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NCT Number: NCT07542327

The Role of Autoantibodies Against G-protein Coupled Receptors in Obesity

The purpose of this study is to explore if GPCR-autoantibodies:

1. are pressent in people living with obesity, and are associated with degree of obesity 2. if it is associated with obesity related diseases

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Southern Denmark, Esbjerg

Esbjerg, Region Syddanmark, 6700, Denmark

Location contact

Anitta Ø Johansen, Chief consultant

CONTACT

[email protected]

+ 21338607 ext. +45

Claus B Juhl, Professor, MD, PhD

PRINCIPAL_INVESTIGATOR

Tobias M Windedal, MD

SUB_INVESTIGATOR

About this study

The present study aims to investigate the role of GLP1-R autoantibodies in a large, deeply phenotyped obesity cohort. In an unblinded exploratory analysis, GLP1-R, GIP-R and ghrelin-R autoantibody levels will be measured using proprietary assay. The central hypothesis is that the presence and concentration of these autoantibodies is positively associated with the degree of obesity. Secondary we hypothesize that the presence and concentration of GLP1-R or GIP-R autoantibodies are associated with the presence of insulin resistance and prediabetes. As an exploratory approach we hypothesize that the presence and concentration of GLP1-R, GIP-R or ghrelin-R autoantibodies is associated with eating behavior as assessed by the validated questionnaire Adult Eating Behavior Questionnaire.

At present, it is unknown whether these autoantibodies exert an inhibitory, neutral, or agonistic effect on GLP1R, GIP-R or ghrelin-R signaling. Furthermore, it remains unclear whether individuals with obesity and diabetes-conditions associated with impaired GLP-1 signaling-exhibit a higher prevalence of GLP1R autoantibodies, or whether these autoantibodies differ functionally between diabetic and non-diabetic individuals. Addressing these questions may help explain interindividual variability in weight loss responses and uncover a novel immuno-endocrine mechanism relevant to obesity and metabolic disease.

The project will take advantage of the South Danish Obesity Initiative (SDOI) cohort. This is an ongoing clinical initiative offering screening of a broad panel of obesity related diseases to individuals with BMI above 30 kg/m² and age between 18 and 60 years. People are referred from their general practitioners or from hospital departments and undergo screening for diabetes, dyslipidemia, obstructive sleep apnea, metabolic-associated steatohepatitis and hypertension. In addition, the participants answer questionnaires including the Adult Eating Behavior Questionnaire. A Danish translation of this questionnaire has been validated, and the questionnaire allows evaluation of eating habits (Kolin M.E.I. et al, 2025. DOI:10.3390/nu17243824). A cohort of people with BMI 18.5 to 30 kg/m² has been assessed with an identical screening program with the purpose of serving as a control group. Only participants who gave informed consent to use their data for research purposes are included in this study. The SDOI screening protocol and initial results have previously been published (Juhl C.B. et al 2024. DOI:10.2147/DMSO.S456028).

In the present study we will include 160 participants from the SDOI cohort, of which 120 will be individuals living with obesity. Where 40 participants will have a BMI above 50 kg/m², 40 will have a BMI 40-50 kg/m², 40 will have a BMI 30-40 kg/m². The remaining 40 participants will be from the control cohort (BMI 18.5 to 25 kg/m²). The groups will be matched on sex and age (within 2 years). Individuals with type 1 diabetes and individuals treated with GLP-1RAs for any indication and individuals who have previously undergone bariatric surgery will not be included in the trial.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inhabitant in the Region of Southern Denmark
  • BMI above 30kg/m2
  • age between 18 and 60 years.

Exclusion criteria

  • individuals previously treated with GLP-1RA medication for any indication
  • Individuals who have previously undergone bariatric surgery
  • Individuals with type 1 diabetes

Treatment and study plan

Primary outcomes

  1. Exploring the pressence and role of GPCR-autoantibodies in obesity

    Time frame: At the time of enrolement

    explore the pressence of GPCR-autoantibodies in people living with obesity, and if there is any association with the degree of obesity

Secondary outcomes

  1. Exploring the association between GPCR-autoantibodies and obesity related diseases

    Time frame: At the time of enrolment

    explore if the pressence of GPCR-autoantibodies is associated with obesity related diseases (pre-diabetes, type 2 diabetes and metabolic syndrome) in people living with obesity

Study contacts

Contact information is provided by the study sponsor or research team.

Claus B Juhl, Professor, MD, PhD

CONTACT

[email protected]

79183120 ext. 45

Tobias M Windedal, MD

CONTACT

[email protected]

42957945 ext. 45

Sponsors and collaborators

Lead sponsor

Claus Bogh Juhl

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 21, 2026
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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