Disorder of Glucose Regulation, Gestational Diabetes Mellitus, Impaired Glucose Tolerance, Metabolic Syndrome, Type 2 Diabetes Mellitus
Conditions
Keywords
gestational diabetes mellitus, type 2 diabetes mellitus, metabolic dysfunction, impaired fasting glucose, impaired glucose tolerance, incretin mimetic
Brief summary
A diagnosis of gestational diabetes mellitus (GDM)has significant implications for the future health of the mother. GDM is often the culmination of years of unrecognized and unmodified diabetes risk factors that lead to overt and occult clinical manifestations during pregnancy. Systematic reviews of older studies conclude that 35-60% women with gestational diabetes will develop type 2 diabetes (DM2) at rates much greater than control groups who did not have glucose intolerance during pregnancy. Liraglutide may potentially delay disease progression in GDM considering the beta -(ß-)cell function improvement in DM2 and ß-cell mass shown to increase in animal models. This study will examine if the addition of liraglutide to metformin therapy is more effective than metformin alone in improving insulin sensitivity and normalizing insulin secretion in at-risk overweight/obese women with prior GDM.
Detailed description
Gestational diabetes is often the culmination of years of unrecognized and unmodified diabetes risk factors that lead to overt and occult clinical manifestations during pregnancy. . Despite the high and increasing rate of type 2 diabetes in Louisiana, the medical community does not have reliable estimates of the number of woman living in southern Louisiana who develop diabetes subsequent to GDM. Systematic reviews of older studies conclude that 35-60% women with gestational diabetes will develop type 2 diabetes at rates much greater than control groups who did not have glucose intolerance during pregnancy. The higher rates were in studies of particular ethnic groups in the U.S. Recently, follow-up programs elsewhere also have identified increasing rates of type 2 diabetes by 5-10 years after GDM: 9-43% type 2 diabetes in Europe and 11-21% in Asia. The frequency of type 2 diabetes is influenced by BMI, weight gain after pregnancy, family history of diabetes, fasting and postchallenge glucose levels during and after pregnancy, postpartum insulin resistance and inadequate β-cell secretion, and the need for pharmacological treatment during pregnancy. However, the risk factors are unable to predict all cases of subsequent type 2 diabetes: the biggest risk factor is a GDM pregnancy. Presently, in the literature, there are described new, more efficient methods of diabetes prevention in groups with a high risk of this disorder, which involve both, lifestyle modification and pharmacological therapies. Lifestyle intervention was found to reduce the incidence of type 2 diabetes by 58% and metformin by 31% as compared with placebo. The use of rosiglitazone in subjects with prediabetes resulted in a 60% reduction of the diabetes incidence rate. Studies are needed for optimal postpartum and long-term health of women who have had GDM. Considerable recent evidence suggests that incretin-based therapies may be useful for the treatment of DM2 because continuous administration of glucagon-like peptide 1 (GLP-1) produces substantial improvements in glucose control and ß-cell function in subjects with type 2 diabetes. Infusion of GLP-1 improves first and second-phase insulin secretion suggesting that early GLP-1 therapy may preserve ß-cell function in subjects with IGT or mild DM2. Whereas native GLP-1 has a very short half-life, the GLP-1 analogue liraglutide has a prolonged action (t1/2=13 h) suitable for once-daily injection. Liraglutide may potentially delay disease progression in GDM considering the ß-cell function improvement in DM2 and ß-cell mass shown to increase in animal models. This study will examine if the addition of liraglutide to metformin therapy is more effective than metformin alone in improving metabolic parameters in at-risk overweight/obese women with prior GDM
Interventions
Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -98 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated
Metformin XR-500 qd for 2 weeks, 500 mg bid 2 weeks; 500 mg am, 1000 mg pm- 2 weeks - 1000 bid final dose Liraglutide- start 0.6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated during the 4-wk non-forced dose-escalation period ( maximum allowed dose of 1.8 mg SC QD)
Sponsors
Study design
Eligibility
Inclusion criteria
* Adult female 18 years to 45 years of age who experienced GDM within 52 weeks of index pregnancy * Actual BMI \>25 kg/ m2 * Written consent for participation in the study * Patient completed lactation * Dysglycemia (impaired fasting glucose \[IFG}, impaired glucose tolerance \[IGT} or IFG/IGT) and/or ß-cell dysfunction postpartum requiring pharmacological intervention (except type 1 or 2 diabetes)
