Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | OTHER |
Not provided
Not provided
Not provided
Not provided
It is estimated that there will be 439-552 million people with type 2 diabetes mellitus (T2DM) globally in 2030. Type 2 Diabetes Mellitus is present in one quarter of patients at the bariatric outpatient clinic. It is undecided which metabolic surgery grants best results in the remission of T2DM and which procedure does that at the lowest rate of surgical complications, long term difficulties and side effects. Non alcoholic fatty liver disease (NAFLD) is present in 80% of all morbidly obese subjects and is a major risk factor for development of insulin resistance and non alcoholic steatohepatis (NASH). It is increasingly recognized that the immune system, possibly driven by innate lymphoid cells (ILC's), and the intestinal microbiome are major players in this obesity related disease and the switch from benign to malign (insulin resistance and T2DM) obesity. However, the exact mechanisms of action behind the surgery-driven switch back from malign to benign obesity are unknown.Primary objective is to evaluate and compare the glycaemic control in T2DM within the first year of LRYGB and LMBG. Secondary aim is to gain insight in the pathophysiological mechanisms that drive the conversion of malign to benign obesity.
Metabolic surgery has proven to be a viable long-term solution in the treatment of morbid obesity and its comorbidities. It induces rapid remission of type 2 diabetes mellitus (T2DM). Type 2 Diabetes Mellitus is present in one quarter of patients at the bariatric outpatient clinic. Non alcoholic fatty liver disease (NAFLD) is present in 80% of all morbidly obese subjects and is a major risk factor for development of insulin resistance and non alcoholic steatohepatis (NASH), with the latter becoming the major indication for liver transplantation in the USA. It is increasingly recognized that the immune system, possibly driven by innate lymphoid cells (ILC's), and the intestinal microbiome are major players in this obesity related disease and the switch from benign to malign (insulin resistance and T2DM) obesity. However, the exact mechanisms of action behind the surgery-driven switch back from malign to benign obesity are unknown. Also, it is undecided which metabolic surgery grants best results in the remission of T2DM and which procedure does that at the lowest rate of surgical complications, long term difficulties and side effects. The Laparoscopic Roux-en-Y Gastric Bypass (LRYGB), an efficient but complex procedure, is the golden standard in the Netherlands. The Laparoscopic Mini Gastric Bypass (LMGB) is technically less challenging and has been introduced to overcome some of the limitations of LRYGB. It has been hypothesized that the LMGB has a more rapid and durable glycaemic control, possibly due to the altered constitution and the augmented length of the biliary limb. There is reason to believe that the improved glycaemic control might become apparent within the first year of surgery and that it might remain thereafter. However, it is unknown what order of magnitude is to be expected and whether subgroups of T2DM patients will benefit the LMGB more. Also, it is unknown whether and to what extent intestinal microbiota and immunological tone can predict the metabolic response (improvement in insulin sensitivity) and NAFLD/NASH reduction and whether differences are expected between these two surgeries. Increased understanding of the pathophysiological mechanisms as well as their relationship to metabolic disturbances are thought to be of crucial importance to discover new diagnostic and therapeutical targets in obesity associated insulin resistance/T2DM and NAFLD/NASH. Primary objective is to evaluate and compare the glycaemic control in T2DM within the first year of LRYGB and LMBG. Secondary aim is to gain insight in the pathophysiological mechanisms that drive the conversion of malign to benign obesity.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Laparoscopic Roux-en-Y gastric bypass | Active Comparator | Laparoscopic Roux-en-Y gastric bypass |
|
| Laparoscopic Mini Gastric Bypass | Experimental | laparoscopic Mini gastric bypass |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| laparoscopic Roux-en-Y gastric bypass | Procedure | laparoscopic Roux-en-Y gastric bypass with a 50 cm biliary limb and a 150 cm alimentary limb |
|
| Measure | Description | Time Frame |
|---|---|---|
| glycaemic control | as measured by the difference in HBa1C | 12 months FU |
| Measure | Description | Time Frame |
|---|---|---|
| glycaemic control | as measured by the difference in HBa1C | 6 and 24 months FU |
| glycaemic control | as measured by the difference in HBa1C and anti-diabetic medication |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Anne-Sophie van Rijswijk, MD | Contact | +31205124460 | anne-sophie.vanrijswijk@slz.nl | |
| Maurits de Brauw, MD PhD | Contact | maurits.debrauw@slz.nl |
| Name | Affiliation | Role |
|---|---|---|
