Development and validation of an interpretable machine learning-based calculator for predicting 5-year weight trajectories after bariatric surgery: a multinational retrospective cohort SOPHIA study.


Journal

The Lancet. Digital health
ISSN: 2589-7500
Titre abrégé: Lancet Digit Health
Pays: England
ID NLM: 101751302

Informations de publication

Date de publication:
10 2023
Historique:
received: 29 11 2022
revised: 04 05 2023
accepted: 11 07 2023
medline: 2 10 2023
pubmed: 1 9 2023
entrez: 31 8 2023
Statut: ppublish

Résumé

Weight loss trajectories after bariatric surgery vary widely between individuals, and predicting weight loss before the operation remains challenging. We aimed to develop a model using machine learning to provide individual preoperative prediction of 5-year weight loss trajectories after surgery. In this multinational retrospective observational study we enrolled adult participants (aged ≥18 years) from ten prospective cohorts (including ABOS [NCT01129297], BAREVAL [NCT02310178], the Swedish Obese Subjects study, and a large cohort from the Dutch Obesity Clinic [Nederlandse Obesitas Kliniek]) and two randomised trials (SleevePass [NCT00793143] and SM-BOSS [NCT00356213]) in Europe, the Americas, and Asia, with a 5 year follow-up after Roux-en-Y gastric bypass, sleeve gastrectomy, or gastric band. Patients with a previous history of bariatric surgery or large delays between scheduled and actual visits were excluded. The training cohort comprised patients from two centres in France (ABOS and BAREVAL). The primary outcome was BMI at 5 years. A model was developed using least absolute shrinkage and selection operator to select variables and the classification and regression trees algorithm to build interpretable regression trees. The performances of the model were assessed through the median absolute deviation (MAD) and root mean squared error (RMSE) of BMI. 10 231 patients from 12 centres in ten countries were included in the analysis, corresponding to 30 602 patient-years. Among participants in all 12 cohorts, 7701 (75·3%) were female, 2530 (24·7%) were male. Among 434 baseline attributes available in the training cohort, seven variables were selected: height, weight, intervention type, age, diabetes status, diabetes duration, and smoking status. At 5 years, across external testing cohorts the overall mean MAD BMI was 2·8 kg/m We developed a machine learning-based model, which is internationally validated, for predicting individual 5-year weight loss trajectories after three common bariatric interventions. SOPHIA Innovative Medicines Initiative 2 Joint Undertaking, supported by the EU's Horizon 2020 research and innovation programme, the European Federation of Pharmaceutical Industries and Associations, Type 1 Diabetes Exchange, and the Juvenile Diabetes Research Foundation and Obesity Action Coalition; Métropole Européenne de Lille; Agence Nationale de la Recherche; Institut national de recherche en sciences et technologies du numérique through the Artificial Intelligence chair Apprenf; Université de Lille Nord Europe's I-SITE EXPAND as part of the Bandits For Health project; Laboratoire d'excellence European Genomic Institute for Diabetes; Soutien aux Travaux Interdisciplinaires, Multi-établissements et Exploratoires programme by Conseil Régional Hauts-de-France (volet partenarial phase 2, project PERSO-SURG).

Sections du résumé

BACKGROUND
Weight loss trajectories after bariatric surgery vary widely between individuals, and predicting weight loss before the operation remains challenging. We aimed to develop a model using machine learning to provide individual preoperative prediction of 5-year weight loss trajectories after surgery.
METHODS
In this multinational retrospective observational study we enrolled adult participants (aged ≥18 years) from ten prospective cohorts (including ABOS [NCT01129297], BAREVAL [NCT02310178], the Swedish Obese Subjects study, and a large cohort from the Dutch Obesity Clinic [Nederlandse Obesitas Kliniek]) and two randomised trials (SleevePass [NCT00793143] and SM-BOSS [NCT00356213]) in Europe, the Americas, and Asia, with a 5 year follow-up after Roux-en-Y gastric bypass, sleeve gastrectomy, or gastric band. Patients with a previous history of bariatric surgery or large delays between scheduled and actual visits were excluded. The training cohort comprised patients from two centres in France (ABOS and BAREVAL). The primary outcome was BMI at 5 years. A model was developed using least absolute shrinkage and selection operator to select variables and the classification and regression trees algorithm to build interpretable regression trees. The performances of the model were assessed through the median absolute deviation (MAD) and root mean squared error (RMSE) of BMI.
FINDINGS
10 231 patients from 12 centres in ten countries were included in the analysis, corresponding to 30 602 patient-years. Among participants in all 12 cohorts, 7701 (75·3%) were female, 2530 (24·7%) were male. Among 434 baseline attributes available in the training cohort, seven variables were selected: height, weight, intervention type, age, diabetes status, diabetes duration, and smoking status. At 5 years, across external testing cohorts the overall mean MAD BMI was 2·8 kg/m
INTERPRETATION
We developed a machine learning-based model, which is internationally validated, for predicting individual 5-year weight loss trajectories after three common bariatric interventions.
FUNDING
SOPHIA Innovative Medicines Initiative 2 Joint Undertaking, supported by the EU's Horizon 2020 research and innovation programme, the European Federation of Pharmaceutical Industries and Associations, Type 1 Diabetes Exchange, and the Juvenile Diabetes Research Foundation and Obesity Action Coalition; Métropole Européenne de Lille; Agence Nationale de la Recherche; Institut national de recherche en sciences et technologies du numérique through the Artificial Intelligence chair Apprenf; Université de Lille Nord Europe's I-SITE EXPAND as part of the Bandits For Health project; Laboratoire d'excellence European Genomic Institute for Diabetes; Soutien aux Travaux Interdisciplinaires, Multi-établissements et Exploratoires programme by Conseil Régional Hauts-de-France (volet partenarial phase 2, project PERSO-SURG).

