Evidence map›Paper›PMID 37910240›Full record

ArticleClinical oral investigations2023

Influence of antiresorptive/antiangiogenic therapy on changes in periodontal and oral tissue structures: a histomorphometrical analysis in rats.

Ausra Ramanauskaite, Katharina Mangold, Ninad Padhye, Karina Obreja, Fanya Borschert, Iulia Dahmer, Frank Schwarz

Open access · hybridAbstract read
In one paragraph

Article in Clinical oral investigations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 2 countries.

Ausra RamanauskaiteDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Katharina MangoldDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Ninad PadhyeDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Karina ObrejaDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Fanya BorschertDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Iulia DahmerDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany.
Frank SchwarzDepartment of Oral Surgery and Implantology, Goethe University, Carolinum, Theodor-Stern-Kai 7; Building 29, 60596, Frankfurt am Main, Germany. f.schwarz@med.uni-frankfurt.de.
Goethe University Frankfurt · DEGoethe Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of this study was to investigate the influence of various antiresorptive and antiangiogenic medications on morphological changes in periodontal and oral tissue structures. MATERIALS AND

methodsFifty-five Wistar rats randomly received dual application (i.e., at baseline and after 12-weeks) one of the following medications: (1) amino-bisphosphonate [zoledronate (Zo)], (2) RANKL inhibitor [denosumab (De)], (3) antiangiogenic [bevacizumab (Be)], (4) Zo + Be, (5) De + Be or (6) no medication [Control (Co)]. Periodontal and oral tissue biopsies were obtained at 17 (n = 21 animals, Phase 1, (De = 3, De + Be = 3, Zo = 5, Be = 3, Zo + Be = 2, Co = 5) and 29 (n = 34 animals, (De = 8, De + Be = 6, Zo = 2, Be = 7, Zo + Be = 4, Co = 7, Phase 2) weeks after the second drug application. The following outcomes were histomorphometrically assessed: periodontal space width in the coronal (PLS-C, mm) and apical sections (PLS- A), number of empty alveolar bone lacunae in the coronal, apical sections and at the apex at respective tooth sites (EL - C, EL- A, EL- Ap), mucosal thickness at edentulous alveolar ridge areas (MT, mm), and, when present, associated areas of inflammatory cell infiltrates (ICI, mm

resultsComparable mean PLS-C, PLS-A, ET-A, ET-C, ET-Ap, and MT values were observed in all experimental groups after Phases 1 and 2. The presence of ICI was identified in 3 animals in the Co group (Phase 1: 1, Phase 2: 2), and 17 animals in the test groups (Phase 1: 4; Phase 2: 14). The estimated ICI surface area was significantly higher in the Zo + Be group, followed by the Zo and Be groups compared to that measured in the Co group. The time (i.e., Phases 1 and 2) was not found to be a predictor for the extent of the ICI area. In all groups, the EL-C, EL-A, and EL-Ap values were significantly higher after Phase 2 compared to those assessed after Phase 1. The MT values were significantly reduced in all groups after Phase 2 compared to those measured after Phase 1.

conclusionsThe present evaluation was not able to find any morphological effects of different antiresorptive and antiangiogenic medications on periodontal and oral tissue structures. The presence of inflammatory cell infiltrates was more frequently observed in the animals administered with antiresorptive and antiangiogenic medications as well as combinations thereof. CLINICAL RELEVANCE: Administration of antiresorptive and antiangiogenic medications may be capable of inducing inflammatory reactions in periodontal tissues.

Indexed as

DiphosphonatesPeriodontiumAnimalsInflammationRatsRats, WistarZoledronic AcidDiphosphonatesZoledronic AcidAnimal experimentAntiangiogenic therapyAntiresorptive therapyHistological techniquePeriodontal spaceTreatment

Identifiers

PMID37910240
PMCPMC10713659
OpenAlexW4388139878

What OpenQuestion holds

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LicenceCC BY
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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.