WEGOVY weight loss study aims to predict who benefits most

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

* Inclusion Criteria Male or female Aged over 18 years Patient included in the WEGOVY® ATU/AP program in one of the 14 participating CSOs: initial Body Mass Index (BMI) ≥ 40 kg/m² (Class III or morbid obesity) and presence of at least one weight-related comorbidity: treated hypertension, treated dyslipidemia, established cardiovascular disease, treated sleep apnea syndrome; and in the absence of therapeutic alternatives Patient has been informed and has not objected to participation in the study Patient affiliated with a French social security scheme * Tagging Criteria to Identify Subpopulations of Interest (for classification purposes only - not a condition for inclusion) \*1 Patients with a history of bariatric surgery: 1. At least 1 year post-bariatric surgery (definitive technique or gastric band still in place) 2. Defined as failure if: Initial %EWL \< 50% (even without weight regain) and/or weight regain \> 20% of lost weight compared to postoperative nadir \*2 Patients with Binge Eating Disorder (BED): Defined by the clinician according to DSM-5 criteria for BED: a. Recurrent episodes of binge eating, characterized by both: Eating, in a discrete period of time, an amount of food that is definitely larger than what most individuals would eat in a similar time under similar circumstances A sense of lack of control over eating during the episode b. The binge eating episodes are associated with three (or more) of the following: Eating much more rapidly than normal Eating until uncomfortably full Eating large amounts of food when not physically hungry Eating alone due to embarrassment Feeling disgusted with oneself, depressed or guilty afterward c. Marked distress regarding binge eating d. The binge eating occurs, on average, at least once a week for 5 months e. The behavior is not associated with regular inappropriate compensatory behavior (e.g., purging, fasting, excessive exercise) and does not occur exclusively during anorexia nervosa or bulimia nervosa \*3 Patients with rare monogenic or syndromic obesity: According to the French national guidelines (PNDS) for rare obesity causes: HAS website 1. Includes: Hypothalamic (lesional) obesity, such as craniopharyngioma Genetic forms of obesity 2. Most frequently encountered syndromes: Prader-Willi syndrome Bardet-Biedl syndrome 16p11.2 deletion or SH2B1 variant LEPR, POMC, PCSK1, and MC4R variants * 4 Older patients: <!-- --> 1. Age \> 60 years * 5 Patients with extreme obesity: a. BMI ≥ 60 kg/m² \*6 Patients with obesity under psychotropic treatment: Presence of one or more of the following treatments at baseline: i. Antidepressants: Agomelatine, Amitriptyline, Citalopram, Clomipramine, Duloxetine, Escitalopram, Fluoxetine, Fluvoxamine, Imipramine, Iproniazid, Mianserin, Milnacipran, Mirtazapine, Moclobemide, Paroxetine, Sertraline, Tianeptine, Venlafaxine, Vortioxetine ii. Antipsychotics: Amisulpride, Aripiprazole, Chlorpromazine, Clozapine, Cyamemazine, Flupenthixol, Fluphenazine, Haloperidol, Levomepromazine, Loxapine, Olanzapine, Pimozide, Pipamperone, Prochlorperazine, Quetiapine, Risperidone/Paliperidone, Sulpiride, Tiapride, Zuclopenthixol iii. Mood stabilizers: Lithium carbonate, Carbamazepine, Lamotrigine, Oxcarbazepine, Sodium divalproate, Valpromide iv. Psychostimulants: Methylphenidate v. Anxiolytics: Antihistamines, anticonvulsants, or other anxiolytic agents \*7 Non-specific patients: Patients not meeting any of the above subpopulation criteria \- Exclusion Criteria Pregnant or breastfeeding women Persons under legal protection or guardianship \- Criteria for Early Study Withdrawal Early withdrawal from the study will occur in the following cases: The patient withdraws their non-opposition to participation The patient discontinues treatment with WEGOVY® prematurely