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| Name | Class |
|---|---|
| Chinese Academy of Sciences | OTHER_GOV |
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Intestinal microflora refers to the trillions of microorganisms living in our gut, which is considered as an independent endocrine organ of human body. Intestinal microbiota plays a very important role in human health. The composition of human intestinal microbiota is affected by a variety of factors, including age, living region, eating habits, nutrition, probiotics, antibiotics and so on. It is found that the imbalance of intestinal microbiota is closely related to the occurrence and development of metabolic diseases including type 2 diabetes mellitus (T2DM). There are great differences in the structure and function of intestinal microbiota between healthy people and T2DM patients, and recently changes of intestinal microbiota have been observed in pre-diabetes. In recent years, it has been found that some commonly used hypoglycemic drugs may regulate and improve the imbalance of intestinal flora of T2DM patients, including metformin, α - glucosidase inhibitor, and Glucagon-like peptide-1(GLP-1) receptor agonist, which have a positive impact on the short chain fatty acid (SCFAs) producing bacteria. However, on the one hand, subjects of those studies were mostly western population and there were just a few studies on the influence of anti-diabetic drug on human gut microbiota in Chinese population, on the other hand, the study of influence of Dipeptidyl peptidase-4(DPP-4) inhibitors, sulfonylureas, sodium-dependent glucose transporters-2(SGLT-2) inhibitors or thiazolidinediones on intestinal microbiota is rare or even absent. This study aims to explore the effect of different hypoglycemic drugs on intestinal flora and find the potential intestinal target of drug action in Chinese population.
In this study, T2DM patients who were free of anti-diabetic drugs or those have taken hypoglycemic drugs and ready to add a new drug were recruited, they were treated with metformin, α - glucosidase inhibitor, DPP-4 inhibitors, sulfonylureas, SGLT-2 inhibitors, or thiazolidinediones according to their state of illness. Faecal specimen will be collected for test of composition of gut microbiota at baseline and 4-week, 8-week,12-week after taking medication. At baseline, patients will take physical examination and blood test, every patient will complete the questionnaire under the direction of doctors to get their general information and diet habits. Physical examination and blood test will repeat at 4-week, 8-week,12-week after treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Glucophage group | Experimental |
| |
| Acarbose group | Experimental |
| |
| Sitagliptin group | Experimental |
| |
| Dapagliflozin group | Experimental |
| |
| Pioglitazone group | Experimental |
| |
| Glimepiride group | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Glucophage 500Mg Tablet | Drug | 0.5g three times daily |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline to post-treatment in composition in gut microbiota analyzed by meta-genome sequencing. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in fasting blood glucose. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in level of TNF-a. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in fasting insulin. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in blood lipid including cholesterol, triglycerides, high-density lipoprotein. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in 2-hour postprandial blood glucose. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in level of IL-6. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in level of IL-8. | Baseline, Week 4, Week 8, Week 12 | |
| Changes from baseline to post-treatment in composition in level of IL-10. | Baseline, Week 4, Week 8, Week 12 |
| Measure | Description | Time Frame |
|---|---|---|
| The linear relationship between gut microbiota and blood glucose and blood lipid level. | Week 4, Week 8, Week 12 | |
| The linear relationship between gut microbiota and inflammation factors level. | Week 4, Week 8, Week 12 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Weigang zhao, MD | Contact | +86 69151876 | xiehezhaoweigang@163.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peking Union Medical College Hospital | Beijing | Beijing Municipality | 100730 | China |
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| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| D008687 | Metformin |
| D013607 | Tablets |
| D020909 | Acarbose |
| D000068900 | Sitagliptin Phosphate |
| C529054 | dapagliflozin |
| D000077205 | Pioglitazone |
| C057619 | glimepiride |
| ID | Term |
|---|---|
| D001645 | Biguanides |
| D006146 | Guanidines |
| D000578 | Amidines |
| D009930 | Organic Chemicals |
| D004304 |
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| Acarbose Tablets |
| Drug |
50mg three times daily |
|
| Sitagliptin tablet | Drug | 100mg once daily |
|
| Dapagliflozin Tablet | Drug | 10mg once daily |
|
| Pioglitazone Tablets | Drug | 30mg once daily |
|
| Glimepiride Tablets | Drug | 2mg once daily |
|
| Changes from baseline to post-treatment in composition in level of C-reative protein. | Baseline, Week 4, Week 8, Week 12 |
| D004700 | Endocrine System Diseases |
| Dosage Forms |
| D004364 | Pharmaceutical Preparations |
| D014312 | Trisaccharides |
| D009844 | Oligosaccharides |
| D011134 | Polysaccharides |
| D002241 | Carbohydrates |
| D014230 | Triazoles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011719 | Pyrazines |
| D045162 | Thiazolidinediones |
| D013844 | Thiazoles |
| D013457 | Sulfur Compounds |