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Morbid ObesityNCT02067585

An Analysis of Lipid and Glucose Metabolism Following Bariatric Surgery

A study testing Standardized Lipid meals in people with Morbid Obesity, run by University of Alberta at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Bariatric surgery induce remarkable weight loss and improvement or resolution of type 2 diabetes. Obesity is the primary risk factor for type 2 diabetes, and 90% of all type 2 diabetics are obese. Type 2 diabetes resolves post-operatively in 84-98% after bypass and 48-68% after restrictive procedures. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Morbid Obesity
What is being tested?
Standardized Lipid meals
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 siteCanada
Study dates
Feb 2010to Sep 2012
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • morbidly obese patients
  • age 18-65
  • with or without type 2 diabetes
  • 12 or more months following LRYGB or LAGB, or patients waiting for mentioned procedures
  • able to provide written informed consent.

Who cannot join

  • chronic liver disease
  • maladaptive eating behavior
  • current pharmacological treatment for obesity
  • for patients following LAGB - ongoing band volume adjustments
  • hypothyroidism
  • treatment with insulin
Show all 13Show fewer
  • revision of a previous bariatric procedure
  • major postoperative complication
  • allergy to soy or any component of the study meal
  • renal failure (glomerular filtration <60mL/min)
  • alcoholism
  • acute illness
  • pregnancy or nursing.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • CAMIS

    Edmonton, Alberta, T5H 3V9

Other trials in Canada

About this study

Bariatric surgery induce remarkable weight loss and improvement or resolution of type 2 diabetes. Obesity is the primary risk factor for type 2 diabetes, and 90% of all type 2 diabetics are obese. Type 2 diabetes resolves post-operatively in 84-98% after bypass and 48-68% after restrictive procedures.

Obesity leads to elevated plasma free fatty acids and subsequently to excessive accumulation of triglyceride in peripheral tissues, which is an independent risk factor for insulin resistance and type 2 diabetes. Bariatric surgery is associated with dramatic decrease in plasma free fatty acids and other lipids.

Read more

This study will clarify the relationship of changes in fatty acid and other lipid metabolism to improved insulin sensitivity after different bariatric procedures ('restrictive' - laparoscopic adjustable gastric band and 'hybrid' - laparoscopic roux-en-y gastric bypass) and compare them with non-surgical obese patients. This will allow the investigators to refine indications for these procedures especially in patients with type 2 diabetes.

The investigators will analyze whether surgical bypass of the upper small bowel plays a critical role in the resolution of type 2 diabetes and improvement in lipid metabolism. The investigators will achieve this by comparing gastric banding and gastric bypass in a collaborative research study involving obesity surgeons, physicians and lipid researchers.

Read the detailed description

Background: Bariatric surgery is the only evidence-based approach to efficacious and sustainable weight loss. It is estimated that about one third of patients undergoing bariatric surgery have type 2 diabetes, with a high rate of resolution of diabetes post-operatively: 84-98% after gastric bypass and 48-68% after purely restrictive procedures(1, 2). Other cardiovascular risk factors such as lipid profile and inflammatory markers also, significantly improve. 25% of the population of Alberta are obese and 2,7% are morbidly obese, one third of them are with type 2 diabetes. Bariatric surgery in these patients will translate into a cure for type II diabetes, dramatic improvements in quality of life, improved longevity and lower health care costs for the system.

Morbid obesity leads to elevated plasma free fatty acids (FFA) and subsequently to excessive accumulation of triglyceride in peripheral tissues. Excessive triglyceride accretion is an independent risk factor for insulin resistance, type II diabetes and cardiovascular complications. Bariatric surgery is associated with dramatic improvements in these comorbid diseases(2). Purely restrictive procedures (laparoscopic adjustable gastric band - LAGB) may differ from hybrid procedures (laparoscopic roux-en-y gastric bypass - LRYGB) in their effect on diabetes and cardiovascular disease. The LAGB is a less complex surgical procedure that can be done on a day surgery basis and has an extremely low peri-operative mortality rate. The LRYGB is much more complex and has a low but important rate of anastomotic leak and mortality.

