Evidence map›Paper›PMID 31707108›Full record

ArticleBone2020

Anti-vascular endothelial growth factor antibody monotherapy causes destructive advanced periodontitis in rice rats (Oryzomys palustris).

J G Messer, E J Castillo, A M Abraham, J M Jiron, R Israel, J F Yarrow, S Thomas, M C Reynolds, R D Wnek, M Jorgensen and 5 more

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 24% 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, 15 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

15 authors at 3 institutions in 2 countries.

J G MesserDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: jgmesser@ufl.edu.
E J CastilloDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: evelynjcastillo@ufl.edu.
A M AbrahamDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: abelabra@ufl.edu.
J M JironDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: jjiron@ufl.edu.
R IsraelDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: ronniei@ufl.edu.
J F YarrowResearch Service, VA Medical Center, Gainesville, FL, United States of America; Division of Endocrinology, Diabetes, and Metabolism, University of Florida College of Medicine, Gainesville, FL, United States of America. Electronic address: Joshua.yarrow@medicine.ufl.edu.
S ThomasDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: sthomas101@ufl.edu.
M C ReynoldsResearch Service, VA Medical Center, Gainesville, FL, United States of America.
R D WnekResearch Service, VA Medical Center, Gainesville, FL, United States of America.
M JorgensenDepartment of Pediatrics, College of Medicine, UF, United States of America. Electronic address: marda@ufl.edu.
N WanionokDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America.
C Van PoznakUniversity of Michigan, Ann Arbor, MI, United States of America. Electronic address: cvanpoz@med.umich.edu.
I BhattacharyyaDepartment of Oral & Maxillofacial Diagnostic Sciences, College of Dentistry, UF, United States of America. Electronic address: IBHATTACHARYYA@dental.ufl.edu.
D B KimmelDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: kimmeldb@comcast.net.
J I AguirreDepartment of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America. Electronic address: aguirrej@ufl.edu.
University of Florida · USFlorida College · USUniversity of Michigan · US

Funding

Role of Periodontitis in Osteonecrosis of the Jaw Pathophysiology in Rice RatsR01DE023783 · NIDCR · UNIVERSITY OF FLORIDA · PI AGUIRRE, JOSE IGNACIO · 2014 to 2018
$1.7M
NIDCR NIH HHS R01 DE023783
6 · The paper itself

Abstract

objectiveAngiogenesis inhibitors (AgI) are commonly used in combination chemotherapy protocols to treat cancer, and have been linked to osteonecrosis of the jaw (ONJ). However, it is unknown if AgI therapy alone is sufficient to induce ONJ. We have previously established an ONJ model in rice rats with localized periodontitis that receive zoledronic acid (ZOL). The purpose of this study was to use this model to determine the role of anti-vascular endothelial growth factor A (anti-VEGF) antibody treatment of rice rats with localized maxillary periodontitis. We hypothesized that rice rats with localized maxillary periodontitis given anti-VEGF monotherapy will develop oral lesions that resemble ONJ, defined by exposed, necrotic alveolar bone.

methodsAt age 4 weeks, 45 male rice rats were randomized into three groups (n = 15): 1) VEH (saline), 2) ZOL (80 μg/kg body weight, intravenously once monthly), and 3) anti-VEGF (5 mg B20-4.1.1/kg body weight, subcutaneously twice weekly). After 24 weeks, rats were euthanized, jaws were excised and a high-resolution photograph of each quadrant was taken to assign a severity grade based on gross appearance. Jaws were then fixed, scanned by MicroCT, decalcified and sectioned for histopathologic and immunohistochemical analyses.

results40-80% of the rats in the three groups developed gross oral lesions. 50% of ZOL rats developed ONJ. In contrast, 80% of the anti-VEGF rats developed destructive advanced periodontitis that was characterized by extreme alveolar bone loss and fibrosis. Anti-VEGF rats never developed exposed, necrotic bone. Furthermore, only anti-VEGF rats developed mild to severe mandibular periodontitis. Compared to VEH rats, more T-cells were found in periodontal lesions of anti-VEGF rats and more cells of the monocyte lineage were found in ONJ lesions of ZOL rats.

conclusionsAnti-VEGF monotherapy administered to a validated rodent model of ONJ caused a destructive advanced form of periodontitis that differed significantly from ONJ.

Indexed as

Bisphosphonate-Associated Osteonecrosis of the JawOsteonecrosisPeriodontitisAnimalsDiphosphonatesMaleRatsSigmodontinaeX-Ray MicrotomographyZoledronic AcidDiphosphonatesZoledronic AcidAnti-angiogenicJawOncologyOral diseasesOsteonecrosis

Identifiers

PMID31707108
PMCPMC6941430
OpenAlexW2987340510

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.