Diabetes Mellitus, Type II
Conditions
Brief summary
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health (NIH) has sponsored a consortium of investigators to conduct a clinical treatment trial, Treatment Options for type 2 Diabetes in Adolescents and Youth (TODAY). The primary objective of the TODAY trial is to compare the efficacy of three treatment arms on time to treatment failure based on glycemic control. The secondary aims are to: * compare and evaluate the safety of the three treatment arms; * compare the effects of the three treatments on the pathophysiology of type 2 diabetes (T2D) with regards to beta cell function and insulin resistance, body composition, nutrition, physical activity and aerobic fitness, cardiovascular risk factors, microvascular complications, quality of life, and psychological outcomes; * evaluate the influence of individual and family behaviors on treatment response; and * compare the relative cost effectiveness of the three treatment arms. The three treatment regimens are: (1) metformin alone, (2) metformin plus rosiglitazone, and (3) metformin plus an intensive lifestyle intervention called the TODAY Lifestyle Program (TLP). The study recruits patients over a three-year period and follows patients for a minimum of two years. Patients are randomized within two years of the diagnosis of T2D.
Detailed description
T2DM has dramatically increased throughout the world in many ethnic groups and among people with diverse social and economic backgrounds. Over the last decade, the increase in the number of children and youth with T2DM has been labeled an epidemic. Before the 1990s, it was rare for most pediatric centers to have patients with T2DM. By 1994, T2DM patients represented up to 16% of new cases of diabetes in children in urban areas, and by 1999, depending on geographic location, the range of percent of new cases due to T2DM was between 8-45% and disproportionately represented in minority populations. T2DM in children and youth, as in adults, is due to the combination of insulin resistance and relative β-cell failure. It appears that there are a host of genetic and environmental risk factors for insulin resistance and limited β-cell reserve. The epidemic of pediatric T2DM is coincident with the rise in the number of children who are overweight or at risk for overweight and with a decrease in the physical activity pattern of youth. There has been a strong association between T2DM and the onset of puberty, a positive family history of T2DM, and elements of the metabolic syndrome such as acanthosis nigricans and polycystic ovarian syndrome (PCOS). Preceding the development of frank diabetes, children and youth experience a period of prediabetes. Prediabetes is defined as either elevated fasting glucose or impaired glucose tolerance. Despite the dramatic increase in the number of cases of prediabetes and T2DM in pediatric populations, there have been no published large-scale studies investigating the pathophysiology, treatment, and complications of these disorders in children and youth. The long-term complications and costs associated with T2DM make such studies imperative. Between 1997 and 2002, the estimated cost of diabetes with regard to direct medical cost increased from $44 billion to $92 billion, and the total cost increased from $98 billion to $132 billion. The vast majority of monies are spent on the long-term complications of this disorder. Since the long-term microvascular and cardiovascular complications relate to duration of diabetes and to control of glycemia, it could be hypothesized that the increasing number of children and youth diagnosed with T2DM, if not effectively treated, could dramatically add to the economic burden of this disease over the ensuing decades. Except in American Indian youth, there are no population-based data available with regard to prevalence of T2DM. Instead, only clinic-based reports indicate that there has been a tremendous increase in the number of children and adolescents with T2DM. T2DM occurs almost exclusively in children and youth who are overweight or at risk for overweight (BMI \> 85th percentile for age). At the time of diagnosis, most pediatric patients are in the midst of Tanner Stage 2-4 puberty. Puberty contributes to insulin resistance due to augmentation of growth hormone secretion, and if these normal pubertal physiologic changes are not compensated for by increased insulin secretion, frank diabetes will develop. Half to three-quarters of patients have a parent and close to ninety percent have at least one first or second degree relative with T2DM. The clinical presentation of T2DM in youth ranges from mild asymptomatic hyperglycemia to severe ketoacidosis. In those who present with clinical symptoms due to hyperglycemia, glycosuria and weight loss are present in 20-40%, ketonuria is present in 33% and ketoacidosis is found in 5-10%. Patients without clinical symptoms are diagnosed as the result of routine blood or urine testing during a health care visit or by investigating a variety of complaints such as chronic infection, sleep apnea, hyperlipidemia, hypertension, and hirsutism or irregular periods associated with PCOS. It may be difficult to distinguish T1DM from T2DM at presentation. The absence of autoantibodies is a prerequisite for the diagnosis of T2DM. In addition, evidence of residual insulin secretion is suggestive of T2DM rather than T1DM. Patients with T2DM have dual abnormalities of insulin resistance and insulin deficiency. It is hypothesized that to achieve the level of glycemic control required to optimize long-term outcome and decrease or prevent microvascular complications, treatment regimens should theoretically be designed to improve insulin resistance and preserve residual β-cell function. The available anti-diabetic agents have not been adequately evaluated in pediatric patients. This is particularly relevant with regard to using combination therapy to improve glycemic control or lifestyle interventions aimed at obesity and sedentary behavior.
