Trials / Unknown
UnknownNCT04924686
Changes of Muramyl Dipeptide in Intestinal and Extra-intestinal Diseases
A Bacterial Bi-functional Peptidoglycan Hydrolase Sheds NOD2 Ligands to Regulate Gut Homeostasis
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 600 (estimated)
- Sponsor
- Zhujiang Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
Nucleotide-binding oligomerization domain 2 (Nod2) signaling is critical for human health.To figure out the clinical relevance of NOD2 ligands, the investigators plan to evaluate the change of NOD2 ligands in inflammatory bowel diseases (IBD), CRC, atherosclerotic cardiovascular disease (ACVD), and type 2 diabetes mellitus (DM2 ).
Detailed description
Previous studies have shown that NOD2 gene mutants were associated with the Crohn's disease (CD), colorectal cancer (CRC) and many other diseases, suggesting the critical role of NOD2 signaling in human physiology and pathogenethesis. However, whether decreased NOD2 ligands also contributed to these diseases is unknown. In this study, the investigators plan to evaluate the change of NOD2 ligands in inflammatory bowel diseases (IBD), CRC, atherosclerotic cardiovascular disease (ACVD), and type 2 diabetes mellitus (DM2 ). For each of the patient, a sex- and age- matched control were chosen. Both the targeted metabolomics (LC-MS-MS methods) and NOD2-transfected cells co-expressing NF-κB luciferase reporters were used to test NOD2 ligands in the fecal and plasma samples.
Conditions
- Colorectal Cancer
- Inflammatory Bowel Disease
- Atherosclerotic Cardiovascular Disease
- Type2 Diabetes Mellitus
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Observational studies, no intervention | Observational studies, no intervention |
Timeline
- Start date
- 2020-05-10
- Primary completion
- 2023-06-10
- Completion
- 2023-08-15
- First posted
- 2021-06-14
- Last updated
- 2021-06-14
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04924686. Inclusion in this directory is not an endorsement.