Krysiak Robert, Szkróbka Witold, Okopień Bogusław
Department of Internal Medicine and Clinical Pharmacology, Medical University of Silesia, Katowice, Poland.
Exp Clin Endocrinol Diabetes. 2018 May;126(5):321-326. doi: 10.1055/s-0043-120342. Epub 2017 Nov 8.
Levothyroxine and selenomethionine were found to reduce thyroid antibody titers in patients with Hashimoto's thyroiditis. The same effect was produced by intensive statin therapy. The aim of the present study was to assess whether hypolipidemic agents modulate the impact of thyroid hormone supplementation and selenomethionine on thyroid autoimmunity.
The study included 62 women with Hashimoto's thyroiditis treated for at least 6 months with levothyroxine and selenomethionine. On the basis of plasma lipids, women were divided into three groups: women with isolated hypercholesterolemia (group A; n=20), women with isolated hypertriglyceridemia (group B; n=17), and women with normal plasma lipids (group C; n=25). Group A were then treated with atorvastatin (20 mg daily), while group B received micronized fenofibrate (200 mg daily). Serum titers of thyroid peroxidase and thyroglobulin antibodies, as well as serum levels of thyrotropin, free thyroxine and free triiodothyronine were measured at the beginning of the study and 6 months later.
Fenofibrate decreased triglycerides and increased HDL cholesterol, while simvastatin decreased total and LDL cholesterol. Fenofibrate reduced titers of thyroid peroxidase and, to a lesser extent, thyroglobulin antibodies. Atorvastatin tended to increase thyroid peroxidase antibodies. No changes in thyrotropin, free thyroxine and free triiodothyronine were observed in any treatment group. Fenofibrate-induced changes in thyroid antibody titers correlated with baseline antibody titers, as well as with treatment-induced changes in HDL cholesterol and insulin sensitivity.
The obtained results indicate that only fibrates may potentiate the effect of selenomethionine and levothyroxine on thyroid autoimmunity in women.
左甲状腺素和硒代蛋氨酸可降低桥本甲状腺炎患者的甲状腺抗体滴度。强化他汀类药物治疗也有同样的效果。本研究的目的是评估降脂药物是否能调节甲状腺激素补充剂和硒代蛋氨酸对甲状腺自身免疫的影响。
该研究纳入了62例接受左甲状腺素和硒代蛋氨酸治疗至少6个月的桥本甲状腺炎女性患者。根据血脂情况,将女性分为三组:单纯高胆固醇血症患者(A组;n = 20)、单纯高甘油三酯血症患者(B组;n = 17)和血脂正常的女性(C组;n = 25)。然后A组接受阿托伐他汀治疗(每日20毫克),而B组接受微粒化非诺贝特治疗(每日200毫克)。在研究开始时和6个月后测量甲状腺过氧化物酶和甲状腺球蛋白抗体的血清滴度,以及促甲状腺激素、游离甲状腺素和游离三碘甲状腺原氨酸的血清水平。
非诺贝特降低了甘油三酯并提高了高密度脂蛋白胆固醇,而辛伐他汀降低了总胆固醇和低密度脂蛋白胆固醇。非诺贝特降低了甲状腺过氧化物酶滴度,并在较小程度上降低了甲状腺球蛋白抗体滴度。阿托伐他汀倾向于增加甲状腺过氧化物酶抗体。在任何治疗组中均未观察到促甲状腺激素、游离甲状腺素和游离三碘甲状腺原氨酸的变化。非诺贝特引起的甲状腺抗体滴度变化与基线抗体滴度以及治疗引起的高密度脂蛋白胆固醇和胰岛素敏感性变化相关。
所得结果表明,只有贝特类药物可能增强硒代蛋氨酸和左甲状腺素对女性甲状腺自身免疫的作用。