Exclusion criteria
Personal or family history of medullary thyroid carcinoma or in patients with Multiple Endocrine Neoplasia syndrome type 2 * History of pancreatitis * Significant cardiovascular, cerebrovascular, renal, or hepatobiliary diseases in the past (viral hepatitis, toxic hepatic damage, jaundice of unknown etiology) * Serum liver enzymes (AST and/or ALT levels) exceeding more than twice normal laboratory values * Uncontrolled hypertension (systolic blood pressure\>150 mm Hg and/or diastolic blood pressure \>90 mm Hg) * Fasting serum triglycerides ≥800 mg/dl at screening. Lipid-lowering medications must have been maintained at the same dose for 3 months prior to enrollment * Hematological profiles considered to be clinically significant * Cholestasis during the past pregnancy * Presence of contradictions for GLP-1 receptor agonist or metformin administration such as allergy or hypersensitivity * Current use of metformin, thiazolidinediones, dipeptidyl peptidase-4 inhibitors or GLP-1 receptor agonist medications. * Use of drugs known to exacerbate glucose tolerance. * Use of prescription or over-the-counter weight-loss drugs * Diabetes postpartum or history of diabetes or prior use of medications to treat diabetes except gestational diabetes * Creatinine clearance less than 60 ml/min * History or currently undergoing chemotherapy or radiotherapy for cancer * Pregnancy planned during the coming two years * Currently breastfeeding *
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Insulin Secretion-Sensitivity Index (IS-SI) | 84 weeks of treatment | IS-SI in liraglutide-metformin (LIRA-MET) therapy compared to metformin alone (PLacebo-MET) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Fasting Blood Glucose (FBG) | 84 weeks of treatment | Fasting glucose levels in LIRA-MET group compared with PL-MET group |
| Mean Glucose During OGTT (MBG) | 84 weeks of treatment | MBG derived from average glucose measured during OGTT in LIRA-MET group compared with PL-MET group |
| Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) | 84 weeks of treatment | HOMA-IR, a measure of insulin resistance derived from fasting values, in LIRA-MET group compared with PL-MET group |
| Matsuda Insulin Sensitivity Index Derived From OGTT | 84 weeks of treatment | OGTT- derived insulin sensitivity index in LIRA-MET group compared with PL-MET group |
| Insulinogenic Index (IGI) /HOMA-IR | 84 weeks of treatment | IGI/HOMA-IR, a measure of early insulin response corrected by fasting insulin resistance, in LIRA-MET group compared with PL-MET group |
| Absolute Body Weight | 84 weeks of treatment | Body weight in LIRA-MET group compared with PL-MET group |
| Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline) | Change from baseline (time 0) to study end (84 weeks) | Change in body weight from baseline to end o f study in LIRA-MET group compared with PL-MET group. The number was derived from final weight minus baseline and normalized to a percent. |
| Body Mass Index (BMI) | 84 weeks of treatment | BMI, a measure of total body adiposity, in LIRA-MET group compared with PL-MET group |
| Waist Circumference (WC) | 84 weeks of treatment | Waist size (measure of truncal adiposity) with LIRA-MET compared to PL-MET |
| Waist-to-Hip Ratio (WHR) | 84 weeks of treatment | Waist circumference divided by hip circumference (a measure of central adiposity) in LIRA-MET group compared with PL-MET group |
| Triglyceride (TRG) Levels | 84 weeks of treatment | TRG concentrations in LIRA-MET group compared with PL-MET group |
| Total Cholesterol (CHOL) Levels | 84 weeks of treatment | CHOL levels in LIRA-MET group compared with PL-MET group |
| High Density Lipoprotein Cholesterol (HDL-C) Levels | 84 weeks of treatment | HDL-C levels in LIRA-MET group compared with PL-MET group |
| Low Density Lipoprotein Cholesterol (LDL-C) Levels | 84 weeks of treatment | LDL-Cholesterol levels in LIRA-MET group compared with PL-MET group |
| Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C) | 84 weeks of treatment | TRG/HDL-Cholesterol levels in LIRA-MET group compared with PL-MET group |
| Systolic Blood Pressure | 84 weeks of treatment | SBP in LIRA-MET group compared with PL-MET group |
| Diastolic Blood Pressure | 84 weeks of treatment | DBP in LIRA-MET group compared with PL-MET group |
| Alanine Aminotransferase (ALT) Levels | 84 weeks of treatment | Hepatic enzyme, ALT, associated with insulin resistance, in LIRA-MET group compared with PL-MET group |
| Aspartate Aminotransferase (AST) | 84 weeks of treatment | The hepatic marker, AST, associated with insulin resistance in LIRA-MET group compared with PL-MET group |
| Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio | 84 weeks of treatment | ALT/AST ratio, used to assess liver function in LIRA-MET group compared with PL-MET group |
| Waist to Height Ratio (WHtR) | 84 weeks of treatment | Waist circumference divided by height (measure of body fat distribution) in LIRA-MET group compared with PL-MET group |
Countries
United States
Participant flow
Recruitment details
153 met criteria and were randomized
Pre-assignment details
166 were consented but 153 met criteria
Participants by arm
| Arm | Count |
|---|---|
| Metformin XR Plus Liraglutide Metformin XR plus Liraglutide Metformin extended release (XR) 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid- 84 weeks (end study) Liraglutide - start .6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated
Metformin XR plus liraglutide: Metformin XR-500 qd for 2 weeks, 500 mg bid 2 weeks; 500 mg am, 1000 mg pm- 2 weeks - 1000 bid final dose Liraglutide- start 0.6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated during the 4-wk non-forced dose-escalation period ( maximum allowed dose of 1.8 mg SC QD) | 78 |
| Metformin XR Plus Placebo Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -84 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated
Metformin XR plus placebo: Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -98 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated | 75 |
| Total | 153 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Allergic reaction | 1 | 0 |
| Overall Study | intolerant to side effects | 4 | 3 |
| Overall Study | Lack of Efficacy | 0 | 3 |
| Overall Study | Pregnancy | 6 | 6 |
| Overall Study | Withdrawal by Subject | 32 | 26 |
Baseline characteristics
| Characteristic | Metformin XR Plus Liraglutide | Metformin XR Plus Placebo | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 78 Participants | 75 Participants | 153 Participants |
| BMI greater than/equal to 25 | 78 Participants | 75 Participants | 153 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 78 Participants | 75 Participants | 153 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 11 Participants | 17 Participants | 28 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 67 Participants | 58 Participants | 125 Participants |
| Region of Enrollment United States | 78 participants | 75 participants | 153 participants |
| Sex: Female, Male Female | 78 Participants | 75 Participants | 153 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 78 | 0 / 75 |
| other Total, other adverse events | 30 / 78 | 14 / 75 |
| serious Total, serious adverse events | 0 / 78 | 0 / 75 |
Outcome results
Insulin Secretion-Sensitivity Index (IS-SI)
IS-SI in liraglutide-metformin (LIRA-MET) therapy compared to metformin alone (PLacebo-MET)
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Insulin Secretion-Sensitivity Index (IS-SI) | 418.4 index | Standard Deviation 387 |
| Metformin XR Plus Placebo | Insulin Secretion-Sensitivity Index (IS-SI) | 333 index | Standard Deviation 206 |
Absolute Body Weight
Body weight in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Absolute Body Weight | 94.2 kilograms | Standard Deviation 18.6 |
| Metformin XR Plus Placebo | Absolute Body Weight | 91.3 kilograms | Standard Deviation 20 |
Alanine Aminotransferase (ALT) Levels
Hepatic enzyme, ALT, associated with insulin resistance, in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Alanine Aminotransferase (ALT) Levels | 32.3 U/L | Standard Deviation 10.7 |
| Metformin XR Plus Placebo | Alanine Aminotransferase (ALT) Levels | 31 U/L | Standard Deviation 9.9 |
Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio
ALT/AST ratio, used to assess liver function in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio | 1.2 ratio of ALT (U/L)/ AST (U/L) | Standard Deviation 0.4 |
| Metformin XR Plus Placebo | Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio | 1.18 ratio of ALT (U/L)/ AST (U/L) | Standard Deviation 0.3 |
Aspartate Aminotransferase (AST)
The hepatic marker, AST, associated with insulin resistance in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Aspartate Aminotransferase (AST) | 27 U/L | Standard Deviation 8 |
| Metformin XR Plus Placebo | Aspartate Aminotransferase (AST) | 28 U/L | Standard Deviation 10.5 |
Body Mass Index (BMI)
BMI, a measure of total body adiposity, in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Body Mass Index (BMI) | 33.8 weight (kg) /height (m) squared | Standard Deviation 5.2 |
| Metformin XR Plus Placebo | Body Mass Index (BMI) | 32.8 weight (kg) /height (m) squared | Standard Deviation 6 |
Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline)
Change in body weight from baseline to end o f study in LIRA-MET group compared with PL-MET group. The number was derived from final weight minus baseline and normalized to a percent.
