Trimboli Pierpaolo, Virili Camilla, Centanni Marco, Giovanella Luca
Department of Nuclear Medicine and Thyroid Centre, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.
Front Endocrinol (Lausanne). 2018 Mar 21;9:118. doi: 10.3389/fendo.2018.00118. eCollection 2018.
Levothyroxine sodium (LT4) is the therapy of choice for hypothyroidism. In the last decade, new LT4 formulations, such as liquid and softgel capsules, became available. Even if some evidence has been reached in the efficacy of liquid LT4 in patients with suboptimal TSH on tablet LT4, the usefulness of softgel LT4 has been rarely studied. This study aimed at evaluating the effect of switching from tablet to softgel LT4 patients without increased need for LT4. TSH was used as proxy of LT4 bioavailability and effectiveness.
During the period from April to August 2017, 19 patients on tablet LT4 treatment for hypothyroidism, mostly due to autoimmune thyroiditis, were enrolled. Subjects with causes of malabsorption or increased requirement of LT4 were previously excluded. Patients finally included were asked to switch from tablet to softgel LT4 formulation at unchanged dose and ingestion fashion (30 min before breakfast). TSH was measured with chemiluminescence immunoassays.
According to exclusion and inclusion criteria, 19 patients were finally selected. One of these had headache 4 days later and come back to tablet LT4, and 18 of them (16W/2M; mean age = 55 years; BMI 22.7 kg/m) completed the study. They were treated with a median LT4 dose of 88 μg/day and showed a median TSH value of 3.33 mIU/L. The rate of cases with TSH ≤ 4.0 mIU/L was 61.1% (11/18 cases). When patients were re-evaluated after 3 months of softgel LT4, we observed that TSH reached levels under 4.0 mIU/L in 16/18 (88.9%) patients, TSH was lower in 11 cases, and in 6 out of 7 patients with pre-switch TSH values over the normal range. Overall, TSH values on softgel LT4 (median 1.90 mIU/L) was significantly lower from that observed during tablet LT4 ( = 0.0039).
These data show that hypothyroid patients with no proven malabsorption may have an improved TSH following 3 months from the switch from tablet to softgel LT4 preparation at unchanged dose.
左甲状腺素钠(LT4)是治疗甲状腺功能减退症的首选药物。在过去十年中,出现了新的LT4制剂,如液体制剂和软胶囊制剂。尽管已有证据表明,对于服用片剂LT4后促甲状腺激素(TSH)未达最佳水平的患者,液体制剂LT4有效,但软胶囊制剂LT4的效用鲜少被研究。本研究旨在评估甲状腺功能减退症患者从片剂LT4转换为软胶囊LT4且LT4需求量未增加时的效果。TSH被用作LT4生物利用度和有效性的替代指标。
在2017年4月至8月期间,招募了19名因甲状腺功能减退症接受片剂LT4治疗的患者,多数病因是自身免疫性甲状腺炎。先前已排除存在吸收不良病因或LT4需求量增加的患者。最终纳入的患者被要求以不变的剂量和服用方式(早餐前30分钟)从片剂LT4转换为软胶囊LT4制剂。采用化学发光免疫分析法测定TSH。
根据排除和纳入标准,最终选定19名患者。其中1名患者在4天后出现头痛,又恢复服用片剂LT4,其余18名患者(16名女性/2名男性;平均年龄 = 55岁;体重指数22.7kg/m²)完成了研究。他们接受的LT4中位剂量为88μg/天,TSH中位值为3.33mIU/L。TSH≤4.0mIU/L的病例比例为61.1%(11/18例)。当患者在服用软胶囊LT4 3个月后重新评估时,我们观察到16/18(88.9%)的患者TSH降至4.0mIU/L以下,11例患者的TSH降低,在转换前TSH值超出正常范围的7例患者中有6例TSH降低。总体而言,软胶囊LT4时的TSH值(中位值1.90mIU/L)显著低于服用片剂LT4时观察到的TSH值(P = 0.0039)。
这些数据表明,在剂量不变的情况下,从片剂LT4转换为软胶囊LT4制剂3个月后,无明确吸收不良的甲状腺功能减退症患者的TSH可能会改善。