Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT06291571 |
| Other study ID # |
324543 |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
June 1, 2024 |
| Est. completion date |
March 1, 2030 |
Study information
| Verified date |
May 2024 |
| Source |
University of Aberdeen |
| Contact |
Indrani Mukhopadhya, PhD |
| Phone |
07889761704 |
| Email |
indrani.mukhopadhya[@]abdn.ac.uk |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
The normal human gut is home to millions of microbes including bacteria, fungi, and viruses,
collectively forming the gut microbiota, which exists in harmony within us. Much research is
still required to fully understand the contribution of microbes resident in the large
intestine in liver diseases. The liver receives blood from the gut carrying all the necessary
nutrients needed for our body but also has to deal with toxins derived from the microbes
residing in the intestines. The gut microbiota is altered in liver disease. We still do not
know clearly how this change impacts liver function and the health of liver patients. The
purpose of our study is to answer this question by assessing the gut microbiota using modern
microbiological and molecular methods. By studying the alterations in the gut microbiota in
patients with liver disease we can understand how they affect our immune system and
metabolism. This will help design novel medicinal products to prevent and treat liver
disease.
Description:
Purpose and design:
The key question of this research study is to elucidate the role of the gut microbiota
(bacteria, fungi and viruses) in the development and progression of liver disease. There is a
large amount of existing literature which suggests that there is a change in the nature of
the gut microbes in liver diseases. However, the specific role of the 'gut virome' in liver
disease is still an emerging field. Its relationship with the bacteria and fungi in the lumen
and interaction with the host immune system needs to be characterised in liver diseases. This
study aims to look at the host-microbe dynamics in liver diseases, which will not only lead
to a better understanding of the pathogenesis of these diseases but also help in designing
therapeutic interventions to prevent progression. The proposal has been peer-reviewed by
colleagues at Aberdeen Royal Infirmary. Wider dissemination of the results will be done
through publications in scientific journals and through public engagement forums.
Recruitment:
Patients will be recruited from the Peter Brunt Gastrointestinal (GI) and Liver clinic, and
the GI and liver ward at Aberdeen Royal Infirmary. Outpatient attendees will be sent
participant information sheets by mail before their clinical attendance along with their
clinic appointment letter, for them to have enough time to understand the information. At
their clinic appointment, they will be consented by a member of the clinical team, and a
collection kit handed to them for a faecal sample. For patients with liver disease receiving
treatment on the ward, we will collect faecal samples after informed consent is obtained.
Information regarding the cause and stage of liver disease will be routinely collected from
the case records of these patients. We would also like to obtain faecal samples from a
subgroup of patients over a longer time course to see the evolution of gut microbiota over
time. We will request two more faecal samples over a period of six months. All the necessary
collection containers and information for delivery of these samples to the research
laboratory at the Institute of Medical Sciences, University of Aberdeen will be provided.
Finally, we may request a blood sample from a subset of patients (n=25) for challenge
studies. A total of 30 ml of blood will be collected from this subgroup of patients. These
patients will be consented specifically by the clinical team.
A very small group of patients will be identified when they are listed for a liver biopsy.
This procedure is done for diagnostic reasons or to stage the disease in a specific cohort of
patients with liver disease. The decision to do the biopsy is taken by their consultant
hepatologist. The biopsy is done in a day-case unit in a planned manner. The patients are
sent an appointment letter to come in for the procedure. The participation information sheets
will be sent along with these letters, to consider the information in advance. They will be
consented by a member of the clinical team on the day of the biopsy.
The liver biopsy is performed by a consultant radiologist. A portion of liver tissue in
excess of that required for diagnostic purposes will be cut off from the main sample. The
portion will not be more than 0.5 cm with at least 2 cm of liver tissue sent to the labs for
clinical and pathological assessment. The portion taken for research will be kept and
transported to the University of Aberdeen lab in a liquid nitrogen flask for work package 3
assessment. Cells will then be isolated from these samples for single-cell RNA sequencing
analysis (ScRNAseq) analysis. Liver tissue will also be utilised to perform spatial
transcriptomics which will localise the exact area of metabolic alteration. These cells will
also be used to create tissue organoids.
There are two liver research nurses and a Hepatology research fellow who will help in
co-ordinating the study. There are five consultant hepatologists and specialist registrars
who will help in identifying prospective patients. We would anticipate the collection of 200
liver disease patient sample sets and a corresponding number of appropriately matched control
subjects over the five-year proposed study period for the wider study. We would anticipate 50
subjects for the liver biopsy sub-group study in the same time period.
