Key result
Uric acid lowering with probenecid or allopurinol has no effect on kidney-specific RAS activity versus placebo.
Why the study?
Higher serum uric acid levels are strongly associated with increased renin-angiotensin system activity and hypertension risk, but the effect of lowering uric acid on RAS activity in humans is unknown and data on blood pressure reduction are conflicting.
Does uric acid lowering with probenecid or allopurinol reduce kidney-specific and systemic RAS activity or blood pressure in overweight or obese adults with serum uric acid ≥5.0 mg/dl?
RCT (n=149)
Double-blind
randomly assigned
Does uric acid lowering with probenecid or allopurinol reduce kidney-specific and systemic RAS activity or blood pressure in overweight or obese adults with serum uric acid ≥5.0 mg/dl?
Absolute Event Rate: -4% vs 1%
p-value: p=0.77
Lowering serum uric acid with probenecid or allopurinol does not reduce renin-angiotensin system activity or blood pressure in overweight/obese adults, challenging the hypothesis that uric acid is a reversible risk factor for hypertension.
Uric acid lowering does not affect RAS activity or BP; challenges observational associations and supports noncausal link in adults.
Background and objectives Higher serum uric acid levels, even within the reference range, are strongly associated with increased activity of the renin-angiotensin system (RAS) and risk of incident hypertension. However, the effect of lowering serum uric acid on RAS activity in humans is unknown, although the data that lowering serum uric acid can reduce BP are conflicting. Design, setting, participants, & measurements In a double-blind placebo-controlled trial conducted from 2011 to 2015, we randomly assigned 149 overweight or obese adults with serum uric acid ≥5.0 mg/dl to uric acid lowering with either probenecid or allopurinol, or to placebo. The primary endpoints were kidney-specific and systemic RAS activity. Secondary endpoints included mean 24-hour systolic BP, mean awake and asleep BP, and nocturnal dipping. Results Allopurinol and probenecid markedly lowered serum uric acid after 4 and 8 weeks compared with placebo (mean serum uric acid in allopurinol, probenecid, and placebo at 8 weeks was 2.9, 3.5, and 5.6 mg/dl, respectively). The change in kidney-specific RAS activity, measured as change in the median (interquartile range) renal plasma flow response to captopril (in ml/min per 1.73 m 2 ) from baseline to 8 weeks, was −4 (−25 to 32) in the probenecid group ( P =0.83), −4 (−16 to 9) in the allopurinol group ( P =0.32), and 1 (−21 to 17) in the placebo group ( P =0.96), with no significant treatment effect ( P =0.77). Similarly, plasma renin activity and plasma angiotensin II levels did not significantly change with treatment. The change in mean (±SD) 24-hour systolic BPs from baseline to 8 weeks was −1.6±10.1 with probenecid ( P =0.43), −0.4±6.1 with allopurinol ( P =0.76), and 0.5±6.0 with placebo ( P =0.65); there was no significant treatment effect ( P =0.58). Adverse events occurred in 9%, 12%, and 2% of those given probenecid, allopurinol, or placebo, respectively. Conclusions In contrast to animal experiments and observational studies, this randomized, placebo-controlled trial found that uric acid lowering had no effect on kidney-specific or systemic RAS activity after 8 weeks or on mean systolic BP. These data do not support the hypothesis that higher levels of uric acid are a reversible risk factor for increased BP.
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McMullan et al. (2017) conducted an RCT in Overweight or obese with elevated serum uric acid (n=149). Probenecid or allopurinol vs. Placebo was evaluated on Kidney-specific RAS activity (change in median renal plasma flow response to captopril from baseline to 8 weeks) (p=0.77). Uric acid lowering with probenecid or allopurinol had no significant effect on kidney-specific RAS activity compared with placebo after 8 weeks (P=0.77).
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