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This study aims to investigate the distribution of gut microbiota-derived metabolites, and to evaluate whether postoperative nutritional intervention can modulate the gut-heart metabolic axis, thereby improving metabolic profiles and clinical outcomes.
Background: Cardiovascular diseases remain the leading cause of mortality worldwide. Recent research has highlighted the role of gut microbiota and its metabolites-such as trimethylamine-N-oxide, phenylacetylglutamine, and p-cresyl sulfate-in the pathogenesis of cardiovascular disease through mechanisms involving inflammation, oxidative stress, and vascular dysfunction. However, little is known about the actual distribution of these metabolites in human cardiac tissues or their correlation with circulating levels. No clinical studies to date have systematically examined both tissue and blood samples in this context.
Methods: Preoperative blood samples and intraoperative cardiac tissue specimens will be collected. Both targeted and untargeted metabolomics analyses will be performed using mass spectrometry to detect key gut microbiota-derived metabolites. A subset of patients will receive postoperative probiotic supplementation. Serial blood will be collected to monitor changes in the metabolome and gut microbial composition.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Probiotic group | Experimental | Received standard postoperative care with probiotic supplementation |
|
| Placebo group | Placebo Comparator | Received standard postoperative care with placebo supplementation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| probiotic supplementation intervention | Other | probiotic supplementation will be administered, while participants continue undergoing standard postoperative care |
|
| Measure | Description | Time Frame |
|---|---|---|
| Trimethylamine-N-oxide | Gut microbiota-derived metabolites | From enrollment to the end of intervention at 3 weeks |
| Phenylacetylglutamine | Gut microbiota-derived metabolites | From enrollment to the end of intervention at 3 weeks |
| P-cresyl sulfate | Gut microbiota-derived metabolites | From enrollment to the end of intervention at 3 weeks |
| Indoxyl sulfate | Gut microbiota-derived metabolites | From enrollment to the end of intervention at 3 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ke-Yun Chao, PhD | Contact | +886-905-301-879 | C00152@mail.fjuh.fju.edu.tw |
| Name | Affiliation | Role |
|---|---|---|
| Ke-Yun Chao, PhD | Fu Jen Catholic University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fu Jen Catholic University Hospital, Fu Jen Catholic University | Recruiting | New Taipei City | 24352 | Taiwan |
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| ID | Term |
|---|---|
| D002318 | Cardiovascular Diseases |
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| Placebo supplementation intervention | Other | Undergo routine standard postoperative care with placebo intervention |
|