Young Adults With Early-onset Obesity Treated With Semaglutide

Background:

The prevalence of obesity in adolescents has increased markedly in the past decades, thus entailing increased cumulative incidences of type 2 diabetes, cardiovascular disease, and chronic kidney disease (1). Adolescents with obesity are at a substantially elevated risk of developing morbid obesity and type 2 diabetes in early adulthood (2,3) and a recent large scale meta-analysis revealed that mortality increased approximately log-linearly with BMI over 25.0 kg/m² in all continents; and that this increment was greater in younger than older people (4). Furthermore, obesity increase the risk of stigmatization with respect to social relationships, entry into the job market, reduced self-esteem and other psychological problems (5). Thus, adolescents with obesity require particular medical attention.

Since 2008, The Childrens Obesity Clinic (TCOC), Department of Pediatrics, Copenhagen University Hospital Holbæk has treated more than 4000 children and adolescents with overweight or obesity using the TCOC protocol which includes regular counselling on diet, exercise, lifestyle and general health. The TCOC protocol has proven successful with a reduction in BMI standard deviation score (SDS) after 1.5 years of treatment obtained in 74% of the children and adolescents (6). In addition, significant improvements in lipid profile (7) the degree of hypertension (8), hepatic steatosis (9) and the presence of visceral fat (9) have been reported.

However, approximately one in four of the children following the TCOC protocol do not achieve a reduction in BMI SDS. Furthermore, for the majority of children who reduce BMI SDS, obesity remains and represents a medical and personal issue. Lifestyle intervention is the method of choice for children with obesity, however, new effective treatment strategies for non-responders are urgently required.

Glucagon-like peptide-1 (GLP-1) is secreted from endocrine cells in the intestine upon meal intake and reduces blood glucose and food intake in a dose-dependent manner (10-13). It has previously been shown that 1) people with obesity have impaired GLP-1 secretion already in the overweight state, indicating that low concentrations of GLP-1 may be part of obesity development (14), 2) weight loss induces a marked increase in GLP-1 response and this increase is part of a successfully maintained weight loss of >10 kg (15), 3) treatment with a GLP-1 receptor agonist (GLP-1 RA) facilitates long term weight loss maintenance (13 kg) accompanied by substantial improvement in metabolic health, compared to similar diet-induced weight loss maintenance (15-17),4) appetite sensation and eating behavior are important factors in maintenance of weight loss (18,19). Pathogenic mutations in the appetite-regulating melanocortin-4 receptor represent the most common cause of early-onset monogenic obesity that has been shown to be a type of obesity that is more resistant to lifestyle interventions (20) and even to bariatric surgery (21). Interestingly, this population is responsive to treatment with GLP-1 RA (liraglutide 3.0 mg daily) (22). This indicates that GLP-1 RAs can overrule lifestyle modification-resistant obesity due to the appetite-inhibiting effect. A new GLP1-1 RA (semaglutide) was approved by the European Medical Agency (EMA) for weight management in adults with obesity in January 2022. Placebo subtracted weight loss with semaglutide 2.4 mg was 13.9 % compared to 4.5% with liraglutide 3.0 mg after 68 weeks in adults with overweight or obesity (23). Thus, semaglutide has a potentially larger treatment effect also in young adults with childhood onset obesity. The treatment effect of semaglutide 2.4 mg in young adults with lifestyle-treatment-resistant childhood onset obesity is currently unknown, why the outcomes of this study is of high clinical and socioeconomic relevance.

Study hypothesis:

Treatment with a GLP-1 RA will facilitate weight loss in young adults with and without treatment-resistant childhood-onset obesity.

Objectives:

1. To treat young adults with obesity, who have been resistant to structured lifestyle intervention (TCOC protocol), with the GLP-1 RA, semaglutide 2.4 mg/ week.
2. To treat young adults with obesity, who have responded insufficiently to the structured lifestyle intervention (TCOC protocol) and still have obesity, with semaglutide 2.4 mg/ week.
3. To identify underlying mechanisms of lifestyle-untreatable versus treatable childhood-onset obesity.
4. Assess the efficacy of an exercise-based strategy to discontinue obesity medication while sustaining a healthy body composition in youth with childhood-onset obesity.

Endpoints:

Primary endpoint:

1. Change in BMI (weight in kg/height in m^2) from before to after semaglutide treatment compared to placebo.

Secondary endpoints (changes from before to after semaglutide treatment compared to placebo):

1. Body composition (fat mass, fat percentage, fat-free mass, visceral fat, liver fat)
2. Changes in metabolic health: (e.g. glucose and insulin for HOMA-IR and Matsuda index, HbA1c, lipids i.e. cholesterol, HDL, LDL, triglycerides, FFA glucose-tolerance status, blood pressure, pulse, and hip and waist circumference, and calculate metabolic syndrome prevalence and metabolic syndrome z-score, and waist-to-height ratio.
3. Body weight
4. Proportion with a reduction in body weight of at least 5%, 10%, 15%, and 20%

The changes in endpoints from baseline (randomization) to after 68 weeks of treatment will be analyzed for all participants treated with semaglutide compared with all participants receiving placebo, and separately in non-responders and insufficient responders to the TCOC protocol, semaglutide compared with placebo.