Interventions
capsule, 1000 mg bid
capsule, 4 mg bid
a lifestyle change (LC) phase of weekly sessions for months 1-6, followed by a bi-weekly lifestyle maintenance (LM) phase through months 7-12, and a continued contact (CC) phase from months 13 through the end of the study. The CC phase sessions are scheduled monthly for the initial 12 months (study months 13-24) and then quarterly or 4 times a year to the end of the study
Sponsors
Study design
Eligibility
Inclusion criteria
(during Screening and Run-in period): * Diabetes by ADA criteria (laboratory determinations of fasting glucose ≥ 126 mg/dL, random glucose ≥ 200 mg/dL, or two-hour OGTT glucose ≥ 200 mg/dL) documented and confirmed in medical record. For patients diagnosed with diabetes during screening who have a normal fasting glucose but an elevated two-hour glucose during an OGTT, the HbA1c must be ≥ 6%. * Duration since diagnosis less than two years by date of randomization. * BMI ≥ 85th percentile documented at time of diagnosis or at screening. * Fasting C-peptide at screening (drawn at least one week after treatment for ketosis or acidosis, if applicable) \> 0.6 ng/mL. * Absence of pancreatic autoimmunity (both GAD and ICA512 negative). * Age 10-17, with randomization prior to 18th birthday. * Signed informed consent/assent forms for the pre-randomization period. * A family member or adult closely involved in the daily activities of the child agrees to participate in the child's treatment. * Fluency in English or Spanish for both child and family member. * Patient and family able to fully participate in trial protocol in the opinion of the investigator.
Exclusion criteria
(during Screening and Run-in period): * Participating in another interventional research study protocol in the past 30 days. * Genetic syndrome or disorder known to affect glucose tolerance other than diabetes. * Patient on inhaled steroids at dose above 1000 mcg daily Flovent equivalent. * Patient on a course of oral steroids within the last 60 days or on oral steroids more than 20 days during the past year. * Patient on medication(s) that are known to affect insulin sensitivity or secretion within the last 30 days. * Patient on medication(s) that are known to cause weight gain within the last 30 days. * Patient on any weight-loss medication(s) within the last 30 days. * Patient on medication(s) known to affect the metabolism of study drug. * Inability to comprehend the lowest grade level at which lifestyle intervention materials are prepared, for both child and participating family member. * Females who are pregnant, planning to become pregnant within two years of enrollment, or who admit sexual activity without appropriate contraception. * Calculated creatinine clearance \< 70 mL/min. * Any transaminase \> 2.5 ULN. If any transaminase 1.5-2.5 times ULN, then patient must be appropriately evaluated by PCP (minimum evaluation includes ceruloplasmin level, alpha-1 antitrypsin phenotype, ANA, anti-smooth muscle antibody, anti-LKM antibody, anti-HCV, and anti-HBc total antibody not IgM, iron, and TIBC) and is eligible if all other causes for elevation are ruled out and it is presumed due only to non-alcoholic fatty liver disease (NAFLD). * Diabetic ketoacidosis (DKA) at any time after diagnosis unless only a single episode of DKA related to a significant medical illness. * Physical limitations preventing patient from being randomized to the lifestyle intervention. * Patient plans to leave the geographic area within one calendar year. * Abnormal reticulocyte count or HbA1c chromatogram at time of screening. * Admitted use of anabolic steroids within the past 60 days. * Other significant organ system illness or condition (including psychiatric or developmental disorder) that would prevent participation in the opinion of the investigator. * Patient participates in a formal weight-loss program. Inclusion Criteria (post Run-in and Randomization): * Duration since diagnosis less than 2 years at randomization. * HbA1c \< 8% on metformin alone. * Age 10-17, with randomization before patient is 18 years old. * Signed consent/assent forms for randomization and the post-randomization phase. * A family member or adult closely involved in the daily activities of the child agrees to participate in the child's treatment. * Fluency in English or Spanish for both child and family member. * Patient and family able to fully participate in trial protocol in the opinion of the investigator.