Rothacker Karen M, Brown Suzanne J, Hadlow Narelle C, Wardrop Robert, Walsh John P
Department of Endocrinology and Diabetes (K.M.R., S.J.B., J.P.W.), Sir Charles Gairdner Hospital, Nedlands, Western Australia 6009, Australia; Department of Clinical Biochemistry (K.M.R., N.C.H., R.W.), PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Western Australia 6009, Australia; Western Diagnostic Pathology (N.C.H.), Myaree, Western Australia 6154, Australia; School of Pathology and Laboratory Medicine, The University of Western Australia (N.C.H.), Crawley, Western Australia 6009, Australia; and School of Medicine and Pharmacology (J.P.W.), The University of Western Australia, Crawley, Western Australia 6009, Australia.
J Clin Endocrinol Metab. 2016 Mar;101(3):1151-8. doi: 10.1210/jc.2015-4011. Epub 2016 Jan 6.
The TSH-T4 relationship was thought to be inverse log-linear, but recent cross-sectional studies report a complex, nonlinear relationship; large, intra-individual studies are lacking.
Our objective was to analyze the TSH-free T4 relationship within individuals.
We analyzed data from 13 379 patients, each with six or more TSH/free T4 measurements and at least a 5-fold difference between individual median TSH and minimum or maximum TSH. Linear and nonlinear regression models of log TSH on free T4 were fitted to data from individuals and goodness of fit compared by likelihood ratio testing.
Comparing all models, the linear model achieved best fit in 31% of individuals, followed by quartic (27%), cubic (15%), null (12%), and quadratic (11%) models. After eliminating least favored models (with individuals reassigned to best fitting, available models), the linear model fit best in 42% of participants, quartic in 43%, and null model in 15%. As the number of observations per individual increased, so did the proportion of individuals in whom the linear model achieved best fit, to 66% in those with more than 20 observations. When linear models were applied to all individuals and averaged according to individual median free T4 values, variations in slope and intercept indicated a nonlinear log TSH-free T4 relationship across the population.
The log TSH-free T4 relationship appears linear in some individuals and nonlinear in others, but is predominantly linear in those with the largest number of observations. A log-linear relationship within individuals can be reconciled with a non-log-linear relationship in a population.
促甲状腺激素(TSH)与甲状腺素(T4)的关系曾被认为是对数线性反比关系,但近期的横断面研究报告称二者关系复杂且呈非线性;尚缺乏大规模的个体内研究。
我们的目的是分析个体内TSH与游离T4的关系。
我们分析了13379例患者的数据,每位患者均有6次或更多次TSH/游离T4测量值,且个体TSH中位数与最低或最高TSH之间至少相差5倍。将游离T4的对数TSH的线性和非线性回归模型拟合到个体数据,并通过似然比检验比较拟合优度。
比较所有模型,线性模型在31%的个体中拟合最佳,其次是四次模型(27%)、三次模型(15%)、零模型(12%)和二次模型(11%)。在剔除最不理想的模型(将个体重新分配到最佳拟合的可用模型)后,线性模型在42%的参与者中拟合最佳,四次模型在43%的参与者中拟合最佳,零模型在15%的参与者中拟合最佳。随着个体观察次数的增加,线性模型拟合最佳的个体比例也增加,在有超过20次观察的个体中达到66%。当将线性模型应用于所有个体并根据个体游离T4中位数进行平均时,斜率和截距的变化表明整个人群中对数TSH与游离T4的关系呈非线性。
对数TSH与游离T4的关系在一些个体中呈线性,在另一些个体中呈非线性,但在观察次数最多的个体中主要呈线性。个体内的对数线性关系与人群中的非对数线性关系可以相互协调。