Identifiants

pubmed: 37652841
pii: S2589-7500(23)00135-8
doi: 10.1016/S2589-7500(23)00135-8
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT01129297', 'NCT02310178', 'NCT00793143', 'NCT00356213']

Types de publication

Randomized Controlled Trial Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e692-e702

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests PP reports a grant from I-Site Université Lille Nord Europe, University of Lille, Métropole Européenne de Lille, Inria, Région Hauts-de-France. RP reports a grant from Swiss National Science; and foundation fees from Johnson & Johnson and the Falik Foundation. RVC reports grants from Johnson & Johnson Medical Brazil, Medtronic Brazil, Jansen Pharmaceuticals, NovoNordisk, and Abbott; and being a member of a Scientific Advisory Board for Baritek and GI Dynamics. CWLR reports grants from the Irish Research Council, Health Research Board, Science Foundation Ireland, and Anabio; being a member of the Global Advisory Board for NovoNordisk, Eli Lilly, Johnson & Johnson, Boehringer Ingelheim, GI Dynamics, Herbalife, and Irish Life Health; and has stock or stock options in Keyron and Beyond BMI. FP reports consulting fees from Novo Nordisk, Eli lilly, Medtronic, and Johnson & Johnson. All other authors declare no competing interests.

Auteurs

Patrick Saux (P)

Université de Lille, Inria, CNRS, Centrale Lille, UMR 9189 - CRIStAL, France.

Pierre Bauvin (P)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1190-EGID, Lille, France.

Violeta Raverdy (V)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1190-EGID, Lille, France.

Julien Teigny (J)

Université de Lille, Inria, CNRS, Centrale Lille, UMR 9189 - CRIStAL, France.

Hélène Verkindt (H)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1190-EGID, Lille, France.

Tomy Soumphonphakdy (T)

Université de Lille, Inria, CNRS, Centrale Lille, UMR 9189 - CRIStAL, France.

Maxence Debert (M)

Université de Lille, Inria, CNRS, Centrale Lille, UMR 9189 - CRIStAL, France.

Anne Jacobs (A)

Nederlandse Obesitas Kliniek, Huis Ter Heide, Netherlands.

Daan Jacobs (D)

Nederlandse Obesitas Kliniek, Huis Ter Heide, Netherlands.

Valerie Monpellier (V)

Nederlandse Obesitas Kliniek, Huis Ter Heide, Netherlands.

Phong Ching Lee (PC)

Department of Endocrinology, Division of Medicine, Singapore General Hospital, Singapore.

Chin Hong Lim (CH)

Department of Upper Gastrointestinal and Bariatric Surgery, Division of Surgery, Singapore General Hospital, Singapore.

Johanna C Andersson-Assarsson (JC)

Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Lena Carlsson (L)

Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Per-Arne Svensson (PA)

Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden; Institute of Health and Care Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Florence Galtier (F)

Endocrinology Department, CHU de Montpellier, University of Montpellier, Montpellier, France; Clinical Investigation Center 1411, INSERM, CHU de Montpellier, University of Montpellier, Montpellier, France.

Guelareh Dezfoulian (G)

Centre Hospitalier Valenciennes, Valenciennes, France.

Mihaela Moldovanu (M)

Centre Hospitalier Valenciennes, Valenciennes, France.

Severine Andrieux (S)

Centre Hospitalier Arras, Arras, France.

Julien Couster (J)

Centre Hospitalier Boulogne-sur-Mer, Boulogne-sur-Mer, France.

Marie Lepage (M)

Centre Hospitalier Boulogne-sur-Mer, Boulogne-sur-Mer, France.

Erminia Lembo (E)

Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy; Università Cattolica del Sacro Cuore Rome, Rome, Italy.

Ornella Verrastro (O)

Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy; Università Cattolica del Sacro Cuore Rome, Rome, Italy.

Maud Robert (M)

Department of Digestive Surgery, Center of Bariatric Surgery, Hopital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Paulina Salminen (P)

Division of Digestive Surgery and Urology, Turku University Hospital, Turku, Finland; Department of Surgery, University of Turku, Turku, Finland.

Geltrude Mingrone (G)

Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy; Università Cattolica del Sacro Cuore Rome, Rome, Italy.

Ralph Peterli (R)

University of Basle, Basle, Switzerland; Clarunis, Department of Visceral Surgery, University Centre for Gastrointestinal and Liver Diseases, St Clara Hospital and University Hospital Basle, Basle, Switzerland.

Ricardo V Cohen (RV)

The Center for Obesity and Diabetes, Oswaldo Cruz German Hospital, São Paulo, Brazil.

Carlos Zerrweck (C)

Clínica Integral de Cirugía para la Obesidad y Enfermedades Metabólicas, Hospital General Tláhuac, Mexico City, Mexico.

David Nocca (D)

Department of Digestive Surgery, CHU de Montpellier, University of Montpellier, Montpellier, France.

Carel W Le Roux (CW)

University College Dublin, Dublin, Ireland.

Robert Caiazzo (R)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1190-EGID, Lille, France.

Philippe Preux (P)

Université de Lille, CNRS, Inria, Centrale Lille, UMR 9189 - CRIStAL, Lille, France. Electronic address: philippe.preux@inria.fr.

François Pattou (F)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1190-EGID, Lille, France. Electronic address: francois.pattou@univ-lille.fr.

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