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment Failure (Loss of Glycemic Control) | Study duration - 2 years to 6.5 years of follow up from randomization | Defined as A1c persistently \>=8% over a 6-month period or persistent metabolic decompensation (inability to wean insulin within 3 months of initiation or the occurrence of a second episode within three months of discontinuing insulin) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Serious Adverse Events | Reported as occurred during study follow-up - 2 years to 6.5 years from randomization. | Number of serious adverse events reported during the trial. Participant could have multiple episodes reported. |
| Insulin Secretion | 24 months | Insulinogenic index determined from OGTT as difference in insulin at 30 minutes minus 0 minutes divided by difference in glucose at 30 minutes minus 0 minutes. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. |
| Body Composition -- BMI | 24 months | Body mass index (BMI) measured in kg per meters squared. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. |
| Body Composition -- Waist Circumference | 24 months | Waist circumference (cm) measured at the iliac crest at its outermost point with the measuring tape placed around the participant in a horizontal plane parallel to the floor at the mark and the measurement teken at the end of normal expiration without the tape compressing the skin. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. |
| Insulin Sensitivity | 24 months | All participants were followed to 24 months. Insulin sensitivity is measured from OGTT as inverse of fasting insulin (mL/uU). The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. |
| Body Composition -- Fat Mass | 24 months | Determined by DXA whole body scan. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. In addition, in about 1/3 of participants DXA scans could not be obtained on participants weighing more than 300 pounds (136 kg), the upper limit in size set by the machine manufacturers. Scans were considered invalid if a body part (e.g., arm, leg) was completely off or partially off the scanner, there was hand-hip overlap, or there was motion or movement during the scan. |
| Comorbidity -- Hypertension | Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization. | A diagnosis was made by an out-of-range value \>=95th percentile or systolic \>=130 or diastolic \>=80 sustained over 6 months or on an anti-hypertensive medication. |
| Comorbidity -- LDL Dyslipidemia | Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization. | A diagnosis was made from out-of-range value \>= 130 mg/dL sustained over 6 months or put on lipid lowering medication. |
| Comorbidity -- Triglycerides Dyslipidemia | Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization. | A diagnosis was made by an out-of-range value \>=150 mg/dL sustained over 6 months or on appropriate lipid lowering medication. |
| Body Composition -- Bone Density | 24 months | Measured by DXA, both whole body scan and AP-spine scan. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. In addition, in about 1/3 of participants DXA scans could not be obtained on participants weighing more than 300 pounds (136 kg), the upper limit in size set by the machine manufacturers. Scans were considered invalid if a body part (e.g., arm, leg) was completely off or partially off the scanner, there was hand-hip overlap, or there was motion or movement during the scan. |
Countries
United States
Participant flow
Recruitment details
Participants were recruited from July 2004 to February 2009. Participants were recruited from the patient populations of pediatric endocrine clinics at the participating study clinical centers, including satellite clinics. Posters announced the study. Study staff approached youth and their families during medical visits.
Pre-assignment details
Prior to randomization, eligible subjects entered a 2-6 month run-in period, with goals of weaning from non-study diabetes medications, tolerating metformin at 1000 mg bid but no less than 500 mg bid, attaining glycemic control on metformin alone, mastering standard diabetes education, and adhering to study medication and visit attendance.
