Bariatric Surgery and HDL-cholesterol
Primary Purpose
Morbid Obesity
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Roux-en-Y gastric bypass
diet and lifestyle modifications
Sponsored by
About this trial
This is an interventional treatment trial for Morbid Obesity
Eligibility Criteria
Inclusion Criteria:
- BMI =/> 35 kg/m2,
- age 30-60 years,
- both sexes
Exclusion Criteria:
- history of major abdominal or bariatric surgery,
- disabling cardiac or pulmonary diseases,
- cancer,
- long-term treatment with oral corticosteroids, and
- mental illness
Sites / Locations
- Catholic University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Roux-en-Y gastric bypass
diet and lifestyle modifications
Arm Description
Both sexes, age between 30 and 60 years, BMI =/> 35 kg/m2
Both sexes, age between 30 and 60 years, BMI =/> 35 kg/m2
Outcomes
Primary Outcome Measures
changes in HDL-cholesterol Baseline to 1 year HDL-cholesterol changes: baseline to 1 year
Secondary Outcome Measures
changes in Apolipoprotein 4 (Apo4) and insulin sensitivity
Full Information
NCT ID
NCT01707771
First Posted
October 10, 2012
Last Updated
October 15, 2012
Sponsor
Catholic University of the Sacred Heart
1. Study Identification
Unique Protocol Identification Number
NCT01707771
Brief Title
Bariatric Surgery and HDL-cholesterol
Official Title
Effect of Gastric Bypass Versus Diet on Cardiovascular Risk Factors
Study Type
Interventional
2. Study Status
Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Catholic University of the Sacred Heart
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Objective: to assess the effect of gastric bypass on HDL-cholesterol concentration and its Apolipoprotein A4 content at 1 year following bariatric surgery in comparison with a hypocaloric diet. Secondary aim was to measure total cholesterol and triglycerides levels as well as insulin sensitivity after interventions.
Summary Background Data: Very few prospective uncontrolled studies have investigated the effects of Roux-en-Y gastric bypass (RYGB) on cardiovascular risk factors. No controlled studies had as primary goal the changes in HDL-cholesterol after gastric bypass.
Methods: Forty subjects with a BMI>40 or ≥35 kg/m2 in the presence of diabetes were enrolled.
Twenty of them were operated of RYGB while 20 received lifestyle modification suggestions and medical therapy for obesity complications (diabetes, hypertension and hyperlipidemia).
Detailed Description
Study design The study was an unblinded, prospective, non randomized clinical trial. Participants were recruited from referrals for treatment of morbid obesity between September 2008 and July 2009. One year follow-up was completed in September 2011.
The aim of the study related to the changes in HDL-cholesterol at 1 year after the intervention. Secondary aims were the changes in Apolipoprotein 4 (Apo4) and insulin sensitivity after the interventions.
Twenty morbidly-obese subjects (11 women and 9 men), whose 14 with normal glucose tolerance and 6 with type 2 diabetes mellitus (T2DM), have been studied before and 1, 2, 3, 6, 9 and 12 months after bariatric surgery.
Twenty morbidly-obese subjects (12 women and 8 men), 15 with normal glucose tolerance and 5 with T2DM, in the waiting list for bariatric surgery were enrolled in the protocol and underwent medical therapy for obesity complications (diabetes, hypertension and hyperlipidemia) and lifestyle modification suggestions.
Participants were eligible for inclusion if they had a BMI of 40 kg/m2 or >35 kg/m2 in presence of type 2 diabetes, were aged 30 to 60 years, and had not sustained weight loss in the previous 1 year. Exclusion criteria were a history of major abdominal or bariatric surgery, disabling cardiac or pulmonary diseases, cancer, long-term treatment with oral corticosteroids, and mental illness.
Roux-&-Y Gastric Bypass (RYGB) involves the use of a surgical stapler to create a small and vertically oriented gastric pouch with a volume usually < 30 ml. The upper pouch is completely divided by the gastric remnant and is anastomosed to the jejunum, 75 cm distally to the Treitz's ligament , through a narrow gastrojejunal anastomosis in a Roux-en-Y fashion. Bowel continuity is restored by an entero-entero anastomosis, between the excluded biliary limb and the alimentary limb, performed at 150 cm from the gastrojejunostomy.
Lifestyle modifications A hypocaloric diet (15 kcal/kgbw containing 55% carbohydrates, 30% lipids and 15% proteins) was prescribed together with the indications to perform 30 minutes brisk walk each day. Patients had open access to a diabetologist every 3 months. Medical therapies, including pharmaceutical agents, were assigned on an individual basis.
