Evidence map›Paper›PMID 38025036›Full record

ArticleJBMR plus2023

Zucker Diabetic-Sprague Dawley Rats Have Impaired Peri-Implant Bone Formation, Matrix Composition, and Implant Fixation Strength.

Kyle D Anderson, Christian Beckmann, Saskia Heermant, Frank C Ko, Bryan Dulion, Imad Tarhoni, Jeffrey A Borgia, Amarjit S Virdi, Markus A Wimmer, D Rick Sumner and 1 more

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 1 institution in 1 country.

Kyle D AndersonDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Christian BeckmannDepartment of Orthopedic Surgery Rush University Medical Center Chicago IL USA.
Saskia HeermantDepartment of Orthopedic Surgery Rush University Medical Center Chicago IL USA.
Frank C KoDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.ORCID https://orcid.org/0000-0001-7305-7946
Bryan DulionDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Imad TarhoniDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Jeffrey A BorgiaDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Amarjit S VirdiDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Markus A WimmerDepartment of Orthopedic Surgery Rush University Medical Center Chicago IL USA.
D Rick SumnerDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.
Ryan D RossDepartment of Anatomy and Cell Biology Rush University Medical Center Chicago IL USA.ORCID https://orcid.org/0000-0003-3760-234X
Rush University Medical Center · US

Funding

Pre and Post-Doctoral Training in Joint HealthT32AR073157 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI D Rick Sumner · 2019 to 2026
$2.3M
NIAMS NIH HHS T32 AR073157
6 · The paper itself

Abstract

An increasing number of patients with type 2 diabetes (T2DM) will require total joint replacement (TJR) in the next decade. T2DM patients are at increased risk for TJR failure, but the mechanisms are not well understood. The current study used the Zucker Diabetic-Sprague Dawley (ZDSD) rat model of T2DM with Sprague Dawley (SPD) controls to investigate the effects of intramedullary implant placement on osseointegration, peri-implant bone structure and matrix composition, and fixation strength at 2 and 10 weeks post-implant placement. Postoperative inflammation was assessed with circulating MCP-1 and IL-10 2 days post-implant placement. In addition to comparing the two groups, stepwise linear regression modeling was performed to determine the relative contribution of glucose, cytokines, bone formation, bone structure, and bone matrix composition on osseointegration and implant fixation strength. ZDSD rats had decreased peri-implant bone formation and reduced trabecular bone volume per total volume compared with SPD controls. The osseointegrated bone matrix of ZDSD rats had decreased mineral-to-matrix and increased crystallinity compared with SPD controls. Osseointegrated bone volume per total volume was not different between the groups, whereas implant fixation was significantly decreased in ZDSD at 2 weeks but not at 10 weeks. A combination of trabecular mineral apposition rate and postoperative MCP-1 levels explained 55.6% of the variance in osseointegration, whereas cortical thickness, osseointegration mineral apposition rate, and matrix compositional parameters explained 69.2% of the variance in implant fixation strength. The results support the growing recognition that both peri-implant structure and matrix composition affect implant fixation and suggest that postoperative inflammation may contribute to poor outcomes after TJR surgeries in T2DM patients. © 2023 The Authors.

Indexed as

ANIMAL MODELSBIOMECHANICSBONE MATRIXDIABETESIMPLANTS

Identifiers

PMID38025036
PMCPMC10652173
OpenAlexW4387573770

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.