Ohzeki T, Hanaki K, Motozumi H, Ohtahara H, Ishitani N, Urashima H, Tsukuda T, Shiraki K, Sasaki S, Nakamura H
Department of Pediatrics, Faculty of Medicine, Tottori University, Yonago, Japan.
Horm Res. 1993;39(5-6):229-34. doi: 10.1159/000182741.
The relation between thyroid-stimulating hormone (TSH) and triiodothyronine (T3) was evaluated in a girl with the selective pituitary type of thyroid hormone resistance for more than 7 years to clarify whether bromocriptine was an effective treatment or not. Levels of T3 (before: 2.44 +/- 0.64 nmol/l, mean +/- SD) and TSH (4.81 +/- 2.52 mU/l) were significantly decreased during therapy (T3: 2.15 +/- 0.44 nmol/l; TSH: 1.59 +/- 0.78 mU/l). T3 x TSH, calculated as one of the indices of pituitary resistance, on bromocriptine therapy (3.229 +/- 1.255 mU/l x nmol/l) was significantly (p < 0.005) smaller than the product before the administration (11.298 +/- 5.891 mU/l x nmol/l). The results suggest that bromocriptine should be one of the agents initially considered for the treatment of pituitary resistance to thyroid hormone.
为明确溴隐亭是否为有效的治疗药物,对一名患有选择性垂体型甲状腺激素抵抗超过7年的女孩,评估了促甲状腺激素(TSH)与三碘甲状腺原氨酸(T3)之间的关系。治疗期间,T3水平(治疗前:2.44±0.64nmol/L,均值±标准差)和TSH水平(4.81±2.52mU/L)显著降低(T3:2.15±0.44nmol/L;TSH:1.59±0.78mU/L)。作为垂体抵抗指标之一计算的T3×TSH,在溴隐亭治疗时(3.229±1.255mU/L×nmol/L)显著(p<0.005)小于给药前的乘积(11.298±5.891mU/L×nmol/L)。结果表明,溴隐亭应是最初考虑用于治疗垂体性甲状腺激素抵抗的药物之一。