PURPOSE: TO evaluate the adverse effect of aluminum hydroxide on levot
hyroxine pharmacokinetics in hypothyroid patients and study the mechan
ism of this effect. DESIGN: An in vivo open study supplemented by in v
itro experiments. SETTING: A university hospital-based outpatient serv
ice. INTERVENTION: Administration for 2 to 4 weeks of an aluminum hydr
oxide-containing preparation to patients balanced on replacement thyro
xine therapy. MEASUREMENTS: Serum thyrotropin (TSH). RESULTS: A signif
icant increase in serum TSH was observed during seven periods of alumi
num hydroxide administration (7.19 +/- 1.3 versus 2.62 +/- 0.8 mU/L; P
= 0.012). In vitro studies indicated a considerable nonspecific adsor
ptive capacity of aluminum hydroxide for thyroxine. CONCLUSIONS: The r
esults indicate an adverse effect of aluminum hydroxide on levothyroxi
ne bioavailability through a mechanism involving nonspecific adsorptio
n, or complexing, of levothyroxine to aluminum hydroxide. We recommend
close monitoring of serum TSH levels in patients receiving oral thyro
id hormone replacement therapy who concurrently take aluminum hydroxid
e-containing medications. Adjustment of the levothyroxine dose, or ces
sation of the antacid, may be necessary.