Time frame: Change from baseline (time 0) to study end (84 weeks)
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline) | -7.2 percent change in weight from baseline | Standard Error 1.3 |
| Metformin XR Plus Placebo | Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline) | -3.1 percent change in weight from baseline | Standard Error 1.4 |
Diastolic Blood Pressure
DBP in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Diastolic Blood Pressure | 77.6 mmHg | Standard Deviation 8.9 |
| Metformin XR Plus Placebo | Diastolic Blood Pressure | 77 mmHg | Standard Deviation 9.9 |
Fasting Blood Glucose (FBG)
Fasting glucose levels in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Fasting Blood Glucose (FBG) | 90 mg/dL | Standard Deviation 6.4 |
| Metformin XR Plus Placebo | Fasting Blood Glucose (FBG) | 91.7 mg/dL | Standard Deviation 8.4 |
High Density Lipoprotein Cholesterol (HDL-C) Levels
HDL-C levels in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | High Density Lipoprotein Cholesterol (HDL-C) Levels | 51 mg/dL | Standard Deviation 12.6 |
| Metformin XR Plus Placebo | High Density Lipoprotein Cholesterol (HDL-C) Levels | 48.7 mg/dL | Standard Deviation 11.7 |
Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)
HOMA-IR, a measure of insulin resistance derived from fasting values, in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) | 2.2 index | Standard Deviation 1.4 |
| Metformin XR Plus Placebo | Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) | 2.45 index | Standard Deviation 1.5 |
Insulinogenic Index (IGI) /HOMA-IR
IGI/HOMA-IR, a measure of early insulin response corrected by fasting insulin resistance, in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Insulinogenic Index (IGI) /HOMA-IR | 0.8 index | Standard Deviation 1.14 |
| Metformin XR Plus Placebo | Insulinogenic Index (IGI) /HOMA-IR | 0.62 index | Standard Deviation 0.38 |
Low Density Lipoprotein Cholesterol (LDL-C) Levels
LDL-Cholesterol levels in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Low Density Lipoprotein Cholesterol (LDL-C) Levels | 110 mg/dL | Standard Deviation 32 |
| Metformin XR Plus Placebo | Low Density Lipoprotein Cholesterol (LDL-C) Levels | 107 mg/dL | Standard Deviation 25 |
Matsuda Insulin Sensitivity Index Derived From OGTT
OGTT- derived insulin sensitivity index in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Matsuda Insulin Sensitivity Index Derived From OGTT | 5.9 index | Standard Deviation 2.9 |
| Metformin XR Plus Placebo | Matsuda Insulin Sensitivity Index Derived From OGTT | 5.4 index | Standard Deviation 3.2 |
Mean Glucose During OGTT (MBG)
MBG derived from average glucose measured during OGTT in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Mean Glucose During OGTT (MBG) | 121.6 mg/dL | Standard Deviation 20.8 |
| Metformin XR Plus Placebo | Mean Glucose During OGTT (MBG) | 118.8 mg/dL | Standard Deviation 18.9 |
Systolic Blood Pressure
SBP in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Systolic Blood Pressure | 122 mmHg | Standard Deviation 12 |
| Metformin XR Plus Placebo | Systolic Blood Pressure | 123 mmHg | Standard Deviation 12 |
Total Cholesterol (CHOL) Levels
CHOL levels in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Total Cholesterol (CHOL) Levels | 183.7 mg/dL | Standard Deviation 36 |
| Metformin XR Plus Placebo | Total Cholesterol (CHOL) Levels | 183.8 mg/dL | Standard Deviation 27 |
Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C)
TRG/HDL-Cholesterol levels in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C) | 2.56 ratio of TRG (mg/dL)/HDL-C (mg/dl) | Standard Deviation 1.5 |
| Metformin XR Plus Placebo | Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C) | 2.95 ratio of TRG (mg/dL)/HDL-C (mg/dl) | Standard Deviation 2.9 |
Triglyceride (TRG) Levels
TRG concentrations in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Triglyceride (TRG) Levels | 120 mg/dL | Standard Deviation 64.5 |
| Metformin XR Plus Placebo | Triglyceride (TRG) Levels | 125 mg/dL | Standard Deviation 76.4 |
Waist Circumference (WC)
Waist size (measure of truncal adiposity) with LIRA-MET compared to PL-MET
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Waist Circumference (WC) | 94.3 centimeters | Standard Deviation 15.2 |
| Metformin XR Plus Placebo | Waist Circumference (WC) | 95.3 centimeters | Standard Deviation 15.2 |
Waist to Height Ratio (WHtR)
Waist circumference divided by height (measure of body fat distribution) in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Waist to Height Ratio (WHtR) | .56 ratio of waist /height | Standard Deviation 0.08 |
| Metformin XR Plus Placebo | Waist to Height Ratio (WHtR) | .57 ratio of waist /height | Standard Deviation 0.07 |
Waist-to-Hip Ratio (WHR)
Waist circumference divided by hip circumference (a measure of central adiposity) in LIRA-MET group compared with PL-MET group
Time frame: 84 weeks of treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Metformin XR Plus Liraglutide | Waist-to-Hip Ratio (WHR) | .81 ratio of waist/hip circumference | Standard Deviation 0.04 |
| Metformin XR Plus Placebo | Waist-to-Hip Ratio (WHR) | .81 ratio of waist/hip circumference | Standard Deviation 0.05 |