Lewis EJ, Lewis JB, Greene T, et al. Sulodexide for kidney protection in type 2 diabetes patients with microalbuminuria: a randomized controlled trial. Am J Kidney Dis. 2011 Nov;58(5):729-36. Epub 2011 Aug 26. (Original) PMID: 21872376
Abstract
BACKGROUND: Sulodexide,
a heterogenous group of sulfated glycosaminoglycans, includes
low-molecular-weight heparin (~80% +/- 8%), high-molecular-weight
heparin (~5% +/- 3%), and dermatan (~20% +/- 8%), with a mean molecular
weight of ~9 kDa. The drug is absorbed orally and has no anticoagulant
effect in the doses used. Small preliminary studies consistently showed
sulodexide to be associated with decreased albuminuria in patients with
diabetes.
STUDY DESIGN: We conducted a multicenter placebo-controlled
double-blinded study to determine the effect of sulodexide on urine
albumin excretion in patients with type 2 diabetic nephropathy. SETTING
&
PARTICIPANTS: Patients with type 2 diabetes and urine
albumin-creatinine ratios (ACRs) of 35-200 mg/g in men and 45-200 mg/g
in women were enrolled. Serum creatinine level was <1.5 mg/dL. Blood
pressure goal was 130/80 mm Hg. A maximum US Food and Drug
Administration-approved dose of an angiotensin-converting enzyme
inhibitor or angiotensin receptor blocker for a minimum of 4 months
before randomization was required.
INTERVENTIONS: The study drug was
sulodexide, 200 mg/d. OUTCOME & MEASUREMENTS: The primary end point
was normoalbuminuria (ACR <20 mg/g and a decrease >25%) or 50%
decrease in baseline ACR.
RESULTS: In 1,056 randomly assigned
patients with a mean baseline ACR of 107.8 +/- 83.7 mg/g, comparing the
sulodexide versus placebo groups, the primary end point was achieved in
16.5% versus 18.4%; normoalbuminuria, in 7.9% versus 6.1%; and a 50%
decrease in albuminuria, in 15.4% versus 17.6%. The relative probability
of any given change in albuminuria was identical in both groups.
LIMITATIONS: We were unable to determine whether the administered sulodexide was absorbed from the gastrointestinal tract.
CONCLUSION:
Sulodexide failed to decrease urine albumin excretion in patients with
type 2 diabetic nephropathy and microalbuminuria.
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