The Association Between Microbiota, Endotoxaemia and the Host Obesity/ Insulin Resistance (MiPOOP Study)

NCT ID: NCT03665961

Last Updated: 2018-09-11

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

35 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-10-25

Study Completion Date

2017-09-26

Brief Summary

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The objectives of this study are to examine the effects of ethnicity, central obesity and dietary components, on the human gut microbiome. The investigators hypothesize that these factors have an influence on the composition of the gut microbiome. Healthy subjects (n=35) provided stool samples for gut microbiome profiling using 16S rRNA sequencing and completed a dietary questionnaire. The serum samples were assayed for a panel of inflammatory cytokines. Their associations with central obesity were examined.

Detailed Description

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Introduction: Perturbance in the composition of human gut microbiota has been associated with metabolic disorders such as obesity, diabetes mellitus and insulin resistance. The objectives of this study are to examine the effects of ethnicity, central obesity and dietary components, on the human gut microbiome. The investigators hypothesize that these factors have an influence on the composition of the gut microbiome.

Methods: Subjects of Chinese (n=14), Malay (n=10) or Indian (n=11) ancestry, median age 39 (range:22-70 years old), were enrolled. The subjects provided stool samples for gut microbiome profiling using 16S rRNA sequencing and completed a dietary questionnaire. The serum samples were assayed for a panel of biomarkers (Interleukin-6, tumour necrosis factor alpha, adiponectin, cleaved cytokeratin 18, lipopolysaccharide binding protein and limulus amebocyte lysate). Central obesity was defined by waist circumference cut-offs in Asians.

Conditions

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Central Obesity

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Central obesity

Cases with central obesity as defined by waist circumference cut-offs ≥ 90 cm in men and ≥ 80 cm in women for Asians

No interventions assigned to this group

No central obesity

Controls with no central obesity

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Provision of signed written informed consent,
* Aged between 21- 75 years old,
* Body Mass Index (BMI) of \> 18 kg/m2,
* Ethnic group of either Chinese, Malay or Indian as evidenced by identification card,
* Subject with absence of impaired glucose tolerance,
* Subject is healthy with no clinically significant disease or condition as determined through their medical history, physical examination; Diabetes mellitus was defined as Type 2 DM fulfilling the WHO criteria and the care of Department of Endocrinology, Changi General Hospital,
* Ability to communicate with investigator and to understand and comply with all requirements of study participation.

Exclusion Criteria

* Subject who are viral Hepatitis (B or C) or HIV positive as per declaration,
* Subject who had bariatric surgery including lap banding, gastric sleeve surgery, cholecystectomy,
* Subject who has \> 5% weight loss in the last 3 months prior to study enrolment as per declaration,
* Subject who are on 'stable' insulin sensitizers such as such as rosiglitazone, metformin for the last 3 months prior to enrolment,
* Pregnant women,
* Subject who has been treated with antibiotics within 6 weeks of enrolment,
* Subject who has usage of lactulose, dietary fibres for purpose of constipation,
* Subject with immune-compromised status; undergoing chemotherapy, on steroid,
* Subject with FMHx or PMHx of autoimmune disease, GI cancers, inflammatory bowel disease, Irritable bowel syndrome and anxiety or depression as per declaration.
Minimum Eligible Age

21 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Genome Institute of Singapore

OTHER

Sponsor Role collaborator

Changi General Hospital

OTHER

Sponsor Role lead

Responsible Party

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John Chen Hsiang

Consultant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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John Chen Hsiang, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Changi General Hospital

Locations

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Changi General Hospital

Singapore, , Singapore

Site Status

Countries

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Singapore

References

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Hsiang JC, Bai WW, Raos Z, Stableforth W, Upton A, Selvaratnam S, Gane EJ, Gerred SJ. Epidemiology, disease burden and outcomes of cirrhosis in a large secondary care hospital in South Auckland, New Zealand. Intern Med J. 2015 Feb;45(2):160-9. doi: 10.1111/imj.12624.

Reference Type BACKGROUND
PMID: 25371019 (View on PubMed)

Ho EXP, Cheung CMG, Sim S, Chu CW, Wilm A, Lin CB, Mathur R, Wong D, Chan CM, Bhagarva M, Laude A, Lim TH, Wong TY, Cheng CY, Davila S, Hibberd M. Human pharyngeal microbiota in age-related macular degeneration. PLoS One. 2018 Aug 8;13(8):e0201768. doi: 10.1371/journal.pone.0201768. eCollection 2018.

Reference Type BACKGROUND
PMID: 30089174 (View on PubMed)

Other Identifiers

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MiPOOP

Identifier Type: -

Identifier Source: org_study_id

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