Participants by arm
| Arm | Count |
|---|---|
| 1 Metformin Alone Metformin alone
Metformin: capsule, 1000 mg bid | 232 |
| 2 Metformin + Rosiglitazone Metformin + Rosiglitazone
Metformin: capsule, 1000 mg bid
Rosiglitazone: capsule, 4 mg bid | 233 |
| 3 Metformin + Lifestyle Program Metformin + Lifestyle Program
Metformin: capsule, 1000 mg bid
Lifestyle Program: a lifestyle change (LC) phase of weekly sessions for months 1-6, followed by a bi-weekly lifestyle maintenance (LM) phase through months 7-12, and a continued contact (CC) phase from months 13 through the end of the study. The CC phase sessions are scheduled monthly for the initial 12 months (study months 13-24) and then quarterly or 4 times a year to the end of the study | 234 |
| Total | 699 |
Baseline characteristics
| Characteristic | 1 Metformin Alone | 3 Metformin + Lifestyle Program | Total | 2 Metformin + Rosiglitazone |
|---|---|---|---|---|
| Age, Continuous | 14.1 years STANDARD_DEVIATION 1.9 | 13.8 years STANDARD_DEVIATION 2 | 14.0 years STANDARD_DEVIATION 2 | 14.1 years STANDARD_DEVIATION 2.1 |
| Body mass index (BMI) | 35.8 kg per m squared STANDARD_DEVIATION 8.1 | 34.1 kg per m squared STANDARD_DEVIATION 7.1 | 34.9 kg per m squared STANDARD_DEVIATION 7.6 | 35.0 kg per m squared STANDARD_DEVIATION 7.7 |
| Body mass index z-score | 2.27 z-score STANDARD_DEVIATION 0.45 | 2.18 z-score STANDARD_DEVIATION 0.46 | 2.23 z-score STANDARD_DEVIATION 0.47 | 2.22 z-score STANDARD_DEVIATION 0.49 |
| Bone density from DXA | 1.09 g per cm squared STANDARD_DEVIATION 0.12 | 1.08 g per cm squared STANDARD_DEVIATION 0.12 | 1.09 g per cm squared STANDARD_DEVIATION 0.13 | 1.10 g per cm squared STANDARD_DEVIATION 0.13 |
| Duration of diabetes | 7.8 months STANDARD_DEVIATION 6 | 7.6 months STANDARD_DEVIATION 5.8 | 7.8 months STANDARD_DEVIATION 5.8 | 8.0 months STANDARD_DEVIATION 5.7 |
| Fat mass from DXA | 33.7 kg STANDARD_DEVIATION 9.9 | 32.6 kg STANDARD_DEVIATION 9.8 | 33.3 kg STANDARD_DEVIATION 10 | 33.5 kg STANDARD_DEVIATION 10.2 |
| Highest household education level College no degree | 77 participants | 63 participants | 218 participants | 78 participants |
| Highest household education level Graduate degree | 35 participants | 38 participants | 114 participants | 41 participants |
| Highest household education level High school, GED, business or technical | 57 participants | 66 participants | 172 participants | 49 participants |
| Highest household education level Less than high school | 60 participants | 62 participants | 182 participants | 60 participants |
| Highest household education level Unknown | 3 participants | 5 participants | 13 participants | 5 participants |
| Insulinogenic index from OGTT | 1.02 uU/mL divided by mg/dL | .87 uU/mL divided by mg/dL | .93 uU/mL divided by mg/dL | .92 uU/mL divided by mg/dL |
| Insulin sensitivity (inverse of fasting insulin from OGTT) | .036 mL/uU | .040 mL/uU | .039 mL/uU | .040 mL/uU |
| Nuclear family + grandparents history of diabetes No | 17 participants | 29 participants | 72 participants | 26 participants |
| Nuclear family + grandparents history of diabetes Unknown | 4 participants | 5 participants | 16 participants | 7 participants |
| Nuclear family + grandparents history of diabetes Yes | 211 participants | 200 participants | 611 participants | 200 participants |
| Nuclear family history of diabetes No | 97 participants | 86 participants | 276 participants | 93 participants |
| Nuclear family history of diabetes Unknown | 4 participants | 5 participants | 16 participants | 7 participants |
| Nuclear family history of diabetes Yes | 131 participants | 143 participants | 407 participants | 133 participants |
| Percent overweight | 82.1 100% X (BMI-50th %ile)/50th %ile STANDARD_DEVIATION 38.3 | 75.6 100% X (BMI-50th %ile)/50th %ile STANDARD_DEVIATION 35.3 | 78.9 100% X (BMI-50th %ile)/50th %ile STANDARD_DEVIATION 37.3 | 79.1 100% X (BMI-50th %ile)/50th %ile STANDARD_DEVIATION 38.1 |
| Race/Ethnicity, Customized American Indian | 12 participants | 13 participants | 41 participants | 16 participants |
| Race/Ethnicity, Customized Asian Non-Hispanic | 3 participants | 3 participants | 11 participants | 5 participants |
| Race/Ethnicity, Customized Black Non-Hispanic | 77 participants | 86 participants | 227 participants | 64 participants |
| Race/Ethnicity, Customized Hispanic | 91 participants | 86 participants | 278 participants | 101 participants |
| Race/Ethnicity, Customized White Non-Hispanic | 49 participants | 46 participants | 142 participants | 47 participants |
| Region of Enrollment United States | 232 participants | 234 participants | 699 participants | 233 participants |
