Medeiros-Neto G A, Marcondes J A, Cavaliere H, Wajchenberg B L, Knobel M
Acta Endocrinol (Copenh). 1985 Sep;110(1):61-5. doi: 10.1530/acta.0.1100061.
Sixteen patients with congenital goitre were submitted to a bovine TSH stimulation test (bTSH), and serum thyroid hormones (T3, T4), TSH and thyroglobulin (Tg) were measured before and after bTSH injection. In 9 patients with an organification defect basal levels of Tg were normal (19.4 +/- 3.1 micrograms/l) rising after bTSH to a mean level +/- SEM of 37.3 +/- 4.1 micrograms/l. Six patients with defective Tg synthesis or release had a mean basal level of serum Tg of 8.7 +/- 1.9 microgram/l (mean +/- SEM) and failed to raise serum Tg concentrations after bTSH (mean +/- SEM: 10.4 +/- 2.1 micrograms/l). In both groups a modest although significant (P less than 0.05) change in serum thyroid hormones after bTSH was noted. We conclude that the bTSH test may be used to distinguish the group with defective Tg synthesis or release from other types of congenital goitre.
16例先天性甲状腺肿患者接受了牛促甲状腺激素刺激试验(bTSH),并在注射bTSH前后测定了血清甲状腺激素(T3、T4)、促甲状腺激素(TSH)和甲状腺球蛋白(Tg)。9例存在有机化缺陷的患者,Tg基础水平正常(19.4±3.1微克/升),注射bTSH后升高至平均水平±标准误为37.3±4.1微克/升。6例Tg合成或释放存在缺陷的患者,血清Tg平均基础水平为8.7±1.9微克/升(平均±标准误),注射bTSH后血清Tg浓度未升高(平均±标准误:10.4±2.1微克/升)。两组在注射bTSH后血清甲状腺激素均有适度但显著(P<0.05)的变化。我们得出结论,bTSH试验可用于将Tg合成或释放存在缺陷的组与其他类型的先天性甲状腺肿区分开来。