Anthropometric measures Body weight was measured to the nearest 0.1 kg with a beam scale and height to the nearest 0.5 cm using a stadiometer (Holatin, Crosswell, Wales, U.K.).
Blood pressure Blood pressure was measured 3 times with an appropriately sized cuff after the participant had rested for 5 minutes, and the last 2 measurements were averaged.
Oral glucose tolerance test A standard 75-g oral glucose tolerance test (OGTT) was performed after an overnight fasting with blood sampling at 0, 30, 60, 90, 120, and 180 min. Samples were placed in chilled tubes, and plasma was separated within 20 min and stored at -80°C.
Analytical methods Blood was drawn in the morning after an overnight fast. The sera and plasma were immediately separated by centrifugation at 4°C and stored at -80°C until assay.
Plasma glucose was measured by the glucose-oxidase method (Beckman, Fullerton, CA). Plasma insulin was assayed by microparticle-enzyme immunoassay (Abbott, Pasadena, CA) with a sensitivity of 1 μU/ml and an intra-assay CV of 6.6%.
Total cholesterol and triglycerides were measured enzymatically. HDL-cholesterol was measured after precipitating apolipoprotein B-containing lipoproteins with dextran sulfate and magnesium chloride.
HbA1c serum levels were measured by high-performance liquid-chromatography (normal range 3.5-6.5%) Apo A4 was assessed by ELISA (Cusabio Biotech, Wuhan, Hubei, China); the detection range is from 15.62 μg/l to 1000 μg/l and the minimum detectable concentration is 4 μg/l.
Insulin Sensitivity Models
The OGTT and fasting plasma glucose and insulin were used to compute the insulin sensitivity. Insulin resistance was assessed using the homeostasis model assessment (HOMA-IR) originally described by Mathew et al. HOMA-IR was calculated using the following equation:
HOMA-IR(μU/ml∙mg/dl)=fasting insulin(μU/ml)∙(fasting glucose (mg/dl))/405 Peripheral insulin sensitivity was assessed by the Oral Glucose Insulin Sensitivity (OGIS) model. OGIS is an index of insulin sensitivity calculated in this case from the 3 hours OGTT and it is an estimate of the glucose clearance during a hyperinsulinemic euglycemic glucose clamp expressed in ml/min per square meter of body surface area.
Statistics All of the data are expressed as means ± SD unless otherwise specified. The Wilcoxon paired-sample test was used for intragroup comparisons. Two-sided P < 0.05 was considered significant. Nonparametric Spearman correlations were used to assess linear relationships between single variables.
We calculated that a total of 30 participants would give 80% power to detect a significant (P < 0.05) difference between the groups. To allow for possible dropouts and add power for analysis of secondary outcomes, we decided to enroll 40 participants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Roux-en-Y gastric bypass
Arm Type
Active Comparator
Arm Description
Both sexes, age between 30 and 60 years, BMI =/> 35 kg/m2
Arm Title
diet and lifestyle modifications
Arm Type
Active Comparator
Arm Description
Both sexes, age between 30 and 60 years, BMI =/> 35 kg/m2
Intervention Type
Procedure
Intervention Name(s)
Roux-en-Y gastric bypass
Intervention Description
Active Comparator: Roux-en-Y gastric bypass
Intervention Type
Behavioral
Intervention Name(s)
diet and lifestyle modifications
Intervention Description
Active Comparator: diet and lifestyle modifications
Primary Outcome Measure Information:
Title
changes in HDL-cholesterol Baseline to 1 year HDL-cholesterol changes: baseline to 1 year
Time Frame
1 year
Secondary Outcome Measure Information:
Title
changes in Apolipoprotein 4 (Apo4) and insulin sensitivity
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
BMI =/> 35 kg/m2,
age 30-60 years,
both sexes
Exclusion Criteria:
history of major abdominal or bariatric surgery,
disabling cardiac or pulmonary diseases,
cancer,
long-term treatment with oral corticosteroids, and
mental illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Geltrude Mingrone, MD
Organizational Affiliation
Catholic University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Catholic University
City
Rome
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
23979288
Citation
Raffaelli M, Guidone C, Callari C, Iaconelli A, Bellantone R, Mingrone G. Effect of gastric bypass versus diet on cardiovascular risk factors. Ann Surg. 2014 Apr;259(4):694-9. doi: 10.1097/SLA.0b013e31829d6989.
Results Reference
derived
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Bariatric Surgery and HDL-cholesterol
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