Key result
One year of treatment with the aldose reductase inhibitor zopolrestat increased resting LVEF (P<0.02) and exercise LVEF (P<0.001) in diabetic patients with neuropathy.
Why the study?
Does the aldose reductase inhibitor zopolrestat improve asymptomatic cardiac abnormalities in diabetic patients with neuropathy?
RCT (n=81)
Blinded
Randomized
Does the aldose reductase inhibitor zopolrestat improve asymptomatic cardiac abnormalities in diabetic patients with neuropathy?
p-value: p=<0.02 for resting LVEF, <0.001 for exercise LVEF
Treatment with the aldose reductase inhibitor zopolrestat for 1 year stabilized and partially reversed asymptomatic left ventricular abnormalities in diabetic patients with neuropathy.
Opens aldose reductase inhibition as a treatment axis for asymptomatic LV dysfunction in diabetic neuropathy; extends neuropathy data to cardiac endpoints.
OBJECTIVE—The goal of this study was to determine whether treatment with an aldose reductase inhibitor (ARI) has beneficial effects on asymptomatic cardiac abnormalities in diabetic patients with neuropathy. RESEARCH DESIGN AND METHODS—Diabetic subjects with neuropathy (n = 81) with either a low diastolic peak filling rate or impaired augmentation of left ventricular (LV) ejection fraction (LVEF) during maximal bicycle exercise were identified by gated radionuclide ventriculography. Coronary artery disease, left ventricular hypertrophy, and valvular heart disease were excluded by clinical evaluation, myocardial perfusion imaging, and echocardiography. Subjects were randomized to receive blinded treatment with either the placebo or the ARI zopolrestat 500 or 1,000 mg daily for 1 year. RESULTS—After 1 year of ARI treatment, there were increases in resting LVEF (P < 0.02), cardiac output (P < 0.03), LV stroke volume (P < 0.004), and exercise LVEF (P < 0.001). In placebo-treated subjects, there were decreases in exercise cardiac output (P < 0.03), stroke volume (P < 0.02), and end diastolic volume (P < 0.04). Exercise LVEF increased with ARI treatment independent of blood pressure, insulin use, or the presence of baseline abnormal heart rate variability. There was no change in resting diastolic filling rates in either group. CONCLUSIONS—Diabetic patients with neuropathy have LV abnormalities that can be stabilized and partially reversed by ARI treatment.
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Johnson et al. (2004) conducted an RCT in Diabetic neuropathy with asymptomatic cardiac abnormalities (n=81). Zopolrestat (aldose reductase inhibitor) vs. Placebo was evaluated on Changes in resting LVEF, cardiac output, LV stroke volume, and exercise LVEF (p=<0.02 for resting LVEF, <0.001 for exercise LVEF). One year of treatment with the aldose reductase inhibitor zopolrestat increased resting LVEF (P<0.02) and exercise LVEF (P<0.001) in diabetic patients with neuropathy.
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