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Metformin in Kidney Disease

Dysmetabolism of Chronic Kidney Disease and Vascular Health

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02252081
Enrollment
125
Registered
2014-09-29
Start date
2014-10-01
Completion date
2019-12-31
Last updated
2021-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease, Chronic Kidney Disease, Metabolic Syndrome

Keywords

metformin, cardiovascular disease, Chronic Kidney Disease, Metabolic Syndrome

Brief summary

Chronic kidney disease (CKD) is a major global health problem associated with substantial costs and resource utilization. Currently, CKD affects more than 500 million people worldwide. Patients with CKD have unacceptably high mortality rates due to cardiovascular (CV) causes, which are not entirely explained by traditional CV risk factors. The mortality rates in advanced CKD are six times higher compared to the Medicare population, with CVD accounting for the overwhelming majority of deaths. Insulin resistance (IR) is common in CKD patients and may represent a central link between CKD and the increased CVD risk observed in this population. Insulin resistance may increase CV risk by impairing and worsening endothelial function, increasing reactive oxygen species, and exacerbating systemic inflammation-hence, insulin resistance is considered a non-traditional CV risk factor in CKD. Obesity (defined by a body mass index \[BMI\] of at least 30 kg/m2) is a major public health problem-the upward trend in obesity prevalence across regions and continents is a worldwide concern. Obesity increases the risk for cardiovascular disease and death. In the general population, obesity hastens death by 9.4 years. Obesity is an independent risk factor for CKD. Besides its contribution to the development of diabetes and hypertension, increased fat mass may also have a direct impact on kidney function. In spite of the increasing prevalence of both obesity and CKD, the impact of obesity in the CKD population is not known, especially in terms of the exaggerated metabolic disturbances associated with their coexistence. It is highly likely that these two conditions have profound interactions that exaggerate the severity of the metabolic derangements when they coexist, particularly in regards to adipokine dysregulation, the risk of insulin resistance, and downstream effects on vascular health. The current proposal will attempt to characterize the relative and combined impact of both obesity and CKD on metabolic disturbances, which may aid in risk stratification and identifying specific targets for intervention. The ultimate goal of this proposal is to understand the relative and combined impact of obesity and CKD on the generation and maintenance of insulin resistance and their impact on cardiovascular health. Specific Aim 2: To study the effects of metformin, an AMPK activator, on metabolic disturbances associated with obesity and moderate CKD. S.A.2.a: To test if metformin will improve LAR in obese patients with moderate CKD compared to placebo. S.A.2.b: To test if metformin will improve markers of systemic inflammation, oxidative stress, endothelial dysfunction in obese patients with moderate CKD compared to placebo. S.A.2.c: To test if metformin will improve atherosclerosis markers and reduce clinical CVD events in obese patients with moderate CKD compared to placebo. Hypothesis: The investigators hypothesize that the administration of metformin in obese CKD patients will significantly improve the adipokine profiles-particularly through a reduction in LAR. Additionally, that it will improve systemic inflammation, oxidative stress and endothelial function, which may or may not be mediated by changes in adipokines. Finally, the investigators hypothesize that improvements in these markers of vascular health will translate into reduced arterial stiffness and less clinical CV events

Interventions

DRUGmetformin

500 to 1500 mg orally per day for 16 weeks if eGFR \> 45 ml/min; 500 to 1000 mg orally per day for 16 weeks if eGFR =\< 45 ml/min

DRUGPlacebo

placebo pill(s) orally per day for 16 weeks

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years old; * Ability to give informed consent; * Life expectancy greater than 6 months; * Estimated GFR 30-59 ml/min/1.73m\^2; * Overweight (BMI \>=25 to \< 30 kg/m\^2) or obese (BMI \>=30 kg/m\^2); or normal (BMI \>=18.5 to \<25 kg/m\^2) if pre-diabetic or insulin resistant.

Exclusion criteria

* Pregnancy or breast feeding; * Presence or history of Diabetes Mellitus type I or II * History of metformin use or any insulin sensitizer or any drug for the treatment of metabolic syndrome over the last one year; * Any acute kidney injury episode in the last 4 months due to the risk of recurrent AKI; * Proteinuria of \> 5 g in 24 hours determined by a 24 hour urine collection or PCR \> 4.5; * Uncontrolled hypertension with systolic blood pressure 160 mmHg and diastolic blood pressure 100 mmHg; * Patients with new changes to their antihypertensive regimen over the last 1 month; * Severe, unstable, or active inflammatory disease; active infection including seropositive HIV, Hepatitis B or C; active connective tissue disorder; or moderate to severe liver disease; * Decompensated heart failure; * Recent hospitalization or surgical procedure within 1 month prior to the study for any cause; * Current active malignancy or cancer history in the prior 5 years (excluding squamous cell and basal cell skin cancers); * Known intolerance to the study drug; * Patient receiving oral or injected steroids * Use of any investigational product or device within 30 days prior to screening, or requirement for any investigational agent prior to completion of all scheduled study assessments;