| Maurits de Brauw, MD PhD | Head of department of Surgery | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| medical Center Slotervaart | Recruiting | Amsterdam | North Holland | 1066EC | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37626349 | Derived | Pyykko JE, Hinnen C, Aydin O, Nieuwdorp M, De Brauw LM, Bruin SC, van Olst N, Gerdes VEA, Sanderman R, Hagedoorn M. Attachment style and post-bariatric surgery health behaviours: the mediating role of self-esteem and health self-efficacy. BMC Psychol. 2023 Aug 25;11(1):248. doi: 10.1186/s40359-023-01273-5. | |
| 36273149 | Derived |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Single-center, open randomized controlled clinical trial
Not provided
Not provided
Not provided
Not provided
|
| laparoscopic Mini gastric bypass | Procedure | laparoscopic Mini gastric bypass with a gastrojejunostomy at 200 centimeters measured from the ligament of Treitz |
|
|
| 6, 12 and 24 months FU |
| Insulin sensitivity | Mixed meal tolerance test for level of insulin sensitivity | baseline, 12, 24 months FU |
| NAFLD/NASH | NAFLD/NASH parameters in liver biopsy measured with the Steatosis, Activity and Fibrosis (SAF) score according to Bedossa et al (2012).For each patient a SAF score summarizing the main histological lesions will be defined. The steatosis score (S) will assess the quantities of larger or median-sized lipid droplets but not foamy microvesicules from 0 to 3 (S0 <5%; S1 5-33%; S2 34-66% and S3>67%). Activity grade (A) from 0-4 is the unweighted addition of hepatocyte ballooning (0-2) and lobular inflammation (0-2). Stage of fibrosis will be assessed using the score described by NASH-CRN as follows; stage 0 (F0) no fibrosis; stage 1 (F1) 1a or 1b perisinusoidal zone 3 or 1c portal fibrosis; stage 2 (F2) persinusoidal and periportal fibrosis without bridging; stage 3 (F3) bridging fibrosis and stage 4 (F4) cirrhosis. A diagnostic algorithm which will be used during this study can be found in the original paper published by Bedossa et al. | day of surgery, reoperation |
| Presence of bacterial DNA/bacterial metabolites - portal vein | in portal vein blood | day of surgery, reoperation |
| Presence of bacterial DNA/bacterial metabolites - liver | in liver | day of surgery, reoperation |
| Presence of bacterial DNA/bacterial metabolites - abdominal adipose tissue | in abdominal adipose tissue depots | day of surgery, reoperation |
| Expression and differentiation of intestinal immunological cells - GALT | in GALT | day of surgery, reoperation |
| Expression and differentiation of intestinal immunological cells - abdominal adipose tissue | in abdominal adipose tissue depots | day of surgery, reoperation |
| Expression and differentiation of intestinal immunological cells - liver | in liver | day of surgery, reoperation |
| Expression and differentiation of intestinal immunological cells - peripheral blood | in peripheral blood | day of surgery, reoperation |
| Expression and differentiation of immunological cells | ILC's, macrophages | 12 and 24 months FU |
| Expression and differentiation of inflammatory markers | IL6, IRX3 and 5 | 12 and 24 months FU |
| Small intestinal and fecal microbiota composition | feces | 2, and 6 weeks, 6 months, as well as 12 and 24 months after surgery |
| Peripheral blood inflammatory markers | ILC's, macrophages, T/B-cells and dendritic cells | 2, and 6 weeks, 6 months, as well as 12 and 24 months after surgery |
| Eating habits | G-food craving questionnaire (FCQ-T) 21 item questionaire scale 0 (never) - 6 (always) | baseline, 12, 24 months FU |
| Eating habits | 10 questions, scale 0-10 for instance 0 not hungry -10 very hungry / satiety / craving salty food / craving sweet food / craving fat food | baseline, 12, 24 months FU |
| Excreted metabolites | urine | baseline, 12, 24 months FU |
| Bio electric impedance | body composition as assesed by bioelectical impedance analysis (BIA): the measurement of body fat in relation to lean body mass. | baseline, 12, 24 months FU |
| Quality of life | Quality of life (IWQOL lite) 5 domain questionaire, 31 items: 1 never true - 5 always true | baseline, 12, 24 months FU |
| Cardiac / ventricular hypertrophy | Electrocardiogram (ECG) | baseline, 12, 24 months FU |
| van Rijswijk A, van Olst N, Meijnikman AS, Acherman YIZ, Bruin SC, van de Laar AW, van Olden CC, Aydin O, Borger H, Beuers UHW, Herrema H, Verheij J, Apers JA, Backhed F, Gerdes VEA, Nieuwdorp M, de Brauw LM. The effects of laparoscopic Roux-en-Y gastric bypass and one-anastomosis gastric bypass on glycemic control and remission of type 2 diabetes mellitus: study protocol for a multi-center randomized controlled trial (the DIABAR-trial). Trials. 2022 Oct 22;23(1):900. doi: 10.1186/s13063-022-06762-3. |
| ID | Term |
|---|---|
| D009767 | Obesity, Morbid |
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D009765 | Obesity |
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D004700 | Endocrine System Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D015390 | Gastric Bypass |
| ID | Term |
|---|---|
| D050110 | Bariatric Surgery |
| D049088 | Bariatrics |
| D000073319 | Obesity Management |
| D013812 | Therapeutics |
| D005763 | Gastroenterostomy |
| D000714 | Anastomosis, Surgical |
| D013514 | Surgical Procedures, Operative |
| D013505 | Digestive System Surgical Procedures |
Not provided
Not provided