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NCT Number: NCT06752018

Inflammation's Impact on Heart Disease and Diabetes

The goal of this observational study is to evaluate the inflammatory response associated with cardiometabolic diseases, and whether these can be reduced by ex vivo treatment with therapeutic agents. Briefly, the study involves two populations: healthy volunteers and severely obese patients undergoing weight-loss surgery. The main questions the study seeks to address are:

1. To investigate if the therapeutic agents modulate the inflammatory response linked to obesity and cardiometabolic disease? 2. What underlying factors contribute to variations in individual responses?

Researchers will examine differences between healthy participants and those undergoing weight-loss surgery to assess the potential impact of weight loss on responsiveness and overall outcomes.

Participants will:

* Undergo initial testing to evaluate their baseline response. * Provide samples during surgery for further analysis. * Participate in follow-up assessments to track changes over time.

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Key information

About this study

The goal of this observational study is to investigate the relationship between treatment responsiveness and inflammation both systemically in blood, and peripherally in tissue biopsies, focusing on its relevance to cardiometabolic disease and associated conditions. The study aims to develop a predictive model to identify individuals most likely to benefit from anti-inflammatory treatments, thus supporting personalized therapeutic strategies.

Main research questions:

  • To investigate if the therapeutic agents modulate the inflammatory response linked to obesity and cardiometabolic disease
  • To determine the underlying factors that contribute to variations in individual responses to anti-inflammatory drugs

Study design:

The study will involve two participant groups:

  • Healthy control group, composedrised of normal weight individuals
  • Obese adult patients, scheduled to undergo bariatric surgery.

Participant procedures:

  • Baseline testing: An initial test will evaluate treatment responsiveness.
  • Tissue sampling: Tissue biopsies are obtained during surgery and undergo detailed analyses, including ex vivo treatments
  • Follow-up assessments: Participants will be reassessed a year after surgery to evaluate long-term outcomes.

Methods:

  • Molecular studies: Whole blood and peripheral tissue biopsies (adipose tissue, liver, muscle and intestinal biopsies) will be analyzed to identify cellular and molecular pathways associated with treatment responsiveness.
  • Predictive modeling: Clinical, molecular, and biochemical data will be integrated to create a model predicting individual responsiveness.
  • Insulin sensitivity analysis: Advanced imaging techniques will measure tissue-specific glucose uptake.

Hypotheses: Impaired ability to regulate the inflammatory response correlates with cardiometabolic disease.

Anticipated Outcomes:

The study seeks to support precision medicine approaches for addressing cardiometabolic disease.

This research builds on previous findings about the role of inflammation in cardiometabolic dysfunction. By differentiating responders from non-responders, the study aims to support targeted therapeutic strategies for inflammation and cardiometabolic health.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Individuals willing and able to give appropriate oral and written informed consent
  • Men and women over 18 years of age.
  • Correct body mass index (BMI) (Lean controls: 18.5-24.9 kg/m2. Obese gastric bypass patients: 35-50 kg/m2)

Exclusion criteria

  • The individual does not follow instructions given in the research study.
  • Pregnancy.
  • Significant gastrointestinal problems.
  • Use of tobacco.
  • The individual consumed alcohol within two days prior to the study visit
  • Active cancer within 5 years.
  • Use of dietary supplements that impact the inflammatory resolution process (e.g., fish oils), and the person is not willing to discontinue the use of the supplements 1 week prior to the visits.
  • Underlying cardiometabolic disease, or medication related to such disease (e.g., blood pressure medication, insulin to treat diabetes, etc.).
  • Underlying inflammatory disease, or medication related to such disease.
  • The individual states that they have increased bleeding tendency or are using anti-coagulant (blood-thinning) medication.
  • For obese patients only: The individual has lost more than 8% of his/her body weight since their clinical referral for surgery or has lost more than 3% of his/her body weight in the 4 months leading up to surgery.

Treatment and study plan

Gastric bypass

Procedure

Roux-en-Y gastric bypass or sleeve gastrectomy

Primary outcomes

  1. Whole blood ROS prooduction

    Time frame: At baseline and 1 year post surgery

    The primary endpoint of the study is the therapeutic agent-induced reduction in reactive oxygen species (ROS) production in whole blood, following stimulation with N-Formylmethionyl-leucyl-phenylalanine (fMLP), escherichia coli (E. coli), and phorbol myristate acetate (PMA).

  2. Whole blood ROS production

    Time frame: At the time of enrollment

    The primary endpoint of the study is the therapeutic agent-induced reduction in ROS production in whole blood, following stimulation with fMPL, E. coli, or PMA

Study contacts

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

Emma Börgeson, MSc

CONTACT

[email protected]

+45 9352 2984

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Registry information

Official study title

Inflammation: a Key Contributor to Heart Disease and Diabetes?

Acronym: INFO

Important dates

Study start
2025
Primary completion
2030
Study completion
2030
First posted
Dec 30, 2024
Registry last updated
Feb 3, 2025

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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