Effect of Farxiga on Renal Function and Size in Type 2 Diabetic Patients With Hyperfiltration



Status:Recruiting
Conditions:Diabetes, Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:30 - 70
Updated:4/27/2018
Start Date:December 20, 2016
End Date:April 2019

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The investigators propose to treat newly diagnosed, hyperfiltering T2DM patients with or
without microalbuminuria with dapagliflozin or metformin for 4 months. The metformin-treated
group will serve as controls for improved glycemic control, since the investigators have
shown that insulin therapy to normalize A1c reduces hyperfiltration and kidney size in T1DM
patients.

Hyperfiltration is a characteristic feature in experimental models of diabetes and is
causally related to an increase in intraglomerular pressure. In newly diagnosed diabetic
patients, both type 1 and type 2, hyperfiltration and enlarged kidney size commonly are
observed, and these hemodynamic/anatomic abnormalities are associated with an increased risk
for the development of diabetic nephropathy.

In poorly controlled diabetic individuals, the filtered load of glucose is markedly increased
and glucose - with sodium - reabsorption by the SGLT2 transporter in the proximal tubule is
augmented. As a consequence sodium delivery to the macula densa is reduced, making the kidney
think that it is under perfused and this results in afferent renal arteriolar vasodilation.
The efferent arteriole of the hyperfiltrating diabetic kidney also is hypersensitive to
angiotensin II despite the absence of systemic RAS activation. The net result of these
hemodynamic changes is an increase in intraglomerular pressure and hyperfiltration. Further,
angiotensin is a potent growth factor and contributes to the increase in size of individual
glomeruli and total kidney size. Since the intraglomerular pressure is related to the radius
(r3) by the Law of LaPlace, the increase in glomerular size also contributes to
hyperfiltration.

Based upon the preceding sequence, it follows that a drug that blocks glucose, along with
sodium, reabsorption in the proximal tubule would enhance sodium delivery to the macula
densa, cause afferent renal arteriolar constriction, reduce intraglomerular
pressure/hyperfiltration, and decrease kidney size. In hyperfiltering diabetic patients with
microalbuminuria, the investigators also would expect the microalbuminuria to decrease.
Consistent with this scenario, animal studies have documented that both acute and chronic
inhibition of SGLT2 decreases hyperfiltration and prevents diabetic nephropathy. A recent
study in hyperfiltering type 1 diabetic patients treated with empagliflozin has provided
additional support for the tubular glomerular feedback hypothesis.

The investigators propose to treat newly diagnosed, hyperfiltering T2DM patients with or
without microalbuminuria with dapagliflozin or metformin for 4 months. The metformin-treated
group will serve as controls for improved glycemic control, since the investigators have
shown that insulin therapy to normalize A1c reduces hyperfiltration and kidney size in T1DM
patients

Inclusion Criteria:

- Newly diagnosed, drug naïve, hyperfiltering and normofiltration patients with type 2
diabetes mellitus (T2DM)

- Hyperfiltration is defined by GFR >135 ml/min•1.73m2

- Normofiltration by a GFR = 90-134 ml/min•1.73m2

- BMI = 20-45 kg/m2

- HbA1c = 7.5% to 12%

- Willingness to participate in the 16 week study protocol

- Hematocrit >34%

- GAD antibody negative

- BP < 145/90 mmHg

Exclusion Criteria:

- > 300 mg/day albumin excretion

- Ingestion of medications known to interfere with the renin-angiotensin system or renal
function, including diuretic therapy

- Hospitalization for unstable angina, history of recent macrovascular
(MI/stroke/TIA/ACS) disease, coronary artery revascularization (within 2 months prior
to enrollment)

- Proliferative diabetic retinopathy

- History of cancer or major organ system disease

- New York Heart class II-IV heart failure Severe hepatic insufficiency and/or
significant abnormal liver function defined as aspartate aminotransferase (AST) and/or
alanine aminotransferase (ALT) > 3x ULN or total bilirubin > 2.0 mg/dL (34.2 µmo/L)

- Treatment with steroids, beta blockers, alpha blockers, antiobesity drugs

- Pregnant or nursing mothers

- Premenopausal females who are not practicing acceptable contraceptive methods
Participation in another trial with an investigational drug within 30 days Alcohol or
drug abuse within the preceding 6 months

- Any condition, psychiatric or medical, which in the opinion of the investigator would
interfere with the successful completion of the study

- Orthostatic hypotension (> 15/10 mmHg decrease upon standing for 3 minutes)

- Positive serologic evidence of current infectious liver disease including Hepatitis B
viral antibody IGM, Hepatitis B surface antigen, Hepatitis C virus antibody and HIV

- Volume depleted patients

- Estimated glomerular filtration rate <60 mL/min•1.73m2. Patients at risk for volume
depletion due to co-existing conditions or concomitant medications, such as loop
diuretics should have careful monitoring of their volume status
We found this trial at
7
sites
4502 Medical Drive
San Antonio, Texas 78284
(210) 567-7000
Phone: 210-567-6691
University of Texas Health Science Center at San Antonio The University of Texas Health Science...
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5801 South Ellis Avenue
Chicago, Illinois 60637
 773.702.1234
Phone: 773-702-7936
University of Chicago One of the world's premier academic and research institutions, the University of...
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303 East Superior Street
Chicago, Illinois 60611
Phone: 312-503-4130
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75 Commercial Road
Melbourne, Victoria 3004
Phone: 61385321362
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Melbourne,
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6400 Sanger Road
Orlando, Florida 32827
Phone: 407-745-2145
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Orlando, FL
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San Antonio, Texas
Phone: 210-358-7200
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Spokane, Washington 99204
Phone: 509-340-0930
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Spokane, WA
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