Mechanistic Insights to Weight Loss Maintenance Through SGLT2 Inhibitors
Study Details
Study Description
Brief Summary
Obesity increases the risk of cardiometabolic diseases such as hypertension and diabetes. Weight loss interventions such as low-calorie diet and physical activity are effective for weight loss in the short term, but weight loss maintenance (WLM) with low-calorie diet and physical activity is challenging. Weight loss is associated with a reduction in the amount of calories needed to maintain the body at rest, called the resting energy expenditure (REE), which may be a probable mechanism for this lack of WLM. Most individuals are unable to adequately change their diet and increase their physical activity levels to overcome this decrease in REE which prevents WLM. Therefore, techniques that increase REE may promote WLM in these individuals. Pre-clinical studies for Empagliflozin - Sodium-glucose Cotransporter-2 (SGLT2) inhibitor have shown an increase in REE. Thus, in addition to reducing the cardiovascular risk, SGLT2 inhibitor may promote WLM by increasing REE. This study aims to promote WLM in obese individuals by increasing the REE using SGLT2 inhibitor therapy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Empagliflozin Arm We will enroll 12 obese participants who have intentionally lost greater than or equal to 5% of body weight through a non-pharmacological structured weight loss program based on diet and exercise within the last 6 months. The participants will take empagliflozin 25mg/day orally for 12 months. |
Drug: Empagliflozin Arm
The subject will be randomized, in a double-blind manner to Empagliflozin 25mg once daily for a period of 12 months
Other: Exercise capacity VO2 maximum determination
Each participant's maximal oxygen capacity will be determined using a modified Bruce treadmill protocol and will also undergo a DEXA scan to determine the body mass.
Other: Exercise Challenge
Each participant will walk at 70 % of his/her VO2max for 20 minutes on treadmill and will also undergo a resting energy expenditure test.
|
| Placebo Comparator: Placebo Arm We will enroll 12 obese participants who have intentionally lost greater than or equal to 5% of body weight through a non-pharmacological structured weight loss program based on diet and exercise within the last 6 months. The participants will take a placebo pill orally once a day for 12 months. |
Other: Control Arm
The subject will be randomized, in a double-blind manner to receive placebo once daily for a period of 12 months
Other: Exercise capacity VO2 maximum determination
Each participant's maximal oxygen capacity will be determined using a modified Bruce treadmill protocol and will also undergo a DEXA scan to determine the body mass.
Other: Exercise Challenge
Each participant will walk at 70 % of his/her VO2max for 20 minutes on treadmill and will also undergo a resting energy expenditure test.
|
Outcome Measures
Primary Outcome Measures
- Change in Resting Energy Expenditure [12 months]
Change in Resting Energy Expenditure between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
Secondary Outcome Measures
- Change in Body Weight [12 months]
Change in Body Weight between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in Body Mass Index [12 months]
Change in Body Mass Index between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in Waist Circumference [12 months]
Change in Waist Circumference between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in HbA1C levels [12 months]
Change in HbA1C levels between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in lipid profile [12 months]
Change in Lipid profile between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in HOMA-IR [12 months]
Change in HOMA-IR between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in ESR [12 months]
Change in ESR between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in CRP [12 months]
Change in CRP between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in IL-6 [12 months]
Change in IL-6 between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in TNF-α [12 months]
Change in TNF-α between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in glucagon-like peptide-1 (GLP-1) [12 months]
Change in glucagon-like peptide-1 (GLP-1) between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in peptide YY (PYY) [12 months]
Change in peptide YY (PYY) between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in ghrelin [12 months]
Change in ghrelin between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in glucose-dependent insulinotropic polypeptide (GIP) [12 months]
Change in glucose-dependent insulinotropic polypeptide (GIP) between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
- Change in glucagon [12 months]
Change in glucagon between the two arms (Empagliflozin v/s Placebo) from baseline and after 12 months of intervention
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age more than or equal to 18 years
-
Body mass index more than or equal to 30 kg/m2 who have lost ≥5% of body weight within the past 6 months without taking any pharmacotherapy for weight loss
Exclusion Criteria:
-
Age less than 18 years at screening.
-
Untreated systolic BP <100 or >160 mmHg at baseline, or diastolic BP <80 or >100 mmHg at baseline
-
Women who are pregnant or breastfeeding or who can become pregnant and not practicing an acceptable method of birth control during the study (including abstinence)
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Taking pharmacotherapy indicated for weight loss, such as GLP-1 agonists or with weight loss as an adverse event
-
History of Type I Diabetes
-
Have any past or present illness of cardiovascular disease, including myocardial infarction, angina, cardiac arrhythmia, diabetes, stroke, TIA, or seizure
-
Current or past (<12 months) history of smoking
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Estimated glomerular filtration rate (GFR) < 60 ml/min/1.73 m2 (CKD-EPI equation) urine albumin creatinine ratio ≥30 mg/g
-
Hepatic Transaminase (AST and ALT) levels >3x the upper limit of normal
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Significant psychiatric illness
-
Anemia (men, Hct < 38%; women, Hct <36%)
-
Inability to exercise on a treadmill
-
Consumption of more than 2 alcoholic drinks daily
-
Any contraindications to empagliflozin
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Alabama at Birmingham | Birmingham | Alabama | United States | 35294 |
Sponsors and Collaborators
- University of Alabama at Birmingham
Investigators
- Principal Investigator: Pankaj Arora, MD, FAHA, University of Alabama at Birmingham
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 300011125