FracturesAnimalsBone DensityFemaleLumbar VertebraeMiceMice, Inbred C57BLSpineX-Ray MicrotomographyBone resorptionFractureOsteoclastsSystemic bone loss

Identifiers

PMID32736144
PMCPMC7502487
OpenAlexW3045626906

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.