Municchi G, Malozowski S, Nisula B C, Cristiano A, Rose S R
Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
J Pediatr. 1992 Aug;121(2):214-20. doi: 10.1016/s0022-3476(05)81191-6.
Because some patients with growth hormone (GH) deficiency are found to be hypothyroid after initiation of treatment with GH, we assessed the predictive value of the nocturnal thyrotropin surge (a sensitive test for central hypothyroidism) in 56 untreated GH-deficient children and adolescents. Eighteen patients had a subnormal thyrotropin surge (mean 18% (range -30% to 46%)), significantly less than that of 96 normal control subjects (mean 124%; 95% confidence limits, 47% to 300%; p less than 0.01); 13 of the 18 had a subnormal total thyroxine (T4) level or a subnormal free T4 level, or both. These 18 patients were given thyroid hormone replacement therapy; GH deficiency was confirmed during treatment with thyroxine. Of the remaining 38 patients, who had no initial evidence of dysfunction of the hypothalamic-pituitary-thyroid axis, 23 were re-examined while they were receiving GH treatment. Hypothyroidism developed in none of those 23 children during GH therapy. The nocturnal thyrotropin surge test and determination of iodothyronine levels were repeated in 14 of these euthyroid patients. There was no significant change in mean thyrotropin surge (129% (range +49% to +300) vs 125% (range +51% to +222%)), mean serum level of total T4 (111 +/- 4 vs 103 +/- 3 nmol/L), mean serum level of free T4 (19 +/- 0.7 vs 18 +/- 0.8 pmol/L), mean serum level of triiodothyronine (2.5 +/- 0.1 vs 2.5 +/- 0.1 nmol/L), or mean serum level of thyrotropin (2.9 +/- 0.3 vs 2.9 +/- 0.5 mU/L (mean +/- SEM)). We conclude that GH treatment does not appreciably alter thyroid function in GH-deficient patients who have no evidence of thyroid axis dysfunction before GH treatment.
由于一些生长激素(GH)缺乏的患者在开始接受GH治疗后被发现存在甲状腺功能减退,我们评估了夜间促甲状腺激素激增(一种用于中枢性甲状腺功能减退的敏感检测方法)在56名未经治疗的GH缺乏儿童和青少年中的预测价值。18名患者的促甲状腺激素激增低于正常水平(平均18%(范围为-30%至46%)),显著低于96名正常对照受试者(平均124%;95%置信区间,47%至300%;p<0.01);这18名患者中有13名总甲状腺素(T4)水平或游离T4水平低于正常,或两者均低于正常。这18名患者接受了甲状腺激素替代治疗;在甲状腺素治疗期间证实存在GH缺乏。其余38名患者最初没有下丘脑-垂体-甲状腺轴功能障碍的证据,其中23名在接受GH治疗时接受了复查。在这23名儿童的GH治疗期间,无一例发生甲状腺功能减退。对其中14名甲状腺功能正常的患者重复进行了夜间促甲状腺激素激增检测和碘甲状腺原氨酸水平测定。促甲状腺激素激增平均值(129%(范围为+49%至+300)对125%(范围为+51%至+222%))、总T4血清平均水平(111±4对103±3 nmol/L)、游离T4血清平均水平(19±0.7对18±0.8 pmol/L)、三碘甲状腺原氨酸血清平均水平(2.5±0.1对2.5±0.1 nmol/L)或促甲状腺激素血清平均水平(2.9±0.3对2.9±0.5 mU/L(平均值±标准误))均无显著变化。我们得出结论,在GH治疗前没有甲状腺轴功能障碍证据的GH缺乏患者中,GH治疗不会明显改变甲状腺功能。