Evidence map›Paper›PMID 38107047›Full record

ArticleThe Saudi dental journal2023

Combination adipose-derived mesenchymal stem cells-demineralized dentin matrix increase bone marker expression in periodontitis rats.

Desi Sandra Sari, Millenieo Martin, Ernie Maduratna, Hari Basuki Notobroto, Ferdiansyah Mahyudin, Ketut Sudiana, Nora Ertanti, Aristika Dinaryanti, Fedik Abdul Rantam

Open access · hybridAbstract read
In one paragraph

Article in The Saudi dental journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
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

9 authors at 2 institutions in 1 country.

Desi Sandra SariDepartment of Periodontics, Faculty of Dentistry, Universitas Jember, Jember 68121, Indonesia.
Millenieo MartinGraduated Student, Faculty of Dentistry, Universitas Jember, Jember 68121, Indonesia.
Ernie MaduratnaDepartment of Periodontics, Faculty of Dentistry Universitas Airlangga, Surabaya 60132, Indonesia.
Hari Basuki NotobrotoDepartment of Biostatistics and Demography, Faculty of Public Health, Universitas Airlangga, Surabaya 60132, Indonesia.
Ferdiansyah MahyudinDepartment of Orthopaedic & Traumatology, Dr Soetomo General Hospital, Surabaya 60132, Indonesia.
Ketut SudianaDepartment of Pathology Anatomy, Faculty of Medicine, Universitas Airlangga, Surabaya 60132, Indonesia.
Nora ErtantiStem Cells Research and Development Center, Universitas Airlangga, Surabaya 60132, Indonesia.
Aristika DinaryantiStem Cells Research and Development Center, Universitas Airlangga, Surabaya 60132, Indonesia.
Fedik Abdul RantamStem Cells Research and Development Center, Universitas Airlangga, Surabaya 60132, Indonesia.
Airlangga University · IDUniversitas Jember · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Periodontal disease is common in both developed and developing countries and affects around 20-50% of the global population, especially in adolescents, adults and the elderly is a public health problem. ADMSCs have the advantage of regenerating damaged tissue with high quality. DDM in the form of slices can improve healing in the mandibular sockets of molar teeth. The combination of ADMSC-DDM is expected to accelerate bone regeneration. Objectives: To analyze the combination of ADMSCs-DDM at increasing bone marker expression in periodontitis rats. Methods: This research is experimental with a randomized control group post-test-only design. A total of 50 male Wistar rats were divided into four groups: 1) normal group (K); 2) CP model (K + ); 3) CP model and treated with DDM scaffold therapy (K(s)); 4) CP model and treated with ADMSCs-DDM combination therapy (K(sc)). Making a CP model with injected LPS Results: The results of the MTT scaffold DDM were significant in the 10%, 50%, and 100% dilution groups (p < 0.05). The results showed there was a substantial difference in the expression of STRO-1 between the study groups (p < 0.05). The (K(sc)) was significantly higher than the (K) in RUNX-2 expression (p < 0.05). OSX expression showed significant results between study groups (p < 0.05). The expression of OCN and COL-I showed a significant difference in all study groups on day 28, where the (K(sc)) was higher than the (K) (p < 0.05). Conclusions: Administration of the ADMSCs-DDM combination can accelerate alveolar bone regeneration on day 28. There is a mechanism of alveolar bone regeneration through the STRO-1, RUNX-2, OSX, and the COL-I pathway in periodontitis models.

Indexed as

Adipose-Derived Mesenchymal Stem CellsAlveolar Bone ResorptionDemineralized Dentin MatrixRegeneration PeriodontalScaffold

Identifiers

PMID38107047
PMCPMC10724358
OpenAlexW4385490901

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.