Evidence map›Paper›PMID 41170560›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Human Atlas of Tooth Decay Progression: Identification of Cellular Mechanisms Driving the Switch from Dental Pulp Repair Toward Irreversible Pulpitis.

Hoang Thai Ha, Sofya Kosmynina, Amandine Verocq, Keremsah Ozen, Ines Tekia, Hugo Bussy, Marie Ramirez, Dima Sabbah, Chloe Goemans, Valerie Vandenbempt and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Hoang Thai HaLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.ORCID https://orcid.org/0000-0002-7287-0764
Sofya KosmyninaLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Amandine VerocqLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Keremsah OzenLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Ines TekiaLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Hugo BussyLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Marie RamirezLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Dima SabbahLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Chloe GoemansLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Valerie VandenbemptSignal Transduction and Metabolism laboratory, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Esteban N GurzovSignal Transduction and Metabolism laboratory, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.ORCID https://orcid.org/0000-0003-4642-0273
Sumeet Pal SinghLaboratory of Regeneration and Stress Biology, Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM-Jacques E. Dumont), Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.
Nicolas BaeyensLaboratoire de Physiologie et Pharmacologie, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, 1070, Belgium.ORCID https://orcid.org/0000-0001-9893-3041

Funding

Fondation ULB, Actions Blanches ULB
6 · The paper itself

Abstract

Dental pulp responses to dental decay, the most prevalent chronic disease worldwide, involve remodeling processes comparable to those observed in other human diseases. By combining volumetric imaging and single-cell analysis at various stages of the disease in human samples, the natural history of how dental pulp responds to decay is uncovered. During the early phases, an arterialization of capillary networks and a progressive outward remodeling of larger vessels are observed. Additionally, neurogenesis of nerve endings and the reprogramming of perivascular progenitor cells into fibroblasts, initiating the physiological reparative response of the stromal tissue, is identified. Vascular and nerve regression, along with a shift in immune response and dental pulp fibrosis, contribute to irreversible pulpitis. These findings establish a foundation for a more comprehensive understanding of how dental tissues respond to injury, thereby prompting a paradigm shift in patient management strategies. Furthermore, this study underscores the potential of the human tooth as a valuable model for investigating other systemic diseases and evaluating treatment responses.

Indexed as

Dental CariesDental PulpPulpitisAdultDisease ProgressionFemaleHumansMaledental pulpfibrosisinflammationneurogenesisodontoblaststooth decayvascular remodeling

Identifiers

PMID41170560
PMCPMC12884820

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.