LAGB and LRYGB vary in their average percent excess weight loss (%EWL)(2). This may contribute to a disparity in their impact on comorbid disease. However, improvements in insulin sensitivity and glucose homeostasis occur early after LRYGB, preceding significant weight loss(3). Postoperative changes in the absorption and metabolism of lipids induced by a malabsorptive procedure may be responsible for these beneficial changes. The relationship of improved insulin sensitivity to changes in lipid metabolism need to be clarified in order to understand the varying impact of LAGB and LRYGB on comorbid disease associated with obesity. The initial decreased caloric intake following Bariatric surgery can improve the response of adipose tissue manifested by favorable changes in adipocytokines. The postoperative rise in adiponectin (4, 7) (an anti-inflammatory mediator) was observed. These changes correlate with weight loss and improvement in insulin resistance.

In obese insulin-resistant subjects, insulin cannot attenuate hydrolysis of stored triglyceride in adipose tissue and consequently this leads to excessive free fatty acids release into circulation and increased delivery of fatty acids to the muscle, liver and pancreas. Excessive uptake of fatty acids into these tissues exacerbates hepatic and muscle insulin resistance and impairs insulin secretion from pancreatic beta cells. Bariatric surgery improves insulin sensitivity which leads to inhibition of hydrolysis of adipose triglycerides and decreased release of free FFA into the circulation. Recently it was shown that not only increased baseline FFA but also altered clearance of FFA normalize after LRYGB (8). Also, postoperative reduction in fat intake and absorption leads to decreased level of FFA in blood. After malabsorptive, weight-reducing procedures the beta cell glucose and fatty acid sensitivity was doubled early in diabetic patients, leading to a decrease in insulin secretion (9).

Beside its contribution to insulin resistance, severe obesity is also associated with an elevated inflammatory state. In obese with type 2 diabetes and metabolic syndrome, the highly sensitive C-reactive protein (CRP) serum concentration, an inflammatory marker, is increased and correlates with the severity of glucose intolerance and with the severity of inflammation (10). Following bariatric surgery, C-reactive protein (CRP) decreases. It has been shown that gastric bypass reduces biochemical cardiac risk factors, particularly, CRP by 80% in addition to triglycerides, total cholesterol, LDL, and lipoprotein A (7, 11).

These changes in lipid and glucose metabolism are seen after restrictive and hybrid procedures to a varying extent. Given the different mechanism of action, technical complexity and safety profiles of LAGB and LRYGB, it is crucial to clarify their impact on co-morbid disease.

Hypothesis:

  1. Postprandial reduction in serum levels of free fatty acids and lipids following LRYGB (a malabsorptive procedure) are greater than following LAGB (a purely restrictive procedure).
  2. Reduced serum levels of free fatty acids and lipids following LRYGB lead to improvements in insulin resistance.

Rationale: Clinical evidence suggests that purely restrictive procedures (LAGB) affect lipid absorption and metabolism differently when compared to hybrid restrictive/malabsorptive procedures (LRYGB). This may be due to the malabsorptive component of LRYGB where ingested food bypasses the duodenum and upper jejunum, both important for lipid digestion and absorption.

Design: A cross-sectional study to characterize lipid absorption and metabolism following bariatric surgical procedures based out of the Weight Wise Clinic at the Royal Alexandra Hospital, Edmonton. Venous blood will be collected after overnight fast, before and after standardized lipid meal, and analyzed for appropriate biochemical indices. The study cohorts will comprise patients after LAGB, LRYGB, in the period of weight stabilization, 12+ months following bariatric surgery. Controls will comprise preoperative patients managed without pharmacologic intervention for their obesity.

Methods: Recruitment and physical examination will be conducted at the Weight Wise Clinic. Studies will begin at the Clinical Investigation Unit, University of Alberta Hospital, at 7 AM after a consumed the night before study meal and then 12-h-overnight fast. Liquid meal will consist of 240 ml of Hormel Great Shake Plus liquid nutritional supplement, 203 Kcal/100mL; 49% calories from fat, mostly unsaturated fatty acids of soy origin; 38% calories from carbohydrates, 13% calories from proteins. Weight measurement will be performed by a nurse. Fasting baseline blood will be drawn and the subjects will consume a second portion of the study meal. The test meal will be drunk with a straw within 15 minutes. Blood withdrawal will be carried out at 10, 20, 30, 90 min, 4 and 6 hrs after the start of ingestion of the standardized meal. Subjects will be allowed to walk or sit, but not to exercise during the test. Drinking of water without sugar will be permitted. Blood will be collected through a venous in-dwelling catheter placed in a cubital vein.

