Aim. Oxidative stress (OS) in subjects with primary hypothyroidism under therapy with L-T4 might be the cause of the side effects commonly found with this treatment. Methods. Twenty-four subjects of both sexes (11 M and 15 F), aged between 41 and 61 years, with primary hypothyroidism were assessed. All the subjects were followed for 30 days during the administration of a fixed dose of 75 μg of L-T4. Levels of T4, T3, TSH, hydroperoxides (as measure of OS ), hs-CRP were determined in plasma before and after the treatment. Side effects (anxiety/agitation, sweating, palpitations and headache) and number of days of discomfort were measured for 15 days before and for two subsequent 15-day periods. Results. Administration of L-T4 satisfactorily balanced the hypothyroidism. A high level of hydroperoxides, 370±27.7 U.CARR. (Carratelli Units: 1 U.CARR. = 0.08 mg of H 2O2/L), was observed before treatment, and L-T4 administration further increased the level up to 435±39.5 U.CARR (p<0.05). The treatment produces a significant increase in hs-CRP, from 3.2±2.32 to 4.0±1.27 mg/L (P<0.05). Side effects, almost absent at the baseline 15-day control, occurred with high frequencies during the treatment: between 9.6±1.14 days/15 days for sweating and 14.1±0.93 days/15 days for palpitations. Some side effects were found to be linearly correlated with hydroperoxides (r=0.641, P<0.01 and r=0.658, P<0.01 respectively) or with hs-CRP, as in the case of anxiety/agitation (r=0.629, P<0.01). Following L-T4 administration the days of discomfort turned out to be particularly prominent during the two subsequent 15-day controls (3.8±0.75 and 4.8±0.78 days respectively). Conclusion. Primary hypothyroidism and therapy with L-T4at a dose of 75 pg/day cause OS. Side effects following L-T4therapy depend on OS and cause daily discomfort and loss of working activity in about 1/3 of the days considered.

Oxidative stress following administration of levothyroxine in subjects suffering from primary hypothyroidism.

BELCARO, Giovanni;FERAGALLI, Beatrice
2011-01-01

Abstract

Aim. Oxidative stress (OS) in subjects with primary hypothyroidism under therapy with L-T4 might be the cause of the side effects commonly found with this treatment. Methods. Twenty-four subjects of both sexes (11 M and 15 F), aged between 41 and 61 years, with primary hypothyroidism were assessed. All the subjects were followed for 30 days during the administration of a fixed dose of 75 μg of L-T4. Levels of T4, T3, TSH, hydroperoxides (as measure of OS ), hs-CRP were determined in plasma before and after the treatment. Side effects (anxiety/agitation, sweating, palpitations and headache) and number of days of discomfort were measured for 15 days before and for two subsequent 15-day periods. Results. Administration of L-T4 satisfactorily balanced the hypothyroidism. A high level of hydroperoxides, 370±27.7 U.CARR. (Carratelli Units: 1 U.CARR. = 0.08 mg of H 2O2/L), was observed before treatment, and L-T4 administration further increased the level up to 435±39.5 U.CARR (p<0.05). The treatment produces a significant increase in hs-CRP, from 3.2±2.32 to 4.0±1.27 mg/L (P<0.05). Side effects, almost absent at the baseline 15-day control, occurred with high frequencies during the treatment: between 9.6±1.14 days/15 days for sweating and 14.1±0.93 days/15 days for palpitations. Some side effects were found to be linearly correlated with hydroperoxides (r=0.641, P<0.01 and r=0.658, P<0.01 respectively) or with hs-CRP, as in the case of anxiety/agitation (r=0.629, P<0.01). Following L-T4 administration the days of discomfort turned out to be particularly prominent during the two subsequent 15-day controls (3.8±0.75 and 4.8±0.78 days respectively). Conclusion. Primary hypothyroidism and therapy with L-T4at a dose of 75 pg/day cause OS. Side effects following L-T4therapy depend on OS and cause daily discomfort and loss of working activity in about 1/3 of the days considered.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/262912
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