| Sex: Female, Male Female | 146 Participants | 154 Participants | 452 Participants | 152 Participants |
| Sex: Female, Male Male | 86 Participants | 80 Participants | 247 Participants | 81 Participants |
| Tanner stage by physical examination 1, 2, or 3 | 23 participants | 30 participants | 79 participants | 26 participants |
| Tanner stage by physical examination 4 or 5 | 209 participants | 204 participants | 620 participants | 207 participants |
| Total annual household income < $25,000 | 81 participants | 92 participants | 259 participants | 86 participants |
| Total annual household income $25,000-49,999 | 83 participants | 66 participants | 210 participants | 61 participants |
| Total annual household income >=$50,000 | 44 participants | 53 participants | 155 participants | 58 participants |
| Total annual household income unknown | 24 participants | 23 participants | 75 participants | 28 participants |
| Waist circumference | 110.4 cm STANDARD_DEVIATION 16.6 | 106.6 cm STANDARD_DEVIATION 16.2 | 108.6 cm STANDARD_DEVIATION 16.7 | 109.0 cm STANDARD_DEVIATION 17 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — |
| other Total, other adverse events | 215 / 232 | 196 / 233 | 213 / 234 |
| serious Total, serious adverse events | 42 / 232 | 34 / 233 | 58 / 234 |
Outcome results
Treatment Failure (Loss of Glycemic Control)
Defined as A1c persistently \>=8% over a 6-month period or persistent metabolic decompensation (inability to wean insulin within 3 months of initiation or the occurrence of a second episode within three months of discontinuing insulin)
Time frame: Study duration - 2 years to 6.5 years of follow up from randomization
Population: The entire cohort of 699 participants was included in the analysis.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| 1 Metformin Alone | Treatment Failure (Loss of Glycemic Control) | Treatment failure | 120 participants |
| 1 Metformin Alone | Treatment Failure (Loss of Glycemic Control) | Did not fail treatment during trial | 112 participants |
| 2 Metformin + Rosliglitazone | Treatment Failure (Loss of Glycemic Control) | Treatment failure | 90 participants |
| 2 Metformin + Rosliglitazone | Treatment Failure (Loss of Glycemic Control) | Did not fail treatment during trial | 143 participants |
| 3 Metformin + Lifestyle Program | Treatment Failure (Loss of Glycemic Control) | Treatment failure | 109 participants |
| 3 Metformin + Lifestyle Program | Treatment Failure (Loss of Glycemic Control) | Did not fail treatment during trial | 125 participants |
Body Composition -- BMI
Body mass index (BMI) measured in kg per meters squared. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time.
Time frame: 24 months
Population: Cohort measured at 24 months and had not experienced treatment failure.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| 1 Metformin Alone | Body Composition -- BMI | 36.7 kg per meters squared | Standard Deviation 9.1 |
| 2 Metformin + Rosliglitazone | Body Composition -- BMI | 38.2 kg per meters squared | Standard Deviation 8.1 |
| 3 Metformin + Lifestyle Program | Body Composition -- BMI | 35.3 kg per meters squared | Standard Deviation 8.4 |
Body Composition -- Bone Density
Measured by DXA, both whole body scan and AP-spine scan. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. In addition, in about 1/3 of participants DXA scans could not be obtained on participants weighing more than 300 pounds (136 kg), the upper limit in size set by the machine manufacturers. Scans were considered invalid if a body part (e.g., arm, leg) was completely off or partially off the scanner, there was hand-hip overlap, or there was motion or movement during the scan.
Time frame: 24 months
Population: Members of the cohort measured at 24 months who did not experience treatment failure.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| 1 Metformin Alone | Body Composition -- Bone Density | 1.15 g/cm squared | Standard Deviation 0.1 |
| 2 Metformin + Rosliglitazone | Body Composition -- Bone Density | 1.15 g/cm squared | Standard Deviation 0.11 |
| 3 Metformin + Lifestyle Program | Body Composition -- Bone Density | 1.15 g/cm squared | Standard Deviation 0.12 |
Body Composition -- Fat Mass
Determined by DXA whole body scan. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time. In addition, in about 1/3 of participants DXA scans could not be obtained on participants weighing more than 300 pounds (136 kg), the upper limit in size set by the machine manufacturers. Scans were considered invalid if a body part (e.g., arm, leg) was completely off or partially off the scanner, there was hand-hip overlap, or there was motion or movement during the scan.
