Key result
A 12-month lifestyle-metformin intervention significantly reduced urinary albumin excretion by 60% (P<0.001) in obese non-diabetic subjects with baseline UAE of 10-29 mg/day.
Why the study?
Does a lifestyle modification-metformin program reduce urinary albumin excretion in overweight/obese non-diabetic subjects with high-normal albuminuria?
Cohort (n=41)
Does a lifestyle modification-metformin program reduce urinary albumin excretion in overweight/obese non-diabetic subjects with high-normal albuminuria?
A lifestyle-metformin intervention significantly reduces urinary albumin excretion in obese, non-diabetic subjects with high-normal albuminuria (10-29 mg/day), suggesting this threshold identifies a reversible adverse cardiovascular risk profile.
Should not yet alter practice for high-normal albuminuria; leaves open whether lifestyle-metformin improves cardiovascular outcomes in obese non-diabetics.
BACKGROUND: We investigated whether levels of albuminuria (urinary albumin excretion (UAE)) below those conventionally accepted as microalbuminuria (<30 mg/day) are sensitive to correction of obesity and obesity-related risk factors. METHODS: The effects of a 12-month lifestyle modification-metformin program were evaluated in otherwise healthy overweight/obese "normoalbuminuric" subjects: group I with UAE of <10 mg/day (n = 23) and group II with UAE of 10-29 mg/day (n = 18). RESULTS: The subjects of group II were older and heavier, and had higher blood pressure (BP) and lower high-density lipoprotein (HDL) levels, than those of group I. Creatinine clearances were also higher in group II (148 +/- 14 ml/min) than in group I (108 +/- 9 ml/min). Although the intervention induced comparable reductions in obesity, BP, lipids and insulin levels in both groups, UAE was significantly reduced in group II (9.1 +/- 1.8 mg/24 h; 60% reduction; P < 0.001), and non-significantly in group I (0.75 +/- 0.5 mg/day; 12% reduction; P > 0.1). Additionally, greater reduction in creatinine clearance was observed in subjects with higher UAE rates. After the intervention, both groups achieved similar UAE rates (5.7 +/- 0.9 and 5.2 +/- 1.0 mg/day; P > 0.10). Basal UAE was related to the subjects' creatinine clearance (r = 0.38; P = 0.04). For both groups together, intervention-induced changes in UAE rates were not significantly related to BP, age, or body weight. However, for group II subjects, BP and UAE reduction were positively associated (r = 0.44; P = 0.03). CONCLUSIONS: UAE of 10-29 mg/day (hyperalbuminuria), below the conventionally used limit to define microalbuminuria, is already associated with a more adverse cardiovascular risk profile, and is exquisitely sensitive to interventions that reduce obesity, BP, and insulin resistance.
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Cubeddu et al. (2007) conducted a cohort in Obesity with normoalbuminuria (n=41). Lifestyle modification and metformin vs. Baseline UAE <10 mg/day (Group I) vs UAE 10-29 mg/day (Group II) was evaluated on Reduction in urinary albumin excretion (UAE) (p=<0.001). A 12-month lifestyle-metformin intervention significantly reduced urinary albumin excretion by 60% (P<0.001) in obese non-diabetic subjects with baseline UAE of 10-29 mg/day.
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