Design outcomes

Primary

MeasureTime frameDescription
Change is Leptin to Adiponectin Ratio (LAR)16 weeks after start of treatmentChange in leptin to adiponectin ratio (LAR) after 4 months of metformin vs. placebo will be assessed as a biomarker of insulin resistance in CKD

Secondary

MeasureTime frameDescription
Change in Flow-mediated Dilation (FMD)16 weeks after the start of treatmentChange in FMD after 4 months of treatment with metformin will be compared to change in the placebo group.
Aortic Pulse-wave Velocity (aPWV)16 weeks after starting treatmentis a measurement of stiffening of the large elastic arteries and atherosclerosis. It is a subclinical marker of cardiovascular disease

Other

MeasureTime frameDescription
Estimated Glomerular Filtration Rate (eGFR)baseline and 16 weeks after starting treatmenteGFR is a measurement of kidney function, this was a descriptive measurement

Countries

United States

Participant flow

Recruitment details

65 patients did not meet inclusion criteria (normal GFR or to low GFR, new diabetes diagnosis, uncontrolled hypertension) or decline to participate.

Participants by arm

ArmCount
Metformin
500 to 1500 mg orally per day for 16 weeks if eGFR \> 45 ml/min; 500 to 1000 mg orally per day for 16 weeks if eGFR =\< 45 ml/min metformin: 500 to 1500 mg orally per day for 16 weeks if eGFR \> 45 ml/min; 500 to 1000 mg orally per day for 16 weeks if eGFR =\< 45 ml/min
30
Placebo
placebo pill(s) orally per day for 16 weeks Placebo: placebo pill(s) orally per day for 16 weeks
30
Total60

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event41
Overall Studynon compliance & others02
Overall StudyWithdrawal by Subject21

Baseline characteristics

CharacteristicPlaceboTotalMetformin
Age, Continuous66 years67 years69 years
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
5 Participants12 Participants7 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
25 Participants48 Participants23 Participants
Sex: Female, Male
Female
6 Participants12 Participants6 Participants
Sex: Female, Male
Male
24 Participants48 Participants24 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
18 / 308 / 30
other
Total, other adverse events
16 / 306 / 30
serious
Total, serious adverse events
2 / 302 / 30

Outcome results

Primary

Change is Leptin to Adiponectin Ratio (LAR)

Change in leptin to adiponectin ratio (LAR) after 4 months of metformin vs. placebo will be assessed as a biomarker of insulin resistance in CKD

Time frame: 16 weeks after start of treatment

Population: analyzed as log transformed using ANCOVA of change, ng/µg (log transformed value)

ArmMeasureGroupValue (MEDIAN)
MetforminChange is Leptin to Adiponectin Ratio (LAR)baseline2.2 ng/micrograms
MetforminChange is Leptin to Adiponectin Ratio (LAR)Week 161.3 ng/micrograms
PlaceboChange is Leptin to Adiponectin Ratio (LAR)baseline1.3 ng/micrograms
PlaceboChange is Leptin to Adiponectin Ratio (LAR)Week 161.4 ng/micrograms
Secondary

Aortic Pulse-wave Velocity (aPWV)

is a measurement of stiffening of the large elastic arteries and atherosclerosis. It is a subclinical marker of cardiovascular disease

Time frame: 16 weeks after starting treatment

ArmMeasureGroupValue (MEDIAN)
MetforminAortic Pulse-wave Velocity (aPWV)baseline aPWV (cm/s)9.6 cm/s
MetforminAortic Pulse-wave Velocity (aPWV)Week16 aPWC (cm/s)9.9 cm/s
PlaceboAortic Pulse-wave Velocity (aPWV)baseline aPWV (cm/s)9.8 cm/s
PlaceboAortic Pulse-wave Velocity (aPWV)Week16 aPWC (cm/s)9.9 cm/s
Secondary

Change in Flow-mediated Dilation (FMD)

Change in FMD after 4 months of treatment with metformin will be compared to change in the placebo group.

Time frame: 16 weeks after the start of treatment

ArmMeasureGroupValue (MEDIAN)
MetforminChange in Flow-mediated Dilation (FMD)baseline5.1 change in percent
MetforminChange in Flow-mediated Dilation (FMD)week 169.5 change in percent
PlaceboChange in Flow-mediated Dilation (FMD)baseline5.0 change in percent
PlaceboChange in Flow-mediated Dilation (FMD)week 166.2 change in percent
Other Pre-specified

Estimated Glomerular Filtration Rate (eGFR)

eGFR is a measurement of kidney function, this was a descriptive measurement

Time frame: baseline and 16 weeks after starting treatment

Population: kidney function measurement

ArmMeasureGroupValue (MEDIAN)
MetforminEstimated Glomerular Filtration Rate (eGFR)baseline GFR49.5 ml/min
MetforminEstimated Glomerular Filtration Rate (eGFR)Week 16 GFR52 ml/min
PlaceboEstimated Glomerular Filtration Rate (eGFR)baseline GFR48.5 ml/min
PlaceboEstimated Glomerular Filtration Rate (eGFR)Week 16 GFR48.7 ml/min

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026