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It is well known that incretin, particular GLP-1enhances satiety and reduces energy intake in controlling appetite and dietary in humans (Flint A, et al. Gutzwiller JP et al.). Recently, incretin-based therapy has been attracted a lot of interest (Hare KJ, Knop FK). However, it is not clear how the incretin-based therapy affects energy and content of dietary intake in patients with type 2 diabetes mellitus (T2DM). Previously, the investigators reported the amount of energy and content of dietary intake in type 2 diabetic Japanese patients with more than 10 years of long time duration after discovery using questionnaire (Inoue K et al.) and the patients were impaired a secretion of active GLP-1 (Kamoi et al).
The investigators examine whether the incretin-based therapy effects on the energy and content of dietary intake in the same patients before and one year after administration of incretin-related drugs using the same method previously (Inoue K et al.).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Incretin-related drugs |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Incretin-related drugs | Drug | DPP-IV inhibitors are administered via per os. GLP-L receptor agonists are administered via subcutaneous injections. |
|
| Measure | Description | Time Frame |
|---|---|---|
| HbA1c | one year |
| Measure | Description | Time Frame |
|---|---|---|
| BMI | One year | |
| Calory of dietary intake | One year | |
| Content of dietary intake |
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Inclusion Criteria:
Exclusion Criteria:
Patients with a serious complication in the heart, liver or kidney
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100 patients
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| Name | Affiliation | Role |
|---|---|---|
| Kyuzi Kamoi, MD | Nagaoka Red Cross Hospital | Principal Investigator |
| Yoshiko Kontai, RD | Universty of Niigata Prefecture | Principal Investigator |
| Kanako Inoue, RD | Universty of Niigata Prefecture | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nagaoka Red Cross Hospital | Nagaoka | Niigata | 940-2085 | Japan |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Result | 1. Flint A, et al. Glucagon-like peptide 1 promotes satiety and suppresses energy intake in humans. J Clin Invest. 1998; 101(3):515-520. 2. Gutzwiller JP, et al. Glucagon-like peptide-1: a potent regulator of food intake in humans. Gut. 1999; 44(1):81-86. 3. Verspohl EJ. Novel therapeutics for type 2 diabetes: incretin hormone mimetics (glucagon-like peptide-1 receptor agonists) and dipeptidyl peptidase-4 inhibitors. Pharmacol Ther. 2009; 124(1):113-38. 4. Hare KJ, Knop FK. Incretin-based therapy and type 2 diabetes. Vitam Horm. 2010; 84:389-41 5. Inoue K, Kontai Y, Kamoi K, et al. Energy and content of dietary intake and life related habituation using questionnaire written by Japanese language in Japanese patients with endocrine and metabolism disorders. Abstract in 14 Annual Scientific Meeting of the Metabolism and Clinical Nutrition Society, held at Yokohama of Japan on15th Jan, 2011 (in Japanese). |
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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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|
| One year |
| D004700 | Endocrine System Diseases |