Evidence map›Paper›PMID 41975015›Full record

ArticleCommunications medicine2026

Geometric morphometrics based diagnostic model for Skeletal Class III patients.

Maria Cristina Faria-Teixeira, Inês M N Carvalho, Alexandra Dehesa-Santos, Francisco Salvado E Silva, Helena Afonso Agostinho, Francisco Do Vale, António Vaz-Carneiro, Leixuri De Frutos-Valle, Shin-Jae Lee, Joao C Guimaraes and 1 more

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Maria Cristina Faria-Teixeira *Complutense University of Madrid, School of Dentistry, Madrid, Spain.
Inês M N Carvalho *Universidade de Lisboa, Faculdade de Medicina, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.ORCID https://orcid.org/0009-0000-3129-5495
Alexandra Dehesa-SantosComplutense University of Madrid, School of Dentistry, Madrid, Spain.
Francisco Salvado E SilvaUniversidade de Lisboa, Faculdade de Medicina, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
Helena Afonso AgostinhoSão João University Hospital of Porto, Porto, Portugal.
Francisco Do ValeUniversity of Coimbra, School of Dentistry, Coimbra, Portugal.
António Vaz-CarneiroUniversidade de Lisboa, Faculdade de Medicina, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
Leixuri De Frutos-ValleComplutense University of Madrid, School of Dentistry, Madrid, Spain.
Shin-Jae LeeDepartment of Orthodontics, Seoul National University School of Dentistry, 101 Daehak-ro, Jongno-gu, Seoul, Korea.
Joao C GuimaraesUniversidade de Lisboa, Faculdade de Medicina, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal. joao.guimaraes@medicina.ulisboa.pt.ORCID http://orcid.org/0000-0002-1664-472X
Alejandro Iglesias-LinaresComplutense University of Madrid, School of Dentistry, Madrid, Spain. aleigl01@ucm.es.

Funding

EC | Research Executive Agency (REA) 952377
6 · The paper itself

Abstract

backgroundSkeletal Class III (SCIII) malocclusion represents a heterogeneous cluster of craniofacial anomalies characterised by a sagittal mesial discrepancy. It is among the most challenging orthodontic conditions to treat because there is no standardisation regarding subphenotype classification or treatment efficacy prediction. This study aimed to develop a data-driven model to identify novel clinically relevant SCIII subphenotypes, contributing to tailored treatment protocols.

methodsA clinical subphenotypic classification model for SCIII was developed using 12 annotated craniofacial landmarks from lateral cephalometric radiographs of 655 adult SCIII patients of white origin. SCIII subphenotypes were identified by applying generalised Procrustes analysis and unsupervised clustering, and a classification model was developed for predicting subphenotypes for new patients. Cross-validation was employed to demonstrate the robustness of our clustering and classification models.

resultsHere we show that our model inferred six distinct subphenotypes that unravelled relevant morphological features in SCIII patients. We further demonstrate the generalisability of our model across ethnicities using an external validation cohort of patients of Korean origin. The identified SCIII subphenotypes exhibit a strong correlation with treatment decision.

conclusionsOur results contribute to the development of an accurate SCIII diagnostic tool (available at https://tools.istars.pt/sciii/ ), moving towards the goal of improving treatment efficacy for this condition.

Identifiers

PMID41975015
PMCPMC13270103

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.