Laboratory analyses: The plasma total cholesterol, low density lipoprotein cholesterol, high density lipoprotein cholesterol, triglycerides, nonesterified fatty acid concentration and the degree of unsaturation, ApoB-48 (intestinally-derived lipoprotein) and apoB-100 (liver-derived lipoprotein), insulin, glucose, CPR, adiponectin, HbA1c, albumin, AST, ALT, ketone bodies will be measured.

Primary outcome: postprandial changes in serum free fatty acids, lipids (cholesterols total, LDL and HDL, triglycerides) and apoB in patients after bariatric surgery and their relationship with insulin sensitivity (glucose, insulin, HOMA index).

The investigators expect that greater reduction in postprandial serum free fatty acids and lipids (cholesterol, triglyceride) after LRYGB will be associated with greater decrease in insulin resistance (HOMA index is expected to decrease), as compared with LAGB. Insulin, plasma glucose and ketone bodies are expected to decrease.

Secondary outcomes: Changes in HbA1c, AST, ALT, albumin, CRP, adiponectin levels will be compared with the changes in fatty acids, lipids and insulin resistance.

The investigators expect that reduced serum free fatty acid level will be associated with decrease in marker of inflammation (CRP), HbA1c, AST, ALT, and increase in anti-inflammatory mediator (adiponectin) after both procedures, but more pronounced after LRYGB.

Sample Size Calculation: Sample size was calculated based on review of literature showing decrease in post-bariatric procedure free fatty acids. A power analysis was performed with a beta of 0.20 and an alpha of 0.05. Assuming that a 30% difference in the level of FFA exists between morbidly obese operated and not operated patients, 16 subjects will need in each arm, total 48 for LAGB, LRYGB and control groups. Thus the study would provide an 80% chance that a difference would be detected if one exists.

Data analysis: Multivariate Analysis for testing statistical significance of improved serum free fatty acid, ApoB and lipid levels and their correlation with insulin sensitivity (glucose, insulin) among multiple groups of data will be performed by a statistician.

Conditions
Morbid Obesity
Being tested
Standardized Lipid meals
Medical subject headings
Obesity, Morbid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Standardized Lipid mealsDietary supplement

    Standardized Lipid meals: 240 ml of Hormel Great Shake Plus liquid nutritional supplement, 203 Kcal/100mL; 49% calories from fat, mostly unsaturated fatty acids of soy origin; 38% calories from carbohydrates, 13% calories from proteins.

Study groups in NCT02067585
Study groupRoleWhat they receive
LAGBExperimentalStandardized Lipid meals will be served to Laparoscopic adjustable gastric banding patients.
Receives: Dietary Supplement: Standardized Lipid meals
LRYGBExperimentalStandardized Lipid meals will be served to the Laparoscopic Rou-en-Y gastric bypass patients.
Receives: Dietary Supplement: Standardized Lipid meals
Non-surgicalExperimentalStandardized Lipid meals will be served to the non-surgical obese patients
Receives: Dietary Supplement: Standardized Lipid meals

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Triglycerides Post-prandial

    Measured: 0 minutes

  2. Triglycerides

    Measured: 30 minutes

  3. Triglyceride

    Measured: 90 minutes

  4. Triglyceride

    Measured: 4 hours

  5. Triglyceride

    Measured: 6 hours

Secondary outcomes (5)
  1. Blood Glucose

    Measured: 0 minute

  2. Glucose

    Measured: 30 minutes

  3. Glucose

    Measured: 90 minutes

  4. Glucose

    Measured: 4 hours

  5. Glucose

    Measured: 6 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2014 (estimated)
  2. Study startFeb 2010
  3. Primary completionAug 2011
  4. Study completionSep 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02067585
Sponsor's protocol ID
Pro00008986
Other IDs
Edmonton Civic Employees
Status last verified
Feb 2017
First submitted
13 Feb 2014
Last updated
11 Apr 2017
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Standardized Lipid meals in people with Morbid Obesity, run by University of Alberta at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Apr 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 11 Apr 2017). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Triglycerides Post-prandial (time frame: 0 minutes). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2017.

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