Time frame: 24 months
Population: Members of the cohort measured at 24 months who did not experience treatment failure.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| 1 Metformin Alone | Body Composition -- Fat Mass | 36.1 kg | Standard Deviation 12 |
| 2 Metformin + Rosliglitazone | Body Composition -- Fat Mass | 39.7 kg | Standard Deviation 10.5 |
| 3 Metformin + Lifestyle Program | Body Composition -- Fat Mass | 32.2 kg | Standard Deviation 9.4 |
Body Composition -- Waist Circumference
Waist circumference (cm) measured at the iliac crest at its outermost point with the measuring tape placed around the participant in a horizontal plane parallel to the floor at the mark and the measurement teken at the end of normal expiration without the tape compressing the skin. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time.
Time frame: 24 months
Population: Members of cohort measured at 24 months who had not experience treatment failure.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| 1 Metformin Alone | Body Composition -- Waist Circumference | 110.8 cm | Standard Deviation 17.5 |
| 2 Metformin + Rosliglitazone | Body Composition -- Waist Circumference | 114.0 cm | Standard Deviation 16.3 |
| 3 Metformin + Lifestyle Program | Body Composition -- Waist Circumference | 108.6 cm | Standard Deviation 16.7 |
Comorbidity -- Hypertension
A diagnosis was made by an out-of-range value \>=95th percentile or systolic \>=130 or diastolic \>=80 sustained over 6 months or on an anti-hypertensive medication.
Time frame: Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization.
Population: Entire cohort.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1 Metformin Alone | Comorbidity -- Hypertension | 57 participants |
| 2 Metformin + Rosliglitazone | Comorbidity -- Hypertension | 53 participants |
| 3 Metformin + Lifestyle Program | Comorbidity -- Hypertension | 45 participants |
Comorbidity -- LDL Dyslipidemia
A diagnosis was made from out-of-range value \>= 130 mg/dL sustained over 6 months or put on lipid lowering medication.
Time frame: Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization.
Population: Entire cohort.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1 Metformin Alone | Comorbidity -- LDL Dyslipidemia | 18 participants |
| 2 Metformin + Rosliglitazone | Comorbidity -- LDL Dyslipidemia | 16 participants |
| 3 Metformin + Lifestyle Program | Comorbidity -- LDL Dyslipidemia | 15 participants |
Comorbidity -- Triglycerides Dyslipidemia
A diagnosis was made by an out-of-range value \>=150 mg/dL sustained over 6 months or on appropriate lipid lowering medication.
Time frame: Data collected at baseline and during follow-up - 2 years to 6.5 years from randomization.
Population: Entire cohort.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1 Metformin Alone | Comorbidity -- Triglycerides Dyslipidemia | 20 participants |
| 2 Metformin + Rosliglitazone | Comorbidity -- Triglycerides Dyslipidemia | 28 participants |
| 3 Metformin + Lifestyle Program | Comorbidity -- Triglycerides Dyslipidemia | 22 participants |
Insulin Secretion
Insulinogenic index determined from OGTT as difference in insulin at 30 minutes minus 0 minutes divided by difference in glucose at 30 minutes minus 0 minutes. The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time.
Time frame: 24 months
Population: Participants who were measured at 24 months and had not experience treatment failure.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| 1 Metformin Alone | Insulin Secretion | .75 uU/mL divided by mg/dL |
| 2 Metformin + Rosliglitazone | Insulin Secretion | .83 uU/mL divided by mg/dL |
| 3 Metformin + Lifestyle Program | Insulin Secretion | .71 uU/mL divided by mg/dL |
Insulin Sensitivity
All participants were followed to 24 months. Insulin sensitivity is measured from OGTT as inverse of fasting insulin (mL/uU). The analysis sample includes only participants with 24 month data who had not experienced the primary outcome by that time.
Time frame: 24 months
Population: Participants who were measured at 24 months and had not experienced treatment failure.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| 1 Metformin Alone | Insulin Sensitivity | 0.037 mL/uU |
| 2 Metformin + Rosliglitazone | Insulin Sensitivity | 0.049 mL/uU |
| 3 Metformin + Lifestyle Program | Insulin Sensitivity | 0.039 mL/uU |
Number of Serious Adverse Events
Number of serious adverse events reported during the trial. Participant could have multiple episodes reported.
Time frame: Reported as occurred during study follow-up - 2 years to 6.5 years from randomization.
Population: Entire cohort.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1 Metformin Alone | Number of Serious Adverse Events | 42 episodes of serious adverse event |
| 2 Metformin + Rosliglitazone | Number of Serious Adverse Events | 34 episodes of serious adverse event |
| 3 Metformin + Lifestyle Program | Number of Serious Adverse Events | 58 episodes of serious adverse event |