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Proof-of-concept trial on the efficacy of sodium tungstate in human obesity.

Diabetes, obesity & metabolism (2010-10-01)
F Hanzu, R Gomis, M J Coves, J Viaplana, M Palomo, A Andreu, J Szpunar, J Vidal
RESUMEN

Considering the poor long-term success of current dietary and pharmacological interventions, we aimed to evaluate the potential effect of sodium tungstate in the treatment of grade I and II obesity (ClinicalTrials.gov identifier: NCT00555074). Prospective, randomized, placebo-controlled, double-blind, proof-of-concept study was carried out. Following a 2-week lead-in period, 30 obese (body mass index, BMI 30.0-39.9 kg/m(2)), non-diabetic subjects were randomized to receive either sodium tungstate (100 mg bid) or placebo for 6 weeks. The primary study endpoint was the absolute change in body weight relative to the time of randomization. Treatment with sodium tungstate [-0.135 ± 0.268 kg (95% CI -0.686 to +0.416 kg)] was not associated with a significant weight loss compared to placebo [-0.063 ± 0.277 kg (95% CI -0.632 to +0.507 kg)] (p = 0.854). Likewise, treatment with sodium tungstate was not associated with significant changes in fat mass (DEXA), resting energy expenditure (indirect calorimetry) or caloric consumption (3-day food records). Our data do not support sodium tungstate as a pharmacological agent in the treatment of human obesity.

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Sigma-Aldrich
Sodium tungstate dihydrate, ACS reagent, ≥99%
Sigma-Aldrich
Sodium tungstate dihydrate, BioUltra, ≥99.0% (T)
Sigma-Aldrich
Sodium tungstate dihydrate, 99.995% trace metals basis