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AI-based diagnosis in mandibulofacial dysostosis with microcephaly using external ear shapes.
Hennocq, Quentin; Bongibault, Thomas; Marlin, Sandrine; Amiel, Jeanne; Attie-Bitach, Tania; Baujat, Geneviève; Boutaud, Lucile; Carpentier, Georges; Corre, Pierre; Denoyelle, Françoise; Djate Delbrah, François; Douillet, Maxime; Galliani, Eva; Kamolvisit, Wuttichart; Lyonnet, Stanislas; Milea, Dan; Pingault, Véronique; Porntaveetus, Thantrira; Touzet-Roumazeille, Sandrine; Willems, Marjolaine; Picard, Arnaud; Rio, Marlène; Garcelon, Nicolas; Khonsari, Roman H.
Afiliação
  • Hennocq Q; Imagine Institute, INSERM UMR1163, Paris, France.
  • Bongibault T; Service de Chirurgie Maxillo-Faciale et Chirurgie Plastique, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Centre de Référence des Malformations Rares de la Face et de la Cavité Buccale MAFACE, Filière Maladies Rares TeteCou, Faculté de Médecine, Université de Paris Cité, Pa
  • Marlin S; Laboratoire 'Forme et Croissance du Crâne', Faculté de Médecine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université Paris Cité, Paris, France.
  • Amiel J; Imagine Institute, INSERM UMR1163, Paris, France.
  • Attie-Bitach T; Laboratoire 'Forme et Croissance du Crâne', Faculté de Médecine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université Paris Cité, Paris, France.
  • Baujat G; Imagine Institute, INSERM UMR1163, Paris, France.
  • Boutaud L; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
  • Carpentier G; Imagine Institute, INSERM UMR1163, Paris, France.
  • Corre P; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
  • Denoyelle F; Imagine Institute, INSERM UMR1163, Paris, France.
  • Djate Delbrah F; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
  • Douillet M; Imagine Institute, INSERM UMR1163, Paris, France.
  • Galliani E; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
  • Kamolvisit W; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
  • Lyonnet S; CHU Lille, Inserm, Service de Chirurgie Maxillo-Faciale et Stomatologie, U1008-Controlled Drug Delivery Systems and Biomaterial, Université de Lille, Lille, France.
  • Milea D; Department of Oral and Maxillofacial Surgery, INSERM U1229-Regenerative Medicine and Skeleton RMeS, Nantes, France.
  • Pingault V; Department of Oral and Maxillofacial Surgery, Nantes University, CHU Nantes, Nantes, France.
  • Porntaveetus T; Department of Paediatric Otolaryngology, AP-HP, Hôpital Necker-Enfants Malades, Paris, France.
  • Touzet-Roumazeille S; Imagine Institute, INSERM UMR1163, Paris, France.
  • Willems M; Imagine Institute, INSERM UMR1163, Paris, France.
  • Picard A; Service de Chirurgie Maxillo-Faciale et Chirurgie Plastique, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Centre de Référence des Malformations Rares de la Face et de la Cavité Buccale MAFACE, Filière Maladies Rares TeteCou, Faculté de Médecine, Université de Paris Cité, Pa
  • Rio M; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Garcelon N; Center of Excellence in Genomics and Precision Dentistry, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
  • Khonsari RH; Imagine Institute, INSERM UMR1163, Paris, France.
Front Pediatr ; 11: 1171277, 2023.
Article em En | MEDLINE | ID: mdl-37664547
ABSTRACT

Introduction:

Mandibulo-Facial Dysostosis with Microcephaly (MFDM) is a rare disease with a broad spectrum of symptoms, characterized by zygomatic and mandibular hypoplasia, microcephaly, and ear abnormalities. Here, we aimed at describing the external ear phenotype of MFDM patients, and train an Artificial Intelligence (AI)-based model to differentiate MFDM ears from non-syndromic control ears (binary classification), and from ears of the main differential diagnoses of this condition (multi-class classification) Treacher Collins (TC), Nager (NAFD) and CHARGE syndromes.

Methods:

The training set contained 1,592 ear photographs, corresponding to 550 patients. We extracted 48 patients completely independent of the training set, with only one photograph per ear per patient. After a CNN-(Convolutional Neural Network) based ear detection, the images were automatically landmarked. Generalized Procrustes Analysis was then performed, along with a dimension reduction using PCA (Principal Component Analysis). The principal components were used as inputs in an eXtreme Gradient Boosting (XGBoost) model, optimized using a 5-fold cross-validation. Finally, the model was tested on an independent validation set.

Results:

We trained the model on 1,592 ear photographs, corresponding to 1,296 control ears, 105 MFDM, 33 NAFD, 70 TC and 88 CHARGE syndrome ears. The model detected MFDM with an accuracy of 0.969 [0.838-0.999] (p < 0.001) and an AUC (Area Under the Curve) of 0.975 within controls (binary classification). Balanced accuracies were 0.811 [0.648-0.920] (p = 0.002) in a first multiclass design (MFDM vs. controls and differential diagnoses) and 0.813 [0.544-0.960] (p = 0.003) in a second multiclass design (MFDM vs. differential diagnoses).

Conclusion:

This is the first AI-based syndrome detection model in dysmorphology based on the external ear, opening promising clinical applications both for local care and referral, and for expert centers.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article