Evidence map›Paper›PMID 32065225›Full record

ArticleEuropean journal of orthodontics2020

Raloxifene administration enhances retention in an orthodontic relapse model.

Niloufar Azami, Po-Jung Chen, Shivam Mehta, Zana Kalajzic, Eliane H Dutra, Ravindra Nanda, Sumit Yadav

Open access · greenAbstract read
In one paragraph

Article in European journal of orthodontics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 23 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

7 authors at 1 institution in 1 country.

Niloufar AzamiDivision of Orthodontics, UConn Health, Farmington, CT, USA.
Po-Jung ChenDivision of Orthodontics, UConn Health, Farmington, CT, USA.
Shivam MehtaDivision of Orthodontics, UConn Health, Farmington, CT, USA.
Zana KalajzicDepartment of Oral Health and Diagnostic Sciences, Division of Oral and Maxillofacial Radiology, UConn Health, Farmington, CT, USA.
Eliane H DutraDivision of Orthodontics, UConn Health, Farmington, CT, USA.
Ravindra NandaDivision of Orthodontics, UConn Health, Farmington, CT, USA.
Sumit YadavDivision of Orthodontics, UConn Health, Farmington, CT, USA.
UConn Health · US

Funding

Mechanism of BMP2 regulation of Mandibular Condylar Cartilage GrowthK08DE025914 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI YADAV, SUMIT · 2017 to 2021
$947k
The role of FGFR3 in the effects of PTH in the Mandibular CondyleK01DE029528 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI DUTRA, ELIANE · 2020 to 2024
$934k
NIDCR NIH HHS K01 DE029528NIDCR NIH HHS K08 DE025914
6 · The paper itself

Abstract

BACKGROUND AND

objectivesOrthodontic relapse is a physiologic process that involves remodelling of the alveolar bone and principle periodontal ligament fibres. Raloxifene is an Food and Drug Administration (FDA)-approved selective oestrogen receptor modulator that inhibits systemic bone loss. In our study, we examined the effects of Raloxifene on alveolar bone modelling and orthodontic relapse in a rodent model. MATERIALS AND

methodsThe efficacy of raloxifene was evaluated in 15-week-old male Wistar rats, 8 in each group (Control, Raloxifene, Raloxifene + 7-day relapse, Raloxifene + 14-day relapse) for a total of 42 days. All animals had 14 days of orthodontic tooth movement with a closed nickel-titanium coil spring tied from incisors to right first molar applying 5-8 gm of force. On the day of appliance removal, impression was taken with silicon material and the distance between first molar and second molar was filled with light-cured adhesive resin cement for retention phase. Raloxifene Retention, Raloxifene Retention + 7D, Raloxifene Retention + 14D groups received 14 daily doses of raloxifene (2.0 mg/kg/day) subcutaneously after orthodontic tooth movement during retention. After 14 days of retention, the retainer was removed and right first molar was allowed to relapse for a period of 14 days. Raloxifene injection continued for the Raloxifene + 14-day relapse group during relapse phase too. Control group received saline injections during retention. Animals were euthanized by CO2 inhalation. The outcome measure included percentage of relapse, bone volume fraction, tissue density, and histology analysis using tartrate-resistant acid phosphatase staining and determining receptor activator of nuclear factor-кB-ligand (RANKL) and osteoprotegerin expression.

resultsRaloxifene Retention + 14D group had significantly less (P < 0.05) orthodontic relapse when compared with other groups. There was a significant increase (P < 0.05) in bone volume fraction and tissue density in the Raloxifene Retention + 14D group when compared with other groups. Similarly, there was significant decrease in number of osteoclasts and RANKL expression in Raloxifene Retention + 14D group when compared with Raloxifene Retention + 7D group (P < 0.05).

conclusionRaloxifene could decrease post-orthodontic treatment relapse by decreasing bone resorption and indirectly enhancing bone formation.

Indexed as

Tooth Movement TechniquesAnimalsBone RemodelingMaleMolarOsteoclastsRaloxifene HydrochlorideRatsRats, WistarRecurrenceRaloxifene Hydrochloride

Identifiers

PMID32065225
PMCPMC7485273
OpenAlexW3006842267

What OpenQuestion holds

Textmetadata
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.