Other prespecified endpoints:

To determine the effect of GLP-1 RA treatment, and compare data between the two intervention groups, excellent responders and a population-based reference group with normal weight development for the above-mentioned and following outcomes:

1. Questionnaires will be given to the participants to determine self-rated quality of life (SF-36 and PedsQL), eating habits (three-factor eating questionnaire, BED-Q), physical activity (IPAQ), food preferences, self-efficacy (G-SES), sleep quality (PSQI), and appetite (VAS)
2. Conventional Magnetic resonance imaging (MRI) and spectroscopy is used to assess effects on fat deposits in liver, viscera, and muscle. Site-specific bone-measurements, collection of bone markers (CTX and P1NP), and DEXA scans will be performed to assess bone-health.
3. To explore the effects on appetite regulation and systemic markers of immuno-metabolism: Hormonal appetite regulation will be measured during meal tests and fasting (eg. GLP-1, Peptide YY, Glucagon, Leptin, Ghrelin, Liver-Expressed Antimicrobial Peptide 2 (LEAP2), Adiponectin, GDF-15, N-lactoyl-phenylalanine, neurotensin, neprilysin) using our standard methodologies. In plasma samples various biomarkers of inflammation will be measured (e.g., sCD163, hsCRP, IL1, IL2, IL4, IL8, IL10, IL12p70, IL13, IL-1Rap IL-6, TNF-α, SAA1, SAA2, ORM1, ORM2, ICAM-1, VCAM-1, tPA, vWF) and oxidation (eg malonyldialdehyde, F2-Isoprostanes, etc.), IPS, sphingolipids, and metabolomics using plasma metabolomics and proteomics technique. We will also measure metabolic disruptors (e.g., per- and polyfluorinated substances (PFAS)) and store cells for induction of pluripotent stem cell cultures (iPSC), and perform peripheral blood mononuclear cells (PBMNCs) isolation, including DNA collection.
4. To explore the effects on immuno-metabolic profile in human subcutaneous (sc) adipose tissue and gene expression profile of adipose tissue and in circulating inflammatory cells (PBMNCs),we will perform RNA sequencing (Illumina sequencing 30 million paired-end reads/sample) and determine the changes in pro-inflammatory (e.g. IL-6, IL1b, MCP-1, resistin, leptin, chemerin, etc.) and anti-inflammatory (e.g. adiponectin) adipocytokines, and in adipocyte differentiation markers such as FAB4, CABPA and PPAR-γ as well as markers of macrophages infiltration (CD163, CD68) and M1/M2 phenotype of them such as CD40, CCR7, CD207 etc. (all by qRTPCR).
5. To explore the effect on food preferences and appetite sensation: Food preferences are assessed by a picture display test where standardized pictures of food items are shown. Subjective appetite sensations will be obtained during a fixed standardized meal using electronic visual analogue scales (VAS) to record hunger, satiety, fullness, prospective food consumption, desire to eat something fatty, salty, sweet or savory, and palatability of the meals.
6. To explore the effect on brain structure and activity using magnetic resonance imaging (MRI): Brain MRI will be conducted in a subset of participants by trained personnel at the Neurobiological Research Unit, at Copenhagen University Hospital, Rigshospitalet. Pre- and post-meal scans will be performed. From brain MRI we will examine functional connectivity (whole-brain, seed-to-voxel analysis (with the hypothalamus as the primary seed and additional regions of interest (ROI)), and ROI-to-ROI analysis), resting-state networks, brain age, and structural measures such as gray matter volume. Resting-state networks will be examined using Independent Component Analysis in the CONN toolbox. Structural measures, including gray matter volume, will be obtained with FreeSurfer software, and brain age will be estimated using the Pyment software package. Each brain MRI session will last approximately one hour.
7. To explore the genetic risk scores correlated to treatment response: All participants are chip genotyped to define polygenic risk scores. DNA material will be extracted from blood samples. The Infinium Global Screening Array will be used to analyze the array with Illumina Genome Studio before the bioinformatic removal of SNPs containing genes mentioned in the "American College Medical Genetics and Genomics" List.
8. To explore the effect on the microbiota: The microbiome will be measured in fecal and saliva samples of participants. Furthermore, fecal and saliva samples were collected from the same individuals when they were children with obesity, allowing for comparison of potential differences already evident in childhood that may indicate later treatment response to lifestyle change and GLP-1RA treatment.
9. To explore the effect on metabolomics in urine: Urine samples are collected at the two test days and will be stored frozen for later analyses for potential changes in the metabolomic profile.
10. Psycho-social aspects of obesity development and treatment response We will evaluate the effect of adversity measures across upbringing and current living conditions and explore eating practices and individual weight trajectories in relation to psychological and social factors.
11. A physical activity tracker will be worn on the wrist throughout the study period to assess habitual physical activity and sleep habits.
12. To explore the effect of post medication phase on limiting weight and fat regain: We will investigate whether a post medication program after GLP-1RA discontinuation, comprising data-driven supervised exercise, sleep, and healthy eating behaviour, can limit weight and fat regain and limit deterioration of metabolic health. We will perform DEXA scans 26 weeks after medication termination to investigate changes in body fat percentage, fat mass, and lean mass. We will investigate changes in the outcomes mentioned above and grip strength.