Ghosh Sujoy, Pramanik Subhodip, Biswas Kaushik, Bhattacharjee Kingshuk, Sarkar Rajib, Chowdhury Subhankar, Mukhopadhyay Pradip
Department of Endocrinology and Metabolism, I.P.G.M.E&R, Kolkata, India.
Biocon Limited, Bengaluru, India.
Eur Thyroid J. 2020 Jan;9(1):19-24. doi: 10.1159/000504218. Epub 2019 Nov 20.
The levothyroxine absorption test for evaluation of pseudomalabsorption in patients with primary hypothyroid is not standardised. An individual in whom a workup for malabsorption is warranted remains undefined.
Twenty-five euthyroid, 25 newly diagnosed hypothyroid, 25 treated hypothyroid with normalised TSH, and 25 hypothyroid subjects with elevated TSH despite adequate dose of levothyroxine for more than 6 months, and 10 euthyroid subjects with true malabsorption were administered levothyroxine (10 μg/kg or maximum 600 μg) to study its absorption profile by measuring free T4 level at hourly intervals for 5 h. : Free T4 peaked at 3 h with marginal insignificant decline at 4 h in all groups. The increments of free T4 (between baseline and 3 h) of the four groups (except malabsorption) were not statistically different. The mean increment of free T4 in true malabsorption was 0.39 ng/dL (95% CI: 0.29-0.52) and it was 0.78 ng/dL (95% CI: 0.73-0.85) (10.4 pmol/L) for other groups combined together. The cut off of free T4 increment at 3 h from baseline above 0.40 ng/dL had a sensitivity of 97% and specificity of 80% (AUC 0.904, < 0.001) to exclude true malabsorption.
Subjects with elevated TSH on adequate dose of LT4 can be reliably diagnosed to be non-adherent to treatment with levothyroxine absorption test. The incremental value above 0.40 ng/dL (5.14 pmol/L) at 3 h may be useful to identify individuals where workup of malabsorption is unwarranted.
用于评估原发性甲状腺功能减退患者假性吸收不良的左甲状腺素吸收试验尚未标准化。对于需要进行吸收不良检查的个体,其定义尚不明确。
对25名甲状腺功能正常者、25名新诊断的甲状腺功能减退者、25名促甲状腺激素(TSH)已正常化的接受治疗的甲状腺功能减退者、25名尽管服用了足够剂量的左甲状腺素超过6个月但TSH仍升高的甲状腺功能减退者,以及10名患有真正吸收不良的甲状腺功能正常者,给予左甲状腺素(10μg/kg或最大600μg),通过每小时测量游离T4水平持续5小时来研究其吸收情况。结果:所有组的游离T4在3小时达到峰值,4小时略有下降但无显著差异。四组(除吸收不良组外)游离T4的增量(基线至3小时之间)无统计学差异。真正吸收不良组游离T4的平均增量为0.39ng/dL(95%可信区间:0.29 - 0.52),其他组合并后的平均增量为0.78ng/dL(95%可信区间:0.73 - 0.85)(10.4pmol/L)。以基线至3小时游离T4增量高于0.40ng/dL作为截断值,排除真正吸收不良的敏感度为97%,特异度为80%(曲线下面积0.904,P<0.001)。
服用足够剂量左甲状腺素(LT4)但TSH升高的患者,可通过左甲状腺素吸收试验可靠地诊断为未坚持治疗。3小时时游离T4增量高于0.40ng/dL(5.14pmol/L)可能有助于识别无需进行吸收不良检查的个体。