Evidence map›Paper›PMID 41430218›Full record

ArticleBMC oral health2025

Regeneration of the pulp-dentin complex in mature teeth using autologous demineralized dentin matrix and dental pulp stem cells: two case reports.

Misako Nakashima, Noriaki Yoshihashi, Hiroyuki Tanaka, Koichiro Iohara

Abstract readCase Reports
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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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

4 authors.

Misako NakashimaFuture Health Medical Corporation, RD Dental Clinic, Kobe, Hyogo, 650-0047, Japan. nakashima-m@rdshikaclinic.com.
Noriaki YoshihashiGood Bridge Medical Corporation, Tooth Clinic Tokyo, Chuo-ku, Tokyo, 104-0031, Japan.
Hiroyuki TanakaJyushokai Corporation, Nagoya RD Dental Clinic, Nagoya, Aichi, 450-0002, Japan.
Koichiro IoharaAir Water Inc. Institute of Regenerative Medicine, Kobe, Hyogo, 650-0047, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegenerating the true pulp-dentin complex in mature teeth with necrotic pulps or apical lesions remains challenging, and consistent clinical evidence of dentin bridge formation is limited. This report describes two adult cases treated with regenerative endodontic therapy (RET) using autologous dental pulp stem cells (DPSCs) and demineralized dentin matrix (DDM). CASE PRESENTATION: In Case 1, a 33-year-old woman developed pulp necrosis with apical periodontitis in a maxillary left central incisor following traumatic subluxation. After canal disinfection, autologous DPSCs isolated from her extracted third molar were transplanted into the canal, and DDM particles were placed at the orifice as a capping scaffold. The contralateral traumatized but still vital incisor was monitored as a control. During 52 weeks of follow-up, the treated tooth regained positive pulp sensibility within 1 week, developed a dentin-like bridge exceeding 3 mm at the orifice, and on 52-week MRI showed high-signal pulp-like tissue comparable to adjacent healthy teeth, whereas the untreated control lost vitality and underwent progressive pulp canal obliteration. In Case 2, a 48-year-old man presented with a maxillary left central incisor that had previously undergone root canal treatment and exhibited severe coronal dentin loss beneath an old crown. Orthodontic extrusion was performed to expose sound supragingival dentin, followed by RET with autologous DPSCs and DDM. Sensibility testing was not feasible due to coronal coverage; however, at 48 weeks CBCT demonstrated a well-defined dentin-like bridge extending from beneath the canal orifice into the coronal pulp chamber. In both cases, quantitative CBCT showed progressive increases in mineral density at the regenerated tissue, reaching approximately 75-80% of adjacent native dentin by the final follow-up. No adverse events were observed, and there were no signs of ankylosis, root resorption, or generalized canal obliteration.

conclusionsThese cases suggest that autologous DPSCs combined with DDM can support dentin-like bridge formation and functional recovery in mature incisors, offering a potential biologically based alternative or adjunct to conventional root canal therapy for preserving structurally compromised teeth.

Indexed as

Dental PulpDental Pulp NecrosisDentinRegenerationRegenerative EndodonticsStem Cell TransplantationAdultFemaleHumansIncisorMaleMiddle AgedPeriapical PeriodontitisStem CellsDemineralized Dentin MatrixDemineralized dentin matrixDental pulp stem cellsDentin bridgePulp-dentin complex regenerationRegenerative endodontics therapy

Identifiers

PMID41430218
PMCPMC12752351

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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.