Feig · JAMA 2008 · randomized, double-blind, placebo-controlled crossover trial · n=30

Effect of allopurinol on blood pressure of adolescents with newly diagnosed essential hypertension: a randomized trial.

Cited 926 times in the scientific literature.

Level 2 - randomized trial

Individual randomized controlled crossover trial

PubMed 18728266 · doi:10.1001/jama.300.8.924 · record verified 2026-08-29

What was done

A randomized, double-blind, placebo-controlled crossover trial evaluated 30 adolescents aged 11 to 17 years with newly diagnosed, never-treated stage 1 essential hypertension and serum uric acid levels ≥ 6 mg/dL. Participants received allopurinol (200 mg twice daily) for 4 weeks and placebo twice daily for 4 weeks, separated by a 2-week washout period, with randomized treatment order. The main outcomes were changes in casual and 24-hour ambulatory blood pressure.

What was found

Allopurinol significantly reduced blood pressure compared with placebo. Mean change in casual systolic BP was -6.9 mm Hg (95% CI, -4.5 to -9.3) for allopurinol vs -2.0 mm Hg (95% CI, 0.3 to -4.3) for placebo (P = .009), and casual diastolic BP change was -5.1 mm Hg (95% CI, -2.5 to -7.8) vs -2.4 mm Hg (95% CI, 0.2 to -4.1; P = .05). Mean change in 24-hour ambulatory systolic BP was -6.3 mm Hg (95% CI, -3.8 to -8.9) for allopurinol vs 0.8 mm Hg (95% CI, 3.4 to -2.9) for placebo (P = .001); ambulatory diastolic BP change was -4.6 mm Hg (95% CI, -2.4 to -6.8) vs -0.3 mm Hg (95% CI, 2.3 to -2.1; P = .004). Twenty of 30 participants achieved normal BP on allopurinol vs 1 on placebo (P < .001).

Why it matters

This study provides clinical evidence that lowering uric acid with allopurinol reduces blood pressure in hyperuricemic adolescents with newly diagnosed essential hypertension.

Limits

The sample size was small (n = 30) from a single pediatric center, and the follow-up duration was short (4 weeks per treatment). Patients with stage 2 hypertension or major systemic comorbidities were excluded, and long-term efficacy and potential adverse effects were not established.

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