Pilot Study of the Human Metagenome in Metabolic Diseases
NCT ID: NCT06363253
Last Updated: 2025-05-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
600 participants
OBSERVATIONAL
2023-08-14
2027-12-31
Brief Summary
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Recruited participants will have their fecal, salivary, urine, serum, and in certain instances, mucosal samples taken, for metagenomic sequencing and metabolite testing.
We hope to uncover various differences and signatures in the metagenome and metabolome in various diseased states, with potential future therapeutic applications in personalised medicine.
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Detailed Description
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The gut bacteriome, and more recently the virome, has been shown to be significantly correlated with the obese phenotype, while gut microbiome dysbiosis is known to occur in individuals with sarcopenia. Clinically, there is an unmet clinical need to better personalize the treatment of patients with metabolic disorders such as obesity and metabolic syndrome, and patients suffering from sarcopenia and frailty as a result of aging. However, the literature regarding the metagenomic signatures associated with these disorders, in particular the non-bacteriome species, bacterial metabolites, and their relationship with host metabolism, were scarce.
Thus we hypothesize, that the human metagenome and metabolome, may play a role in influencing chronic inflammatory disorders related to metabolic disorders, such as obesity and diseases related to aging like sarcopenia and aging.
This is a cohort study, involving metagenomic sequencing and metabolomic analysis, of patients metagenome and metabolome, in various diseased states. A cohort of healthy control patients without obesity or sarcopenia will also be recruited.
Samples collected will include fecal, salivary, serum, urine, mucosal samples for metagenomic sequencing and metabolomic testing.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Obese
Patients with BMI \> 27.5 kg/m2
No specific intervention
Patient will undergo their routine clinical treatment for their related clinical condition (eg. anti-obesity or bariatric intervention for obese group; muscle strengthening interventions or necessary treatment for their concomitant medical condition for the sarcopenia group).
Follow-up testing will include repeat assessment of the subjects metagenome and metabolome over time, and after intervention
Control subjects will have no interventions performed as well.
Sarcopenic
Patients who are sarcopenic, defined by the Asian Working Group on Sarcopenia 2014 criteria, which is defined as
1. having low handgrip strength (\<26kg for males; \<18kg for females) AND/OR
2. Low gait speed (\<0.8m/s) AND
3. Low muscle mass (\<7.0kg/m2 for males; \<5.7kg/m2 for females)
No specific intervention
Patient will undergo their routine clinical treatment for their related clinical condition (eg. anti-obesity or bariatric intervention for obese group; muscle strengthening interventions or necessary treatment for their concomitant medical condition for the sarcopenia group).
Follow-up testing will include repeat assessment of the subjects metagenome and metabolome over time, and after intervention
Control subjects will have no interventions performed as well.
Controls
Healthy volunteers who are not obese (BMI \<27.5kg/m2), OR who are screened and found to not be sarcopenic
No specific intervention
Patient will undergo their routine clinical treatment for their related clinical condition (eg. anti-obesity or bariatric intervention for obese group; muscle strengthening interventions or necessary treatment for their concomitant medical condition for the sarcopenia group).
Follow-up testing will include repeat assessment of the subjects metagenome and metabolome over time, and after intervention
Control subjects will have no interventions performed as well.
Interventions
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No specific intervention
Patient will undergo their routine clinical treatment for their related clinical condition (eg. anti-obesity or bariatric intervention for obese group; muscle strengthening interventions or necessary treatment for their concomitant medical condition for the sarcopenia group).
Follow-up testing will include repeat assessment of the subjects metagenome and metabolome over time, and after intervention
Control subjects will have no interventions performed as well.
Eligibility Criteria
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Inclusion Criteria
* Sarcopenic patients, defined as 1) low handgrip strength (\<26 for males; \<18kg for females), AND/OR low gait speed (\<0.8m/s) AND low muscle mass (\<7.0kg/m2 for males; \<5.7kg/m2 for females)
\- Healthy subjects without sarcopenia, and not obese (BMI\<27.5kg/m2)
Exclusion Criteria
* Presence of intestinal stoma, hence inability to collect fecal samples
21 Years
99 Years
ALL
Yes
Sponsors
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Singapore General Hospital
OTHER
Lee Kong Chian School of Medicine, Nanyang Technological University
UNKNOWN
Duke-NUS Graduate Medical School
OTHER
Sengkang General Hospital
OTHER
Responsible Party
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Chue Koy Min
Clinical Assistant Professor
Locations
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Sengkang General Hospital
Singapore, , Singapore
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CIRB Ref: 2023/2073
Identifier Type: -
Identifier Source: org_study_id
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