Characterisation of Endothelial Cells in Different Inflammatory Pathologies (JEDI-2)

Royal Surrey County Hospital NHS Foundation Trust

Status: Enrolling

Conditions: Vasoplegia; Sepsis

Treatments: Other: Endothelial cell biopsy

Study type: Observational

Funder types: Other

Identifiers

NCT06613256

24SURN320251

Details and patient eligibility

About

The goal of this observational study is to characterise changes in gene expression in endothelial cells in patients with either sepsis or post major abdominal surgery.

The main question we plan to answer is: 'What molecular pathways are differentially expressed during inflammatory pathologies?'

Full description

The immune system is a complex network of cells and molecules that protects the body from infection and injury. When the immune system is activated, it produces inflammation, which is a natural response to help heal the body. However, too much inflammation can be harmful and lead to serious complications, such as sepsis, low blood pressure, organ failure and death.

The interaction of cells that line the blood vessels (endothelial cells, EC) with the immune system, is believed to be the root cause of these symptoms. When exposed to inflammation, the instructional molecules (RNA) inside the EC change. This leads to a change of operation promoting the severe symptoms previously mentioned.

Researchers have developed new safe techniques to collect these cells from the blood vessels of patients to study disorders like diabetes, heart disease and stroke. This technique involves gently inserting a metal guidewire into an arm vein to collect ECs.

This study plans to collect ECs from patients undergoing surgery or admitted to intensive care. We also plan to collect control samples from healthy volunteers. Samples will be collected over the duration of the patients to RSFT. The RNA will be removed from the cells and counted to highlight changes in instructions in the cells.

Data from this study will potentially highlight new pathways involved in inflammation and help classify how some patients will react to current treatments. To obtain this data, this study will be split into 2 parts. Part 1 focuses on collecting one sample from a patient when they are at their most unwell states and comparing that to a sample from a healthy person. Part 2 will focus on key mRNA molecules identified during Part 1 and identifying how their expression changes over time.

Enrollment: 105 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Healthy volunteer

• Adult ≥ 18 years
• Able and willing to give consent

Surgical patients

• Adult ≥ 18 years
• Patients admitted to RSFT for planned major surgery

Critically ill patients

• Adult ≥ 18 years
• Emergency admission to ICU at RSFT
• Meets the sepsis 3.0 definition

Exclusion criteria

Healthy volunteer

• Not currently a patient within the hospital
• Absence of inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, diabetes, cardiovascular disease and CKD.
• Not on immunomodulatory medications, such as corticosteroids
• History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation)

Surgical patients

• Patients with restricted liberty, prisoners or under legal protection
• Anticipated prohibitively difficult venous cannulation
• Presenting with inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, sepsis, diabetes with end organ damage, cardiovascular disease and CKD
• Currently prescribed immunomodulatory medication or immunocompromised
• Received chemotherapy within 2 weeks of predicted sampling
• Receiving vasopressor support prior to surgery
• History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation)

Critically ill patients

• Patients with restricted liberty, prisoners or under legal protection• Anticipated prohibitively difficult venous cannulation
• Presenting with inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, diabetes with end organ damage, cardiovascular disease and CKD.
• Currently prescribed immunomodulatory medication or immunocompromised
• Received chemotherapy within 2 weeks of predicted sampling.
• History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation)

Trial design

105 participants in 5 patient groups

Part 1 - control patients

Description:

25 healthy volunteers 1 X Endothelial cell biopsy

Treatment:

Other: Endothelial cell biopsy

Part 1 - surgical patients

Description:

20 surgical patients 1 X Endothelial cell biopsy Samples collected at 24 hours post knife to skin to capture peak inflammation

Treatment:

Other: Endothelial cell biopsy

Part 1 - sepsis patients

Description:

20 sepsis patients 1 X Endothelial cell biopsy Samples collected on admission to ICU

Treatment:

Other: Endothelial cell biopsy

Part 2 - surgical patients

Description:

20 surgical patients 3 X Endothelial cell biopsy Samples collected pre-surgery, 24 hours and 48 hours post knife to skin

Treatment:

Other: Endothelial cell biopsy

Part 2 - sepsis patients

Description:

20 sepsis patients 3 X Endothelial cell biopsy Samples collected on admission, 24 hours and 48 hours post admission to ICU

Treatment:

Other: Endothelial cell biopsy