Control subjects will be healthy volunteers recruited from the University of Aberdeen and
Aberdeen Royal Infirmary. The study will be advertised through pamphlets. The control
participants will be contacted by the research team and will be given the participation
information sheets which will be sent by email or handed over in person, 24 hours before
consent is obtained. This will ensure they have time to read and understand the research
study. An initial screening meeting will take place during which the volunteer will meet a
member of the research team. They will be asked to complete a basic health questionnaire
detailing age, weight and details of any relevant health conditions and regular medication to
ensure that they meet the inclusion/exclusion criteria for the study. If they meet the
inclusion criteria, then they will be asked to sign a consent form and will then be formally
recruited into the study. They will be given a study number that will be used at all times to
keep their identity anonymous.
A subject log will be maintained for all the patients and controls recruited in the study
which will be kept securely in a locked cabinet in the University of Aberdeen.
Methodology
The study will be carried out in the University of Aberdeen, Institute of Medical Sciences
and Rowett Institute research laboratories. The study aims to elucidate the role of the gut
microbiota and host immune response in liver disease through three work packages as described
below:
Work package 1: Investigation of the alteration of gut microbiota in liver diseases
This work package involves collection of faecal samples from eligible patients and healthy
controls for the following assessments:
A) To investigate the alteration of the gut microbiota in patients with liver diseases:
Molecular analyses will require DNA and RNA extraction from faecal samples collected from
patients. PCR based assessment will be employed using both universal and also group/species
directed approaches to study microbial diversity. Following PCR analysis, other analytical
methods may be employed including (but not exclusively) clone library construction and Sanger
sequencing and also probing based approaches. Omics based approaches like 16sRNA gene
sequencing, metagenomics, metatranscriptomics, metabolomics and metaproteomics will also be
used to study microbial diversity and function.
B) Isolate and characterise the pathogenic potential of specific microbes which are
associated with liver diseases: Microbiological assessment of faecal samples will allow us to
enumerate specific microbes (bacteria, viruses, and fungi) from samples using conventional
microbiology culture techniques. These isolates will then be identified and assessed for
their pathogenetic potential. This will involve genomic assessment of pathogenicity utilising
techniques like whole genome sequencing to characterise specific traits. We will also perform
metabolomic assessment of pathogenic microbes to look for alteration in pathways pertaining
to bile salt, alcohol, and short chain fatty acid metabolism. This will involve
transcriptomic assessment of the pathogenic strains as well as gas chromatography to study
the by-products of their metabolism.
Work package 2: Assessment of host response to specific microbes in liver diseases This work
package will involve collection of 30 ml of blood from patients and controls. This group of
subjects will be consented specifically for blood testing. This blood will be used to
generate macrophages which will be needed for the challenge studies. Pathogenic microbes
identified in Study 1 will be assessed for their pro-inflammatory potential through challenge
experiments on cell lines, tissue organoids and experimental animal models. Blood taken at
the time of recruitment will be assessed for evidence of inflammatory mediators following
challenge with infectious agents identified in Study 1. Whole blood collected ~ 30 ml (2
tablespoons) will have a panel of bacterial/viral and fungal cells added and these will be
incubated for up to 48 hours. Evidence of inflammatory development will be studied using
molecular techniques including (but not exclusively) ELISA and flow cytometric analysis. In a
proportion of subjects, blood will be taken to extract peripheral blood monocyte cells
(PBMCs) to assess the systemic immune response against these putative pathogens.
Work package 3: Characterise the changes in the liver immune microenvironment by analysing
liver biopsies from patients. This work package will be done to elucidate the inflammatory
changes that are occurring within the liver in response to the gut pathogens. A small
subgroup of patients who are undergoing liver biopsy for clinical reasons will be consented
for a small portion of liver tissue in excess of what is required for diagnostic purposes.
The larger portion will be sent off for pathological assessment. This small excess portion
will be cut off from the liver biopsy by the radiologist and handed over immediately to a
member of the research team. This will be transported in a liquid nitrogen flask to the
University of Aberdeen lab for processing. Hepatocytes will then be isolated from these liver
biopsy samples for single-cell RNA sequencing analysis (ScRNAseq). Liver tissue will also be
utilized to perform spatial transcriptomics which will localize the exact area of metabolic
alteration.
